NLRP3 inflammasome activation in gestational diabetes mellitus placentas is associated with hydrogen sulfide synthetase deficiency.

The placenta may play a key role in the activation of inflammation and initiation of insulin resistance (IR) during gestational diabetes mellitus (GDM) pathogenesis. Interleukin (IL)-1β and IL-18, regulated by NLR family pyrin domain containing-3 (NLRP3) inflammasome, are important inflammatory cytokines in the initiation of maternal IR during GDM. However, the mechanism responsible for the regulatory of NLRP3 inflammasome in placenta remains unknown. Hydrogen sulfide (H2S) exerts anti-inflammatory function partially via suppressing the activation of the NLPR3 inflammasome. The present study aimed to investigate the role of NLRP3 inflammasome, H2S synthetase cystathionine-γ-lyase (CSE) and cystathionine-β-synthetase (CBS) in placenta in the pathogenesis of GDM. Clinical placenta samples were collected from pregnant women with GDM (n=16) and healthy pregnant women at term (n=16). Western blot analysis was performed to detect the protein expression levels of NLRP3, cleaved caspase-1, CBS and CSE in the placenta samples. Pearson's correlation analysis was performed to assess the correlation between NLRP3 inflammasome and H2S synthetase. Human placental cells were cultured and treated with different concentrations of NaHS (0, 10, 25 and 50 nmol/l) or L-cysteine (0, 0.25, 0.50 and 1.00 mmol/l). In addition, western blot analysis was performed to detect the protein expression levels of NLRP3 and cleaved caspase-1, while ELISA was performed to measure the production of IL-1β and IL-18 in the culture media. The results demonstrated that the expression levels of NLRP3 and cleaved caspase-1 increased, while the expression levels of CBS and CSE decreased in the placenta samples. In addition, the expression levels of NLRP3 and cleaved caspase-1 were inversely correlated with the expression levels of CBS and CSE. Notably, NaHS and L-cysteine significantly suppressed the expression levels of NLRP3 and cleaved caspase-1, and the production of IL-1 and IL-18 in human placental cells. Taken together, the results of the present study suggest that H2S synthetase deficiency in placenta may contribute to excessive activation of NLRP3 inflammasome in GDM. Copyright: © Wu et al.

Introduction

Gestational diabetes mellitus (GDM) is a form of diabetes first recognized during pregnancy, which is characterized by glucose intolerance and insulin resistance (IR) (1). Epidemiological studies have reported that GDM affects ~15.5-19.9% of all pregnant women in China (2,3). GDM is associated with several adverse events, including stillbirth, fetal macrosomia and development of type 2 DM later in life (4-6). The activation of inflammation in placenta and adipose tissue plays key roles in IR during the pathogenesis of GDM (7,8). Several inflammatory cytokines derived from placenta and adipose tissue participate in the activation of inflammation and initiate or aggravate IR during pregnancy (9-11). The placenta is a highly specialized organ during pregnancy that releases various cytokines and hormones, and contributes to the maternal IR (12-14). Since IR significantly improves immediately after delivery in GDM women (15,16), it is speculated that the placenta may play a key role in the activation of inflammation and initiation of IR during GDM pathogenesis. However, the mechanism responsible for the regulation of inflammation in GDM placenta remains unclear.

Interleukin (IL)-1β and IL-18 are important inflammatory cytokines in the initiation of maternal IR during GDM (17-19). The animal experimental study by Schulze et al (20) reported that treatment with an anti-IL-1β antibody improved glucose-tolerance of GDM mice. The nucleotide binding and oligomerization domain-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome participates in the regulation of IL-1β and IL-18 production (21,22). The NLRP3 inflammasome can be activated by a wide range of pathogens and cellular damages, resulting in the generation of cleaved caspase-1, and produces IL-1β and IL-18 (21,22). Previous studies have demonstrated that activation of the NLRP3 inflammasome is significantly elevated in patients with obesity, dyslipidemia and diabetes (23-25). According to the animal experimental study by Zhang et al (26), the expression levels of NLRP3 and caspase-1 are elevated in the placenta tissues of GDM mice. However, given that the expression of the NLRP3 inflammasome has not yet been investigated in clinical GDM placenta samples, further studies are required to determine the mechanism of the excessive activation of the NLPR3 inflammasome in placenta of GDM.

