TRP Channels in Angiogenesis and Other Endothelial Functions.

dc.contributor.authorSmani, Tarik
dc.contributor.authorGómez, Luis J
dc.contributor.authorRegodon, Sergio
dc.contributor.authorWoodard, Geoffrey E
dc.contributor.authorSiegfried, Geraldine
dc.contributor.authorKhatib, Abdel-Majid
dc.contributor.authorRosado, Juan A
dc.date.accessioned2025-01-07T15:15:57Z
dc.date.available2025-01-07T15:15:57Z
dc.date.issued2018-12-03
dc.description.abstractAngiogenesis is the growth of blood vessels mediated by proliferation, migration, and spatial organization of endothelial cells. This mechanism is regulated by a balance between stimulatory and inhibitory factors. Proangiogenic factors include a variety of VEGF family members, while thrombospondin and endostatin, among others, have been reported as suppressors of angiogenesis. Transient receptor potential (TRP) channels belong to a superfamily of cation-permeable channels that play a relevant role in a number of cellular functions mostly derived from their influence in intracellular Ca2+ homeostasis. Endothelial cells express a variety of TRP channels, including members of the TRPC, TRPV, TRPP, TRPA, and TRPM families, which play a relevant role in a number of functions, including endothelium-induced vasodilation, vascular permeability as well as sensing hemodynamic and chemical changes. Furthermore, TRP channels have been reported to play an important role in angiogenesis. This review summarizes the current knowledge and limitations concerning the involvement of particular TRP channels in growth factor-induced angiogenesis.
dc.identifier.doi10.3389/fphys.2018.01731
dc.identifier.issn1664-042X
dc.identifier.pmcPMC6287032
dc.identifier.pmid30559679
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC6287032/pdf
dc.identifier.unpaywallURLhttps://www.frontiersin.org/articles/10.3389/fphys.2018.01731/pdf
dc.identifier.urihttps://hdl.handle.net/10668/27000
dc.journal.titleFrontiers in physiology
dc.journal.titleabbreviationFront Physiol
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Sevilla (IBIS)
dc.page.number1731
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectTRP channels
dc.subjectTRPC
dc.subjectTRPM
dc.subjectTRPV
dc.subjectVEGF
dc.subjectangiogenesis
dc.subjectendothelial cells
dc.titleTRP Channels in Angiogenesis and Other Endothelial Functions.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number9

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