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Gli1+ Cells Couple with Type H Vessels and Are Required for Type H Vessel Formation

机译:Gli1 +细胞与H型血管结合是H型血管形成所必需的

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摘要

Mesenchymal stem/stromal cells (MSCs) reside in the perivascular niche and modulate tissue/organ homeostasis; however, little is known about whether and how their localization and function are linked. Particularly, whether specific MSC subsets couple with and regulate specialized vessel subtypes is unclear. Here, we show that Gli1 cells, which are a subpopulation of MSCs couple with and regulate a specialized form of vasculature. The specific capillaries, i.e , CD31 EMCN type H vessels, are the preferable vascular subtype which Gli1 cells are adjacent to in bone. Gli1 cells are further identified to be phenotypically coupled with type H endothelium during bone growth and defect healing. Importantly, Gli1 cell ablation inhibits type H vessel formation associated with suppressed bone generation and regeneration. Mechanistically, Gli1 cells initiate angiogenesis through Gli and HIF-1α signaling. These findings suggest a morphological and functional framework of Gli1 cells modulating coupled type H vasculature for tissue homeostasis and regenerative repair.
机译:间充质干/基质细胞(MSC)驻留在血管周围的壁iche中,并调节组织/器官的动态平衡。但是,关于它们的定位和功能是否以及如何链接的了解甚少。特别是,尚不清楚特定的MSC亚群是否与特定的血管亚型结合并对其进行调节。在这里,我们显示了Gli1细胞,它是MSC的一个亚群,并与它们调控着特定形式的脉管系统。特定的毛细血管,即CD31 EMCN H型血管,是骨骼中Gli1细胞相邻的优选血管亚型。进一步确定Gli1细胞在骨生长和缺陷修复过程中与H型内皮细胞表型偶联。重要的是,Gli1细胞消融可抑制与抑制骨生成和再生有关的H型血管形成。从机制上讲,Gli1细胞通过Gli和HIF-1α信号启动血管生成。这些发现表明,Gli1细胞的形态和功能框架可调节H型脉管系统的组织稳态和再生修复。

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