Atherosclerosis is the formation of fibrofatty lesions in the arterial wall (Libby et al., 2019). It is mainly characterized by endothelial cell dyskinesia, inflammatory cell recruitment and vascular smooth muscle cell dedifferentiation (Gimbrone and García-Cardeña, 2016; Wang et al., 2018). Review the evolution of atherosclerosis, which affects younger adults more than ever and is involved in the majority of deaths. As a systemic disease, its main affected sites include cardiovascular, cerebrovascular and peripheral vessels (Poznyak et al., 2020). When present, the disease typically manifests as most myocardial infarctions and numerous strokes, as well as disabling peripheral arterial disease. The occurrence and development of atherosclerosis is a complex process, and the current exploration of the pathogenesis of atherosclerosis highlights the influence of mutations in bone marrow and stem cells on the risk of cardiovascular disease (Libby, 2021). The influence of related pathways on inflammation may further modulate the progression of atherosclerosis (Zhu et al., 2018). Currently, various experimental data indicate that atherosclerosis is a chronic, immune, inflammatory vascular disease driven primarily by innate immune responses of myeloid cells (Ling et al., 2021). Chronic vascular inflammation can attract cells of the innate and adaptive immune systems to lesions, thereby inhibiting or accelerating atherosclerosis (Kobiyama and Ley, 2018; Saigusa et al., 2020). Traditionally, atherosclerosis has been considered a cholesterol storage disease. The accumulation of low-density lipoprotein triggers vascular inflammation. Macrophages absorb lipoprotein through micropinocytosis or aggregate in the form of cholesterol crystals. As cholesterol continues to flow in, macrophages gradually transform into foam cells (Wolf and Ley, 2019). Compelling experimental and clinical data suggest that inflammation is fundamentally involved in the pathophysiology of atherogenesis (Libby and Hansson, 2019). Inflammation may serve as a link between various factors and atherosclerosis, but it does not replace lipid risk (Libby, 2021). Inflammation is associated with infiltration of various immune cells, most notably macrophages, T cells (Williams et al., 2020). Stem cells are cells with the potential for self-renewal and differentiation, and a key role in the pathogenesis of atherosclerosis has been demonstrated (Orlandi, 2015). Inflammatory pathways in stem cells are regulated by multiple transcription factors and co-regulatory molecules (Rahman et al., 2016). However, the signaling pathways that regulate inflammation and cytokine production are still not completely understood. Atherosclerosis is a multifactorial disease. As the disease progresses, it is gradual and hidden, and for a long time there is no apparent discomfort. It is hard to get noticed. Once it occurs, it will seriously endanger human health (Raggi et al., 2018).

Surface markers of stem cells have been proposed by relevant laboratories based on biological characteristics and characterization, and different stem cell populations have been defined according to these markers (Chambers et al., 2021). These minimal positive markers that can be used to identify this stem cell population mainly include Cluster of differentiation 34 (CD34), SOX10, c-kit and Stro1, although some of them are still controversial, a relatively strict definition of stem cell characterization has been made (Mildmay-White and Khan, 2017). In addition, the expression of Sca1, Class Ⅵ intermediate filament protein (Nestin), and Glioma-associated oncogene homology 1 (Gli1) can also reflect stem cell-related properties (Calderone, 2012; Bobryshev et al., 2015; Kramann et al., 2016). However, due to the heterogeneity of stem cells and the lack of comprehensive and robust definitions of cell surface markers, there are overlapping relationships among stem cell markers.

Therefore, we could combine multiple stem cell markers to evaluate the characteristics of stem cell populations. Markers expressed by stem cells are present in all three layers of the arterial wall and bone morrow. Stem cells can specialize to form smooth muscle cells, endothelial cells, fibroblasts and osteocytes. Under certain conditions, circulating stem cells can also migrate to injured areas to participate in repair of injury and neointima formation (Jiang et al., 2021). In addition to the incomplete definition of stem cell markers, there is still no effective means to judge the process of stem cells, especially the process of differentiation into Smooth muscle cell (SMC). Thus, more studies and attempts are needed to elucidate the phenotypic differences before and after stem cell differentiation (Figure 1).

