- Open Access
S100B is required for maintaining an intermediate state with double-positive Sca-1+ progenitor and vascular smooth muscle cells during neointimal formation
Stem Cell Research & Therapy volume 10, Article number: 294 (2019)
Accumulation of vascular smooth muscle cells (VSMCs) within the neointimal region is a hallmark of atherosclerosis and vessel injury. Evidence has shown that Sca-1-positive (Sca-1+) progenitor cells residing in the vascular adventitia play a crucial role in VSMC assemblages and intimal lesions. However, the underlying mechanisms, especially in the circumstances of vascular injury, remain unknown.
Methods and results
The neointimal formation model in rats was established by carotid artery balloon injury using a 2F-Forgaty catheter. Most Sca-1+ cells first appeared at the adventitia of the vascular wall. S100B expressions were highest within the adventitia on the first day after vessel injury. Along with the sequentially increasing trend of S100B expression in the intima, media, and adventitia, respectively, the numbers of Sca-1+ cells were prominently increased at the media or neointima during the time course of neointimal formation. Furthermore, the Sca-1+ cells were markedly increased in the tunica media on the third day of vessel injury, SDF-1α expressions were obviously increased, and SDF-1α levels and Sca-1+ cells were almost synchronously increased within the neointima on the seventh day of vessel injury. These effects could effectually be reversed by knockdown of S100B by shRNA, RAGE inhibitor (SPF-ZM1), or CXCR4 blocker (AMD3100), indicating that migration of Sca-1+ cells from the adventitia into the neointima was associated with S100B/RAGE and SDF-1α/CXCR4. More importantly, the intermediate state of double-positive Sca-1+ and α-SMA cells was first found in the neointima of injured arteries, which could be substantially abrogated by using shRNA for S100B or blockade of CXCR4. S100B dose-dependently regulated SDF-1α expressions in VSMCs by activating PI3K/AKT and NF-κB, which were markedly abolished by PI3K/AKT inhibitor wortmannin and enhanced by p65 blocker PDTC. Furthermore, S100B was involved in human umbilical cord-derived Sca-1+ progenitor cells’ differentiation into VSMCs, especially in maintaining the intermediate state of double-positive Sca-1+ and α-SMA.
S100B triggered neointimal formation in rat injured arteries by maintaining the intermediate state of double-positive Sca-1+ progenitor and VSMCs, which were associated with direct activation of RAGE by S100B and indirect induction of SDF-1α by activating PI3K/AKT and NF-κB.
Coronary artery disease (CAD) is mainly attributed to atherosclerosis and seriously threatens human health because of high morbidity and mortality . Accumulation of vascular smooth muscle cells (VSMCs) within the neointimal region is a hallmark of atherosclerosis and vessel injury . Published data have shown that adventitial (Adv) Sca-1-positive (Sca-1+) progenitor cells have multiple differentiation potential into VSMCs and likely contribute to intimal lesions in vivo . Percutaneous coronary intervention (PCI) is one of the most effective treatment options of CAD and is widely used . Despite this, it is still necessary to recognize VSMC assemblages and PCI postoperative restenosis to provide novel prophylactic and therapeutic drug targets for vascular diseases, especially CAD.
Sca-1+ progenitor cells reside in the inner side of the vascular adventitia; they originate neither from the bone marrow nor from the circulating cells based on genetic tracing and bone marrow transplantation [5,6,7]. Later studies reveal that Sca-1+ progenitor cells occur late during vascular development after the arterial media is fully formed, whereas VSMCs have already acquired a differentiated phenotype in the meantime [8, 9]. Differentiated VSMCs in the outer media can migrate into the inner adventitia and lose expression of VSMC markers, gain expression of progenitor cell markers, and contribute to a subpopulation of Sca-1+ progenitor cells [10, 11]. However, the underlying mechanisms, especially in the circumstances of vascular injury, remain unknown.
S100B, a member of the S100 multigenic family expressing small (9 kDa and 14 kDa) Ca2+-binding proteins of the EF-hand type, is mainly localized in astrocytes under normal physiological conditions . Previous evidence has suggested that S100B was involved in neointimal formation mediated by VSMC phenotypic transformation through interaction with receptor for advanced glycation end-products (RAGE) . Recent studies have shown that S100B induced migration and infiltration of inflammatory cells, leading to human diseases such as cerebral ischemic disease and muscular dystrophy [14, 15]. Of interest, S100B/RAGE have shown multiple roles in regulating stem cell function including proliferation, differentiation, and stemness under physiological and pathological conditions [16,17,18,19]. Thus, these results suggested a potential link between S100B and Sca-1+ cells in mediating neointimal formation.
Published data have shown that migration of stem cells into the intima plays a key role in neointimal formation [8,9,10,11]. Stromal cell-derived factor-1 α (SDF-lα), one of the crucial signal molecules and landmarks of cell migration, was actually involved in triggering migration of Sca-1+ progenitor cells into the neointima by activating its receptor CXCR4 in the process of neointimal formation after vessel damage . Considering the traits of common action of S100B and SDF-lα as inflammatory factors, S100B levels reached the peak at 2–6 h after tissue injury [21, 22], while SDF-lα expressions peaked 24 h after heart and vessel injury [23, 24], indicating that S100B could have a potential role in inducing SDF-lα expression in the injured vessels, and involving in the development of neointimal formation through SDF-lα signaling.
In this study, we found that Sca-1+ progenitor cells first increased in the inner adventitia of the vascular bed followed by in the neointima; S100B expression increased in a time-dependent manner in the sequence of adventitia, media, and neointima during neointimal formation. Furthermore, S100B could play a crucial role in maintaining the intermediate state with double-positive Sca-1+ progenitor cells and VSMCs during injury-induced neointimal formation, which was associated with RAGE and SDF-1/CXCR4 signaling.
According to the Guide for the Care and Use of Laboratory Animals (Chinese version), all animals were raised in specific-pathogen-free (SPF) grade animal laboratories. The model preparations of balloon-injured carotid artery in rats were approved by the Committee of Experimental Animals Care of Hubei University of Medicine.
