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生还是死:内皮细胞在发育、修复和疾病中的可塑性。

To be or not to be: endothelial cell plasticity in development, repair, and disease.

机构信息

Division of Developmental Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, 20892, USA.

出版信息

Angiogenesis. 2021 May;24(2):251-269. doi: 10.1007/s10456-020-09761-7. Epub 2021 Jan 15.

Abstract

Endothelial cells display an extraordinary plasticity both during development and throughout adult life. During early development, endothelial cells assume arterial, venous, or lymphatic identity, while selected endothelial cells undergo additional fate changes to become hematopoietic progenitor, cardiac valve, and other cell types. Adult endothelial cells are some of the longest-lived cells in the body and their participation as stable components of the vascular wall is critical for the proper function of both the circulatory and lymphatic systems, yet these cells also display a remarkable capacity to undergo changes in their differentiated identity during injury, disease, and even normal physiological changes in the vasculature. Here, we discuss how endothelial cells become specified during development as arterial, venous, or lymphatic endothelial cells or convert into hematopoietic stem and progenitor cells or cardiac valve cells. We compare findings from in vitro and in vivo studies with a focus on the zebrafish as a valuable model for exploring the signaling pathways and environmental cues that drive these transitions. We also discuss how endothelial plasticity can aid in revascularization and repair of tissue after damage- but may have detrimental consequences under disease conditions. By better understanding endothelial plasticity and the mechanisms underlying endothelial fate transitions, we can begin to explore new therapeutic avenues.

摘要

内皮细胞在发育过程中和整个成年期都表现出非凡的可塑性。在早期发育过程中,内皮细胞具有动脉、静脉或淋巴管的特性,而一些特定的内皮细胞则会发生额外的命运变化,成为造血祖细胞、心脏瓣膜和其他细胞类型。成年内皮细胞是体内寿命最长的细胞之一,它们作为血管壁的稳定组成部分的参与对于循环系统和淋巴系统的正常功能至关重要,但这些细胞在损伤、疾病甚至血管的正常生理变化过程中,也表现出显著的改变其分化特性的能力。在这里,我们讨论内皮细胞在发育过程中如何被特化为动脉、静脉或淋巴管内皮细胞,或者转化为造血干细胞和祖细胞或心脏瓣膜细胞。我们将比较来自体外和体内研究的发现,重点关注斑马鱼作为探索驱动这些转变的信号通路和环境线索的有价值模型。我们还讨论了内皮细胞的可塑性如何有助于损伤后组织的再血管化和修复——但在疾病条件下可能会产生有害的后果。通过更好地了解内皮细胞的可塑性和内皮细胞命运转变的机制,我们可以开始探索新的治疗途径。

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