β-Cell MicroRNAs: Small but Powerful.

Noncoding RNA and especially microRNAs (miRs) have emerged as important regulators of key processes in cell biology, including development, differentiation, and survival. Currently, over 2,500 mature miRs have been reported in humans, and considering that each miR has multiple targets, the number of genes and pathways potentially affected is huge. Not surprisingly, many miRs have also been implicated in diabetes, and more recently, some have been discovered to play important roles in the pancreatic islet, including β-cell function, proliferation, and survival. The goal of this Perspective is to offer an overview of this rapidly evolving field and the miRs involved, reveal novel networks of β-cell miR signaling, and provide an outlook of the opportunities and challenges ahead.

Introduction

The perceived role of noncoding RNA has greatly changed over the past two decades. What was once thought to be largely “junk” is now understood to play an important regulatory role within the cell. Among the types of noncoding RNAs, microRNAs (miRs) have been shown to regulate key processes of cell biology, including differentiation and survival (1,2). These short nucleotide sequences (21–23 nt) are located either intergenically or within a host gene (3,4) and are transcribed under the control of RNA polymerase II (5), although transcription via RNA polymerase III has also been observed (6). Primary miR transcripts are processed into precursor miR by Drosha (7,8) and into mature miR by Dicer (9), and the mature miR strand combines with Argonaute proteins (Ago) into a RNA-induced silencing complex (RISC) (10) that binds to target sequences generally located in the 3′ untranslated region (UTR) of mRNAs (11). This target sequence is complementary (though often imperfectly so) to the mature miR, and specificity is primarily conferred by the first seven or eight nucleotides, known as the “seed” sequence (12). Upon binding to its gene target, the miR/RISC complex causes translational repression and/or degradation of the targeted mRNA sequence, as previously reviewed in detail (13), resulting in the downregulation of the protein encoded by the gene target. There also have been a few isolated reports of noncanonical effects, including miRs interacting with the coding sequence or the 5′UTR of target genes and thereby leading to translational repression (14–16). Surprisingly, in muscle cells, miR-1 has recently been shown to enter the mitochondria and to increase rather than to repress translation of mitochondrial DNA–encoded proteins (17). This effect was still dependent on Ago2 and on specific base-pairing of the miR with the target gene mRNA. In contrast, the same miR decreased the translation of target genes in the cytoplasm (17). It was therefore hypothesized that miRs may stimulate translation if Ago2 is present but its functional partner GW182 is excluded and if the target mRNA lacks a poly-A tail and 5′ cap, all of which is the case in mitochondria. While such mitochondrial effects have yet to be shown in pancreatic β-cells, they would be expected to have a major impact, especially considering the unique susceptibility of β-cells to alteration in bioenergetics and oxidative stress (18). Interestingly, miR-184, a miR highly expressed in human β-cells, has been suggested to be involved in noncanonical pathways and has been shown to directly target Ago2 (19).

According to version 21 of the online database for miRs (www.mirbase.org), there are 2,588 mature miRs found in Homo sapiens (20). The fact that each miR has multiple targets dramatically increases the number of potential genes targeted and pathways affected. It is therefore not surprising that many miRs have also been implicated in diabetes and its complications, as previously reviewed (21,22). However, the miR field is rapidly evolving and an increasing number of miRs have recently been shown to play important roles specifically in the pancreatic islet. By combining this knowledge and putting the data into context, this Perspective helps to provide an updated overview and reveal novel miR signaling networks with the potential impact on the life and death of islet β-cells.

Identifying MiRs Expressed In Islet β-Cells

MiR profiling experiments have been performed to determine the expression of miRs in various tissues, and these studies have yielded an atlas for mammalian miR expression (23) and profiles from different species and various tissues, which are available online (smiRNAdb; http://www.mirz.unibas.ch/cloningprofiles) (24). These data have also been used to estimate relative abundance and tissue specificity of miRs in human islets and MIN6 mouse insulinoma cells (25). Furthermore, recent studies have used MIN6 cells (26), mouse islets (19), primary intact human islets (27), and human β-cells (27) sorted by flow cytometry for in-depth RNA sequencing, providing some indication of miR expression levels in pancreatic islets and β-cells. In addition, others have compared the enrichment of miR species in flow-sorted human islet α- and β-cell fractions using a quantitative PCR-based miR array platform (28). The expression levels and enrichment of the miRs reported to play a role in islet β-cell biology and discussed in this review are provided in Table 1. The most highly expressed miR was miR-375, and not surprisingly, miR-375 represents the best studied miR in β-cell biology and has been found to be involved in inhibition of insulin secretion (29) and compensatory β-cell proliferation (30). The top β-cell–enriched miR (>100-fold higher expression in β-cells as opposed to α-cells) was miR-204, and miR-204 has recently been shown to play an important role in the control of insulin production (31). These findings support the notion of expression level and/or enrichment being important; however, considering the fact that miRs are very potent regulatory molecules, it is not surprising that miRs with lower expression levels and/or no specific β-cell enrichment are capable of affecting β-cell biology (e.g., miR-34a) (32). Finally, some miRs may be expressed at very low levels or even be undetectable in human islets under normal, physiological conditions but might be upregulated under pathological circumstances, which would then affect β-cell function (e.g., miR-199a) (33). In the following paragraphs, only miRs that have been demonstrated to control key processes of islet β-cell biology, such as insulin production and secretion, proliferation or differentiation, and apoptosis or survival, are briefly discussed. Their β-cell effects are summarized in Table 2 and the overlap of their functions is shown in Fig. 1.

Table 1

Expression and β-cell enrichment of miRs discussed

miRs	Human β-cells	Human islets	Mouse islets	Mouse MIN6 cells	β-Cell enrichment
miR-375	5,804,575	2,046,518	636,788	369,695	2
miR-7	670,521	259,457	842,839	423	3
let-7a	668,000	343,033	227,187	4,481	5
miR-148a	389,911	176,002	742,453	15,457	56
miR-26a	389,655	132,411	46,550	25,539	3
miR-182	327,398	152,455	33,286	38,695	10
miR-184	151,568	58,167	56,873	143
miR-30d	111,933	149,301	61,834	12,796	3
miR-200c	60,837	72,125	153,868	1,297	3
miR-21	60,031	284,834	27,077	1,514	5
miR-24	34,032	69,287	58,673	390	6
miR-204	32,817	8,346	890	11	108
miR-200b	22,134	14,969	27,367	2,236	2
miR-30a-5p	21,116	117,912	174,538	9,278	4
miR-16	18,254	10,389	3,215	5,186	3
miR-29a	15,815	13,379	39,338	1,375	3
miR-15a	2,914	1,982	684	89	16
miR-19b	2,081	1,321	56
miR-152	1,656	1,659	44,121	211
miR-29b	1,212	1,500	1,984		3
miR-342	1,017	586	300	449
miR-9	687	2,028	275
miR-96	514	499	500	312	23
miR-15b	442	330	133	149
miR-195	213	516	244		2
miR-34a	190	503	62
miR-199a-3p			168	4
miR-145	49	804	206		2
miR-124a	41	120	17
miR-33a		92	34
miR-338-3p			193	72

MiRs are listed in order of their expression level in human β-cells as assessed by RNA sequencing. Numbers represent read counts in sorted human β-cells (27), intact human islets (27), C57BL/6J mouse islets (19), and MIN6 cells (26). Enrichment in human β-cells in comparison with α-cells was assessed by a quantitative PCR-based miR array; numbers represent fold enrichment (28).

Table 2

β-Cell–relevant miRs and their genomic location and function and references

Mature miR	Precursor miR coding regions (human)	Function in the β-cell	References
let-7	mir-let-7a-1: chr9: 94175957-94176036	Targets IRS2 and regulates β-cell insulin signaling.	72
	mir-let-7a-2: chr11: 122146522-122146593
	mir-let-7a-3: chr22: 46112749-46112822
miR-7	mir-7-1: chr9: 83969748-83969857	Inhibits insulin secretion by targeting SNARE and vesicle-related proteins. Possibly affects β-cell proliferation by targeting parts of the mTOR pathway and differentiation by targeting the transcription factor Pax6.	40, 48, 70, 77, 78, 83–86
	mir-7-2: chr15: 88611825-88611934
	mir-7-3: chr19: 4770670-4770779
miR-9	mir-9-1: chr1: 156420341-156420429	Inhibits insulin secretion by targeting the deacetylase Sirt1 and the transcription factor Onecut2.	35, 60
	mir-9-2: chr5: 88666853-88666939
	mir-9-3: chr15: 89368017-89368106
miR-15	mir-15a: chr13: 50049119-50049201	MiR-15a increases insulin biosynthesis, possibly by targeting UCP2. May also increase apoptosis by targeting Bcl-2. May alter differentiation and development by targeting Ngn3.	64, 74, 103
	mir-15b: chr3: 160404588-160404685	MiR-15b targets Ngn3, overexpression during development reduces total number of endocrine cells.	74
miR-16	mir-16-1: chr13: 50048973-50049061	Targets Ngn3, overexpression reduces total number of endocrine cells.	74
	mir-16-2: chr3: 160404745-160404825
miR-19	mir-19b-1: chr13: 91351192-91351278	May be important in development and insulin synthesis as it targets NeuroD1 and decreases insulin mRNA.	67
	mir-19b-2: chrX: 134169671-134169766
miR-21	mir-21: chr17: 59841266-59841337	Sensitizes β-cells to cytokine-induced apoptosis.	32, 101
miR-24	mir-24-1: chr9: 95086021-95086088	Increased in db/db mice. Knockdown results in decreased insulin mRNA via de-repression of transcriptional repressors. Overexpression decreases insulin secretion and proliferation. Targets menin, Hnf1a, and NeuroD1.	65, 66, 71
	mir-24-2: chr19: 13836287-13836359
miR-26	mir-26a-1: chr3: 37969404-37969480	Knockdown decreases insulin mRNA via upregulation of repressors. May play a role in development by targeting TET enzymes, which are oxidizers of DNA.	65, 73
	mir-26a-2: chr12: 57824609-57824692
miR-29	mir-29a: chr7: 130876747-130876810	Inhibits GSIS by targeting SNARE protein syntaxin-1, Onecut2, and Mct1. Overexpression also causes β-cell apoptosis via downregulation of Mcl1.	25, 26, 36, 57, 58
	mir-29b-1: chr7: 130877459-130877539
	mir-29b-2: chr1: 207802443-207802523
miR-30	mir-30a: chr6: 71403551-71403621	MiR-30a-5p plays a key role in glucotoxicity and targets NeuroD1.	38
	mir-30d: chr8: 134804876-134804945	MiR-30d increases insulin expression by increasing the transcription factor MafA. Protects from TNF-α–induced toxicity by downregulating MAP4K4.	51, 54
miR-33	mir-33a: chr22: 41900944-41901012	Targets ABCA1 transporter protein to control cholesterol efflux from cells and consequently decreases insulin secretion from β-cells.	34, 63
miR-34	mir-34a: chr1: 9151668-9151777	Expressed during differentiation of β-cells. Can cause β-cell apoptosis, possibly by targeting Bcl-2.	32, 78, 96, 99, 101, 105
miR-96	mir-96: chr7: 129774692-129774769	Decreases insulin secretion by increasing granuphilin and decreasing the GTPase effector Noc2.	37
miR-124	mir-124a-1: chr8: 9903388-9903472	Decreases insulin secretion by targeting GTPase Rab27a and indirectly affecting SNARE proteins. Highly expressed late in development. Targets FoxA2, which is involved in β-cell differentiation.	37, 50, 51, 53
	mir-124a-2: chr8: 64379149-64379257
	mir-124a-3: chr20: 63178500-63178586
miR-145	mir-145: chr5: 149430646-149430733	Decreases GSIS by targeting ABCA1.	34
miR-148	mir-148a: chr7: 25949919-25949986	Targets ABCA1. Knockdown decreases insulin mRNA via upregulation of transcriptional repressors.	34, 65
miR-152	mir-152: chr17: 48037161-48037247	Increased in offspring of mothers fed a low-protein diet, negatively affecting insulin secretion.	33
miR-182	mir-182: chr7: 129770383-129770492	Knockdown decreases insulin mRNA via upregulation of transcriptional repressors.	65
miR-184	mir-184: chr15: 79209788-79209871	Negatively regulates β-cell proliferation by targeting Ago2.	19, 95, 96
miR-195	mir-195: chr17: 7017615-7017701	Increased in regenerating mouse pancreas and decreases Ngn3.	74, 95
miR-199	mir-199a-1: chr19: 10817426-10817496	Mediates negative effects of low-protein maternal diet on insulin secretion by targeting mTOR signaling.	33, 96
	mir-199a-2: chr1: 172144535-172144644
miR-200	mir-200b: chr1: 1167104-1167198	MiR-200b increases β-cell apoptosis by targeting Zeb1.	100
	mir-200c: chr12: 6963699-6963766	MiR-200c increases β-cell apoptosis by targeting Dnajc3, Jazf1, Xiap, and Rps6kb1.	106
miR-204	mir-204: chr9: 70809975-70810084	Decreases insulin transcription by targeting MafA.	31
miR-338	mir-338: chr17: 81125883-81125949	MiR-338-3p is reduced in states of β-cell expansion such as pregnancy and is antiproliferative and proapoptotic.	97
miR-342	mir-342: chr14: 100109655-100109753	Mediates negative effects of low-protein maternal diet on insulin secretion by targeting mTOR signaling.	33
miR-375	mir-375: chr2: 219001645-219001708	Decreases GSIS by targeting Mtpn, decreases insulin gene expression by targeting PDK1, and increases compensatory β-cell proliferation.	26, 27, 29, 30, 38, 41, 42, 45, 46, 77, 78, 86, 95

