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

Yi Chi Fu, Jen Tsung Yang, Hui Wen Chen, June Hsieh Wu*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

5 Scopus citations

Abstract

Background: 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.

Original languageEnglish
Pages (from-to)1915-1919
Number of pages5
JournalClinica Chimica Acta
Volume411
Issue number23-24
DOIs
StatePublished - 14 12 2010

Keywords

  • Annexin A5
  • Cell membrane
  • Enzyme-linked immunosorbent assay
  • Flow cytometry
  • Lipoprotein (a)
  • Phosphatidylserine

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