Known as ‘the third endogenous gaseous signaling transmitter’, hydrogen sulfide (H2S) exerts biological functions, including anti-inflammatory, anti-oxidative stress and anti-apoptosis (27,28). Our previous study demonstrated that H2S suppresses activation of the NLPR3 inflammasome in adipocytes (29). Teng et al (30) reported that H2S concentration significantly decreases in parturient women with GDM, suggesting that decreasing H2S may be involved in the pathogenesis of GDM. H2S is synthesized by L-cysteine in a range of mammalian tissues mainly by cystathionine-γ-lyase (CSE) and cystathionine-β-synthetase (CBS) (31). Our previous study demonstrated that human placenta samples express H2S synthetase, CSE and CBS, and deficiency of CSE and CBS in the placenta is associated with preeclampsia (32). Previous studies have also reported that deficiency in H2S synthetase is associated with other pregnancy complications, including premature labor (33) and fetal growth restriction (34). Thus, H2S may participate in the pathogenesis of GDM by regulating activation of the NLPR3 inflammasome in placentas. The present study aimed to investigate the expression of the NLPR3 inflammasome and H2S synthetases, CSE and CBS in clinical GDM placenta samples. In addition, the regulatory effect of H2S on the NLPR3 inflammasome in the cultured extravillous trophoblast cell line, HTR-8/SVneo was investigated.

Materials and methods

Clinical samples

Human placenta tissues were collected from pregnant women with GDM (n=16) and healthy pregnant women at term (n=16) who underwent elective cesarean section between January 2019 and December 2020 at the Chinese PLA 903rd Hospital and Women's Hospital School of Medicine Zhejiang University. The clinical characteristics of the pregnant women are presented in Table I. The present study was approved by the Medical Ethics Committee of the Chinese PLA 903rd Hospital (ethics approval data and no. 2017/03/05) and written informed consent was provided by all participants prior to the study start. Clinical placenta samples were collected within 30 min of cesarean birth, and three small pieces of tissues from separate lobules were randomly taken from each placenta. The tissues were washed with normal saline, immediately frozen in liquid nitrogen and subsequently stored at -80˚C until subsequent experimentation.

Table I

Clinical characteristics of the pregnant women enrolled in the present study.

Clinical characteristic	Normal pregnant women (n=16)	GDM pregnant women (n=16)	P-value
Maternal age, years	31.10±3.28	32.42±4.51	0.300
Gestational age, week	38.60±0.94	38.05±1.22	0.125
BMI, kg/m2	26.75±1.75	27.60±3.34	0.326
Blood pressure, mmHg
Systolic	116.05±11.17	117.58±10.65	0.665
Diastolic	73.45±9.67	73.37±9.17	0.979
Blood glucose, mmol/l
OGTT 0 h	4.46±0.31	4.88±0.56	0.043[a]
OGTT 1 h	6.59±1.13	10.94±2.12	<0.001[b]
OGTT 2 h	5.89±0.75	9.66±1.92	<0.001[b]
HbA1c, %	4.95±0.27	5.28±0.45	0.014[a]
Infant birth weight, g	3407.75±349.45	3315.79±417.34	0.459

aP<0.05;

bP<0.01. GDM, gestational diabetes mellitus; BMI, body mass index.

Human placental cell culture and treatment

The human first trimester extravillous trophoblast cell line, HTR-8/SVneo was gifted by Professor Xin Ni at the Research Center for Molecular Metabolomics, Xiangya Hospital Central. Cells were recovered and incubated in RPMI-1640 media supplemented with 10% fetal bovine serum (both purchased from Gibco; Thermo Fisher Scientific, Inc.) at 37˚C with 5% CO2 and 95% air, until they reached ~90% confluence.

Cells were subsequently digested with 0.25% trypsin. Subsequently, 1x105 cells seeded into 12-wells plates. To investigate the role of H2S in regulating the NLPR3 inflammasome, cells were treated with different concentrations of NaHS (0, 10, 25 and 50 nmol/l; (Sigma-Aldrich; Merck KGaA) or L-cysteine (0, 0.25, 0.50 and 1.00 mmol/l; Sigma-Aldrich; Merck KGaA) for 24 h. The present study also investigated the role of the NLPR3 inflammasome in the production of IL-1β and IL-18, using the NLPR3 inflammasome inhibitor, N-acetyl-tyrosyl-valyl-alanyl-aspartyl chloromethyl ketone (Ac-YVAD-CMK; Sigma-Aldrich; Merck KGaA).