Single-cell Ribonucleic Acid sequencing of SMCs has shown that only a modest fraction of smooth muscle cells is capable of proliferation and differentiation, and the field is moving toward an in-depth phenotypic characterization of SMCs (Liu and Gomez, 2019). In addition to medial smooth muscle, other non-smooth muscle cells, such as stem cells, endothelial cells, and derived cells, are also involved in neointima and atherogenesis of smooth muscle cells in sclerosing lesions (Wang et al., 2018). Increased stem cell proliferation accelerates clonal hematopoiesis during atherosclerosis (Heyde et al., 2021). Since the discovery of vascular stem cells, continued exploration has considerably improved our understanding of their properties and functions. Vascular stem cells are mostly quiescent but are activated in response to injury and are involved in repairing the endothelium and forming neointima (Zhang et al., 2018). In the process of SMC undergoing multiple phenotypic transitions, the expression of mesenchymal stem cell-like markers can replace cell types (Liu and Gomez, 2019). Vascular stem cells have the differentiation potential to participate in vascular remodeling, mainly by activating resident stem cells after injury, improving the ability of SMC aggregation and stem cell migration, and accelerating neointimal hyperplasia (Jiang et al., 2021). Mesenchymal stem cells also inhibit inflammatory activation of macrophages by inducing cholesterol efflux (Groenen et al., 2021). On the other hand, the important contribution of stem cell-derived exosomes in regulating stem cell differentiation, inflammation and immune response to improve atherosclerosis has been gradually recognized (Ling et al., 2021). However, due to the lack of powerful molecular markers to identify and judge stem cell differentiation processes, the cellular behavior and molecular mechanisms of vascular stem cell differentiation into SMC are still unclear. In the future, using phenotypic differences before and after stem cell differentiation to assess changes in stem cell differentiation process and cell characteristics is crucial to elucidate the behavior of vascular stem cells and the signaling pathways involved, which may provide new opportunities to promote the understanding of the functional properties of these cells and the application of clinical therapy (Jiang et al., 2021).

The study of Hu et al. (2004) confirmed that there are a large number of progenitor cells that can differentiate into smooth muscle cells in the adventitia of blood vessels, and these progenitor cells are not derived from bone marrow, but participate in the formation of atherosclerosis. Sca1+ adventitial precursor cells are heterogeneous, maintain their original state in homeostasis, differentiate into a variety of effector cell types upon activation, and contribute to neointima formation and medial wall repair (Jolly et al., 2022). For a long time, it has been believed that the phenotype of smooth muscle cells in atherosclerotic lesions is different from that of medial cells, and adventitial precursor cells such as Sca1+ progenitor cells can migrate from adventitia to intima, differentiate into smooth muscle cells, and participate in atherosclerosis (Hu et al., 2004; Tang et al., 2020; Wu et al., 2021).

Endothelial cell dysfunction is known to cause endothelial inflammation as well as monocyte aggregation, promoting vascular remodeling and neointima formation (Gerhardt and Ley, 2015). However, the application of cell fate mapping and single-cell sequencing technologies has driven the study of adventitia-mediated vascular remodeling, making adventitial biology a worthwhile aspect of the field to explore (Kuwabara and Tallquist, 2017). Sca1+ progenitor cells migrate from the outer membrane to the inner membrane and participate in the formation of neointima, and are affected by multiple factors in the process. KLF transcription factor 4 (Klf4) helps maintain the Sca1 progenitor phenotype, but Klf4 has little effect on neointima formation and selectively promotes adventitial remodeling (Lu et al., 2020), ETS variant transcription factor 2 (ETV2) promotes differentiation of Sca1 progenitors into endothelial cells, however endothelial injury models suggest that Sca1 progenitors transduced with ETV2 are unable to participate in neointima formation and vascular remodeling (Le Bras et al., 2018), However, SMCs promote the migration of stem/progenitor cells from the adventitia to the neointima by releasing C-C motif chemokine ligand 2 (CCL2) and C-X-C motif chemokine ligand 1 (CXCL1) (Yu et al., 2016).

In recent years, in order to elucidate the role of Sca1+ progenitor cells in the process of vascular injury and intimal lesions, Wu et al. (2021) created a model in which Mesenchyme Homeobox 1 (Meox1) controls Sca1+ stem cells to participate in neointima formation. The study demonstrated that Meox1 promotes blood vessels through the Ras homolog family member A (RhoA)—cell division cycle 42 (Cdc42)—C-X-C motif chemokine receptor 4 (CXCR4) pathway Sca1+ progenitor cells in the adventitia migrate to the intima, and then differentiate into SMCs to participate in the formation of neointima. Tang et al. used single-cell sequencing to identify that Sca1-derived smooth muscle cells have a stronger proliferation potential than pristine smooth muscle cells after severe vascular injury. The study showed that Yap transcription factors are involved in SMC-derived expansion, so the Hippo- Yes-associated protein (Yap) pathway may be activated to participate in vascular repair (Wu et al., 2021). In addition, the integrin pathway (Xiao et al., 2007), Signal transducer and activator of transcription 3 (STAT3)- Mitogen-activated protein kinase (MAPK) pathway (Xie et al., 2017), Dickkopf wnt signaling pathway Inhibitor 3 (DKK3)/wnt family member (WNT) signaling pathway (Karamariti et al., 2018), Phosphatidylinositol 3-kinase (PI3K)/Akt serine/threonine kinase (AKT) and Nuclear factor kappa B subunit (NF-kB) signaling pathway (Wu et al., 2019) are involved in the differentiation of Sca1+ progenitor cells into smooth muscle. However, the mechanism of pathway of Sca1+ progenitor cells affecting angiogenesis and intima formation has not been widely recognized due to different methods of progenitor cell extraction and intervention measures.

