» Articles » PMID: 36072343

Molecular Basis for Pericyte-induced Capillary Tube Network Assembly and Maturation

Overview
Specialty Cell Biology
Date 2022 Sep 8
PMID 36072343
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Enhancing human capillary tube network assembly and maturation through upregulated expression of pericyte-derived TIMP-3.

Yrigoin K, Bernard K, Castano M, Cleaver O, Sumanas S, Davis G Front Cell Dev Biol. 2024; 12:1465806.

PMID: 39544367 PMC: 11560913. DOI: 10.3389/fcell.2024.1465806.


Pericyte-to-Endothelial Cell Communication via Tunneling Nanotubes Is Disrupted by a Diol of Docosahexaenoic Acid.

Kempf S, Popp R, Naeem Z, Fromel T, Wittig I, Klatt S Cells. 2024; 13(17.

PMID: 39273001 PMC: 11394577. DOI: 10.3390/cells13171429.


Characterization of Proteome Changes in Aged and Collagen VI-Deficient Human Pericyte Cultures.

Moriggi M, Torretta E, Cescon M, Russo L, Gregorio I, Braghetta P Int J Mol Sci. 2024; 25(13).

PMID: 39000224 PMC: 11241165. DOI: 10.3390/ijms25137118.


Selective mural cell recruitment of pericytes to networks of assembling endothelial cell-lined tubes.

Yrigoin K, Davis G Front Cell Dev Biol. 2024; 12:1389607.

PMID: 38961866 PMC: 11219904. DOI: 10.3389/fcell.2024.1389607.


The role of pericyte in ocular vascular diseases.

Shi L, Ge H, Ye F, Li X, Jiang Q J Biomed Res. 2024; :1-10.

PMID: 38808554 PMC: 11629158. DOI: 10.7555/JBR.37.20230314.


References
1.
Cai Y, Schrenk S, Goines J, Davis G, Boscolo E . Constitutive Active Mutant TIE2 Induces Enlarged Vascular Lumen Formation with Loss of Apico-basal Polarity and Pericyte Recruitment. Sci Rep. 2019; 9(1):12352. PMC: 6710257. DOI: 10.1038/s41598-019-48854-2. View

2.
Horton W, Barrett E . Microvascular Dysfunction in Diabetes Mellitus and Cardiometabolic Disease. Endocr Rev. 2020; 42(1):29-55. PMC: 7846151. DOI: 10.1210/endrev/bnaa025. View

3.
Sun Z, Kemp S, Lin P, Aguera K, Davis G . Endothelial k-RasV12 Expression Induces Capillary Deficiency Attributable to Marked Tube Network Expansion Coupled to Reduced Pericytes and Basement Membranes. Arterioscler Thromb Vasc Biol. 2021; 42(2):205-222. PMC: 8792373. DOI: 10.1161/ATVBAHA.121.316798. View

4.
Yuan L, Sacharidou A, Stratman A, Le Bras A, Zwiers P, Spokes K . RhoJ is an endothelial cell-restricted Rho GTPase that mediates vascular morphogenesis and is regulated by the transcription factor ERG. Blood. 2011; 118(4):1145-53. PMC: 3148162. DOI: 10.1182/blood-2010-10-315275. View

5.
Salvador J, Davis G . Evaluation and Characterization of Endothelial Cell Invasion and Sprouting Behavior. Methods Mol Biol. 2018; 1846:249-259. DOI: 10.1007/978-1-4939-8712-2_16. View