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Effect of Endothelial Nitric Oxide Synthase on Epidermal Permeability Barrier Recovery After Disruption

Overview
Journal Br J Dermatol
Specialty Dermatology
Date 2010 Jul 29
PMID 20662836
Citations 3
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Abstract

Background: We previously demonstrated that neuronal nitric oxide synthase (nNOS) in epidermal keratinocytes is associated with epidermal permeability barrier homeostasis.

Objectives: In the present study, we examined the contributions of inducible nitric oxide synthase (iNOS) and endothelial nitric oxide synthase (eNOS) to epidermal permeability barrier homeostasis.

Methods: We measured the barrier recovery rate after tape stripping of the epidermis of iNOS and eNOS knockout mice, and carried out electron-microscopic observation of the epidermis after acetone treatment.

Results: The barrier recovery rate of eNOS knockout mice was significantly faster than that of the wild-type control, while no significant difference was observed between iNOS knockout mice and wild-type mice. Electron-microscopic observation at 1 h after acetone treatment indicated that barrier recovery of both nNOS and eNOS mice was faster than that of wild-type mice, and lamellar body secretion was accelerated in both types of knockout mice.

Conclusions: These results suggested that both nNOS and eNOS play roles in epidermal barrier homeostasis and lamellar body secretion.

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Role of nitric oxide in regulating epidermal permeability barrier function.

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Inducible nitric oxide synthase is required for epidermal permeability barrier homeostasis in mice.

Dang E, Man G, Zhang J, Lee D, Mauro T, Elias P Exp Dermatol. 2020; 29(10):1027-1032.

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Sphingosine 1-phosphate protects primary human keratinocytes from apoptosis via nitric oxide formation through the receptor subtype S1P₃.

Schmitz E, Potteck H, Schuppel M, Manggau M, Wahydin E, Kleuser B Mol Cell Biochem. 2012; 371(1-2):165-76.

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