For the identification of molecular phenotypes after arterial injury, they used an arterial anastomosis model and collected tissue samples after 2 weeks (short-term) and 5 weeks (longterm) of injury. The results show that Sca1-derived cells express Calponin 1 (CNN1) and Transgelin (SM22) at both stages. However, the former has not acquired a mature SMC phenotype and does not express Smooth muscle myosin heavy chain 11 (MYH11), while the latter has acquired a mature SMC phenotype and can express MYH11 (Tang et al., 2020). In the future, we can use the differences in molecular phenotypes to identify smooth muscle cells derived from Sca1+, which provides new methods and theoretical ideas for future studies. This method is also suitable for further exploring the migration mechanism of Sca1+ progenitor cells corresponding to hyperlipidemia (Kokkinopoulos et al., 2017), which can promote the discovery of therapeutic targets for vascular lesions in the future (Jolly et al., 2022), and open up new therapeutic prospects for vascular related pathological diseases.

Recently, more and more studies have found that the adult stem cell transcription factor SOX10 contributes to tissue encapsulation and microvascular formation (Wang et al., 2017). In the past, smooth muscle differentiation and proliferation was widely believed to play a crucial role in vascular remodeling and disease. However, recent research has shown that vascular stem cells also play an influential role. Pluripotent vascular stem cells can differentiate into neuron-like and mesenchymal stem cell-like cells, and then participate in vascular remodeling and neointima formation of smooth muscle cells. This study defines a “Vascular mesenchymal stem cell (MVSC)—Mesenchymal stem cell (MSC)—SMC” differentiation pathway, distinct from SMC dedifferentiation (Tang et al., 2012b). Since MYH11-negative cells were found to have multi-directional differentiation potential in the early stage of the experiment, studies using MYH11 as lineage tracing found that the neointima 3 weeks after injury contained proliferating cells derived from mature SMCs (Nemenoff et al., 2011), and MYH11 as a late marker of SMC (Yang et al., 2020), the switch of this phenotype after vascular injury intrigued us, Yuan et al. (2017) used lineage tracing in transgenic mice and experimented with a wire injury model and a ligation model, the results showed that SOX10+ cells may be one of the sources of heterogeneous neointima. SOX10+ vascular stem cells are quiescent under normal conditions, and arterial media only express SOX10 after vascular injury to promote proliferation and migration, thereby filling the media and creating neointima.

Yuan et al. (2017) differentiated the neointima into types Ⅰ and Ⅱ, derived from smooth muscle cells and SOX10+ cells, respectively. 2 weeks after injury, lineage tracing results indicated that Smooth muscle actin alpha 2 (ACTA2) was extremely expressed and CNN1 was lowly expressed, but MYH11 was not expressed, which is in line with the concept that vascular stem cells affect angiogenesis intimal hyperplasia after injury, and provides a more adequate theory in accordance with. Additional studies have found that macrophage-derived Matrix metallopeptidase 8 (MMP8) promotes the differentiation of SOX10+ progenitor cells into smooth muscle cells by regulating the ADAM metallopeptidase domain 10 (ADAM10)/Notch receptor 1 (Notch1) signaling pathway (Yang et al., 2020). In addition, the KIT Proto-Oncogene (KIT) pathway has also been confirmed that the neural sheath transcription factor SOX10 plays a key role in the cell survival process (Su et al., 2020).

In the future, we can use molecular phenotype-specific expression of smooth muscle cells from different sources to distinguish smooth muscle cells derived from stem cells. An in-depth study of the mechanisms and pathways associated with the differentiation of SOX10+ progenitor cells into smooth muscle cells, using this as an entry point, has the potential to provide new theoretical ideas for interventions in vascular disease and remodeling, and potentially discover new therapeutic targets.

