The effects of a biodegradable Mg-based alloy on the function of VSMCs via immunoregulation of macrophages through Mg-induced responses.

BACKGROUND: Restenosis is one of the worst side effects of percutaneous coronary intervention (PCI) due to neointima formation resulting from the excessive proliferation and migration of vascular smooth muscle cells (VSMCs) and continuous inflammation. Biodegradable Mg-based alloy is a promising candidate material because of its good mechanical properties and biocompatibility, and biodegradation of cardiovascular stents. Although studies have shown reduced neointima formation after Mg-based CVS implantation in vivo, these findings were inconsistent with in vitro studies, demonstrating magnesium-mediated promotion of the proliferation and migration of VSMCs. Given the vital role of activated macrophage-driven inflammation in neointima formation, along with the well-demonstrated crosstalk between macrophages and VSMCs, we investigated the interactions of a biodegradable Mg-Nd-Zn-Zr alloy (denoted JDBM), which is especially important for cardiovascular stents, with VSMCs via macrophages.
METHODS: JDBM extracts and MgCl2 solutions were prepared to study their effect on macrophages. To study the effects of the JDBM extracts and MgCl2 solutions on the function of VSMCs via immunoregulation of macrophages, conditioned media (CM) obtained from macrophages was used to establish a VSMC-macrophage indirect coculture system.
RESULTS: Our results showed that both JDBM extracts and MgCl2 solutions significantly attenuated the inflammatory response stimulated by lipopolysaccharide (LPS)-activated macrophages and converted macrophages into M2-type cells. In addition, JDBM extracts and MgCl2 solutions significantly decreased the expression of genes related to VSMC phenotypic switching, migration, and proliferation in macrophages. Furthermore, the proliferation, migration, and proinflammatory phenotypic switching of VSMCs were significantly inhibited when the cells were incubated with CMs from macrophages treated with LPS + extracts or LPS + MgCl2 solutions.
CONCLUSIONS: Taken together, our results suggested that the magnesium in the JDBM extract could affect the functions of VSMCs through macrophage-mediated immunoregulation, inhibiting smooth muscle hyperproliferation to suppress restenosis after implantation of a biodegradable Mg-based stent. 2021 Annals of Translational Medicine. All rights reserved.

Introduction

Atherosclerosis is one of the leading causes of morbidity and mortality in developed countries (1). In recent decades, the incidence of atherosclerosis has been increasing rapidly in developing countries due to the increasing popularity of western lifestyles, resulting in this disease becoming a global health concern (2,3). Percutaneous coronary intervention (PCI), which involves implanting a stent into a diseased artery, is regarded as an effective and widely acceptable atherosclerosis treatment (4). However, restenosis is still one of the major challenges associated with PCI in the clinic. Neointima formation is reported to be the main cause of restenosis, primarily due to excessive proliferation and migration of vascular smooth muscle cells (VSMCs) (5,6).

VSMCs, which are major cellular components of the vasculature, are involved in various physiological and pathological changes in the vascular wall (7,8). Because these cells are not terminally differentiated, VSMCs exhibit phenotypic and functional plasticity and play an important role in responding to vascular injury (8). Under physiological conditions, VSMCs exhibit a quiescent-contractile phenotype and regulate blood pressure and the redistribution of blood flow (8,9). The quiescent-contractile phenotype of VSMCs is characteristic of the stable expression of specific proteins, such as α-smooth muscle actin (α‐SMA), SM22α, SM myosin heavy chain (MHC), myocardin (MyoC), and H1-calponin (9,10). Once the vessel is injured or stimulated by external signals, VSMCs can switch from the contractile phenotype to the pro-inflammatory phenotype. The latter phenotype exhibits decreased expression of the proteins mentioned above and increased proliferation and motility, thereby promoting vascular wall repair (7). However, excessive VSMC phenotypic transformation is a critical pathomechanism of some vascular diseases, such as atherosclerosis, cerebral microangiopathy, and hypertension (10-12).

