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Effect of lipoprotein (a) on annexin A5 binding to cell membrane.

AbstractBACKGROUND:
High blood lipoprotein (a) [Lp(a)] concentration is a risk factor for a thrombotic event. Annexin A5 is involved in anticoagulation on the endothelial surface. How Lp(a) affects the annexin A5 function is not clear. This study investigates annexin A5 binding on the cell membrane in the presence of Lp(a).
METHODS:
Lp(a) was isolated from human blood plasma by ultracentrifugation and annexin A5 protein was purchased commercially. The cell membrane was prepared from primary human umbilical vein endothelial cells (HUVEC) and cultured cell line HepG2 by sucrose density gradient centrifugation. Enzyme-linked immunosorbent assays (ELISA) were used to examine annexin A5 binding to the cell membrane in the presence of Lp(a). Flow cytometry was used to analyze the binding of fluorescence-labeled annexin A5 to phosphatidylserine (PS)-translocated intact cells in the presence of Lp(a).
RESULTS:
Annexin A5 binding to the cell membrane was attenuated by a high concentration of Lp(a) in both HUVEC and HepG2 membrane surfaces. The phenomenon was also observed with annexin A5 surface labeling of HepG2 cells and flow cytometry analysis.
CONCLUSIONS:
The results imply that Lp(a) interferes with annexin A5 binding to the procoagulant PS which translocates to the membrane surface under stress condition and therefore may increase the risk for thrombosis.
AuthorsYi-Chi Fu, Jen-Tsung Yang, Hui-Wen Chen, June Hsieh Wu
JournalClinica chimica acta; international journal of clinical chemistry (Clin Chim Acta) Vol. 411 Issue 23-24 Pg. 1915-9 (Dec 14 2010) ISSN: 1873-3492 [Electronic] Netherlands
PMID20705065 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2010 Elsevier B.V. All rights reserved.
Chemical References
  • Annexin A2
  • Annexin A5
  • Ligands
  • Lipoprotein(a)
  • Phosphatidylserines
Topics
  • Annexin A2 (metabolism)
  • Annexin A5 (metabolism)
  • Biological Transport (drug effects)
  • Cell Membrane (drug effects, metabolism)
  • Dose-Response Relationship, Drug
  • Endothelial Cells (cytology, drug effects, metabolism)
  • Flow Cytometry
  • Hep G2 Cells
  • Humans
  • Ligands
  • Lipoprotein(a) (metabolism, pharmacology)
  • Phosphatidylserines (metabolism)
  • Protein Binding (drug effects)
  • Stress, Physiological (drug effects)

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