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循环血管祖细胞在损伤形成和血管愈合中的作用:来自动物模型的经验教训。

Contribution of circulating vascular progenitors in lesion formation and vascular healing: lessons from animal models.

作者信息

Tanaka Kimie, Sata Masataka

机构信息

Department of Cardiovascular Medicine, University of Tokyo Graduate School of Medicine, Tokyo, Japan.

出版信息

Curr Opin Lipidol. 2008 Oct;19(5):498-504. doi: 10.1097/MOL.0b013e32830dd566.

Abstract

PURPOSE OF REVIEW

It is a widely accepted view that vascular repair results from migration and proliferation of adjacent cells in animal models. On the contrary, accumulating evidence suggests that bone marrow can give rise to endothelial-like cells and smooth muscle like cells that potentially contribute to vascular healing, remodeling, and lesion formation under physiological and pathological conditions. The aim of this article is to review recent findings obtained from animal models of vascular diseases regarding bone marrow derived progenitor cells.

RECENT FINDINGS

Studies using chimeric animals revealed that bone marrow derived cells exist at the sites of vascular healing and lesion formation after injury. High-resolution histological analyses revealed that those bone marrow derived cells do express some markers for endothelial cells or smooth muscle cells. Peripheral mononuclear cells could differentiate into endothelial-like cells or smooth muscle like cells in vitro according to the culture conditions.

SUMMARY

Circulating progenitors significantly contribute to vascular repair and lesion formation. These findings provide the basis for the development of new therapeutic strategies that involve targeting the mobilization, homing, differentiation, and proliferation of bone marrow- derived vascular progenitor cells.

摘要

综述目的

在动物模型中,血管修复是由相邻细胞的迁移和增殖导致的,这是一种被广泛接受的观点。相反,越来越多的证据表明,骨髓可产生内皮样细胞和平滑肌样细胞,在生理和病理条件下,这些细胞可能有助于血管愈合、重塑和病变形成。本文旨在综述从血管疾病动物模型中获得的关于骨髓来源祖细胞的最新研究结果。

最新研究结果

使用嵌合动物的研究表明,骨髓来源的细胞存在于损伤后血管愈合和病变形成的部位。高分辨率组织学分析显示,那些骨髓来源的细胞确实表达一些内皮细胞或平滑肌细胞的标志物。外周血单个核细胞在体外可根据培养条件分化为内皮样细胞或平滑肌样细胞。

总结

循环祖细胞对血管修复和病变形成有显著贡献。这些发现为开发新的治疗策略提供了基础,这些策略涉及靶向骨髓来源的血管祖细胞的动员、归巢、分化和增殖。

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