In recent years, biodegradable metallic stents, such as magnesium (Mg)-based stents, have been regarded as promising biomedical implants due to their good mechanical properties, biocompatibility, and biodegradability, which help to avoid sequelae such as late in-stent restenosis and neoatherosclerosis after implantation (6,12-14). Moreover, the rapid degradation of Mg-based stents, whose main degradation product is Mg ions, alters the vascular microenvironment, further affecting the immune response and revascularization in the vessel wall (15,16). In fact, although previous data have demonstrated provascularization and proangiogenic effects of Mg-based alloys in vitro and in vivo (15-17), only a few reports have studied the effects of alloys on VSMCs. Waksman et al. examined the biocompatibility of bioabsorbable Mg alloys in porcine coronary arteries, and the results showed that there was significantly less neointima formation in segments with Mg alloy stents than in those with stainless steel stents (18). Notably, this in vivo finding seems to be inconsistent with previous in vitro reports, showing that the Mg-based alloy extract promoted the proliferation and migration of VSMCs (19). To date, the underlying mechanism of these seemingly contradictory effects of Mg-based alloys in vivo and in vitro has remained unclear and needs to be elucidated.

In addition to the contribution of excessive VSMC proliferation and migration, neointima formation is also driven by local inflammation after PCI by means of early neutrophil recruitment followed by prolonged macrophage accumulation in stented arteries (20,21). Restenosis resulting from intimal hyperplasia and the failure of re-endothelization was reportedly correlated with an excessive inflammatory response (20). Macrophages play an essential role in the inflammatory response after PCI in terms of their polarization into M1-type (proinflammatory) and M2-type (anti-inflammatory) cells (22-26). M2 macrophages play a vital role in resolving inflammation by switching gene expression toward anti-inflammatory molecules (27). In particular, the complicated interaction between macrophages and VSMCs during vascular injury, which further leads to intimal hyperplasia, has been well demonstrated (28). Herein, we hypothesized that Mg-based alloys might affect the migration and proliferation of VSMCs via immunoregulation by macrophages. The present study aimed to explore the potential mechanisms by which Mg in Mg-based alloys regulated intimal hyperplasia using a macrophage-VSMC coculture system in vitro.

We present the following article in accordance with the Materials Design Analysis Reporting (MDAR) checklist (available at https://dx.doi.org/10.21037/atm-21-1375).

Methods

JDBM extract preparation

The composition of the Mg-Nd-Zn-Zr alloy ingot (denoted as JDBM), which was especially designed for vascular stents, has been described in previous studies. The composition of the biodegradable JDBM alloy is as follows (mass percent): Mg: >97%, Nd: 2.1%, Zn: 0.21%, Zr: 0.5%, Mn: 0.009%, Si: 0.006%, Cu: 0.005%, Fe: 0.002% (29-32). JDBM discs (18 mm in diameter and 2.0 mm in height) were immersed in an ultrasonic cleaning bath with ethanol and acetone for 10 min and then sterilized by exposure to ultraviolet light for 1 h before use. JDBM extracts were prepared according to the ISO 10993 guidelines. Briefly, JDBM discs were immersed in DMEM (High glucose, Gibco, USA) supplemented with 10% fetal bovine serum (FBS) (Gibco, USA) and 1% penicillin-streptomycin (PS) (HyClone, USA) with a surface area/volume ratio of 1.25 cm2/mL at 37 °C and 5% CO2 for 72 h. After that, the extracts were then harvested, filtered by a 0.2 µm filter, and stored at 4 °C (30). To avoid the cytotoxicity of full-strength extract (30), the JDBM extracts were further diluted to 15% and 5% with fresh complete DMEM supplemented with 10% FBS (Gibco, USA) and 1% PS (HyClone, USA). Subsequently, we detected the concentration of Mg ions from JDBM by inductively coupled plasma atomic emission spectrometry (ICP-AES, Perkin-Elmer Optima 2000, USA), and the concentration of Mg ions from the 15% JDBM extract was approximately 150 ppm (ppm equals 1 mg of substance per liter, mg/L). As the molecular weight of Mg is 24 g/mol, we prepared MgCl2 solution at 6 mM of the final Mg ion concentration similar to that of the 15% extract (150 mg/L). Then, 2 mM MgCl2 solutions were prepared to simulate the Mg ion concentration of the 5% extract (50 mg/L). Finally, the Mg, Nd, Zn, and Zr ion concentrations were determined by ICP-AES, and pH of the complete DMEM medium (control), JDBM extracts, and MgCl2 solutions were determined by a pH detector (PB-10, Sartorius, Germany). ICP-AES is a method of emission spectroscopy that excites atoms and ions with a plasma, causing it to emit electromagnetic radiation at wavelengths characteristic of a particular element. For pH detection, the pH meter was calibrated with pH buffer solutions (4.00 and 6.86) before detecting the pH values of the solutions.