Western blotting

Placental tissues (~30-40 mg) were homogenized using RIPA lysis buffer (Beyotime Institute of Biotechnology) containing protease inhibitor cocktail tablet (Roche Diagnostics). Cultured human placental cells were scraped off the plate using RIPA lysis buffer containing protease inhibitor cocktail tablet (Roche Diagnostics). The lysates were subsequently centrifuged in the speed of 12,000 x g at 4˚C for 15 min and the supernatant was collected. The concentration of protein in the supernatant was determined using the BCA kit (Beyotime Institute of Biotechnology). According to the concentration of protein, samples containing 30 µg of protein were used for western blot analysis. The protein samples were separated via 4 and 10% SDS-PAGE, transferred onto nitrocellulose membranes and blocked by 5% skim milk at room temperature for 2 h. The membranes were incubated with primary antibodies against NLRP3 (1:1,000; ab263899; Abcam), cleaved caspase-1 (1:1,000; ab179515; Abcam) and β-actin (1:8,000; cat. no. A5441; Sigma-Aldrich; Merck KGaA) overnight at 4˚C. Following the primary incubation, membranes were incubated with a goat anti-rabbit secondary HRP-conjugated antibody (1:5,000; cat. no. BA1054; Wuhan Boster Biological Technology, Ltd.) at room temperature for 1 h. Protein bands were visualized using the enhanced chemiluminescence substrate kit (Merck KGaA) and ChemiScope 6000EXP and the band intensities were calculated by ImageJ (version 1.51b; National Institutes of Health). Then ratio of band intensities to β-actin was obtained to quantify the relative protein expression levels.

ELISA

Following treatment, the culture media of the human placental cells was collected and IL-1β and IL-18 production was determined using the IL-1β ELISA kit (cat. no. F10770) and IL-18 ELISA kit (cat. no. F10920) (both Shanghai Westang Biotech), according to the manufacturer's instructions. All experiments were performed in duplicate.

Statistical analysis

Data are presented as the mean ± SEM in SPSS (version 20; IBM Corp.). Each experiment in HTR-8/SVneo was repeated four times. All data were tested for homogeneity of variance using the Bartlett's test before analyzing the significance. Unpaired Student's t-test was used to compare differences between two groups, while one-way ANOVA followed by Bonferroni's post hoc test was used to compare differences between multiple groups. Pearson's analysis was used to analyze the correlation between two indexes. P<0.05 was considered to indicate a statistically significant difference.

Results

Expression levels of NLRP3, cleaved caspase-1, CBS and CSE in GDM and healthy placentas

To investigate the role of H2S in the excessive activation of the NLPR3 inflammasome in GDM placenta, the expression levels of NLRP3, cleaved caspase-1, and the H2S synthetases CBS and CSE in placentas were determined. As presented in Fig. 1A-D, the expression levels of NLRP3 and cleaved caspase-1 increased, while the expression levels of CBS and CSE decreased in GDM placentas compared with healthy placentas. The correlation between NLRP3 and cleaved caspase-1 with the H2S synthetases were analyzed. As presented in Fig. 2A-D, the levels of CBS and CSE were inversely correlated with NLRP3 and cleaved caspase-1 in GDM placentas.

Figure 1

Comparison of NLRP3, cleaved caspase-1, CBS and CSE expression levels between healthy placentas and GDM placentas. (A) Western blot analysis was performed to detect the protein expression levels of (A) NLRP3, (B) cleaved caspase-1, (C) CBS and (D) CSE in healthy placentas and GDM placentas. Representative protein bands are presented on top of the corresponding histogram. Data are presented as the mean ± SEM. *P<0.05. NLRP3, NLR family pyrin domain containing-3; CBS, cystathionine-β-synthetase; CSE, synthetase cystathionine-γ-lyase; GDM, gestational diabetes mellitus.

Figure 2

Correlation between NLRP3, cleaved caspase-1 and CBS and CSE in GDM placentas. Pearson's correlation analysis was performed to determine the correlation between NLRP3, cleaved caspase-1 and CBS and CSE in GDM placentas. (A) CSE was inversely correlated with NLRP3 in GDM placentas. (B) CSE was inversely correlated with cleaved caspase-1 in GDM placentas. (C) CBS was inversely correlated with NLRP3 in GDM placentas. (D) CBS was inversely correlated with cleaved caspase-1 in GDM placentas. NLRP3, NLR family pyrin domain containing-3; CBS, cystathionine-β-synthetase; CSE, synthetase cystathionine-γ-lyase; GDM, gestational diabetes mellitus.