Nestin is an intermediate filament protein expressed in neuroepithelial stem cells or mesenchymal stem cells (Suguta et al., 2007), and as a well-known stem cell marker, it can be used as a description of stem cell-like progenitor cells in development and tissue repair (Saboor et al., 2016). Nestin was not detected in undamaged arteries, but was detected in the neointima of injured arteries (Wan et al., 2012). Nestin is also upregulated in revascularized arteries after vascular injury, especially in the neointima, suggesting that Nestin expression is involved in vascular remodeling (Oikawa et al., 2010). After further dissecting the role of Nestin in neointima, we found that Nestin is expressed in arterial neointima after balloon injury and in smooth muscle cells in human coronary lesions, representing an adaptive proliferation expression. Phenotype, and the absence of Nestin has profound effects on proliferation and migration, which together suggest that Nestin is involved in both physiological and pathological vascular remodeling processes (Tardif et al., 2015; Calderone, 2018). Although the origin of stem cells is debated, more and more studies have shown that it is certainly involved in vascular remodeling (Psaltis and Simari, 2015). On the premise that Nestin+ smooth muscle cells are derived from stem cells, we speculate that the cells may be differentiated from mesenchymal stem cells (Suguta et al., 2007; Wan et al., 2012), although there is no completely convincing research on the source of Nestin cells. Explained, but the differentiation of Nestin+ pluripotent stem cells into pericytes and smooth muscle cells is widely recognized to be involved in vascular remodeling and neovascular hyperplasia after arterial injury. Heparan sulfate variant 7 (HS7) was recently found to co-localize with Nestin, and HS7 activates AKT and MAPK transduction pathways when promoting angiogenesis and neural stem cell proliferation (Chan et al., 2020), which still needs more research support.

To obtain in vitro and in vivo expression profiles of Nestin in vascular smooth muscle cells, Oikawa et al. (2010) analyzed the localization of Nestin in vascular smooth muscle cells using the premise that 5-Bromodeoxyuridinc (Brud)+ is approximately equivalent to Nestin+. Nestin immune responses gradually decrease over time and disappear after 20 weeks of birth. Based on the properties of Nestin as a stem cell, the data suggest that Nestin+ cells maintain progenitor properties until at least 6 weeks after birth. After 2 weeks of embryos, immunohistochemistry showed that the Nestin signal coexisted with SM22 Deoxyribonucleic acid (DNA), a marker for vascular smooth muscle cells, but not fused with the signal of factor VIII-associated antigen (Oikawa et al., 2010). Saboor et al. (2016) detected the Nestin+ cells in the pulmonary artery, the smooth muscle cellspecific marker SMA positive, and the endothelial marker Platelet endothelial cell adhesion molecule 1 (CD31) negative , which is consistent with the former conclusion. In addition, this marker CNN1 was inversely correlated with Nestin expression and vascular smooth muscle proliferation in the study (Saboor et al., 2016). As a mid-to-late marker for evaluating the role of SMC in neointima, CNN1 was negatively correlated with the proliferation of vascular smooth muscle (Yang et al., 2020), suggesting that Nestin-positive cells represent a certain number of stem cells involved in vascular remodeling and neointima after arterial injury membrane formation (Yang et al., 2020). It provides a certain theoretical basis and methodology for follow-up studies of stem cells involved in atherosclerosis and neointima formation. Certain specific phenotypes of stem cell markers can also provide innovative ideas for the study and treatment of vascular diseases.

MSCs play an essential role in maintaining homeostasis and promoting repair after injury (Chen et al., 2020). Zhao et al. (2014) used lineage tracing in a mouse incisor model to find that Gli1 labeled perivascular MSC-like cells in mouse incisors, which expressed canonical MSC markers and possessed the potential for multilineage differentiation in vitro. Gli1+ cells are pluripotent stem cells of periodontal tissue and play a key role in periodontal tissue renewal and damage repair (Men et al., 2020).

Gli1+ MSC cells are mainly localized in pericyte niches of microvasculature and adventitia of larger vessels, and are resident cells that arise from tissue rather than circulation. Gli1+ cells have dual roles in organ fibrosis and angiogenesis (Zhao et al., 2014; Kramann et al., 2015). On the one hand, Gli1+ cells can serve as precursors of fibroblasts and differentiate into fibroblasts through proliferation after vascular injury, and Gli1+ stromal cells also play a key role in myelofibrosis (Schneider et al., 2017). Gli1+ cells retain MSC expression during fibrosis, which defines immature perivascular cells (Kramann et al., 2015). On the other hand, the periarterial Gli1+ cell portion does not express the classical MSC marker, but can generate Chondroitin sulfate proteoglycan (NG2) pericytes that express the marker (Zhao et al., 2014), and NG2 pericytes represent a subpopulation of MSCs and obtain markers of mature pericytes (Kramann et al., 2015), functions in emergency repair and intimal generation following vascular injury (Zhao et al., 2014).