Cell culture and treatments

RAW264.7 macrophage-like cells were cultured in DMEM complete medium supplemented with 10% FBS and 1% PS in a humidified 5% CO2 incubator at 37 °C. To study the effects of JDBM extracts and MgCl2 solutions on macrophages, cells were activated by lipopolysaccharide (LPS, 1 mg/mL, Invitrogen, USA) for 6 h and then washed with phosphate-buffered saline (PBS) 3 times. After that, the activated RAW264.7 cells were treated with or without 5% extract, 15% extract, 2 mM MgCl2, or 6 mM MgCl2 for another 72 h. To prepare conditioned media (CM), at the end of the culture time, the supernatants of each group were sequentially collected, centrifuged for 5 min at 1,500 rpm, mixed with fresh DMEM complete medium at a ratio of 1:1, and stored at −80 °C until use. A7r5 VSMCs were cultured in different CMs for another 72 h before a series of functional assays.

Cell proliferation and viability assays

The cell counting kit-8 (CCK-8) assay (Dojindo, Japan) evaluated cell proliferation and viability according to the manufacturer’s instructions. Briefly, RAW264.7 cells or A7r5 cells were seeded into 96-well plates and then treated as described above. Then, the cell media culture was removed, and the cells were washed with PBS twice. After that, 100 µL of DMEM containing 10% CCK-8 solution (Dojindo, Kumamoto, Japan) was added to each well, followed by incubation for 3 h in a humidified 5% CO2 incubator at 37 °C. Finally, the absorbance was measured in a microplate reader (BioTek, Winooski, VT, USA) at a 450 nm test wavelength.

Apoptosis and necrosis detection by flow cytometry

Annexin V-FITC and propidium iodide (PI) (BD, USA) were used to measure cell apoptosis and necrosis according to the manufacturer’s instructions. The target protein of Annexin V-FITC is Annexin V, and PI is a fluorescent dye that binds to DNA. The cells were treated, harvested, and washed with cold PBS. Then, the cells were suspended in 1× Annexin binding buffer and stained with Annexin V-FITC and PI for 15 min in the dark at room temperature. Finally, apoptotic and necrotic cells were analyzed by flow cytometry (FACS, Canto II, BD, USA). For the gating strategies, forward versus side scatter (FSC vs. SSC) gating was used to identify cells of interest based on size and granularity (complexity), then a two-parameter density plot was used to distinguish specific cell populations by creating a plot of Annexin V vs. PI. Each quadrant represented a specific cell population: (I) Annexin V-/PI-: living cells; (II) Annexin V+/PI-: early apoptotic cells; (III) Annexin V+/PI+: late apoptotic cells; (IV) Annexin V-/PI+: necrotic cells.

Cell cycle analysis by flow cytometry

A7r5 cells were harvested after being cultured in different CMs for 72 h. The cells were washed once with cold PBS, fixed in ice-cold 70% ethanol, and then stored at −20 °C overnight. After that, the cells were washed with PBS, suspended in 500 µL of PBS containing 100 µg/mL RNase A and 150 µg/mL PI (Beyotime, China), and incubated at 4 °C for 30 min. Finally, the cells were collected and analyzed by FACS (Canto II, BD, USA).