The study was performed in strict adherence with the ethical guidelines for biomedical research involving human subjects in China and was approved by the Institutional Review Board of Shiyan Renmin Hospital, Hubei University of Medicine. Written informed consent was obtained from all participating individuals. Human umbilical cords were collected before disposal after babies were born in Shiyan Renmin Hospital.
Human umbilical cord mesenchymal stem cell isolation and culture
To isolate human umbilical cord mesenchymal stem cells (hUCMSCs), the media layer of fresh human umbilical cord was carefully removed; the adventitial tissues were collected and cut into 0.5-mm-thick pieces for culture on 10-cm plates in a CO2 incubator at 37 °C for 3 h before adding the stem cell growth medium . After 5–7 days of incubation, the migrated cells from the adventitial tissues were digested with 0.25% pancreatic enzymes and collected for purification. The ratio of Sca-1+ progenitor cells in hUCMSCs was evaluated by immunofluorescence assay of Sca-1.
Primary VSMCs were cultured from the aorta of Sprague–Dawley rats (280–300 g) as previously described . VSMCs were cultured and reached 60% confluence; the cells were transfected with Ad-Null, Ad-S100B, or Ad-sh100B for 24 h. The culture media were changed thereafter.
To detect the relationship between S100B and SDF-1α, the cells were transfected with Ad-S100B with different multiplication of infection (MOI) for 3 days.
For experiments on inhibition, VSMCs were transduced with Ad-Null, Ad-S100B, or Ad-sh100B followed by treatment with vehicle (CTL) or selective inhibitors of NF-κB (PDTC, 50 μM), PI3K (WM, wortmannin, 50 nM), MAP kinase (PD, PD98059, 50 μM), or p38 MAPK (SB, SB203580, 30 μM).
To observe the effects of S100B on Sca-1+ progenitor cell migration, conditioned medium (CM) was prepared from the VSMC cultures. Briefly, the corresponding CM of VSMCs was collected 3 days after transfecting with Ad-Null (CM-Ctrl) and Ad-S100B (CM-S100B) as previously described .
Carotid artery balloon injury model and adenoviral gene transfer
Carotid artery balloon injury model was performed as described previously  with a 2F-Forgaty catheter (CA92614-5686, Edwards Life sciences LLC Co.). The arterial segment from the proximal edge of the omohyoid muscle to the carotid bifurcation was washed with saline and incubated with 100 μl of saline or adenovirus expressing S100B shRNA (5 × 109 pfu) or AMD3100 (10 μM) via a fixed catheter for 20 min . Seven or 14 days later, the rats were euthanized with isoflurane, and the balloon-injured and adenovirus-dwelled segments were perfused with saline and collected for follow-up detection and analysis.
Common carotid artery segments were cut with serial sectioning to a thickness of 5 μm. Hematoxylin and eosin (H&E) staining was carried out for morphometric analyses. The images of five fields of view cross sections were randomly captured using a 80i Nikon microscope (Nikon, Inc). Using special software (Image-Pro Plus, Media Cybernetics), areas of the lumen, internal elastic lamina, and external elastic lamina were determined by two double-blinded pathologists, and the ratio of intimal and medial area (I/M) was calculated with following formula: I/M ratio (%) = [IEL area-lumen area]/[EEL area-IEL area] × 100 (%) .
After rehydration and antigen retrieval, artery sections in different time points were blocked with 5% goat serum and permeabilized with 0.01% Triton X-100 in PBS, and incubated with S100B (ab52642, Abcam) antibody at 4°C overnight followed by incubation with HRP-conjugated secondary antibody for immunochemistry staining. The sections were counterstained with hematoxylin. Using special software (Image-Pro Plus, Media Cybernetics), the gray value of the interest protein expression in the target area was extracted precisely, and mean gray value (MGV) is calculated. Ratio of the interest protein expression in target area analyzed with the following formula: the ratio = MGV in treatment group/MGV in control group × 100 (%).
To confirm the dynamic process of Sca-1+ progenitor cell migration from the adventitia to intima during the process of neointimal formation, the artery sections from different time points were incubated with Sca-1 (ab4336, Abcam) antibody followed by fluorescent dye-conjugated secondary antibody (Jackson ImmunoResearch) and counterstained with DAPI (Sigma) .
To detect SDF-1α expression in the VSMCs of injured vessels using co-immunofluorescent staining, the artery sections from different time points were incubated with α-SMA (sc-130616, Santa Cruz, 1:100) and SDF-1α (ab9797, Abcam, 1:100) antibodies followed by fluorescent dye-conjugated secondary antibody and counterstained with DAPI.
To observe the intermediate state of double-positive Sca-1+ progenitor and VSMCs using co-immunofluorescent staining of Sca-1 and α-SMA, the artery sections were incubated 7 or 14 days after treatment with Ad-shS100bB or AMD 3100; subsequently, corresponding fluorescent dye-conjugated secondary antibody was used, and the tissues were counterstained with DAPI.
To observe the expression of RAGE and CXCR4 in Sca-1+ progenitor cells 7 days after the vessels were injured in vivo, the sections were rinsed with PBS and fixed with 4% paraformaldehyde, then blocked with 5% goat serum, permeabilized with 0.01% Triton X-100 in PBS, and incubated with anti-Sca-1 (ab4336, Abcam), anti-RAGE (ab54741, Abcam), and anti-CXCR4 (ab124824, Abcam) followed by TRITC-conjugated secondary antibody (Jackson ImmunoResearch) and counterstained with DAPI.
To observe the expression of RAGE and CXCR4 in Sca-1+ progenitor cells in vitro, Sca-1+ stem cells cultured on coverslips were rinsed with PBS and fixed with 4% paraformaldehyde, then blocked with 5% goat serum, permeabilized with 0.01% Triton X-100 in PBS, and incubated with anti-Sca-1, anti-RAGE, and anti-CXCR4 followed by TRITC-conjugated secondary antibody and counterstained with DAPI.
The images of five fields of view cross sections were randomly captured using a 80i Nikon fluorescence microscope (Nikon, Inc). Using Image-Pro Plus software (Media Cybernetics), the fluorescence intensity value of the interest gene expression within the target area is precisely extracted, and mean fluorescence intensity value (MFI) is calculated. Ratio of the interest protein expression in target area was analyzed with the following formula: the ratio = MFI in treatment group/MFI in control group × 100 (%).
