The DOI matches its Crossref record; 383 of the 383 references it cites were found in a registry or an index.
Transient Receptor Potential Channels in the Vasculature
Open accessAbstract
The mammalian genome encodes 28 distinct members of the transient receptor potential (TRP) superfamily of cation channels, which exhibit varying degrees of selectivity for different ionic species. Multiple TRP channels are present in all cells and are involved in diverse aspects of cellular function, including sensory perception and signal transduction. Notably, TRP channels are involved in regulating vascular function and pathophysiology, the focus of this review. TRP channels in vascular smooth muscle cells participate in regulating contractility and proliferation, whereas endothelial TRP channel activity is an important contributor to endothelium-dependent vasodilation, vascular wall permeability, and angiogenesis. TRP channels are also present in perivascular sensory neurons and astrocytic endfeet proximal to cerebral arterioles, where they participate in the regulation of vascular tone. Almost all of these functions are mediated by changes in global intracellular Ca 2+levels or subcellular Ca 2+signaling events. In addition to directly mediating Ca 2+entry, TRP channels influence intracellular Ca 2+dynamics through membrane depolarization associated with the influx of cations or through receptor- or store-operated mechanisms. Dysregulation of TRP channels is associated with vascular-related pathologies, including hypertension, neointimal injury, ischemia-reperfusion injury, pulmonary edema, and neurogenic inflammation. In this review, we briefly consider general aspects of TRP channel biology and provide an in-depth discussion of the functions of TRP channels in vascular smooth muscle cells, endothelial cells, and perivascular cells under normal and pathophysiological conditions.
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Cioffi, D. L., Wu, S., Chen, H., ALEXEYEV, M. F., Croix, C. M. S., Pitt, B. R., Uhlig, S., & Stevens, T. (2012) · Circulation Research · doi:10.1161/circresaha.112.269506 · Cited by 73
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PLC-mediated PI(4,5)P2 hydrolysis regulates activation and inactivation of TRPC6/7 channels
Itsuki, K., Imai, Y., Hase, H., Okamura, Y., Inoue, R., & Mori, M. X. (2014) · The Journal of General Physiology · doi:10.1085/jgp.201311033 · Cited by 70
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Kochukov, M. Y., Balasubramanian, A., Noel, R. C., & Marrelli, S. P. (2012) · Journal of Vascular Research · doi:10.1159/000342461 · Cited by 51
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Cell-Cell Contact Formation Governs Ca2+ Signaling by TRPC4 in the Vascular Endothelium
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VR1-Mediated Depressor Effects During High-Salt Intake: Role of Anandamide
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Self-citationCa2+/calmodulin‐dependent protein kinase II function in vascular remodelling
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Tsagogiorgas, C., Wedel, J., Hottenrott, M. C., Schneider, M. O., Binzen, U., Greffrath, W., Treede, R., Theisinger, B., Theisinger, S., Waldherr, R., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043525 · Cited by 43
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Saleh, S. N., Albert, A. P., & Large, W. A. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.166678 · Cited by 43
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Pkd1-inactivation in vascular smooth muscle cells and adaptation to hypertension
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Amplification of EDHF‐type vasodilatations in TRPC1‐deficient mice
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Jurek, S., Hirano-Kobayashi, M., Chiang, H. H., Kohane, D. S., & Matthews, B. D. (2014) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2013-0163oc · Cited by 31
Capsaicin-induced nonneural vasoconstriction in canine mesenteric arteries
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Regulation of Cerebral Artery Smooth Muscle Membrane Potential by Ca2+‐Activated Cation Channels
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Self-citationControl of urinary bladder smooth muscle excitability by the TRPM4 channel modulator 9-phenanthrol
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Metadata
- Authors
- Earley, S., & Brayden, J. E.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2015-04
- Volume
- 95
- Issue
- 2
- Pages
- 645-690
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2117597411
- Cited by
- 420
- References
- 383
- FWCI
- 4.38
- Type
- journal article
- Language
- en
- Open access
- green
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