MiRs with established effects on β-cell biology are listed in numerical order.

Figure 1

Key β-cell processes and the miRs involved. MiRs are grouped based on their currently known primary function(s); those with multiple functions in the β-cell are listed in the cross sections of the Venn diagram.

MiRs and Insulin Secretion AND Production

The most prominent function of β-cells is the production and secretion of insulin, and miRs play a variety of different yet important roles in this process (Table 2).

Insulin Secretion: Preventing Excess

Several miRs (e.g., miR-7, -9, -29, -30, -33, -96, -124, -145, and -375) have been shown to target components of the secretory machinery and thereby to control insulin secretion (29,34–40). They constitute the largest group of miRs with an established role in β-cell biology (Fig. 1). Given the importance of a well-orchestrated and fine-tuned insulin response, it is not surprising that this process is controlled at an additional level by these miRs. However, it is striking that all of the miRs have an overall inhibitory effect on insulin exocytosis, suggesting that the ultimate goal is to prevent any excessive insulin secretion and any potentially life-threatening hypoglycemia.

The first miR studied functionally in pancreatic β-cells and shown to regulate insulin secretion was miR-375 (29). MiR-375 is highly and specifically expressed in human pancreatic islets (α- and β-cells) (27,41) and in MIN6 mouse insulinoma cells (29) (Table 1) and is easily detectable in INS-1 cells (42). However, it is also emerging as a miR frequently downregulated in various cancers (43). Overexpression of miR-375 decreases glucose-stimulated insulin secretion (GSIS) in MIN6 cells (29) by targeting myotrophin/V-1 (Mtpn), a protein involved in vesicular transport (44), and this results in decreased insulin exocytosis independent of intracellular calcium signaling (29). In addition, miR-375 has been linked to decreased insulin gene expression through the targeting of 3′phosphoinositide-dependent protein kinase 1 (PDK1) in INS-1E cells (45). β-Cell expression of miR-375 has been reported to be regulated by pancreatic duodenal homeobox 1 (PDX1) and neurogenic differentiation transcription factor (NeuroD1), both crucial transcription factors for β-cell development and necessary for β-cell function and insulin transcription. PDX1 and NeuroD1 were shown to bind to the miR-375 locus in NIT1 mouse insulinoma cells, as well as MIN6 cells (46). In addition, it has been demonstrated in INS-1 832/13 cells and in isolated rat islets that cyclic adenosine monophosphate (cAMP) negatively regulates miR-375 transcription by decreasing the binding of RNA polymerase II to the miR-375 promoter (42). Analysis of the miR-375 promoter further identified important cis-acting elements for the control of miR-375 expression (41,47).

MiR-7 also regulates insulin secretion via targeting of the mRNA of key vesicle fusion and SNARE proteins and proteins involved in vesicular trafficking, membrane targeting, and cytoskeletal rearrangement. β-Cell–specific deletion of miR-7a-2 in mice increases insulin secretion and significantly improves glucose tolerance (40). The precursors of miR-7 are encoded by three different genomic loci (7-1, 7-2, and 7-3 in humans and 7a-1, 7a-2, and 7b in mice) and the latter two have been shown to be induced by NeuroD1 in MIN6 cells (48). MiR-7 is also increased in mouse models of diabetes and negatively regulates GSIS (40). Consistent with the increase in mouse models of diabetes and the detrimental effects on GSIS, miR-7 was also found to be increased in cadaveric human islets of diabetic donors as compared with those of obese nondiabetic donors (40), confirming the role of this miR in human islet pathophysiology.

MiR-124a is increased in the islets of humans with type 2 diabetes (39) and targets multiple proteins related to insulin secretion by both direct and indirect regulation. Overexpression of miR-124a in MIN6 cells increases basal insulin release but causes a decrease in GSIS by directly targeting the GTPase Rab27a (37,39), which is involved in the fusion of secretory vesicles with the plasma membrane (49). Additional targets include SNARE proteins (37), Sirtuin 1 (Sirt1), NeuroD1, and the transcription factor forkhead box A2 (FoxA2) (39). It is via FoxA2 that miR-124a regulates PDX1 as well as the ATP-sensitive potassium channel subunits Kir6.2 and Sur-1 (50). Studies of the upstream regulation of miR-124a in β-cells have reported that its expression can be increased by glucose as shown by a miR microarray in MIN6 insulinoma cells (51). In contrast, incubation with high glucose was found to decrease miR-124 expression in primary rat islets (52). Consistent with this latter finding, proapoptotic and glucose-induced thioredoxin-interacting protein (TXNIP) inhibited β-cell miR-124a expression in both rat INS-1 cells and mouse islets (53).

β-Cell function has also been shown to improve in db/db mice in response to miR-30a-5p suppression, and knockdown of miR-30a-5p reversed glucotoxicity-associated β-cell dysfunction, including insulin gene expression and GSIS, in primary rat islets (38). MiR-30a-5p was further found to be upregulated in response to glucotoxicity and to directly target NeuroD1. Another family member, miR-30d, was found to be increased by high glucose in the aforementioned MIN6 miR microarray along with miR-124a (51). MiR-30d overexpression has been described to increase insulin gene expression in MIN6 cells and mouse islets, supposedly via an increase in the insulin transcription factor MafA (51,54), but the direct miR-30d target mediating this effect remains unknown. On the other hand, miR-30d has been shown to directly downregulate the tumor necrosis factor α (TNF-α)–activated protein kinase, mitogen-activated 4 protein kinase 4 (MAP4K4), and thereby protecting MIN6 β-cells from the detrimental effects of cytokine TNF-α exposure (54).

MiR-96 has been studied together with miR-124a and has been shown to inhibit insulin exocytosis and secretion in MIN6 cells by increasing granuphilin (37). Granuphilin decreases insulin exocytosis (55) by stabilizing a fusion-incompetent form of syntaxin-1a, thus increasing docking yet inhibiting fusion of insulin granules (55) and consequently decreasing secretion (37). Furthermore, miR-96 decreases the GTPase effector Noc2 (37), which also affects the β-cell capacity to respond to secretory stimuli (56).

The miR-29 family (miR-29a/b/c) has been shown by multiple reports to regulate β-cell insulin secretion and to directly target syntaxin-1, a t-SNARE protein involved in insulin exocytosis (36). MiR-29 increases in response to glucose in INS-1E β-cells and human and rat islets (57), and the corresponding decrease in syntaxin-1 has a negative effect on GSIS. Overexpression of miR-29 in MIN6 cells and in dissociated mouse islets results in a similar decrease in GSIS and occurs along with a decrease in the transcription factor Onecut2, one of the predicted targets of miR-29 that negatively regulates the expression of granuphilin (58). MiR-29a and miR-29b have also been associated with the downregulation of monocarboxylate transporter (Mct1) (25). As the ATP/ADP ratio is crucial to insulin secretion, targeting of Mct1, which allows circulating pyruvate to enter the β-cell, may play a role in the effect of miR-29 on glucose sensing and, subsequently, insulin secretion.

Like miR-29, miR-9 also decreases the expression of Onecut2, consequently increasing granuphilin and decreasing insulin exocytosis in INS-1 cells (35). In addition, miR-9 has been demonstrated to target Sirt1, an NAD-dependent deacetylase known to affect insulin secretion (59) and suspected also to be involved in the control of GSIS by miR-9 (60).

Given that they are located in introns of the sterol regulatory element–binding proteins (SREBP-1/2), miR-33a/b are typically studied in the context of insulin signaling in extrapancreatic tissues (61). However, miR-33a is also relevant to β-cell function as it has been shown to target ATP-binding cassette (ABC) transporters, such as ABCA1 (34). ABCA1 promotes the efflux of cholesterol and increased miR-33a results in β-cell cholesterol accumulation, mediating a subsequent decrease in insulin secretion in both mouse and human islets (62,63).

Another miR that decreases GSIS through ABCA1 targeting is miR-145. Investigators discovered miR-145 as a potent ABCA1 regulator by searching for miRs that may regulate ABCA1 by using a combination of eight different miR target prediction software programs (34). Inhibition of miR-145 in mouse islets resulted in an increase in ABCA1 protein levels and an improvement in GSIS. MiR-145 also regulated total islet cholesterol and was found to be decreased in response to glucose in vitro (34).

Insulin Production: Keeping It Steady

Obviously, β-cell function requires proper control not only of insulin secretion but also of insulin production, and both processes are impaired in diabetes. Recently, a few miRs have been discovered to modulate insulin production by inhibiting insulin transcription (e.g., miR-204 [31]) or enhancing insulin biosynthesis (e.g., miR-15, -24, -26, -148, and -182 [64,65]) and to mediate the epigenetic downregulation of insulin production in the context of maternal malnutrition (e.g., miR-199 and -342 [33]).

MiR-204 is the most highly enriched miR in islet β-cells (Table 1) and was first linked to diabetes based on its marked upregulation in a miR microarray study in which the prodiabetic protein TXNIP was overexpressed in INS-1 β-cells (31). Islet miR-204 expression is indeed increased in multiple diabetes models, and by directly targeting and downregulating the insulin transcription factor MafA, miR-204 causes a decrease in insulin production in INS-1 cells and human islets. MiR-204 is encoded within an intron of the transient receptor potential melastatin 3 (TRPM3) gene and therefore also shares the promoter with TRPM3. Given this information, the transcription factor mediating the TXNIP-induced increase in miR-204 was discovered. Signal transducer and activator of transcription 3 (STAT3) acts as a repressor of the TRPM3/miR-204 promoter, and TXNIP was found to decrease STAT3 phosphorylation and activity (31), making this signaling pathway one of the few with at least one known trans-acting factor capable of controlling miR expression.

In contrast, by targeting transcriptional repressors of insulin, miR-24, miR-26, miR-148, and miR-182 have been demonstrated to promote β-cell insulin content (65). After finding that a global decrease of miRs by a tamoxifen-inducible RIP-Cre Dicer knockout led to a diabetic phenotype and decreased insulin levels, the role of some miRs found to be highly expressed in β-cells was investigated further (65). Among them, knockdown of miR-24, miR-26, miR-148, and miR-182 resulted in decreased insulin mRNA levels in primary islets (65). This effect was found to be at least partially mediated by a de-repression of two transcriptional repressors of insulin, Sry-related HMG box 6 (Sox6) and basic helix-loop-helix family, member E22 (Bhlhe22). On the other hand, miR-24 also targets NeuroD1 and hepatic nuclear factor 1 homeobox A (Hnf1a), genes related to maturity-onset diabetes of the young, and inhibits insulin secretion and β-cell proliferation (66). Furthermore, miR-24 expression has been shown to be increased in db/db and high-fat diet–fed mice and in islets exposed to oxidative stress (66).

MiR-15a overexpression has also been shown to increase insulin biosynthesis in mouse islets, possibly by targeting uncoupling protein 2 (UCP2), which, in turn, alters the ATP/ADP ratio (64). Interestingly, high glucose increases miR-15a levels in the short-term, whereas exposure to high glucose downregulates miR-15a in the long-term (64), consistent with the notion of chronic glucotoxicity.

Although it had no significant effect on total insulin levels, miR-19b overexpression has been shown to inhibit insulin mRNA expression in MIN6 cells. MiR-19 also targets the 3′UTR of NeuroD1 and has been found to be increased in pancreatic progenitor cells (67).

During pregnancy, a low-protein diet for the mother can cause harmful effects to the developing fetus, including an increased susceptibility to type 2 diabetes (68). Offspring of mice fed a low-protein diet were found to have insulin secretory defects due to impaired insulin biosynthesis, reduced β-cell insulin content, decreased mammalian target of rapamycin (mTOR), and increased expression of miR-152, miR-199a-3p, miR-342, and miR-7 (33). Also, overexpression of miR-152 led to a decrease in GSIS. Furthermore, inhibition of miR-342 and miR-199a-3p restored insulin content and secretion back to normal (33). Interestingly, miR-375 expression also has been reported to be increased in offspring of low-protein diet–fed mothers, and normalization of miR-375 levels restored β-cell insulin secretion in rat models (69). Together, this suggests that multiple miRs might be affected by and involved in this epigenetic phenomenon caused by a maternal low-protein diet.

MiRs and β-Cell Proliferation and Differentiation

Proliferation and Differentiation: Maintaining the Balance

A considerable number of miRs have been associated with pancreatic β-cell development by affecting proliferation or differentiation (e.g., miR-375 [30], miR-7 [70], miR-124a [50], miR-24 [71], let-7a [72], miR-26a [73], miR-184 [19], miR-195, miR-15, and miR-16 [74]) (Table 2). Not surprisingly, many of them have also been associated with mature β-cell function (Fig. 1). On the other hand, β-cell de-differentiation has recently emerged as an important contributing factor to the loss of functional β-cell mass (75), and it is therefore conceivable that the downregulation of miRs that promote β-cell differentiation may be involved in this process. Indeed, de-differentiation of β-cell–derived cells for in vitro expansion has been found to be associated with a decrease in miR-375 expression (76). In addition, miR-7a transgenic mice have been reported to have diabetes and impaired insulin secretion and show signs of β-cell de-differentiation (40). On the other hand, an initial study to identify miRs highly expressed during development revealed miR-375 and miR-7 to be increased during differentiation of human islets (77). Investigation of miRs involved in human embryonic stem cell differentiation into insulin-producing cells further confirmed the relevance of miR-375 and miR-7 and implicated a number of others (e.g., miR-146 and -34a) in this process (78).

Interestingly, miR-375 knockout mice develop hyperglycemia despite increased β-cell insulin exocytosis (30). Although the hyperglycemia is primarily due to an increase in glucagon levels (consistent with the relative high expression level of miR-375 in α-cells), pancreatic β-cell mass was found to be severely decreased in miR-375–deficient mice. In addition, miR-375 levels were increased in islets of leptin-deficient ob/ob mice, which typically have a compensatory increase in islet mass. On the other hand, double mutant mice deficient in both leptin and miR-375 showed a more than 70% reduction in β-cell mass compared with ob/ob control mice, and further analysis determined that miR-375 targets a number of growth-inhibiting genes and thereby may enhance compensatory β-cell proliferation (30). In vitro experiments overexpressing miR-375 have also shown that miR-375 can induce mesenchymal stem cells from human placenta to become insulin-producing cells (79) and help differentiate induced pluripotent stem cells into insulin-producing islet-like cell clusters (80).

In addition to its role in insulin secretion, miR-7 has also been implicated in the control of β-cell proliferation. Interestingly, miR-7 targets five unique mRNAs involved in the signaling pathway of mTOR (70), a serine/threonine protein kinase known to be involved in β-cell proliferation (81). Inhibition of miR-7 in primary adult pancreatic islets leads to the activation of mTOR signaling and β-cell proliferation, suggesting that miR-7 acts as an inhibitor of β-cell proliferation (70). However, no alteration in β-cell mass was observed in β-cell–specific miR-7a-2 knockout mice (40). MiR-7 loss- and gain-of-function experiments in β-cells have also revealed a regulation of the transcription factor paired box 6 (Pax6). Pax6 is crucial for the development of endocrine cells and proper glucose homeostasis (82). When knocked down in cultured pancreatic rudiments of mouse embryos, an explant model of pancreatic development, the lack of miR-7 increased the number of insulin-positive cells, while the overexpression of miR-7 caused a decrease in Pax6 and insulin content (83). In contrast, whole-body knockdown of miR-7 using intrauterine morpholino injections during early embryonic development has been shown to decrease total β-cell number and insulin expression and to impair glucose tolerance postnatally (84). This suggests that the role of miR-7 expression may be dependent on the developmental stage and the cell distribution of its expression. MiR-7 has been reported to be a highly abundant miR in endocrine cells (85,86), and its expression increases throughout the progression of development and differentiation of human islets (77) as well as in the developing mouse pancreas (84). This is in alignment with its high expression level observed in sorted human β-cells (Table 1). Together, these findings implicate miR-7 as an important miR for maintaining fully differentiated β-cells, while limiting their potential for proliferation.

MiR-124a expression is upregulated later in mouse embryonic pancreatic development (e.g., embryonic day 18.5), indicating a possible role in differentiation (50). As previously mentioned, miR-124a has been demonstrated to target the transcription factor FoxA2 in MIN6 cells, which, in addition to affecting insulin secretion, is also known to play a role in differentiation via PDX1 (87).

Although miR-24 was mentioned above in regard to its role in regulating insulin content, this miR has also been demonstrated to target menin, a ubiquitously expressed nuclear protein involved in cell cycle (88) and tumor suppression (89) and the gene mutated in multiple endocrine neoplasia 1 (MEN1). Menin has also been shown to be involved in the control of pancreatic islet expansion (90) and pancreatic tumorigenesis, as demonstrated by menin knockout mice, which develop islet hyperplasia and tumors (91). In MIN6 and betalox5 cells, targeting of menin by miR-24 led to cellular proliferation and increased cell viability (71), suggesting that miR-24 may play a role in β-cell growth.

Interestingly, menin has also been shown to affect arsenite-resistant protein 2 (ARS2), which is part of the nuclear RNA cap-binding complex. This complex is important for the production of certain miRs, including the highly expressed miR let-7a. Menin promotes the processing of let-7a from primary miRs to precursor miRs (72), and let-7a targets insulin receptor substrate 2 (IRS2), which is crucial for compensatory β-cell proliferation (92). It is therefore hypothesized that the negative effect of menin on β-cell mass is mediated by an increase in let-7a and a subsequent decrease in IRS2 (72).

Pancreatic cell proliferation, endocrine differentiation, and islet cell number have been found to be significantly increased in miR-26a transgenic mice (73), and miR-26a has been shown to target ten-eleven translocation (TET) and thymine-DNA glycosylase (TDG) enzymes (73). TET enzymes are oxidizers of DNA, whereas TDG plays a role in base excision (93). Both of these miR-26a targets have been implicated in development (94).

MiR-184 targets Ago2, one of the primary components of RISC (19). Loss of miR-184 and increases in Ago2 result in increased β-cell proliferation in mice. Interestingly, miR-184 has been found in abundance in normal human islets but not in islets from glucose-intolerant donors (95), and its expression was found to be silenced in islets of humans with type 2 diabetes (96) and ob/ob mice. When miR-184 was restored in ob/ob mice, compensatory β-cell expansion was prevented (19). Together, these data from several independent studies implicate miR-184 as a negative regulator of β-cell proliferation and explain its decrease in diabetic models as an attempt at compensation in response to increased metabolic demand. They thereby support the role of this miR in the control of compensatory β-cell mass expansion.

MiR-338-3p is also thought to play a major role in the control of compensatory β-cell expansion associated with pregnancy and obesity and was found to be significantly downregulated in islets of rats at 14 days of gestation (97). Knockdown of miR-338-3p in INS-1 cells or rat islets increased β-cell proliferation. MiR-338-3p knockdown also protected against cytokine- or palmitate-induced apoptosis, whereas overexpression of miR-338-3p led to increased apoptosis in dispersed rat islets. Interestingly, the G protein–coupled receptor GPR30 activation by 17β-estradiol seemed to negatively regulate β-cell miR-338-3p expression (97), which may explain the observed in vivo downregulation of this miR during pregnancy.

During pancreas development, Neurogenin3 (Ngn3) pushes precursor cells toward an endocrine fate (98), and miR-15a/b, miR-16, and miR-195 were reported to be higher in the regenerating pancreas of partially pancreatectomized mice and to target Ngn3 (74). Inhibition of each of these miRs in regenerating mouse pancreatic tissue resulted in an increase in Ngn3, as well as in its downstream factors, Nkx2.2 and NeuroD1. Conversely, overexpression of these miRs in developing mouse pancreatic bud explants led to a reduction in the total number of endocrine cells (74), suggesting that these miRs may play an important role in the control of islet cell development and differentiation.

MiRs and β-Cell Apoptosis and Survival

Apoptosis and Survival: Walking a Fine Line

β-Cell apoptosis is a critical factor in the pathogenesis and progression of diabetes, and a number of miRs have been shown to be involved, including miR-34a (32), miR-146 (99), miR-21 (32), miR-29 (58), and, most recently, miR-200 (100) (Figs. 1 and 2 and Table 2). It is also important to note that a subset of miRs has been demonstrated to be upregulated by proinflammatory cytokines (101). Cytokines are known to damage β-cell function and contribute to β-cell apoptosis, but the exact mechanisms are still not fully understood. Interestingly, exposure of MIN6 cells or human islets to interleukin-1β (IL-1β) and TNF-α was found to cause an increase in miR-21, miR-34a, and miR-146a expression. These miRs are also increased during prediabetic insulitis in the NOD mouse model of type 1 diabetes and knockdown of miR-34a and miR-146a protected MIN6 cells from cytokine-induced cell death (101), raising the possibility that these miRs might be involved in β-cell cytokine toxicity.

Figure 2

MiR-200 signaling and β-cell apoptosis. MiR-200 is upregulated in diabetes and in response to glucose/diabetes-induced TXNIP. It directly targets the 3′UTR of the antiapoptotic factors Dnajc3, Jazf1, Rps6kb1, and Xiap and the antiapoptotic and EMT-related factor Zeb1. In addition, it indirectly leads to an increase in proapoptotic Bax and tumor suppressor Trp53. Together, this results in increased β-cell apoptosis and further worsening of the diabetes. By inhibiting EMT, miR-200 may also alter the state of β-cell differentiation, which, in turn, may affect diabetes development by limiting β-cell expansion. Numbers in parentheses refer to corresponding references.

Because of its regulation by the tumor suppressor p53 and its targeting of genes involved in development, differentiation, cell cycle, and apoptosis, miR-34a has been studied heavily in the context of cancer (102,103). In fact, a miR-34 mimic is currently in clinical trials for cancer (16,104). Recent reports, however, have also found a connection between this miR and β-cell apoptosis. MiR-34a was increased in islets of diabetic db/db mice, and inhibition of miR-34a partially protected palmitate-treated cells from apoptosis (99). The knockdown of miR-34a in INS-1 cells also resulted in an increase in the number of β-cells and reduced apoptosis in the absence and presence of cytokines (32). It appears that the mechanism by which miR-34a affects β-cell apoptosis is by targeting the antiapoptotic molecule B-cell lymphoma 2 (Bcl-2). Overexpression of miR-34a in MIN6 cells reduced Bcl-2 levels, whereas inhibition of miR-34a abolished the palmitate-induced decrease in Bcl-2 (105). Combined, these multiple independent β-cell studies and extensive cancer literature make a strong case for miR-34a playing a role in the regulation of β-cell death.

MiR-21 has also been positively associated with β-cell apoptosis, and overexpression resulted in decreased numbers of INS-1 β-cells in culture and an increase in their sensitivity to cytokine-induced apoptosis (32). Furthermore, miR-21 was increased alongside miR-34a and miR-146 in response to IL-1β and TNF-α in MIN6 cells and human pancreatic islets (101). Interestingly, miR-21, miR-34a, and miR-146 have also been found to be upregulated in the islets of prediabetic NOD mice (58). However, unlike miR-34a and miR-146, the knockdown of miR-21 did not protect MIN6 cells from cytokine-induced apoptosis (101).

Mentioned previously based on its ability to regulate insulin secretion, miR-29 is also increased in NOD mice with prediabetes and is upregulated in response to cytokines (58). Overexpression of miR-29 led to increased apoptosis in dispersed human islets and in MIN6 cells, and miR-29 was found to confer these effects by targeting the antiapoptotic protein and Bcl-2 family member, myeloid cell leukemia 1 (Mcl1) (58).

Most recently, two independent articles reported the involvement of miR-200 in diabetic β-cell apoptosis (100,106). A schematic summarizing the combined findings is shown in Fig. 2. Initially, members of the miR-200 family (miR-200a/b/c/141/429) were discovered to be increased in islets of diabetic ob/ob mice and in response to overexpression of the glucose-induced proapoptotic protein, TXNIP (31,100). While TXNIP has previously been shown to be highly upregulated in diabetes (107), it is not clear at this point whether these increased TXNIP levels are necessary to confer the miR-200 increase in response to diabetes. In any case, miR-200b was then shown to induce apoptosis in β-cells, as demonstrated by overexpression in INS-1 cells as well as human islets (100). MiR-200b was also found to target and decrease the expression of zinc finger E-box binding homeobox 1 (Zeb1) and knockdown of Zeb1 recapitulated the effect of miR-200b on β-cell apoptosis, indicating that targeting Zeb1 may be the mechanism conferring the apoptotic effect of miR-200b. Furthermore, the fact that Zeb1 is a crucial modulator of E-cadherin and epithelial-mesenchymal transition (EMT) (108) raised the possibility that miR-200b may also have an impact on β-cell differentiation and development (100).

Consistent with these initial findings, members of the miR-200 family that share the AAUACUG seed sequence (i.e., miR-200b, -200c, and -429) have also been demonstrated to play a crucial role in β-cell apoptosis in vivo (106). These miRs were shown to be increased in the islets of diabetic db/db mice, and overexpression of the most abundant member of the miR-200 family, miR-200c, was found to cause apoptosis in mouse islets and MIN6 cells. Importantly, the lack of miR-200 protected mice from streptozotocin-induced diabetes and from diabetes in the Akita mouse model. The study also revealed multiple miR-200c targets, the downregulation of which contributed to the β-cell apoptosis associated with the miR-200c overexpression phenotype, including DnaJ homolog, subfamily C, member 3 (Dnajc3); JAZF zinc finger 1 gene (Jazf1); ribosomal protein S6 kinase, 70kDa, polypeptide 1 gene (Rps6kb1); and X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase (Xiap). In addition, Belgardt et al. (106) found that miR-200c upregulated the activity of the tumor suppressor Trp53, further promoting apoptosis. Interestingly, although the upregulation of miR-200 in diabetes and the resulting increase in β-cell apoptosis has been confirmed by both studies in various models, a number of different downstream targets and pathways have been implemented. However, this diversity is very much in line with the notions that each miR regulates multiple targets, each miR family member targets a distinct set of genes, and often a combination of different pathways is necessary to elicit the full biological effect.

Revealing a MiR-NeuroD1 Signaling Network

The transcription factor NeuroD1 plays a critical role in β-cell development and function (109). It was striking to recognize that a variety of different miRs regulate NeuroD1 directly or indirectly, whereas others are being regulated by NeuroD1, giving rise to an intricate signaling network (Fig. 3). MiR-19b (67), miR-24 (66), miR-30a-5p (38), and miR-124a (39) have been shown to directly target the 3′UTR of NeuroD1 and thereby downregulate its expression. In addition, NeuroD1 expression is under the control of Ngn3, and miR-15a/b, miR-16, and miR-195 have been reported to target Ngn3 and thereby indirectly regulate NeuroD1 (74). In turn, NeuroD1 has been shown to bind to the promoter region of miR-375 (46) and to activate the promoters of miR-7a-2 and miR-7b (48), raising the possibility that it might regulate the expression of these miRs. While the physiological effects of some of the miRs suggested to regulate NeuroD1 will still have to be confirmed and the effects of NeuroD1 on miR-375 and miR-7 expression remain to be determined, this emerging miR-transcription factor network represents an example of how different miRs can converge onto one important pathway to provide tight regulation and an additional level of control.

Figure 3

MiR-NeuroD1 signaling network. MiR-19b, miR-24, miR-30a-5p, and miR-124a target the 3′UTR of NeuroD1 and thereby downregulate its expression. NeuroD1 is also under the transcriptional control of Ngn3, and miR-15a/b, miR-16, and miR-195 target the 3′UTR of Ngn3 and thereby indirectly regulate NeuroD1. In turn, NeuroD1, like PDX1, has been shown to bind to the miR-375 promoter as well as to activate the miR-7 promoter. Together, the cross talk of these miRs and transcription factors provides a multilevel control of NeuroD1 signaling, β-cell development, differentiation, and insulin production. Numbers in parentheses refer to corresponding references.