Nuclear translocation analysis
To confirm if the effects of Ad-S100B on SDF-1α expression involved the activation of NF-kBp65 and p52, the nuclear translocation of NF-kBp65 and p52 was analyzed in VSMCs exposed to Ad-S100B. The cells cultured on coverslips were rinsed with PBS and fixed with 4% paraformaldehyde, then blocked with 5% goat serum, permeabilized with 0.01% Triton X-100 in PBS, and incubated with anti-NF-kBp65 (sc-109, 1:250, Santa Cruz) and anti-NF-kBp52 (sc-7386, 1:250, Santa Cruz) antibodies, followed by TRITC or FITC-conjugated secondary antibody (Jackson ImmunoResearch) and counterstained with DAPI.
Cells samples were then mingled with RIPA buffer containing protease inhibitor mix for extracting total proteins. Protein concentration was measured using the BCA Protein Assay Kit. Briefly, 20-μg protein samples were separated on 4–12% SDS-polyacrylamide gels and electro-transferred onto PVDF membranes (Bio-Rad). The membranes were incubated at 4 °C overnight with antibodies against S100B (ab52642,1: 500, Abcam); SDF-1α (ab9797, 1:500, Abcam) or AKT (#9272 s, 1:500, Cell Signaling); pAKT (#4058 s, 1:500, Cell Signaling); extracellular signal-regulated kinase (ERK1/2, SC-94, SC-154, 1:500, Cell Signaling); pERK1/2 (4370 s, 1:500, Cell Signaling); mitogen-activated protein kinase (p38MAPK, #9211, 1:500, Cell Signaling); p-p38MAPK (SC-7973, 1:500, Cell Signaling); or α-Tubulin (T6074, Sigma) in blocking buffer containing 5% milk followed by incubation with HRP-conjugated secondary antibody (Sigma).
Transwell invasion assays
To determine the functions of S100B and SDF-1α in regulating Sca-1+ progenitor stem cell migration, CM-Ctrl or CM-Ad-S100B were used to explore the cells’ migration using the transwell system with or without neutralizing antibodies, namely S100B, RAGE inhibitor SPF-ZM1, or AMD3100. After 48-h incubation, cells were fixed with 100% methanol and stained with crystal violet (0.1%). The cells within the upper membranes were removed, and those within the bottom membranes were imaged under a light microscope and mounted for quantitative analysis. Images of three different fields of view of each of the transwell membrane were acquired with an optical microscope under × 10 magnifications. Each of the three independent experiments was repeated in triplicate. Migration indexes were calculated as follows: treatment group cells number/control group cells number.
All data were expressed as mean ± SD and then evaluated with two-tailed, unpaired Student’s t test or compared by one-way ANOVA followed by the t test. P < 0.05 was considered to indicate statistical significance.
Sca-1+ progenitor cell migration and S100B expression during balloon injury-induced neointimal formation
To explore the relationship between Sca-1+ progenitor cell migration and S100B expression during injury-induced neointimal formation, we detected the expressions of Sca-1 and S100B in balloon-injured carotid artery by immunohistochemical staining. As shown in Fig. 1a–c, accompanied by the progressive increase of neointimal formation in the injured artery, S100B expressions were gradually induced in a time-dependent manner and showed increased expression in the sequence of adventitia, media, and neointima. Indeed, compared with the sham group, the increased S100B expressions were first found in the artery on day 1 after the injury. Within the injured artery, the S100B expressions were greater at the adventitia of the vessel wall than at the media on the first day after injury (Fig. 1d, e). By contrast, S100B levels at the adventitia were lower than at the media or neointima 14 days after injury (Fig. 1d, e).
Importantly, following the changed characteristics of S100B in the injured artery, the numbers of Sca-1+ progenitor cells gradually increased at the adventitia of the vessel wall in a time-dependent manner and peaked on the seventh day after the injury. Sca-1+ progenitor cells appeared on the first day of injury at the vascular wall media and then gradually increased and reached peak levels on the seventh day after injury. Notably, Sca-1+ progenitor cells in the intima or neointima were not observed at least 3 days after the injury, markedly increased on the seventh day, and peaked 14 days after the injury (Fig. 1f–j and Additional file 1: Figure S1). These results indicated that Sca-1+ progenitor cells showed increased traits in the sequence of adventitia, media, and neointima.
Combining the results of S100B and Sca-1+ progenitor cells, the appearance of Sca-1+ progenitor cells at the adventitia, media, and neointima of the vessel wall were associated with S100B expressions.
S100B promoted Sca-1+ progenitor cell migration into neointima via RAGE
To confirm whether S100B was involved in the process of Sca-1+ progenitor cell migration into the neointima, the number of Sca-1+ progenitor cells in the media and neointima were assessed after local application of Ad-shS100B within the balloon-injured carotid artery. As shown in Fig. 2a, b, the numbers of Sca-1+ progenitor cells in Ad-shS100B-treated arteries were prominently decreased not only at the vascular wall media but also at the neointima, as compared with Ad-Null-treated arteries, indicating that S100B participated in the course of Sca-1+ progenitor cell migration into the neointima. Meanwhile, the I/M ratios were lower in Ad-shS100B-treated arteries than Ad-Null-treated arteries (Fig. 2c). These results proved that S100B could trigger neointimal formation by inducing Sca-1+ progenitor cell migration into the neointima.
Given that S100B is a ligand for RAGE, we tested whether released S100B in VSMCs promoted Sca-1+ progenitor cell migration through its receptor RAGE. As seen in Fig. 2d, e and Additional file 1: Figure S1, Sca-1+ progenitor cells expressed RAGE and the migratory response of Sca-1+ progenitor cells to CM of VSMCs treated with Ad-S100B (CM-AdS100B) were substantially increased. The migration action of Sca-1+ progenitor cells mediated by CM-AdS100B was evidently abrogated by FPS-ZM1 (RAGE inhibitor) or neutralizing antibody of S100B, thereby indicating that S100B could induce Sca-1+ progenitor cell migration through RAGE.
