Short survival of phosphatidylserine-exposing red blood cells in murine sickle cell anemia.

Abstract:

:Several transgenic murine models for sickle cell anemia have been developed that closely reproduce the biochemical and physiological disorders in the human disease. A comprehensive characterization is described of hematologic parameters of mature red blood cells, reticulocytes, and red cell precursors in the bone marrow and spleen of a murine sickle cell model in which erythroid cells expressed exclusively human alpha, gamma, and betaS globin. Red cell survival was dramatically decreased in these anemic animals, partially compensated by considerable enhancement in erythropoietic activity. As in humans, these murine sickle cells contain a subpopulation of phosphatidylserine-exposing cells that may play a role in their premature removal. Continuous in vivo generation of this phosphatidylserine-exposing subset may have a significant impact on the pathophysiology of sickle cell disease.

journal_name

Blood

journal_title

Blood

authors

de Jong K,Emerson RK,Butler J,Bastacky J,Mohandas N,Kuypers FA

doi

10.1182/blood.v98.5.1577

subject

Has Abstract

pub_date

2001-09-01 00:00:00

pages

1577-84

issue

5

eissn

0006-4971

issn

1528-0020

journal_volume

98

pub_type

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