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Review
. 2014 Apr;28(2):155-79.
doi: 10.1016/j.hoc.2013.12.002. Epub 2014 Jan 22.

Hemoglobin s polymerization and red cell membrane changes

Affiliations
Review

Hemoglobin s polymerization and red cell membrane changes

Frans A Kuypers. Hematol Oncol Clin North Am. 2014 Apr.

Abstract

Different pathways lead from the simple point mutation in hemoglobin to the membrane changes that characterize the altered interaction of the sickle red blood cell with its environment, including endothelial cells, white blood cells, and platelets. Polymerization and oxidation-induced damage to both lipid and protein components of the red cell membrane, as well as the generation of bioreactive membrane material (microparticles), has a profound effect on all tissues and organs, and defines the vasculopathy of the patient with sickle cell disease.

Keywords: Membrane lipids; Microparticles; Oxidative damage; Polymerization.

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