Taken together, S100B could trigger neointimal formation by inducing Sca-1+ progenitor cell migration into the neointima through RAGE.
S100B maintains an intermediate state of double-positive Sca-1+ progenitor cells and VSMCs
We determined how S100B was involved in neointimal formation, apart from promoting Sca-1+ progenitor cell migration into the vessel neointima. Double immunofluorescence staining of Sca-1 and α-SMA in the artery showed that Sca-1+ progenitor cells did not express α-SMA at the vascular adventitia (Fig. 3a–c). A few Sca-1+ progenitor cells were positive for α-SMA at the tunica media. Of interest, most Sca-1+ progenitor cells in the neointima of injured arteries acquired the phenotype of α-SMA. By contrast, Sca-1+ progenitor cells in the neointima of Ad-shS100B-treated arteries lost the phenotype of Sca-1 while acquiring a stronger phenotype of α-SMA (Fig. 3a–c, Additional file 1: Figure S2). Furthermore, the I/M ratios were obviously reduced in Ad-shS100B-treated arteries (Additional file 1: Figure S3). These results proved that an intermediate state of double-positive Sca-1+ progenitor cells and α-SMA in the injured arteries was essential for neointimal development, which was associated with S100B.
Meanwhile, Sca-1+ progenitor cells from the adventitia of the umbilical cord showed spontaneous differentiation potential into VSMCs with positive α-SMA (Fig. 3D, E), and the effect was obviously enhanced by overexpression of S100B. More importantly, the enhanced differentiation potential by Ad-S100B was clearly canceled by the RAGE inhibitor, SPF-ZM1.
Hence, increased S100B expression is necessary in the development of neointimal formation for maintaining the intermediate state of double-positive Sca-1+ progenitor cells and VSMCs.
S100B and SDF-1α expression during balloon injury-induced neointimal formation
SDF-1α/CXCR4 plays crucial roles in controlling stem cell migration . We explored whether S100B-induced Sca-1+ progenitor cell migration into the vessel neointima involved SDF-1α/CXCR4. As shown in Fig. 4a–d, following the changed characteristics of S100B in the injured artery, SDF-1α expressions were gradually increased at the vessel wall adventitia in a time-dependent manner and peaked on the third day after injury. SDF-1α expressions were slightly increased on the first day of injury at the vascular wall media and then gradually increased and reached peak levels 14 days after the injury. Of note, SDF-1α expressions in the intima or neointima were not found at least 3 days after injury, markedly increased on the seventh day, and peaked on day 14 after the injury (Fig. 4a–c).
To observe the relationship of S100B and SDF-1α in VSMCs, Ad-S100B was used for transfection into VSMCs with different MOIs. As shown in Fig. 4d, e, S100B induced the expression of SDF-1α in VSMCs in an MOI-dependent manner, reaching peak values at 50 MOI.
Combining the results of S100B and Sca-1+ progenitor cells (Figs. 1 and 2), SDF-1α could participate in the process of S100B-mediated Sca-1+ progenitor cell migration into the neointima upon arterial injury.
S100B knockdown reduced Sca-1+ progenitor cell migration into the neointima through SDF-1α/CXCR4
SDF-1α can trigger cell migration through CXCR4 . To confirm whether S100B was involved in CXCR4 in Sca-1+ progenitor cells, we used immunofluorescence staining (Fig. 5a) and found that Sca-1+ progenitor cells in the vascular adventitia expressed CXCR4. Considering the evidence of S100B-induced SDF-1α in VSMCs (Fig. 2), we found that knockdown of S100B by shRNA in the injured arteries reduced SDF-1α levels in the VSMCs of the vessel wall neointima and media (Fig. 5b–d). More importantly, when the injured arteries were treated with AMD3100, the numbers of Sca-1+ progenitor cells were dramatically reduced in the vascular wall media and neointima (Fig. 5e, f). Finally, to further corroborate whether CXCR4 in Sca-1+ progenitor cells referred to released SDF-1α-mediated cell migration by S100B, Sca-1+ progenitor cells from human umbilical cord adventitia were cultured and showed traits of CXCR4 expression (Fig. 5g). Furthermore, the migratory response of Sca-1 progenitor cells to CM of VSMCs treated with Ad-S100B (CM-AdS100B) was evidently abrogated by CXCR4 blocker, AMD3100, thereby indicating that released SDF-1α by S100B induced Sca-1+ progenitor cell migration through CXCR4 (Fig. 5h).
Thus, the process of S100B-mediated Sca-1+ progenitor cell migration into the neointima of injured arteries involved SDF-1α/CXCR4.
S100B maintains the intermediate state of double-positive Sca-1+ progenitor cells and VSMCs through SDF-1α/CXCR4
Considering the special role of S100B in maintaining the intermediate state of double-positive Sca-1+ progenitor cells and VSMCs, it was necessary to assess the involvement of S100B-mediated SDF-1α/CXCR4 activation. Double immunofluorescence staining of Sca-1+ and α-SMA in the artery showed that Sca-1+ progenitor cells showed very faint expression of α-SMA at the vascular adventitia of injured arteries (Fig. 6a), but almost acquired phenotype of α-SMA in the AMD3100 group (Fig. 6b). Interestingly, a few Sca-1+ progenitor cells in the vehicle group were present and showed α-SMA expression at the tunica media. However, there were very few Sca-1+ progenitor cells in the AMD3100 group that simultaneously expressed α-SMA. More importantly, most Sca-1+ progenitor cells in the neointima of the vehicle groups acquired the α-SMA phenotype. By contrast, cells in the neointima of AMD3100-treated arteries lost the Sca-1+ phenotype and acquired stronger α-SMA phenotype because of less Sca-1+ progenitor cells and more α-SMA+ cells (Fig. 6a–d, Additional file 1: Figure S4). Furthermore, the I/M ratios in AMD3100-treated arteries were obviously reduced (Additional file 1: Figure S5). These results showed that the maintained intermediate state of double-positive Sca-1+ progenitor cells and VSMCs by S100B at least partly involved SDF-1α/CXCR4.
S100B induced SDF-1α expression in VSMCs through NF-kB signaling
To further determine how S100B regulated SDF-1α expression in VSMCs, multiple signaling pathways were detected in S100B-overexpressingVSMCs. As shown in Fig. 7a and Additional file 1: Figure S6, overexpression of S100B did not change the total levels of ERK1/2 and Akt, but increased pAkt, pERK1/2, and pp38MAPK levels. Meanwhile, S100B-induced SDF-1α expression in VSMCs could not be abolished by ERK1/2 inhibitor PD98059 or p38MAPK inhibitor SB203580 but was eliminated by PI3K/Akt inhibitor wortmannin. Notably, SDF-1α expression mediated by S100B in VSMCs could be enhanced by NF-κB blocker PDTC (Fig. 7b, c). Indeed, S100B activated NF-κB p65 and p52 by promoting nuclear translocation of p65 and p52. As shown in Fig. 7d, overexpression of S100B induced p52 nuclear translocation; these specific effects could obviously be abolished by wortmannin and enhanced by PDTC. These results proved that NF-kB and PI3K/Akt signal pathways referred to S100B-induced SDF-1α expression in VSMCs.
To our best knowledge, this study presented three novel findings. First, S100B triggered adventitia Sca-1+ progenitor cell migration into neointimal and accelerated neointimal formation through binding into RAGE. Secondly, SDF-1α induced by S100B in VSMC promoted Sca-1+ progenitor cell migration through activating CXCR4. And lastly, for the first time, S100B maintained the intermediate state of double positive of Sca-1+ progenitor cells and VSMCs through activating RAGE and/or SDF-1α/CXCR4, which were associated with PI3K/Akt and NF-kB signaling pathways.
Published data have shown that the mobilization and recruitment of abundant Sca-1+ progenitor cells from the adventitia and media of vascular walls were mainly responsible for intimal VSMC accumulation during vascular remodeling such as intimal hyperplasia and arterial sclerosis [5, 6, 8, 30,31,32,33,34]. Herein, our study showed that Sca-1+ progenitor cells not only existed in the adventitia and media but also migrated to the intima during vascular injury and participate in the formation of neointima. Furthermore, we reported for the first time to our best knowledge that Sca-1+ progenitor cells existed within the adventitia and media on the first day after vessel injury; there were more Sca-1+ progenitor cells at the adventitia than at the media on the third day of vessel injury, and peaked at the neointima on the seventh day of vessel injury, indicating that adventitial Sca-1+ progenitor cells in damaged vessels migrate in a time-dependent manner into the intima and were involved in the process of neointimal formation.
The roles of S100B/RAGE in stem cell proliferation and differentiation have been previously observed [16,17,18,19, 35]. Our previous study showed that S100B/RAGE participated in neointimal formation as a result of induced VSMC accumulation . The present study provided new evidence that S100B expression was greatest at the adventitia on the first day after vessel injury; S100B levels gradually increased from the media to the neointima in a time-dependent manner after vascular injury. Moreover, along with the increasing trend of S100B expression in the sequence of the three vascular layers, the numbers of Sca-1+ progenitor cells were prominently increased at the adventitia, media, or neointima during the time course of neointimal formation. By contrast, knockdown of S100B by shRNA obviously decreased the numbers of Sca-1+ progenitor cells within the neointima in vivo, and the RAGE blocker markedly eliminated its migration induced by CM treated with Ad-S100B in vitro. These results suggested that S100B could directly trigger Sca-1+ progenitor cell migration and neointimal formation by activating RAGE.
In addition to the gradually increased trends of S100B, our results have shown that SDF-1α expressions increased gradually in the injured vessels, and SDF-1α was later S100B at the adventitia, consistent with previous studies that serum S100B reached its peak before SDF-lα in case of cardiac and neuronal injuries [21,22,23,24]. Subsequently, SDF-1α expressions were not only increased within the media or neointima, accompanied by in vivo increase of S100B, but the VSMCs also showed a gradual increase of SDF-lα levels with increased MOI Ad-S100B in vitro. More importantly, local application of Ad-shS100B in the injured vessels significantly reduced SDF-lα expression in the neointima. Furthermore, NF-κB p65 inhibitor PDTC enhanced the expression of S100B-induced SDF-1α in VSMCs, which was different from the role of activated NF-κB p65 by RAGE in inducing SDF-1α expression in the diabetic kidney . NF-κBp52 activation requires Akt-mediated phosphorylation and nuclear translocation [37,38,39,40], which was consistent with our results in that blockade of Akt using wortmannin could completely abolish S100B-induced SDF-1α expression. These results indicated that S100B was a likely inducer of SDF-lα, which could be related to Akt-NF-κBp65-p52 signaling.
The SDF-1α/CXCR4 axis played a crucial role in neointimal formation through activating Sca-1+ progenitor cells [41, 42]. Our results further showed that the knockdown of S100B by shRNA not only reduced the levels of SDF-lα in injured vessels but also decreased the numbers of Sca-1+ progenitor cells at the neointima, leading to inhibition of its formation. Furthermore, AMD3100, as a CXCR4 inhibitor, also reduced cell numbers and neointimal area in vivo and partially abrogated its migration induced by CM treated with Ad-S100B in vitro. In short, these results demonstrated that S100B could indirectly induce Sca-1+ progenitor cell migration and neointimal formation by manipulating the SDF-1α/CXCR4 axis.
Interestingly, VSMCs in the vessel wall were mostly quiescent but could exhibit a contractile phenotype in adults. Under pathophysiological conditions such as vascular injury, contractile VSMCs presented in the media switched to a proliferative phenotype that could facilitate their ability to migrate to the intima and proliferate to contribute to neointimal formation. Considering the heterogeneity of VSMCs [2, 43], a recent unique phenomenon was noted wherein differentiated VSMCs in the outer media could migrate into the inner adventitia and acquire Sca-1 expression, as one of the progenitor cell markers [10, 11], while simultaneously losing the VSMC phenotype; this provided novel evidence for involvement of a small VSMC subpopulation in neointimal formation, apart from the VSMC phenotype switch. However, the origin and differentiation of VSMCs from Sca-1+ progenitor cells during cardiovascular development and in adults have been identified in the vascular wall adventitia and media . Regardless of the differences in the abovementioned views, unique features of the intermediate state with double-positive Sca-1+ progenitor cells and VSMCs could play an important role in maintaining and promoting neointimal formation after vessel injury. Indeed, previous studies have shown that acquiring and maintaining the intermediate state were required during stem cell differentiation [22,23,24]. The present study not only identified the intermediate state of Sca-1 and α-SMA in the injured artery but also the involvement of S100B in acquiring and maintaining the intermediate state. In line with the role of S100B in regulating stemness of ovarian cancer stem-like cells [45, 46], when knocking down S100B, Sca-1+ progenitor cells within the media and neointimal lost the progenitor cell traits and acquired more contractile phenotypes of VSMCs including α-SMA, leading to the reduction of neointimal area and thickness. Furthermore, S100B-induced SDF-1α referred to preservation of the intermediate state, and the specific effects could be in part abrogated by AMD3100, which was similar to the role of AMD3100 in promoting differentiation of stem cells into cardiomyocytes [47,48,49].
Increased Sca-1+ progenitor cells gradually appeared in the sequence of adventitia, media, and neointima after vessel injury, accompanied by induced S100B expressions in the corresponding vessel wall locations during the process of neointimal formation. Furthermore, S100B triggered neointimal formation in the injured arteries by maintaining an intermediate state of double-positive stem cells and VSMCs that was associated with RAGE and/or SDF-1α/CXCR4 (Fig. 8).
Availability of data and materials
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Protein kinase B
Coronary artery disease
C-X-C motif chemokine receptor 4
Extracellular signal-regulated kinase1/2
Human umbilical cord mesenchymal stem cells
Mitogen-activated protein kinase
Multiplication of infection
Nuclear Factor Kappa-B
Percutaneous coronary intervention
Receptor for advanced glycation end products
S100 calcium-binding protein B
Stem cell antigen-1
Stromal cell-derived factor 1 alpha
Vascular smooth muscle cell
Alpha smooth muscle actin
Lim GB. Coronary artery disease: interventional narrowing of the coronary sinus in refractory angina. Nat Rev Cardiol. 2015;12(4):196.
Bennett MR, Sinha S, Owens GK. Vascular smooth muscle cells in atherosclerosis. Circ Res. 2016;118(4):692–702.
Kokkinopoulos I, Wong MM, Potter CMF, Xie Y, Yu B, Warren DT, Nowak WN, Le Bras A, Ni Z, Zhou C, Ruan X, Karamariti E, Hu Y, Zhang L, Xu Q. Adventitial SCA-1+ progenitor cell gene sequencing reveals the mechanisms of cell migration in response to hyperlipidemia. Stem Cell Reports. 2017;9(2):681–96.
Al-Lamee RK, Nowbar AN, Francis DP. Percutaneous coronary intervention for stable coronary artery disease. Heart. 2019;105(1):11–9.
Hu Y, Zhang Z, Torsney E, Afzal AR, Davison F, Metzler B, Xu Q. Abundant progenitor cells in the adventitia contribute to atherosclerosis of vein grafts in ApoE-deficient mice. J Clin Invest. 2004;113(9):1258–65.
Psaltis PJ, Harbuzariu A, Delacroix S, Witt TA, Holroyd EW, Spoon DB, Hoffman SJ, Pan S, Kleppe LS, Mueske CS, Gulati R, Sandhu GS, Simari RD. Identification of a monocyte-predisposed hierarchy of hematopoietic progenitor cells in the adventitia of postnatal murine aorta. Circulation. 2012;125(4):592–603.
Chen Y, Wong MM, Campagnolo P, Simpson R, Winkler B, Margariti A, Hu Y, Xu Q. Adventitial stem cells in vein grafts display multilineage potential that contributes to neointimal formation. Arterioscler Thromb Vasc Biol. 2013;33(8):1844–51.
Psaltis PJ, Puranik AS, Spoon DB, Chue CD, Hoffman SJ, Witt TA, Delacroix S, Kleppe LS, Mueske CS, Pan S, Gulati R, Simari RD. Characterization of a resident population of adventitial macrophage progenitor cells in postnatal vasculature. Circ Res. 2014;115(3):364–75.
Xie Y, Potter CMF, Le Bras A, Nowak WN, Gu W, Bhaloo SI, Zhang Z, Hu Y, Zhang L, Xu Q. Leptin induces Sca-1(+) progenitor cell migration enhancing neointimal lesions in vessel-injury mouse models. Arterioscler Thromb Vasc Biol. 2017;37(11):2114–27.
Chappell J, Harman JL, Narasimhan VM, Yu H, Foote K, Simons BD, Bennett MR, JørgensenHF. Extensive proliferation of a subset of differentiated, yet plastic, medial vascular smooth muscle cells contributes to neointimal formation in mouse injury and atherosclerosis models. Circ Res 2016; 119(12):1313–1323.
Majesky MW, Horita H, Ostriker A, Lu S, Regan JN, Bagchi A, Dong XR, Poczobutt J, Nemenoff RA, Weiser-Evans MC. Differentiated smooth muscle cells generate a subpopulation of resident vascular progenitor cells in the adventitia regulated by Klf4. Circ Res. 2017;120(2):296–311.
Donato R, Sorci G, Riuzzi F, Arcuri C, Bianchi R, Brozzi F, Tubaro C, Giambanco I. S100B’s double life: intracellular regulator and extracellular signal. Biochim Biophys Acta. 2009;1793(6):1008–22.
Cao T, Zhang L, Yao LL, Zheng F, Wang L, Yang JY, Guo LY, Li XY, Yan YW, Pan YM, Jiang M, Chen L, Tang JM, Chen SY, Wang JN. S100B promotes injury-induced vascular remodeling through modulating smooth muscle phenotype. Biochim Biophys Acta Mol Basis Dis. 2017;1863(11):2772–82.
Zhou S, Zhu W, Zhang Y, Pan S, Bao J. S100B promotes microglia M1 polarizationand migration to aggravate cerebral ischemia. Inflamm Res. 2018;67(11–12):937–49.
