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Phospholipases A2 and neural membrane dynamics: implications for Alzheimer's disease.

Abstract
Phospholipases A(2) (PLA(2)s) are essential enzymes in cells. They are not only responsible for maintaining the structural organization of cell membranes, but also play a pivotal role in the regulation of cell functions. Activation of PLA(2) s results in the release of fatty acids and lysophospholipids, products that are lipid mediators and compounds capable of altering membrane microdomains and physical properties. Although not fully understood, recent studies have linked aberrant PLA(2) activity to oxidative signaling pathways involving NADPH oxidase that underlie the pathophysiology of a number of neurodegenerative diseases. In this paper, we review studies describing the involvement of cytosolic PLA(2) in oxidative signaling pathways leading to neuronal impairment and activation of glial cell inflammatory responses. In addition, this review also includes information on the role of cytosolic PLA(2) and exogenous secretory PLA(2) on membrane physical properties, dynamics, and membrane proteins. Unraveling the mechanisms that regulate specific types of PLA(2)s and their effects on membrane dynamics are important prerequisites towards understanding their roles in the pathophysiology of Alzheimer's disease, and in the development of novel therapeutics to retard progression of the disease.
AuthorsJames C-M Lee, Agnes Simonyi, Albert Y Sun, Grace Y Sun
JournalJournal of neurochemistry (J Neurochem) Vol. 116 Issue 5 Pg. 813-9 (Mar 2011) ISSN: 1471-4159 [Electronic] England
PMID21214562 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Review)
Copyright© 2011 The Authors. Journal of Neurochemistry © 2011 International Society for Neurochemistry.
Chemical References
  • Amyloid beta-Peptides
  • Phospholipases A2
  • Calcium
Topics
  • Alzheimer Disease (pathology)
  • Amyloid beta-Peptides (metabolism)
  • Animals
  • Calcium (metabolism)
  • Cell Membrane (metabolism)
  • Humans
  • Inflammation (metabolism)
  • Models, Biological
  • Neurons (pathology)
  • Nonlinear Dynamics
  • Phospholipases A2 (metabolism)
  • Signal Transduction (physiology)

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