Physiological role of vascular endothelial growth factors as homeostatic regulators.
Authors
Bates, DBeazley-Long, N
Benest, A
Ye, X
Ved, N
Hulse, R
Barratt, S
Machado, M
Donaldson, L
Harper, S
Peiris-Pagès, Maria
Tortonese, D
Oltean, S
Foster, R
Affiliation
Cancer Biology, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Queen's Medical Centre, NottinghamIssue Date
2018-06-18
Metadata
Show full item recordAbstract
The vascular endothelial growth factor (VEGF) family of proteins are key regulators of physiological systems. Originally linked with endothelial function, they have since become understood to be principal regulators of multiple tissues, both through their actions on vascular cells, but also through direct actions on other tissue types, including epithelial cells, neurons, and the immune system. The complexity of the five members of the gene family in terms of their different splice isoforms, differential translation, and specific localizations have enabled tissues to use these potent signaling molecules to control how they function to maintain their environment. This homeostatic function of VEGFs has been less intensely studied than their involvement in disease processes, development, and reproduction, but they still play a substantial and significant role in healthy control of blood volume and pressure, interstitial volume and drainage, renal and lung function, immunity, and signal processing in the peripheral and central nervous system. The widespread expression of VEGFs in healthy adult tissues, and the disturbances seen when VEGF signaling is inhibited support this view of the proteins as endogenous regulators of normal physiological function. This review summarizes the evidence and recent breakthroughs in understanding of the physiology that is regulated by VEGF, with emphasis on the role they play in maintaining homeostasis.Citation
Physiological role of vascular endothelial growth factors as homeostatic regulators. 2018, 8(3): 955-979 Compr PhysiolJournal
Comprehensive PhysiologyDOI
10.1002/cphy.c170015PubMed ID
29978898Type
ArticleLanguage
enISSN
2040-4603ae974a485f413a2113503eed53cd6c53
10.1002/cphy.c170015
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