Sagheddu R, Chiappalupi S, Salvadori L, Riuzzi F, Donato R, Sorci G. Targeting RAGE as a potential therapeutic approach to Duchenne muscular dystrophy. Hum Mol Genet. 2018;27(21):3734–46.
Yang T, Cheng J, Yang Y, Qi W, Zhao Y, Long H, Xie R, Zhu B. S100B mediates stemness of ovarian cancer stem-like cells through inhibiting p53.Stem Cells 2017; 35(2):325–336.
Li D, Li K, Chen G, Xia J, Yang T, Cai P, Yao C, Yang Y, Yan S, Zhang R, Chen H. S100B suppresses the differentiation of C3H/10T1/2 murine embryonic mesenchymal cells into osteoblasts. Mol Med Rep. 2016;14(4):3878–86.
Tan B, Shen L, Yang K, Huang D, Li X, Li Y, Zhao L, Chen J, Yi Q, Xu H, Tian J, Zhu J. C6 glioma-conditioned medium induces malignant transformation of mesenchymal stem cells: possible role of S100B/RAGE pathway. Biochem Biophys Res Commun 2018; 495(1):78–85.
Tubaro C, Arcuri C, Giambanco I, Donato R. S100B protein in myoblasts modulates myogenic differentiation via NF-kappaB-dependent inhibition of MyoD expression. J Cell Physiol 2010; 223(1):270–282.
Akhtar S, Gremse F, Kiessling F, Weber C, Schober A. CXCL12 promotes the stabilization of atherosclerotic lesions mediated by smooth muscle progenitor cells in Apoe-deficient mice. Arterioscler ThrombVasc Biol. 2013;33(4):679–86.
Tanaka Y, Marumo T, Shibuta H, et al. Serum S100B, brain edema, and hematoma formation in a rat model of collagenase-induced hemorrhagic stroke. Brain Res Bull, 2009, 78(4–5):0–163.
Bozkurt A, Yardan T, Ciftcioglu E, et al. Time course of serum S100B protein and neuron-specific enolase levels of a single dose of chlorpyrifos in rats. Basic Clin. Pharmacol. Toxicol. 2010;107(5):893–8.
Ma J, Ge J, Zhang S, Sun A, Shen J, Chen L, Wang K, Zou Y. Time course of myocardial stromal cell-derived factor 1 expression and beneficial effects of intravenously administered bone marrow stem cells in rats with experimental myocardial infarction. Basic Res Cardiol. 2005;100(3):217–23.
Schober A, Knarren S, Lietz M, Lin EA, Weber C. Crucial role of stromal cell-derived factor-1alpha in neointima formation after vascular injury in apolipoprotein E-deficient mice. Circulation. 2003;108(20):2491–7.
Santos Nascimento D, Mosqueira D, Sousa LM, Teixeira M, Filipe M, Resende TP, Araújo AF, Valente M, Almeida J, Martins JP, Santos JM, Bárcia RN, Cruz P, Cruz H, Pinto-do-Ó P. Human umbilical cord tissue-derived mesenchymal stromal cells attenuate remodeling after myocardial infarction by proangiogenic, antiapoptotic, and endogenous cell-activation mechanisms. Stem Cell Res Ther. 2014;5(1):5.
Nagasawa T. CXC chemokine ligand 12 (CXCL12) and its receptor CXCR4. J Mol Med (Berl). 2014;92(5):433–9.
Lamfers ML, Lardenoye JH, de Vries MR, Aalders MC, Engelse MA, Grimbergen JM, van Hinsbergh VW, Quax PH. In vivo suppression of restenosis in balloon-injured rat carotid artery by adenovirus-mediated gene transfer of the cell surface-directed plasmin inhibitor ATF.BPTI. Gene Ther. 2001;8(7):534–41.
Chen SJ, Yue J, Zhang JX, Jiang M, Hu TQ, Leng WD, Xiang L, Li XY, Zhang L, Zheng F, Yuan Y, Guo LY, Pan YM, Yan YW, Wang JN, Chen SY, Tang JM. Continuous exposure of isoprenaline inhibits myoblast differentiation and fusion through PKA/ERK1/2-FOXO1 signaling pathway. Stem Cell Res Ther. 2019;10(1):70.
Kawaguchi N, Zhang TT, Nakanishi T. Involvement of CXCR4 in Normal and Abnormal Development. Cells. 2019;8(2).
Zengin E, Chalajour F, Gehling UM, Ito WD, Treede H, Lauke H, Weil J, Reichenspurner H, Kilic N, Ergün S. Vascular wall resident progenitor cells: a source for postnatal vasculogenesis. Development. 2006;133(8):1543–51.
Cho HJ, Cho HJ, Lee HJ, Song MK, Seo JY, Bae YH, Kim JY, Lee HY, Lee W, Koo BK, Oh BH, Park YB, Kim HS. Vascular calcifying progenitor cells possess bidirectional differentiation potentials. PLoS Biol. 2013;11(4):e1001534.
Sainz J, Al Haj Zen A, Caligiuri G, Demerens C, Urbain D, Lemitre M, Lafont A. Isolation of “side population” progenitor cells from healthy arteries of adult mice. Arterioscler Thromb Vasc Biol. 2006;26(2):281–6.
Tang Z, Wang A, Yuan F, Yan Z, Liu B, Chu JS, Helms JA, Li S. Differentiation of multipotent vascular stem cells contributes to vascular diseases. Nat Commun. 2012;3:875.
Yu B, Wong MM, Potter CM, Simpson RM, Karamariti E, Zhang Z, Zeng L, Warren D, Hu Y, Wang W, Xu Q. Vascular stem/progenitor cell migration induced by smooth muscle cell-derived chemokine (C-C motif) ligand 2 and chemokine (C-X-C motif) ligand 1 contributes to neointima formation. Stem Cells. 2016;34(9):2368–80.
Meng X, Chen M, Su W, Tao X, Sun M, Zou X, Ying R, Wei W, Wang B. The differentiation of mesenchymal stem cells to vascular cells regulated by the HMGB1/RAGE axis: its application in cell therapy for transplant arteriosclerosis. Stem Cell Res Ther. 2018;9(1):85.