Effect of H2S on the expression of the NLPR3 inflammasome in placental cells

Our previous study demonstrated that the expression of the NLPR3 inflammasome decreases via H2S in adipocytes (29). To investigate the role of H2S in the regulation of the NLPR3 inflammasome in placenta, placental cells were cultured and treated with H2S donor NaHS or H2S precursor L-cysteine. As presented in Fig. 3A-D, treatment with NaHS and L-cysteine significantly inhibited the expression levels of NLRP3 and cleaved caspase-1, in dose-dependent manners.

Figure 3

Effects of NaHS and L-cysteine on the expression levels of NLRP3 and cleaved caspase-1 in human placental cells. Western blot analysis was performed to detect the protein expression levels of NLRP3 and cleaved caspase-1 in cells. NaHS regulated the expression levels of (A) NLRP3 and (B) cleaved caspase-1 in human placental cells. L-cysteine regulated the expression levels of (C) NLRP3 and (D) cleaved caspase-1 in human placental cells. Representative protein bands are presented on top of the corresponding histogram. Data are presented as the mean ± SEM (n=4). *P<0.05 and **P<0.01. NLRP3, NLR family pyrin domain containing-3.

Effect of H2S on the production of IL-1β and IL-18 in placental cells

Activation of the NLPR3 inflammasome releases IL-1β and IL-18 (21,22). To confirm the role of H2S in the regulation of the NLPR3 inflammasome in placenta, the contents of IL-1β and IL-18 in the culture media of placental cells were determined. As presented in Fig. 4, treatment with NaHS and L-cysteine decreased the production of IL-1β and IL-18, in dose-dependent manners.

Figure 4

Effects of NaHS and L-cysteine on the contents of IL-1β and IL-18 in the culture media of human placental cells. ELISA was performed to determine IL-1β and IL-18 contents. NaHS regulated the contents of (A) IL-1β and (B) IL-18 in the culture media. L-cysteine regulated the contents of (C) IL-1β and (D) IL-18 in the culture media. Data are presented as the mean ± SEM (n=4). *P<0.05 and **P<0.01. IL, interleukin.

Effect of the NLRP3 inflammasome inhibitor on the production of IL-1β and IL-18 in placental cells

To confirm the role of the NLRP3 inflammasome in the production of IL-1β and IL-18 in placental cells, the NLRP3 inflammasome inhibitor, Ac-YVAD-CMK was used. As presented in Fig. 5, treatment with Ac-YVAD-CMK decreased the release of IL-1β and IL-18.

Figure 5

Effects of the NLRP3 inflammasome inhibitor, Ac-YVAD-CMK on the contents of IL-1β and IL-18 in the culture media of human placental cells. ELISA was performed to determine the contents of IL-1β and IL-18 in the culture media. Ac-YVAD-CMK regulated the contents of (A) IL-1β and (B) IL-18 in the culture media. Data are presented as the mean ± SEM (n=4). **P<0.01. NLR family pyrin domain containing-3; Ac-YVAD-CMK, N-acetyl-tyrosyl-valyl-alanyl-aspartyl chloromethyl ketone; IL, interleukin; LG, low glucose; HG, high glucose.

Discussion

The results of the present study demonstrated that the reduced expression of H2S synthetases, CSE and CBS was correlated with the excessive activation of the NLPR3 inflammasome in GDM placenta. H2S significantly suppressed the activation of the NLPR3 inflammasome in human placental cells in vitro. Furthermore, the NLPR3 inflammasome was involved in the production of IL-1β and IL-18 in human placental cells.

Known as a highly specialized organ during pregnancy, the placenta serves as the interface between maternal and fetal circulation (35). In recent years, the key role of the placenta in the occurrence and development of GDM has been reported by multiple studies (36-38). Currently, IR is the critical pathophysiological characteristic of GDM, which is also found during normal pregnancy. Placenta derived hormones, cytokines and gaseous signaling transmitter can induce IR by interfering with insulin receptor signal transduction (12-14). Furthermore, the dysregulation of hormones, cytokines and gaseous signaling transmitter in placenta may aggravate IR and trigger abnormal glucose metabolism (12-14). Thus, the present study investigated the key molecules in the placenta responsible for the pathogenesis of GDM.