Current theories suggest that the formation of atherosclerotic plaques is caused by the dedifferentiation of mature vascular smooth muscle cells after injury to differentiate into osteoblastlike cells that drive calcification of the media and intima (He et al., 2020), while dedifferentiated smooth muscle cells may derive from Gli1+ adventitial precursor cells, which is not mutually exclusive with the former model (Baker and Péault, 2016). An increasing number of studies have shown that stem/progenitor cells present in the vessel wall, such as smooth muscle precursor cells, migrate to the intima to differentiate into smooth muscle cells, and thus participate in atherosclerotic lesions and neointima formation (Baker and Péault, 2016; Kramann et al., 2016; He et al., 2020). Gli1 represents a specific marker in MSC tissue, and adventitial progenitors are thought to play a role in angiogenesis and disease development (Psaltis and Simari, 2015).

Through lineage tracing of Gli1+ vascular cells, Kramann et al. (2016) showed that adventitial cells migrate into the capsular-media and neointima, and subsequently differentiate into smooth muscle cell-like outlines, which in turn differentiate into osteoblasts, which drive the process of vascular calcification. Using a well-established model of femoral artery wire injury (Sata et al., 2000), they demonstrated through inducible genetic fate tracing that Gli1+ progenitors are an important source of adventitial cells for vascular smooth muscle cells and contribute to arterial wall repair after acute injury (Kramann et al., 2016), mainly reflected in the Gli1+MSC cells involved in the formation of neointima (Kramann et al., 2016; Song et al., 2020). Gli1+ cells obtained the expression of smooth muscle cell marker α-SMA (ACTA2), smooth muscle protein and calponin in the middle and late stages of isolation or under the condition of adding Platelet-derived growth factorbb (PDGF-BB) and Transforming growth factor beta (TGF-β). In contrast, none of these markers could be detected (Kramann et al., 2016). Furthermore, single-cell transcriptional analysis showed that numerous Gli1+ adventitial precursor cells naturally express Transgelin (SM22) (Baker and Péault, 2016; Kramann et al., 2016). Studies have shown that induction of the Hedgehog/Klf4 pathway is the basis for the reprogramming of smooth muscle cell-derived stem progenitor cells (Lu et al., 2020). We speculate that Gli1+ progenitor cells are also present in human arteries and that molecular phenotype-specific expression of Gli1+ cells provide a new theoretical avenue for followup studies, but whether they can be used as progenitor mesenchymal stem cells and for vascular calcification remains open. Treatment targets still need to be studied further.

The crucial role of smooth muscle cells in the progression of atherosclerotic lesions is universally recognized (Bennett et al., 2016), but the origin of smooth muscle cells in the neointima remains controversial. In the past, it was thought that the medial smooth muscle cells dedifferentiate and then migrate to the intima to proliferate to form the neointima (Ross, 1999), and more and more studies have shown that there are a large number of progenitor cells in the adventitia of atherosclerotic lesions, and these progenitor cells can It expresses markers such as c-kit, Sca1, and CD34, and is involved in neointima formation and atherosclerotic lesions, and may be the source of endothelial cells and smooth muscle cells (Torsney et al., 2007). In addition to medial smooth muscle cells, bone marrowderived smooth muscle precursor cells as well as vascular-resident stem/progenitor cells may be involved in this process (Takamiya et al., 2006; Wang et al., 2007; Skartsis et al., 2014; Chen et al., 2018; Ni et al., 2019).

Endogenous c-kit+ stem/progenitor cells have been reported to play a role in tissue repair by differentiating into endothelial cells and smooth muscle cells during the repair of injured arteries (Ellison et al., 2013). Blockade of c-kit attenuates neointima formation (Skartsis et al., 2014; Chen et al., 2018), conversely demonstrating an important role for c-kit in intima formation. Chen et al. (2018) established a vascular injury model and used genetic lineage tracing to find that c-kit+ stem cells mainly differentiate into monocytes/macrophages and granulocytes during intima formation, which promote inflammatory aggregation after injury, thereby infiltrating neointimal lesions. Interestingly, they suggest that the potential of c-kit+ cells to differentiate into endothelial cells and smooth muscle cells is low during intima formation, and that it is mainly through intima infiltration and differentiation that lesion formation is facilitated. Although c-kit+ cells are present in both the vessel wall and bone marrow, data demonstrate that bone marrow-derived c-kit+ cells are the main source of neointima formation (Chen et al., 2018), Progenitors cells expressing the c-kit marker are recruited to the vessel wall and differentiate mainly into monocytes/macrophages and granulocytes, rarely into endothelial and smooth muscle cells, causing vascular inflammation to promote remodeling after injury (Chen et al., 2018). Vascular inflammation plays a key role in the process of neointimal hyperplasia and vascular remodeling (Libby, 2021). On the other hand, cytokine mobilization of c-kit+ stem cells to promote re-endothelialization after angioplasty is a feasible strategy (Takamiya et al., 2006). In a mouse arterial transplantation model, smooth muscle cells in the neointima are populated with c-kit+ cells derived from non-bone marrow, and bone marrowderived c-kit+ cells can produce leukocytes, which together promote neointima formation (Ni et al., 2019). This does not conflict with Chen et al. exclusively. The former study in a mouse allograft model showed that c-kit+ cells can act as a major contributor to the accumulation of neointimal smooth muscle cells, and bone marrow-derived c-kit+ cells may also be an influential factor in neointima formation (Ni et al., 2019). The latter believes that endothelial cells and smooth muscle cells are fewer generated mainly in the natural pathophysiological process of the neointima, and cannot be the main source of endothelial repair and smooth muscle accumulation after vascular injury (Chen et al., 2018). Differences in results may be related to the vascular disease model employed and the severity of vascular injury.