Emerging Concepts and Remaining Challenges

MiRs and Their Many Gene Targets

To date, a multitude of miRs have been linked to islet β-cell biology (Table 1 and 2). They add an additional level of control but also an enormous amount of complexity to the regulation of β-cell function, development, and survival that often still remains underappreciated. MiRs are very potent regulatory molecules, and even small changes in their expression can have major effects that are further multiplied by the fact that each miR typically has many gene targets. Consistent with this notion, several miRs were found to have multiple functions in the β-cell (Fig. 1). The number of targets from one miR locus may further increase due to slight variations in the miR sequence, resulting in multiple isoforms (known as isomiRs) (110). These variants typically involve a shift in the seed sequence of the miR due to processing or posttranscriptional editing. Moreover, a number of noncanonical pathways have recently been described for miR function, including targeting complementary sequences outside of the 3′UTR, localizing to organelles rather than the cytoplasm and leading to translational activation rather than repression of mitochondrial genes (16,17). At this point, it is not clear whether these examples are isolated cases or if they just represent the tip of the iceberg of an even more complex miR regulatory network. In any case, the potential role of such noncanonical pathways in the pancreatic β-cell still remains to be elucidated.

Among miRs and isomiRs highly expressed in β-cells, miR-29 and let-7 were identified as the top two predicted regulatory hubs in type 2 diabetes (26). This means that these miRs scored highly on a bioinformatics analysis that determined the number of conserved predicted targets for each miR among genes in the human type 2 diabetes network. These predicted targets included genes identified in type 2 diabetes genome-wide association studies, such as Camk1d, Glis3, Jazf1, and Slc16a1. Furthermore, isomiRs of miR-375 were found to be likely hubs for type 2 diabetes (26). Taking these findings into consideration, it is tempting to speculate that miRs might play a significant role in the genetics/epigenetics of diabetes, and it will be important for future studies to keep this aspect in mind. In fact, a recent study demonstrated that the expression of a cluster of miRs in an imprinted locus was downregulated in islets of organ donors with type 2 diabetes as compared with control subjects without diabetes (111). While some of these cluster miRs were predicted to target genes playing important roles in β-cell biology (e.g., IAPP), the (patho)physiological role of these miRs still remains to be proven experimentally.

MiR Expression and Upstream Regulation

Over the past 10 years since the initial discovery of miR-375 regulating β-cell insulin secretion, a lot of advances have been made in regard to miRs and their role in islet β-cell function. However, some major challenges still remain. For one, classic transient loss- or gain-of-function experiments are often not able to reveal changes in miR expression and downstream function, and more chronic alterations, such as the creation of stable cell lines and complicated knockout or transgenic mouse models, are necessary. In addition, while the tools and programs to predict putative miR targets have improved dramatically, clearly facilitating the analysis of any downstream effects, identification of the specific upstream factors regulating the expression of any given miR has remained notoriously difficult. In addition, epigenetics such as DNA methylation may play an important role in the regulation of some miRs (111), consistent with their more chronic control pattern and the often observed lack of an acute response. To date, the responsible transcription factors conferring some of the observed changes in miR expression are only known for very few β-cell miRs, e.g., miR-375 (PDX1, NeuroD1), miR-7 (NeuroD1) (46,48), and miR-204 (STAT3) (31). It obviously will be important to identify the cis- and trans-acting factors responsible for the regulation of miR expression in order to recognize novel patterns and fully characterize the physiological role of β-cell miRs.

MiR Cross Talk With Transcription Factors and Other Noncoding RNAs

Aside from the well-accepted concept of one miR targeting many different pathways, the example of the miR-NeuroD1 signaling network revealed that there might also be convergence of different miRs onto one pathway (Fig. 3). It also suggested that cross talk exists between miRs and key transcription factors. While miRs act primarily as posttranscriptional regulators of gene expression, their ability to directly target different transcription factors (e.g., NeuroD1 [38,39,66,67], MafA [31], FoxA2 [50]) also allows them to indirectly control gene transcription. On the other hand, the function of miRs has been suggested to be modulated by competitive endogenous RNAs acting as sponges. These RNAs have been reported to be circular RNAs (112), large noncoding RNAs (lncRNAs) (113), or RNAs encoding pseudogenes (114). However, more recent work has put this theory of RNAs acting as miR sponges in question by demonstrating that the abundance of miR targets does not significantly alter the miR effects on gene expression, at least in the context of normal cell biology (115).

In contrast, lncRNAs are gaining more and more recognition as a biologically important class of noncoding RNAs that is highly regulated and capable of controlling gene expression. Recent studies have demonstrated a high degree of tissue specificity for lncRNAs, revealing more than 1,100 lncRNAs specific to islet cells (116). LncRNAs are thought to be involved in β-cell differentiation, and a subset was found to be dysregulated in the islets of humans with type 2 diabetes. Some islet lncRNAs have also been mapped to genomic loci associated with type 2 diabetes. As an example of their regulatory function, knockdown of HI-LNC25 in cultured human β-cells causes a decrease in the mRNA expression of GLIS3, a gene that codes for an islet Kruppel-like zinc finger protein transcription factor and is mutated in a form of monogenic diabetes (116). On the basis of the findings in NOD islets and MIN6 cells treated with proinflammatory cytokines, lncRNAs have also recently been suggested to be differentially regulated during the development of type 1 diabetes. Moreover, their overexpression has been shown to make β-cells more susceptible to apoptosis (117). The implications of lncRNAs for islet function and development and in the context of imprinted genomic loci have recently been reviewed (118,119). However, it is obvious that this is just the beginning and a lot more work will be necessary to elucidate the role of lncRNAs in β-cell biology and the pathophysiology of diabetes.

Summary

MiRs are small but very powerful regulators of β-cell biology. Their effects are not limited to a certain pathway or any particular set of functions, and their target genes include a variety of different proteins involved in all aspects of cell biology. However, a common theme that seems to emerge is that all genes targeted play important roles in β-cell development, function, and/or survival and therefore may have been deemed “worthy” of this extra level of control. They also seem to share the distinctive feature of being part of processes that leave very little room for error and therefore require additional checks and balances. In fact, it has been suggested that miRs help canalize general genetic programs of development and thereby buffer any random deviations to ensure stable phenotypes (120). They are also thought to contribute to gene regulatory networks that promote robustness and stability of physiological processes such as glucose homeostasis (121). Thus, continuing to peel off the different layers of these regulatory networks not only will provide insight into the various roles of noncoding RNAs but also should help yield a better understanding of β-cell biology and of the molecular processes driving the development of diabetes.