Sanajou D, GhorbaniHaghjo A, Argani H, Roshangar L, Ahmad SNS, Jigheh ZA, Aslani S, Panah F, Rashedi J, Mesgari Abbasi M. FPS-ZM1 and valsartan combinationprotects better against glomerular filtration barrier damage instreptozotocin-induced diabetic rats. J Physiol Biochem. 2018;74(3):467–78.
Jayasooriya RG, Lee KT, Kang CH, Dilshara MG, Lee HJ, Choi YH, Choi IW, Kim GY. Isobutyrylshikonin inhibits lipopolysaccharide-induced nitric oxide and prostaglandin E2 production in BV2 microglial cells by suppressing the PI3K/Akt-mediated nuclear transcription factor-κB pathway. Nutr Res. 2014;34(12):1111–9.
Lin YW, Lee LM, Lee WJ, Chu CY, Tan P, Yang YC, Chen WY, Yang SF, Hsiao M, Chien MH. Melatonin inhibits MMP-9 transactivation and renal cell carcinoma metastasis by suppressing Akt-MAPKs pathway and NF-κB DNA-binding activity. J Pineal Res. 2016;60(3):277–90.
Caporali S, Levati L, Graziani G, Muzi A, Atzori MG, Bonmassar E, Palmieri G, Ascierto PA, D'Atri S. NF-κB is activated in response to temozolomide in an AKT-dependent manner and confers protection against the growth suppressive effect of the drug. J Transl Med. 2012;10:252.
Madrid LV, Mayo MW, Reuther JY, Baldwin AS Jr. Akt stimulates the transactivation potential of the RelA/p65 subunit of NF-kappa B through utilization of the Ikappa B kinase and activation of the mitogen-activated protein kinase p38. J Biol Chem. 2001;276(22):18934–40.
Hu A, Huang J, Li S, Gao Y, Wu L, Deng J, Liu J, Gong Q, Li L, Xu S. Involvement of stromal cell-derived factor-1α (SDF-1α), stem cell factor (SCF), fractalkine (FKN) and VEGF in TSG protection against intimal hyperplasia in rat balloon injury. Biomed Pharmacother. 2019;110:887–894.
Zernecke A, Schober A, Bot I, von Hundelshausen P, Liehn EA, Möpps B, Mericskay M, Gierschik P, Biessen EA, Weber C. SDF-1alpha/CXCR4 axis is instrumental in neointimal hyperplasia and recruitment of smooth muscle progenitor cells. Circ Res. 2005;96(7):784–91.
Komatsu S, Kitazawa T, Ikebe M. Visualization of stimulus-specific heterogeneous activation of individual vascular smooth muscle cells in aortic tissues. J Cell Physiol. 2018;233(1):434–46.
Wang G, Jacquet L, Karamariti E, Xu Q. Origin and differentiation of vascular smooth muscle cells. J Physiol. 2015;593(14):3013–30.
Riuzzi F, Sorci G, Donato R. S100B protein regulates myoblast proliferation and differentiation by activating FGFR1 in a bFGF-dependent manner. J Cell Sci. 2011;124(Pt14):2389–400.
Shim JH, Lee TR, Shin DW. Novel in vitro culture condition improves the stemness of human dermal stem/progenitor cells. Mol Cells. 2013;36(6):556–63.
Hatzistergos KE, Saur D, Seidler B, Balkan W, Breton M, Valasaki K, Takeuchi LM, Landin AM, Khan A, Hare JM. Stimulatory effects of mesenchymal stem cells on cKit+ cardiac stem cells are mediated by SDF1/CXCR4 and SCF/cKit signaling pathways. Circ Res. 2016;119(8):921–30.
Chen M, Xie HQ, Deng L, Li XQ, Wang Y, Zhi W, Yang ZM. Stromal cell-derived factor-1 promotes bone marrow-derived cells differentiation to cardiomyocyte phenotypes in vitro. Cell Prolif. 2008;41(2):336–47.
Tang JM, Wang JN, Zhang L, Zheng F, Yang JY, Kong X, Guo LY, Chen L, Huang YZ, Wan Y, Chen SY. VEGF/SDF-1 promotes cardiac stem cell mobilization and myocardial repair in the infarcted heart. Cardiovasc Res. 2011;91(3):402–11.
This study was supported by grants from Hubei Science & Technology Department Foundation (2018ACA162, 2016CFA027 to JMT), National Natural Science Foundation of China (81670272 to JMT), Hubei University of Medicine Innovation Team (FDFR201601 to JMT), and Hubei University of Medicine PI Foundation (HBMUPI201807 to JMT).
Ethics approval and consent to participate
The study was authorized by the Institutional Review Board of Hubei University of Medicine. Following the guide for the Care and Use of Laboratory Animals (Chinese version), all rats were housed and used for experiments in the SPF-grade animal center in accordance with the guidelines. The procedures for balloon injury in rats were permitted by the Care of Experimental Animals Committee of Hubei University of Medicine.
Consent for publication
The authors declare that they have no competing interests.
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Figure S1. Sca-1+ progenitor cells were increased in the sequence of adventitia, media, and neointima, showing the traits of RAGE expression during balloon injury-induced neointimal formation. Figure S2. S100B knockdown by shRNA reduced the number of Sca-1+/α-SMA- cells while increasing Sca-1−/α-SMA+ cells within the media or intima determined by image-Pro Plus software. Figure S3. S100B knockdown on by shRNA decreased the I/M ratios of the injured arteries. Figure S4. AMD3100 reduced the number of Sca-1+/α-SMA- cells while increasing Sca-1−/α-SMA+ cells within the media or intima. Figure S5. AMD3100 decreased the I/M ratios of the injured arteries. Figure S6. Semi-quantitative assay for the indicated proteins and phosphorylated proteins as determined by western blot. (DOCX 1427 kb)
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Wu, Y., Liu, X., Guo, L. et al. S100B is required for maintaining an intermediate state with double-positive Sca-1+ progenitor and vascular smooth muscle cells during neointimal formation. Stem Cell Res Ther 10, 294 (2019) doi:10.1186/s13287-019-1400-0
- Intermediate state