Journal
CELLULAR SIGNALLING
Volume 24, Issue 6, Pages 1333-1343Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2012.01.009
Keywords
Phospholipase C epsilon; G protein-coupled receptor; Ras family GTPase; Cardiovascular function; Diabetes; Inflammation
Categories
Funding
- National Institutes of Health [GM R01 053536, GM R01 036927, DK R01 045817, DK R01 069575]
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Receptor-initiated phospholipase C activation and generation of IP3 and DAG are important common triggers for a diversity of signal transduction processes in many cell types. Contributing to this diversity is the existence and differential cellular and subcellular distribution of distinct phospholipase C isoforms with distinct regulatory properties. The recently identified PLC epsilon enzyme is an isoform that is uniquely regulated by multiple upstream signals including ras-family GTP binding proteins as well as heterotrimeric G-proteins. In this review we will consider the well documented biochemical regulation of this isoform in the context of cell and whole animal physiology and in the context of other G protein-regulated PLC isoforms. These studies together reveal a surprisingly wide range of unexpected functions for PLC epsilon in cellular signaling, physiology and disease. (c) 2012 Elsevier Inc. All rights reserved.
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