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周细胞诱导毛细血管管网组装和成熟的分子基础。

Molecular basis for pericyte-induced capillary tube network assembly and maturation.

作者信息

Kemp Scott S, Lin Prisca K, Sun Zheying, Castaño Maria A, Yrigoin Ksenia, Penn Marlena R, Davis George E

机构信息

Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida School of Medicine, Tampa, FL, United States.

出版信息

Front Cell Dev Biol. 2022 Aug 22;10:943533. doi: 10.3389/fcell.2022.943533. eCollection 2022.

DOI:10.3389/fcell.2022.943533
PMID:36072343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9441561/
Abstract

Here we address the functional importance and role of pericytes in capillary tube network assembly, an essential process that is required for vascularized tissue development, maintenance, and health. Healthy capillaries may be directly capable of suppressing human disease. Considerable advances have occurred in our understanding of the molecular and signaling requirements controlling EC lumen and tube formation in 3D extracellular matrices. A combination of SCF, IL-3, SDF-1α, FGF-2 and insulin ("Factors") in conjunction with integrin- and MT1-MMP-induced signaling are required for EC sprouting behavior and tube formation under serum-free defined conditions. Pericyte recruitment to the abluminal EC tube surface results in elongated and narrow tube diameters and deposition of the vascular basement membrane. In contrast, EC tubes in the absence of pericytes continue to widen and shorten over time and fail to deposit basement membranes. Pericyte invasion, recruitment and proliferation in 3D matrices requires the presence of ECs. A detailed analysis identified that EC-derived PDGF-BB, PDGF-DD, ET-1, HB-EGF, and TGFβ1 are necessary for pericyte recruitment, proliferation, and basement membrane deposition. Blockade of these individual factors causes significant pericyte inhibition, but combined blockade profoundly interferes with these events, resulting in markedly widened EC tubes without basement membranes, like when pericytes are absent.

摘要

在此,我们探讨周细胞在毛细血管管网组装中的功能重要性和作用,这是血管化组织发育、维持和健康所必需的关键过程。健康的毛细血管可能直接具备抑制人类疾病的能力。我们对控制内皮细胞(EC)在三维细胞外基质中形成管腔和管道的分子及信号需求的理解取得了显著进展。在无血清特定条件下,内皮细胞的芽生行为和管道形成需要干细胞因子(SCF)、白细胞介素-3(IL-3)、基质细胞衍生因子-1α(SDF-1α)、成纤维细胞生长因子-2(FGF-2)和胰岛素(“因子”)的组合,以及整合素和MT1-基质金属蛋白酶(MT1-MMP)诱导的信号。周细胞募集到内皮细胞管腔外表面会导致管径变长变窄,并沉积血管基底膜。相比之下,没有周细胞的内皮细胞管会随着时间的推移继续变宽和缩短,且无法沉积基底膜。周细胞在三维基质中的侵入、募集和增殖需要内皮细胞的存在。详细分析表明,内皮细胞衍生的血小板源性生长因子-BB(PDGF-BB)、血小板源性生长因子-DD(PDGF-DD)、内皮素-1(ET-1)、肝素结合表皮生长因子(HB-EGF)和转化生长因子β1(TGFβ1)对于周细胞的募集、增殖和基底膜沉积是必需的。阻断这些单个因子会导致周细胞显著抑制,但联合阻断会严重干扰这些事件,导致内皮细胞管明显变宽且无基底膜,就像没有周细胞时一样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/9441561/6c12df8f2843/fcell-10-943533-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/9441561/5c4f3c9686fc/fcell-10-943533-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/9441561/6db029a5c995/fcell-10-943533-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/9441561/6c12df8f2843/fcell-10-943533-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/9441561/5c4f3c9686fc/fcell-10-943533-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/9441561/6db029a5c995/fcell-10-943533-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51d/9441561/6c12df8f2843/fcell-10-943533-g003.jpg

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