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Nociceptive TRP Channels: Sensory Detectors and Transducers in Multiple Pain Pathologies

TRP Channels in Skin Biology and Pathophysiology

Departments of Neurosurgery, Biological Chemistry and Neuroscience, Neurosurgery Pain Research Institute, Johns Hopkins School of Medicine, 725 N. Wolfe St., Baltimore, MD 21205, USA
Author to whom correspondence should be addressed.
Academic Editors: Arpad Szallasi and Susan M. Huang
Pharmaceuticals 2016, 9(4), 77;
Received: 25 October 2016 / Revised: 8 December 2016 / Accepted: 9 December 2016 / Published: 14 December 2016
Ion channels of the Transient Receptor Potential (TRP) family mediate the influx of monovalent and/or divalent cations into cells in response to a host of chemical or physical stimuli. In the skin, TRP channels are expressed in many cell types, including keratinocytes, sensory neurons, melanocytes, and immune/inflammatory cells. Within these diverse cell types, TRP channels participate in physiological processes ranging from sensation to skin homeostasis. In addition, there is a growing body of evidence implicating abnormal TRP channel function, as a product of excessive or deficient channel activity, in pathological skin conditions such as chronic pain and itch, dermatitis, vitiligo, alopecia, wound healing, skin carcinogenesis, and skin barrier compromise. These diverse functions, coupled with the fact that many TRP channels possess pharmacologically accessible sites, make this family of proteins appealing therapeutic targets for skin disorders. View Full-Text
Keywords: transient receptor potential; skin; pain; itch; dermatitis; epidermis transient receptor potential; skin; pain; itch; dermatitis; epidermis
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MDPI and ACS Style

Caterina, M.J.; Pang, Z. TRP Channels in Skin Biology and Pathophysiology. Pharmaceuticals 2016, 9, 77.

AMA Style

Caterina MJ, Pang Z. TRP Channels in Skin Biology and Pathophysiology. Pharmaceuticals. 2016; 9(4):77.

Chicago/Turabian Style

Caterina, Michael J., and Zixuan Pang. 2016. "TRP Channels in Skin Biology and Pathophysiology" Pharmaceuticals 9, no. 4: 77.

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