Commentary: Cyclic Adenosine Monophosphate Regulation of Normal and Psoriatic Epidermis

Publisher Website
Google Scholar
Abstract
An article previously published in the Archives1 proposed decreased activity in the cyclic adenosine monophosphate (cAMP) cascade as one potential molecular explanation of the following three characteristics of lesional epidermis in psoriasis: (1) increased cellular proliferation, (2) increased glycogen, and (3) decreased cellular differentiation. In nonepidermal cells, cAMP was known to decrease proliferation, decrease glycogen, and increase differentiation. The cAMP hypothesis assumed that, at the level of molecular regulation, epidermal and nonepidermal cells would be similar rather than dissimilar. If so, decreased cascade activity in different epidermal layers would be one explanation for three lesional characteristics. EPIDERMAL HOMEOSTASIS If the cAMP hypothesis is a tenable explanation for misregulated epidermal proliferation in psoriasis, it must be compatible with our current understanding of proliferative homeostasis. This is the mechanism used to maintain low-level cell proliferation that is sufficient to provide new cells to replace those sloughed from the surface of relatively

This publication has 38 references indexed in Scilit: