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Corticotropin releasing hormone and related peptides can act as bioregulatory factors in human keratinocytes
Authors:Andrzej T Slominski  Birgit Roloff  Blazej Zbytek  Edward T Wei  Klaus Fechner  Jonathan Curry  Jacobo Wortsman
Institution:(1) Department of Pathology, Medical Center, Loyola University, 2160 First South Avenue, 60153 Maywood, Illinois;(2) Department of Histology and Immunology, Medical University of Gdansk, Gdansk, Poland;(3) Department of Pharmacology, School of Public Health, University of California, Berkeley, California;(4) Institute of Molecular Pharmacology, Berlin, Germany;(5) Department of Medicine, Southern Illinois University, Springfield, Illinois
Abstract:Summary Following previous findings in human skin of the functional expression of genes for the corticotropin releasing hormone (CHR) receptor type 1 (CRH-R1) and CRH itself, we searched for local phenotypic effects for peptides related to CRH. We now report that CRH, sauvagine, and urocortin inhibit proliferation of human HaCaT keratinocytes in a dose-dependent manner. The peptides produced variable cyclic adenosine 3′∶5′-monophosphate stimulation with CRH having the highest potency. Binding of iodine 125 CRH to intact keratinocytes was inhibited by increasing doses of CRH, sauvagine, or urocortin, all showing equal inhibitory potency. Immunocytochemistry identified CRH-R1 immunoreactivity in HaCaT keratinocytes. In conclusion, CRH (exogenous or produced locally) and the related urocortin and sauvagine peptides can modify human keratinocyte phenotype through a receptor-mediated pathway.
Keywords:CRH  urocortin  sauvagine  CRH receptors  keratinocytes  skin
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