Transwell migration and wound healing assays

For the transwell migration assay, A7r5 cells were seeded at a density of 5×104/mL in 100 µL of serum-free DMEM in the upper chamber of the inserts (8 µm pore size, Corning, USA), and different CMs were added to the lower chambers. After 8 h of incubation in a humidified 5% CO2 incubator at 37 °C, the cells on the upper side of the insert were removed, and cells on the bottom side were washed with PBS, fixed with 4% paraformaldehyde for 10 min, and stained with hematoxylin and eosin. Finally, images were captured, and the cell number was determined by counting 5 random microscopic fields (×200).

For the wound healing assay, A7r5 cells were seeded at a density of 5×105 cells/well in a 6-well plate. After incubation for 24 h, adherent A7r5 cells were scratched with pipette tips and washed with PBS. Different CMs were added to the cells and incubated for 48 h, and then NIH ImageJ 1.46 software was used to quantify the migration ability of cells by subtracting the scratch distance at 0 h from the area at 48 h.

Real-time quantitative PCR (RT-qPCR)

Total RNA was isolated using TRIzol reagent (Invitrogen, USA), and cDNA was synthesized with a ReverTra Ace qPCR RT kit (Toyobo, Japan) according to the manufacturer’s instructions. Subsequently, qPCR was performed with SYBR Green real-time PCR master mix (Toyobo, Japan). The quantity and quality of RNA were determined by NanoDrop 2000 spectrophotometer (Thermo Fisher Scientific, USA). The expression levels of target genes were evaluated using the ΔΔCt method and were normalized to GAPDH. The primer sequences of the target genes are listed in Table S1.

Statistical analysis

The data are presented as the mean ± standard deviation (SD). Statistical analysis was performed using the Mann-Whitney U test or one-way ANOVA with Tukey’s honestly significant difference (HSD) test and SPSS software. The differences were considered significant at a P value <0.05.

Results

The cytotoxic effects of JDBM extracts and MgCl solutions on macrophages

Since Mg ions are the main degradation product of Mg-based alloys, we investigated the role of Mg ions from JDBM in this study by preparing 15% and 5% JDBM extracts and MgCl2 solutions with equivalent Mg ion concentrations of 6 and 2 mM, respectively (). The control group, which was comprised of a DMEM complete medium, also contained a low concentration of Mg (), providing a basal Mg level for cells.

Figure 1

The cytotoxicity of JDBM extracts and MgCl2 solutions on RAW264.7 cells. (A) The magnesium concentration and pH of JDBM extracts and MgCl2 solutions were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) and a pH detector, respectively, and each experiment was repeated 3 times. After incubation with JDBM extracts or MgCl2 solutions for 3 days, the viability of RAW264.7 cells was determined by the cell counting kit-8 (CCK-8) assay (n=8), (B) and the percentages of apoptotic and necrotic cells were determined by flow cytometry. Forward versus side scatter (FSC vs. SSC) gating was used to identify cells of interest based on size and granularity (complexity), then a two-parameter density plot was used to distinguish specific cell populations by creating a plot of Annexin V vs. propidium iodide (PI). Each quadrant represents a specific cell population: (I) Annexin V-/PI-: living cells; (II) Annexin V+/PI-: early apoptotic cells; (III) Annexin V+/PI+: late apoptotic cells; (IV) Annexin V-/PI+: necrotic cells (C). Statistical analysis was performed by one-way ANOVA, and P value <0.05 was considered as significant.

Then, we evaluated the cytotoxic effects of JDBM extracts and MgCl2 solutions on macrophages. After incubation for 72 h, the cell viability and percentages of apoptotic and necrotic cells were similar between groups, indicating that neither JDBM extracts nor MgCl2 solutions exerted cytotoxic effects on macrophages ().

The effects of JDBM extracts and MgCl solutions on the polarization of macrophages

After the macrophages were treated with LPS for 6 h, the activated macrophages were incubated with JDBM extracts and MgCl2 solutions for another 72 h. As shown in , compared with the control treatment, the 15% JDBM extract and 6 mM MgCl2 solution significantly downregulated the expression of proinflammatory genes, such as Tnfa and Il-6, while the 5% JDBM extract and 2 mM MgCl2 solution significantly inhibited Tnfa but not Il-6 expression. Moreover, the 15% JDBM extract and 6 mM MgCl2 solution significantly downregulated the expression of M1-associated genes (iNOS and Cd86) and significantly upregulated the expression of M2-associated genes (Cd163 and Cd206). However, the 5% JDBM extract and 2 mM MgCl2 solution only significantly regulated some M1- and M2-related genes (iNOS and Cd163), and the expression of Cd86 and Cd206 was similar in the different groups ().

Figure 2

The effects of JDBM extracts and MgCl2 solutions on proinflammatory cytokine expression and the polarization of RAW264.7 cells. After treatment with JDBM extracts and MgCl2 solutions for 3 days, the expression of Tnfa (A) and Il-6 (B) in RAW264.7 cells was determined by quantitative reverse transcription PCR (RT-qPCR). M1 macrophage-associated markers (C,D) and M2 macrophage-associated markers (E,F) were also measured by RT-qPCR. * P<0.05 vs. the control group. Error bars represent the standard deviation (SD) of quadruplicate experiments. Statistical analysis was performed by the Mann-Whitney U test, and P value <0.05 was considered as significant.

The effects of JDBM extracts and MgCl2 solutions on the expression of genes related to VSMC phenotypic switching, migration, and proliferation in macrophages

Furthermore, we evaluated the effect of JDBM extracts and MgCl2 solutions on the expression of genes related to VSMC phenotypic switching, migration, and proliferation in macrophages. The results showed that the 15% JDBM extract and 6 mM MgCl2 solution could significantly downregulate the expression of matrix metalloproteinases (Mmp-2 and Mmp-9), which are regulators of extracellular matrix (ECM) composition and facilitate the migration of VSMCs (). In addition, these treatments significantly decreased the expression of platelet-derived growth factor subunit B (Pdgfb), transforming growth factor beta (Tgfb), and vascular cell adhesion molecule 1 (Vcam-1), all of which have been reported to play roles in promoting VSMC phenotypic switching, proliferation, and migration (). Unexpectedly, it was interesting to note that the JDBM extracts and MgCl2 solutions with low but not high concentrations of Mg2+ (2 mM) could increase the expression of vascular endothelial growth factor (Vegf) in macrophages (). This is in line with previous studies which showed the interaction between M2 macrophages and VEGF. On the one hand, M2 macrophages could secrete VEGF to stimulate angiogenesis, while on the other hand, VEGF contributes to macrophage recruitment and M2 polarization (33-36).

Figure 3

The effects of JDBM extracts and MgCl2 solutions on the expression of genes related to vascular smooth muscle cell (VSMC) phenotypic switching, migration, and proliferation in RAW264.7 cells. After treatment with JDBM extracts and MgCl2 solutions for 3 days, gene expression was determined by quantitative reverse transcription PCR (RT-qPCR) (A-F). *P<0.05 vs. the control group. Error bars represent the standard deviation (SD) of quadruplicate experiments. Statistical analysis was performed by the Mann-Whitney U test, and P value <0.05 was considered as significant.

The cytotoxic effects of CMs on VSMCs

To study the effects of JDBM on the function of VSMCs via macrophage-mediated immunoregulation, CMs were obtained from macrophages to establish an indirect VSMC-macrophage coculture system. A7r5 cells were cultured in different CMs for 72 h, and the cytotoxic effects of the CMs were determined. The results showed that the percentages of apoptotic and necrotic cells and cell cytotoxicity were similar between groups (). The amount of spontaneous apoptosis determined by the Bax/Bcl-2 ratio was also similar between groups (). Furthermore, the CMs from different groups did not affect the cellular morphology of VSMCs (). These results indicated that none of the CMs exerted cytotoxic effects on VSMCs and could be used in further studies.

