1 Department of Emergency, Guangdong General Hospital , Guangdong Academy of Medical Sciences, Guangzhou, China .
2 Department of Cardiology, The First Affiliated Hospital, School of Medicine, Zhejiang University , Hangzhou, China .
Antioxid Redox Signal. 2018 Jul 10;29(2):219-235. doi: 10.1089/ars.2017.7171. Epub 2017 Jul 5.
Atherosclerosis is a major cause for the death of human beings, and it takes place in large- and middle-sized arteries. The pathogenesis of the disease has been widely investigated, and new findings on vascular stem/progenitor cells could have an impact on vascular regeneration. Recent Advances: Recent studies have shown that abundant stem/progenitor cells present in the vessel wall are mainly responsible for cell accumulation in the intima during vascular remodeling. It has been demonstrated that the mobilization and recruitment of tissue-resident stem/progenitor cells give rise to endothelial and smooth muscle cells (SMCs) that participate in vascular repair and remodeling such as neointimal hyperplasia and arteriosclerosis. Interestingly, cell lineage tracing studies indicate that a large proportion of SMCs in neointimal lesions is derived from adventitial stem/progenitor cells.
The influence of stem/progenitor cell behavior on the development of atherosclerosis is crucial. An understanding of the regulatory mechanisms that control stem/progenitor cell migration and differentiation is essential for stem/progenitor cell therapy for vascular diseases and regenerative medicine.
Identification of the detailed process driving the migration and differentiation of vascular stem/progenitor cells during the development of atherosclerosis, discovery of the environmental cues, and signaling pathways that control cell fate within the vasculature will facilitate the development of new preventive and therapeutic strategies to combat atherosclerosis. Antioxid. Redox Signal. 00, 000-000.
动脉粥样硬化是人类死亡的主要原因,发生在大动脉和中动脉。该疾病的发病机制已被广泛研究,血管干细胞/祖细胞的新发现可能对血管再生产生影响。
最近的研究表明,血管壁中存在丰富的干细胞/祖细胞,主要负责血管重塑过程中内膜中的细胞积累。已经证明,组织驻留干细胞/祖细胞的动员和募集产生参与血管修复和重塑的内皮细胞和平滑肌细胞(SMCs),如新生内膜增生和动脉粥样硬化。有趣的是,细胞谱系追踪研究表明,新生内膜病变中的大量 SMC 来源于血管外膜干细胞/祖细胞。
干细胞/祖细胞行为对动脉粥样硬化发展的影响至关重要。了解控制干细胞/祖细胞迁移和分化的调节机制对于血管疾病和再生医学的干细胞/祖细胞治疗至关重要。
确定在动脉粥样硬化发展过程中驱动血管干细胞/祖细胞迁移和分化的详细过程,发现控制血管内细胞命运的环境线索和信号通路,将有助于开发新的预防和治疗策略来对抗动脉粥样硬化。抗氧化。氧化还原信号。00,000-000。