Regulation of Cellular Communication by Signaling Microdomains in the Blood Vessel Wall
- 1 April 2014
- journal article
- review article
- Published by Elsevier in Pharmacological Reviews
- Vol. 66 (2) , 513-569
Abstract
It has become increasingly clear that the accumulation of proteins in specific regions of the plasma membrane can facilitate cellular communication. These regions, termed signaling microdomains, are found throughout the blood vessel wall where cellular communication, both within and between cell types, must be tightly regulated to maintain proper vascular function. We will define a cellular signaling microdomain and apply this definition to the plethora of means by which cellular communication has been hypothesized to occur in the blood vessel wall. To that end, we make a case for three broad areas of cellular communication where signaling microdomains could play an important role: 1) paracrine release of free radicals and gaseous molecules such as nitric oxide and reactive oxygen species; 2) role of ion channels including gap junctions and potassium channels, especially those associated with the endothelium-derived hyperpolarization mediated signaling, and lastly, 3) mechanism of exocytosis that has considerable oversight by signaling microdomains, especially those associated with the release of von Willebrand factor. When summed, we believe that it is clear that the organization and regulation of signaling microdomains is an essential component to vessel wall function.Keywords
This publication has 892 references indexed in Scilit:
- Paracrine signaling through plasma membrane hemichannelsBiochimica et Biophysica Acta (BBA) - Biomembranes, 2013
- Manipulating Connexin Communication Channels: Use of Peptidomimetics and the Translational OutputsThe Journal of Membrane Biology, 2012
- Cytoplasmic Amino Acids within the Membrane Interface Region Influence Connexin OligomerizationThe Journal of Membrane Biology, 2012
- Regulation of eNOS in Caveolae2012
- Spontaneous Lung Dysfunction and Fibrosis in Mice Lacking Connexin 40 and Endothelial Cell Connexin 43The American Journal of Pathology, 2011
- Enhanced connexin 43 expression delays intra‐mitoitc duration and cell cycle traverse independently of gap junction channel functionJournal of Cellular Biochemistry, 2010
- Epoxyeicosatrienoic acids and endothelium-dependent responsesPflügers Archiv - European Journal of Physiology, 2010
- Limiting transport steps and novel interactions of Connexin-43 along the secretory pathwayHistochemistry and Cell Biology, 2009
- Impact of Actin Rearrangement and Degranulation on the Membrane Structure of Primary Mast Cells: A Combined Atomic Force and Laser Scanning Confocal Microscopy InvestigationBiophysical Journal, 2009
- SNAPs, a family of NSF attachment proteins involved in intracellular membrane fusion in animals and yeastCell, 1990