Figure 4

The biocompatibility of conditioned medias (CMs) with A7r5 cells. CMs, which were derived from RAW264.7 cells treated with JDBM extracts or MgCl2 solutions, were added to A7r5 cells and incubated for 72 h. (A) The percentages of apoptotic and necrotic A7r5 cells were determined by flow cytometry. Each quadrant represents a specific cell population: (I) Annexin V-/PI-: living cells; (II) Annexin V+/PI-: early apoptotic cells; (III) Annexin V+/PI+: late apoptotic cells; (IV) Annexin V-/PI+: necrotic cells. (B) The cytotoxicity of cells was analyzed by lactate dehydrogenase (LDH) assays (n=3) (B), and the ratio of Bax/Bcl-2 was determined by quantitative reverse transcription PCR (RT-qPCR). Error bars represent the standard deviation (SD) of quadruplicate experiments (C-E). (F) The morphology of A7r5 cells was observed by microscopy. Scale bar =25 µm. Statistical analysis for LDH assays was performed by one-way ANOVA, and statistical analysis for RT-qPCR was performed by the Mann-Whitney U test. P value <0.05 was considered as significant.

The effects of CMs on the cell cycle and proliferation of VSMCs

Increased proliferation has been reported to be a characteristic of VSMC switching to a proinflammatory phenotype. Therefore, we evaluated the effect of different CMs on the cell cycle and proliferation of VSMCs. As shown in , compared with the control group CM, CMs from macrophages treated with high concentrations of JDBM extract and MgCl2 solutions induced G1-phase cell cycle arrest and the loss of p21 and Cyclin D1. In addition, all CMs from macrophages treated with JDBM extracts and MgCl2 solutions significantly decreased the proportions of VSMCs in S phase. Not surprisingly, as shown in , compared with the control group CM, all CMs from macrophages treated with JDBM extracts and MgCl2 solutions significantly inhibited the proliferation of VSMCs in a dose-dependent manner.

Figure 5

The effects of conditioned medias (CMs) on the proliferation of A7r5 cells. A7r5 cells were treated with different CMs for 72 h. The cell cycle was analyzed by flow cytometry (n=3) (A-D). Cell cycle proteins were measured with quantitative reverse transcription PCR (RT-qPCR), and error bars represent the standard deviation (SD) of triplicate experiments (E,F). The cellular growth rate was analyzed by the cell counting kit-8 (CCK-8) assay (n=8) (G). *P<0.05 vs. the control group. Statistical analysis for the cell cycle assay was performed by one-way ANOVA, and statistical analysis for RT-qPCR and the CCK-8 assay was performed by the Mann-Whitney U test. P value <0.05 was considered as significant.

The effects of CMs on the migration of VSMCs

Next, a transwell migration assay was used to study the effects of CMs on the migration of VSMCs. The results showed that, compared with the control group CM, CMs from macrophages treated with JDBM extracts and MgCl2 solutions significantly inhibited the migration of VSMCs in a dose-dependent manner (). The wound healing assay () further confirmed these results. show the statistical analysis data. These results suggested that JDBM extracts and MgCl2 solutions could significantly inhibit the migration of VSMCs via macrophage-mediated immunoregulation.

Figure 6

The effects of conditioned medias (CMs) on the migration of A7r5 cells. (A,C) A7r5 cells were seeded on transwell plates with different CMs for 8 h, and the results were observed by microscopy. Scale bar =100 µm. (B,D) The cells were scratched, and different CMs were added and incubated for 48 h to observe the migration rate by microscopy. Scale bar =200 µm. The data are presented as the mean ± standard deviation (SD) (n=3). *P<0.05 vs. the control group. Statistical analysis was performed by one-way ANOVA, and P value <0.05 was considered as significant.

The effects of CMs on the polarization of VSMCs

In addition to the effects of different CMs on proliferation and migration, the effects of different CMs on the polarization of VSMCs were also evaluated by measuring the gene expression of VSMC contractile markers, including sm-MHC, α-Sma, Myoc, and Sm22α. The results showed that compared with the control group CM, CMs from macrophages treated with JDBM extracts and MgCl2 solutions significantly upregulated the expression of sm-MHC and Myoc. However, the expression of α-Sma and Sm22α was similar in the different groups (). These results indicated that JDBM extracts and MgCl2 solutions could significantly inhibit the phenotypic switching of VSMCs to a proinflammatory phenotype via macrophage-mediated immunoregulation.

Figure 7

The effects of conditioned medias (CMs) on the polarization of A7r5 cells. A7r5 cells were treated with CMs for 72 h, then phenotype-related markers were determined by quantitative reverse transcription PCR (RT-qPCR). Error bars represent the standard deviation (SD) of quadruplicate experiments. *P<0.05 vs. the control group. Statistical analysis was performed by one-way ANOVA, and P value <0.05 was considered as significant.

Discussion

Restenosis after PCI, which is mainly due to intimal hyperplasia, remains a significant clinical problem, such as in coronary artery bypass graft failure (21,37). Intimal hyperplasia is mainly caused by the proliferation and migration of VSMCs and excessive inflammation due to activated macrophages (25). Biodegradable Mg-based alloys, which have been reported to be promising candidates for cardiovascular stents, were shown to reduce neointima formation in vivo (18,38). In contrast, in vitro studies showed that Mg ions could promote the proliferation and migration of VSMCs (14). These seemingly contradictory results suggest the presence of complex regulatory effects on the phenotypic change in VSMCs induced by Mg-based alloys in vivo. This study aimed to elucidate the mechanisms underlying the seemingly contradictory results from in vivo and in vitro studies. We simulated the physiological environment using a macrophage-VSMC coculture system in vitro and demonstrated that JDBM extract could affect VSMC phenotypic switching, migration, and proliferation by macrophage-mediated immunoregulation, in which Mg ions play a vital role. Three major results were observed: (I) JDBM extracts and MgCl2 solutions significantly alleviated the inflammatory response induced by LPS in macrophages by reversing the polarization of proinflammatory M1 macrophages to an anti-inflammatory M2 phenotype; (II) JDBM extracts and MgCl2 solutions significantly decreased the expression of genes related to VSMC phenotypic switching, migration, and proliferation in macrophages; and (III) CMs derived from LPS-activated macrophages treated with JDBM extracts or MgCl2 solutions inhibited VSMC proliferation, migration, and phenotypic switching from a contractile phenotype to a proinflammatory phenotype ().

Figure 8

Schematic illustration of the potential mechanism underlying the effect of JDBM on vascular smooth muscle cells (VSMCs) through macrophage-mediated immunoregulation. Magnesium reverses the lipopolysaccharide (LPS)-induced polarization of M1-type macrophages to M2-type macrophages and inhibits the expression of genes related to VSMC phenotypic switching, migration, and proliferation in macrophages, further inhibiting the phenotypic switching, migration, and proliferation of VSMCs.

