Open Access. Powered by Scholars. Published by Universities.®

Medicine and Health Sciences Commons

Open Access. Powered by Scholars. Published by Universities.®

Medical Microbiology

PDF

2010

Institution
Keyword
Publication
Publication Type

Articles 31 - 32 of 32

Full-Text Articles in Medicine and Health Sciences

Fluprostenol-Induced Mapk Signaling Is Independent Of Aging In Fischer 344/Nniahsd X Brown Norway/Binia Rat Aorta, Kevin M. Rice, Ernest M. Walker, Sunil K. Kakarla, Satyanarayana Paturi, Miaozong Wu, Sumit Narula, Eric R. Blough Jan 2010

Fluprostenol-Induced Mapk Signaling Is Independent Of Aging In Fischer 344/Nniahsd X Brown Norway/Binia Rat Aorta, Kevin M. Rice, Ernest M. Walker, Sunil K. Kakarla, Satyanarayana Paturi, Miaozong Wu, Sumit Narula, Eric R. Blough

MIIR Faculty Research

The factors that regulate vascular mechanotransduction and how this process may be altered with aging are poorly understood and have not been widely studied. Recent data suggest that increased tissue loading can result in the release of prostaglandin F2 alpha (PGF2α) and other reports indicate that aging diminishes the ability of the aged aorta to activate mitogen activated protein kinase (MAPK) signaling in response to increased loading. Using ex vivo incubations, here we investigate whether aging affects the ability of the aorta to induce phosphorylation of extracellular signal-regulated kinase 1/2 (ERK½-MAPK), p38-MAPK, and Jun N-terminal kinase (JNK-MAPK) activation following stimulation …


Study Of Polytopic Membrane Protein Topological Organization As A Function Of Membrane Lipid Composition, Mikhail Bogdanov, Philip N Heacock, William Dowhan Jan 2010

Study Of Polytopic Membrane Protein Topological Organization As A Function Of Membrane Lipid Composition, Mikhail Bogdanov, Philip N Heacock, William Dowhan

Faculty and Staff Publications

A protocol is described using lipid mutants and thiol-specific chemical reagents to study lipid-dependent and host-specific membrane protein topogenesis by the substituted-cysteine accessibility method as applied to transmembrane domains (SCAM). SCAM is adapted to follow changes in membrane protein topology as a function of changes in membrane lipid composition. The strategy described can be adapted to any membrane system.