Ni et al. (2019) found that Stem cell factor (SCF)/c-kit axis migration can activate the downstream MAPK and Jun Proto-Oncogene (JUK) pathways to induce differentiation into smooth muscle cells, and glucose metabolism also plays a key role in the induction of differentiation. Previous related studies have shown that c-kit precursor cells promote angiogenesis in tissue grafts by regulating the Wnt/Klf4 pathway (Campagnolo et al., 2015). These findings provide current insights into the mechanisms of neointima, and these studies of c-kit+ cells provide theoretical foundations and potential targets for subsequent stem cell therapies for vascular diseases.

Stro-1 is a cell membrane one-way protein that is translocated from the endoplasmic reticulum to the cell membrane in the presence of intracellular calcium depletion (Barkhordarian et al., 2011). As one of the most famous markers of bone marrow mesenchymal stem cells, Stro-1 plays a unique role in the research of bone marrow mesenchymal stem cells (Lin et al., 2011). Immunofluorescence staining showed that Stro-1 was present in nerve fibers, vascular smooth muscle cells, pericytes, and endothelial cells (Yoshiba et al., 2012). Stro-1+ cells are mesenchymal stem cells with multi-lineage differentiation potential, including chondrocyte differentiation, adipocyte differentiation, smooth muscle cells (Kobayashi et al., 2004), which can participate in the repair process after tissue damage. Progenitors expressing Stro-1 are recruited in the perivascular setting and maintain the inflammatory response by enhancing chemotaxis to neutrophils and monocytes/macrophages (Ward, 2010). Stro-1 antigen, as a typical surface antigen of bone marrow stem cells, has inflammatory/immune effects during arterial disease (Ryer et al., 2015). Stro-1 + stem cells are induced to migrate selectively, while mesenchymal stem cells and pericytes have strong osteogenic potential (Doherty et al., 1998; Dennis et al., 2002; Chmilewsky et al., 2013), increased differentiation of osteoblasts may promote tissue repair and vascular remodeling (I et al., 2011). Studies of arterial intima in patients with pulmonary hypertension have shown that the Stro-1+ stem cell population has the ability to differentiate into adipocytes and osteoblasts, thus contributing to vascular lesions (Firth et al., 2010). Dental pulpderived mesenchymal stem cells generate reparative odontoblast-like cells (Yoshiba et al., 2012), and injection of a mixture of hyaluronic acid, butyric acid and retinoic acid can lead to the recruitment of Stro-1+ stem cells and enhance MSC-mediated cytotoxicity in vivo (Lionetti et al., 2010). In vascular lesions, the myofibroblast phenotype predominates in endarterectomy tissue (Firth et al., 2010), and meaningfully, mechanical stress has been shown to promote the expression of SMC-like properties of bone marrow stromal cells (Kobayashi et al., 2004). Immunofluorescence and blotting indicated that both α-SMA were expressed, while the proportion of SM-MHC increased with the prolongation of culture time, and was mainly expressed in the later stage of cell differentiation (Kobayashi et al., 2004). The neointima is derived from mesenchymal progenitor cells of the bone marrow, which in turn repair vascular damage (Kobayashi et al., 2004). However, bone marrow-derived cells are not the only players involved in vascular repair and homeostasis, and cells with morphological and immunophenotypic properties of mesenchymal stem cells are also present in human elastic and muscular arteries (Pasquinelli et al., 2010). With regard to the proliferation and osteogenic differentiation of periodontal ligament and dental pulp stem cells, studies have demonstrated that MAPK pathway and Wnt/β-catenin signaling pathway (Torsney and Xu, 2011) play an indispensable role and are closely related to the differentiation of mesenchymal cells into smooth muscle. The association of cellular processes requires additional study.

By detecting the expression of Stro-1, it was preliminarily identified that bone marrow stromal precursor cells can form fibroblasts (Firth et al., 2010), which in turn proved the contribution of bone marrow-derived circulating progenitor cells. At the same time, mechanical stress can promote the expression of smooth muscle-like properties, which reflects the effect of vascular pressure on the neointima (Kobayashi et al., 2004), and high glucose can induce endothelial cell-mesenchymal transformation into chondrocyte-like cells, which are then involved in the calcification of the vascular media (Tang et al., 2012a). Both influences are involved in the progression of neoplasia and atherosclerosis through the pathway of Stro-1+ mesenchymal cells. It provides us with a current strategy to understand the pathogenesis of vascular disease and the prevention of arteriosclerosis.

Stem/progenitor cells may be involved in vascular repair and intima formation processes. Vascular progenitor cells including endothelial progenitor cells and CD34⁺ cells migrate to the intima during vascular injury and differentiate into vascular smooth muscle cells (Torsney and Xu, 2011). The presence of angiogenic mesenchymal cells in the human thoracic aorta, including both CD34 and ckit cell populations, is associated with proliferative markers (Pasquinelli et al., 2007). In the study of the great saphenous vein, it was found that CD34+/CD31-cells have the potential to differentiate into pericytes (Campagnolo et al., 2010), and pericytes can already differentiate into adipocytes to form lipid nuclei, thereby promoting the formation of plaques in atherosclerotic lesions (Canfield et al., 2000). In a mouse vascular graft model, Tasi suggested that the neointima is heterogeneous, expressing stem cell markers including Sca1, c-kit, CD34, and that the smooth muscle cells in the plaques are derived from the vessel wall rather than myeloid cells (Tsai et al., 2012). However, the contribution of the CD34⁺ resident stem cells of the progenitor cells to the new smooth muscle cells is limited. CD34⁺ stem cells isolated from adventitia can differentiate into smooth muscle cells in vitro and express the early marker SM22 and rarely the late marker SM-MHC, but the vessels are damaged. Rather than participating in intima formation, smooth muscle cells are produced in small numbers and only migrate to the media and maintain equilibrium (Shen et al., 2016). At the same time, it has been shown in stem cell targeted therapy that bone marrow mesenchymal stem cells can replace damaged cells and promote neointima formation in atherosclerosis. This effect is worthy of recognition (Hashem et al., 2021).

The existence and localization of CD34⁺ stem cells in the blood vessel wall are relatively clear, but there are still differences in the formation of atherosclerotic plaques and neointima by adventitial CD34⁺ resident stem cells, which may be related to the selection of arterial and venous sites or the experimental method adopted. Related to differences in animal models, studies have found that CD34⁺ stem cell-derived SMCs are mediated by Ras Homolog Family Member A (RhoA) and Ca²⁺/CaM/Myosin Light Chain Kinase (MLCK)-dependent pathways (Vazão et al., 2011), and more studies are needed to explore this mechanism. However, the efficacy of bone marrow mesenchymal stem cells on neointima deserves recognition and offers excellent prospects for the prevention and treatment of vascular diseases.

Octamer-binding transcription factor 4 (Oct4) was first discovered in early embryos and germ cells, and as an animal transcription factor, it determines the formation of pluripotent stem cells (Nichols et al., 1998). Generally, Oct4 expression is restricted to pluripotent stem cells, and recent studies have found that under pathological conditions, Oct4 activation in a variety of tumors (Gkountela et al., 2019) and atherosclerotic lesions (Cherepanova et al., 2016; Alencar et al., 2020) is associated with migration of cell types (Ding et al., 2021). During the development of atherosclerosis, Oct4 is activated as a key transcription factor that maintains stem cell dedifferentiation and plays an important role in the regulation of the phenotypic transition of vascular smooth muscle cells (Cherepanova et al., 2016), but this evidence is controversial. After using smooth muscle cell-specific knockdown of Oct4, Cherepanova found a decrease in plaque stability, which may be related to the reduced number of SMCs within the lesions due to impaired SMC migration (Cherepanova et al., 2016). In view of the regulation of stem cell pluripotency genes on the pathogenesis of advanced atherosclerotic lesions, Alencar believes that activation of Oct4 may play a beneficial role in the stabilization of atherosclerotic plaques, which is consistent with the former view, and found that Klf4 and Oct4 showed virtually opposite genome-wide influence regulation on the arteriosclerosis protective phenotype (Alencar et al., 2020). Activation of Oct4 in vascular smooth muscle has a protective effect on arteriosclerosis.