Increasing evidence has suggested the vital role of inflammation in the initiation and development of neointimal hyperplasia and subsequent restenosis (39). An upregulation in cell adhesion molecules (CAMs) is the initial event observed after PCI by recruiting leukocytes of monocyte and granulocyte lineage to the damaged vessel wall, followed by monocyte-derived macrophages invading the forming neointima and clustering around the stent struts (37). Other inflammatory cells, including T cells and neutrophils, have also been reported to be involved in the vascular response to injury and the development of neointimal hyperplasia (39,40). These inflammatory cells secrete various mitogens that play crucial roles in VSMC dedifferentiation, migration, and proliferation (39). Among the inflammatory cells mentioned above, the diversity and plasticity of macrophages play important roles in multiple biological processes after PCI, including tissue repair, inflammation, foreign body reaction, and restenosis (41). In this study, we showed that JDBM extracts were capable of inhibiting the inflammatory response in LPS-activated macrophages, as well as skewing M1/M2 polarization towards the anti-inflammatory M2 type. These results indicated that consistent with previous studies on biodegradable Mg-based alloys (15,32,38), JDBM had a significant biological effect on the modulation of macrophage function, which could further influence VSMC dedifferentiation, migration, and proliferation. Numerous signaling pathways have been demonstrated in previous studies to be involved in M2 macrophage polarization, including the NF-κB, JAK-STAT, Akt-p18-mTOR-LXR, and PTEN/PI3k/AKT pathways, among others (41-43). Of note, the transient receptor potential cation channel subfamily M member 7 (TRPM7), which is a predominant Mg2+ channel in mammalian cells, plays a pivotal role in regulating the functions of macrophages (44). Our previous studies reported that Mg from the degradation products of JDBM inhibited the inflammatory response of THP-1 cell-derived macrophages through the TRPM7-PI3K-AKT1 signaling axis.

Furthermore, Mg ions scavenged intracellular reactive oxygen species (ROS) to prevent the inflammatory response based on the LPS-induced activation of the TLR-4-MYD88-NF-κB/MAPK signaling pathway (29). However, up to now, studies on the regulation of macrophage polarization by Mg ions are still limited. Further studies, for instance, high-throughput multi-omic analyses, are still needed to reveal the underlying mechanism of Mg on macrophages.

In fact, the crosstalk between macrophages and VSMCs has been well documented in vascular disorders such as atherosclerosis, in-stent restenosis, and vein graft disease (45,46). Furthermore, there is an emerging understanding that there is an interaction between macrophages and VSMCs, and the macrophage secretion profile influences the VSMC phenotype (28,47). For example, PDGF-BB, which has been regarded as one of the most potent mitogens and chemoattractants for VSMCs, was reported to induce phenotypic switching, proliferation, migration, and MMP-2 upregulation in VSMCs (48,49). Morisaki et al. reported that macrophages modulate the phenotype of cultured rabbit aortic smooth muscle cells through the secretion of PDGF (50). A similar research group reported that PDGF suppressed the expression of the smooth muscle cell differentiation markers α-SMA, SM-MHC, and α-tropomyosin in vivo (51). Yang et al. reported that macrophage-derived MMP-8 determined smooth muscle cell differentiation from adventitial stem/progenitor cells and promoted neointimal hyperplasia (52). A recent study also showed that extracellular vesicles derived from macrophage foam cells could promote VSMC migration and adhesion (53). In addition, it was found that some miRNAs were also involved in the crosstalk between macrophages and VSMCs. MiR-195 could inhibit the proinflammatory profile of macrophages and impact crosstalk with smooth muscle cells (45). In this study, we reported that Mg-based JDBM extracts and MgCl2 solutions significantly decreased some macrophage-derived genes, which were reported to promote VSMC phenotypic switching, proliferation, and migration. These results could at least partly explain our later observation of the effect of the different CMs on the proliferation, migration, and polarization of VSMCs.

Our study also has some limitations. First, we used only cell lines and not confirmed in primary human cells because it is hard for us to obtain the primary human cells. Second, we used CM to establish a macrophage-VSMC coculture system in vitro to study the indirect role of Mg on VSMCs via macrophages. However, the microenvironment and intercellular interactions in vivo are quite complex; thus, the results from in vitro studies can only partly represent the physiological conditions in vivo. In addition, the molecular mechanism underlying the regulation of Mg on VSMCs via macrophages was not determined in this study, and further research will be done shortly.

Conclusions

In summary, in the present study, we provide novel insights into the mechanism by which Mg-based alloys function in preventing restenosis, namely, that Mg ion from the Mg-based alloys could influence VSMC phenotype through modulating macrophage functions. The protective effects of Mg-based alloys make them an exciting therapeutic prospect in further clinical applications of Mg-based vascular stents.

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