The overactive inflammatory response may be the initiating factor for IR. Cytokines of the IL-1 family critically regulate the inflammatory response by controlling several inflammation processes (39,40). Both IL-1β and IL-18, which are classic pro-inflammatory cytokines of the IL-1 family, participate in the initiation of IR of GDM and type 2 DM (17-19). The production of IL-1β and IL-18 is regulated by the NLRP3 inflammasome in different types of tissues and cells. The NLRP3 inflammasome complex is composed of NLRP3, ASC and pro caspase-1. Activation of the inflammasome recruits and cleaves pro caspase-1, which results in the formation of cleaved caspase-1. Subsequently, cleaved caspase-1 converts pro-IL-1β and pro-IL-18 into the mature forms, IL-1β and IL-18 (21,22). According to the animal experimental study by Zhang et al (26), the expression levels of NLRP3 and cleaved caspase-1 are elevated in the placenta tissues of GDM mice. The results of the present study demonstrated that the expression levels of NLRP3 and cleaved caspase-1 were elevated in the clinical placenta samples collected from pregnant women with GDM. Taken together, the results of the present study suggest that excessive activation of the NLRP3 inflammasome in the placenta may be involved in the development of GDM.

Further research on the mechanism of the regulation of the NLRP3 inflammasome in the placenta is required. H2S is a lately identified gaseous signaling transmitter that mediates a variety of biological activities, including, anti-apoptotic and anti-oxidative stress (27,28). During pregnancy, the abnormal production of H2S and the dysregulation of the H2S synthetases, CBS and CSE are associated with various pregnancy complications (32,41,42). The results of the present study demonstrated that the expression of the H2S synthetases, CBS and CSE were significantly downregulated in GDM placenta samples, which was consistent with the findings reported by Teng et al (30). Our previous study investigated the regulatory effect of H2S on the NLRP3 inflammasome in the pathogenesis of vascular complications of type 2 DM, and the results demonstrated that H2S significantly suppressed activation of the NLRP3 inflammasome in adipocyte (23). Other studies have also reported the role of H2S in regulating the NLRP3 inflammasome. For example, Jia et al (43), Zheng et al (44) and Su et al (45) reported the inhibitory effect of H2S on the NLRP3 inflammasome in diabetic myocardial injury model, diabetes-accelerated atherosclerosis model and renal injury model.

The results of the present study demonstrated an inverse correlation between the H2S synthetases and the NLRP3 inflammasome in GDM placentas, suggesting that H2S may participate in regulating the NLRP3 inflammasome in placenta. The effect of H2S on the NLRP3 inflammasome in vitro was also investigated. In human placental cells, both the H2S donor and precursor decreased the expression levels of NLRP3 and cleaved caspase-1, as well as the production of IL-1β and IL-18. In addition, the NLRP3 inflammasome inhibitor decreased the production of IL-1β and IL-18 in human placental cells. Collectively, these results suggest that H2S plays a regulatory role in the activation of the NLRP3 inflammasome, and H2S synthetase deficiency results in excessive activation of the NLRP3 inflammasome and excessive production of IL-1β and IL-18 in GDM placenta.

Most previous studies focused on the downstream biological effects of H2S (29,32,43-45); however, the mechanism responsible for the upstream regulatory factor for the expression of CBS and CSE, and the production of H2S remains unclear. Recently, several studies investigated the upstream regulatory mechanism for the expression of CBS and CSE, and the production of H2S, and the results demonstrated that high fat (46,47), high salt (48), hypoxia (49) and oxidative stress (50) inhibited the expression of CBS and CSE, and the production of H2S. Conversely, vitamin D supplementation increased CSE expression and the production of H2S (51). Other clinical studies have reported that high-fat and high-salt diet, vitamin D deficiency during pregnancy (52-54), hypoxia and oxidative stress in the placenta (55,56) are associated with the pathogenesis of GDM. Taken together, these results suggest that high-fat and high-salt diet, vitamin D, hypoxia and oxidative stress may be upstream regulatory factors for the expression of CBS and CSE, and the production of H2S in GDM. However, further studies are required to determine the specific mechanism responsible for the expression of CBS and CSE, and the production of H2S in GDM.

In conclusion, the results of the present study demonstrated the role of the NLRP3 inflammasome and H2S in the occurrence and development of GDM. Excessive activation of the NLRP3 inflammasome may be induced by the H2S synthetase deficiency in the placenta, and activation of the NLRP3 inflammasome mediates the elevated production of IL-1β and IL-18, thus initiating maternal IR and causing abnormal glucose metabolism.