However, arterial injury-induced neointima formation and diet-induced atherosclerosis differ in pathological and mechanistic as well as genetic factors (Ding et al., 2021), knockout of Oct4 significantly impairs perivascular cell migration and promotes Vascular leakage, which in turn inhibits angiogenesis (Hess et al., 2019). Activation of the stem cell factor Oct4 is involved in the remodeling of the vascular network after vascular injury (Hess et al., 2019). The level of Oct4 in the arterial intima is significantly increased after carotid artery injury (Ding et al., 2021), which in turn regulates the formation of neointima. The expression and localization of Oct4 mainly depends on the co-localization of a-SMA in the endocardium and proliferating cell nuclear antigen (PCNA) in the nucleus of vascular smooth muscle cells. Clear in vitro experiments also proved that the overexpression of Oct4 promotes the proliferation and migration of smooth muscle cells (Yang et al., 2020). Studies have also shown that Oct4 promotes the generation of smooth muscle cells from pluripotent stem cells and regulates the transcriptional activation of SM22 through the DDK3/Wnt signaling pathway (Karamariti et al., 2013), thereby promoting the repair and regeneration of blood vessels.

Despite epigenetic silencing during gastrulation (Hess et al., 2019), the stem cell factor Oct4 can be activated under specific conditions to play a protective role during atherosclerotic lesions and angiogenesis. Given that Oct4 can play an important role in the process of stem/progenitor cell differentiation, it is seldom expressed in somatic cells and has fewer potential side effects, and may become a new target for vascular therapy in the future (Ding et al., 2021). However, the mechanisms and factors responsible for Oct4 activation in somatic cells and the SMC phenotypic transition need to be further investigated in order to identify therapeutic targets (Table 1).

Summarizing the roles of the above-mentioned various stem/progenitor cells in the differentiation process of phenotypic changes, we found that in stem/progenitor cells positive for a variety of stem cell markers, the Wnt/β-catenin pathway plays an essential role in promoting SMC proliferation in stem cells. It plays an influential role in the process of endothelial cell fibrosis and reendothelialization, activation of Wnt signaling pathway can induce differentiation of stem cells and reprogramming of SMC (Karamariti et al., 2013; Campagnolo et al., 2015; Lu et al., 2020; Yang et al., 2020), mainly including two signal activation pathways, Dickkopf3 and Hedgehog. Channel activation favors adventitial remodeling and fibrosis, and promotes SMC proliferation and reendothelial in the neointima (Campagnolo et al., 2015). After being stimulated by vascular injury, the secretion of Vascular Endothelial Growth Factor (VEGF) and TGF-β stimulates the upregulation of the MAPA pathway, the phosphorylation of JUN, and the elevated expression of osteogenic genes in Stro-1 stem cells (Li et al., 2021). SMC proliferation after phenotype conversion of Nestin+ stem cells (Chan et al., 2020), Thereby promoting angiogenesis and osteogenic differentiation, these conclusions need additional research support. Activation of the RhoA/Rho kinase signaling pathway can regulate actin polymerization and MLCK phosphorylation (Vazão et al., 2011; Ni et al., 2019), improve contractility and viability at the cellular level, and promote SMC proliferation and angiogenesis. In addition, some signaling pathways are activated in specific stem cell markers, PI3K/Akt signaling pathway promotes SMC differentiation dependent on SDF-1α expression (Wu et al., 2019), Rac Family Small GTPase 1 (Rac1)/Cdc pathway can participate in intimal formation as a co-control Sca1+ stem cell (Ni et al., 2019), Ca²⁺/CaM signaling pathway mediates cell contraction of stem cells (Vazão et al., 2011). To date, there has been insufficient research on the activation of signaling pathways during stem cell differentiation after vascular injury, and additional theoretical support is needed. Due to the complex biological properties of SMCs, Huize Pan conducted a singlecell analysis of the process of SMC phenotype changes in atherosclerosis, revealing that SMC-derived intermediate cells have the characteristics of differentiation into macrophages and fibrosis, prompting the expression of The pathways regulated in the process of type switching mainly include NF-κB signaling pathway, PI3K/Akt signaling pathway, G protein-coupled receptor (GPCR) pathway, Hedgehog/Notch/Wnt signaling pathway, which is consistent with the above conclusions in the stem cell field in recent years on differentiation process pathways. If there is an intersection, these pathways may be activated in both differentiation modes, and there may be differences in the regulation of the differentiation process after activation, or it may be caused by the overlap of the downstream pathways in the two differentiation modes, which needs to be explored in-depth (Table 2).