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PMID: 12010804 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Normal hemostasis but defective hematopoietic response to growth factors in mice deficient in phospholipid scramblase 1.

Blood ·Vol. 99 ·No. 11 ·2002-06-01 ·Pages 4030-8

Zhou Q, Zhao J, Wiedmer T, Sims PJ

Abstract

Phospholipid scramblase 1 (PLSCR1) is an endofacial plasma membrane protein proposed to participate in transbilayer movement of phosphatidylserine and other phospholipids. In addition to its putative role in the reorganization of plasma membrane phospholipids, PLSCR1 is a substrate of intracellular kinases that imply its possible participation in diverse signaling pathways underlying proliferation, differentiation, or apoptosis. Because PLSCR1 is prominently expressed in a variety of blood cells, we evaluated PLSCR activity in platelets and erythrocytes, and cytokine-dependent growth of hematopoietic precursor cells, of PLSCR1 knock-out mice. Adult PLSCR1(-/-) mice showed no obvious hematologic or hemostatic abnormality, and blood cells from these animals normally mobilized phosphatidylserine to the cell surface upon stimulation. Whereas blood cell counts in adult PLSCR1(-/-) mice were normal, in both fetus and newborn animals neutrophil counts were significantly depressed relative to age-matched wild type (WT). Furthermore, when compared with WT, hematopoietic precursor cells from PLSCR1(-/-) mice showed defective colony formation and impaired differentiation to mature granulocytes as stimulated by stem cell factor and granulocyte colony-stimulating factor (G-CSF). By contrast, PLSCR1(-/-) cells showed normal colony formation stimulated by interleukin-3 or granulocyte-macrophage CSF, and expansion of megakaryocytic and erythroid progenitors by thrombopoietin or erythropoietin was unaffected. Stem cell factor and G-CSF were also found to induce marked increases in PLSCR1 levels in WT cells. Consistent with in vitro assays, PLSCR1(-/-) mice treated with G-CSF showed less than 50% of the granulocytosis observed in identically treated WT mice. These data provide direct evidence that PLSCR1 functionally contributes to cytokine-regulated cell proliferation and differentiation and suggest it is required for normal myelopoiesis.

MeSH Terms
Animals Animals, Newborn Apoptosis/drug effects Bleeding Time Blood Platelets/physiology Bone Marrow Cells/cytology Ca(2+) Mg(2+)-ATPase/deficiency,genetics,metabolism Carrier Proteins/genetics,metabolism Cells, Cultured Colony-Forming Units Assay Fetus Gene Expression Regulation, Enzymologic/drug effects Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology Granulocytes/physiology Growth Substances/pharmacology Hematopoiesis/drug effects,physiology Hemostasis/physiology Liver/cytology,physiology Membrane Proteins/deficiency,genetics,metabolism Mice Mice, Knockout Phospholipid Transfer Proteins Platelet Activation Reference Values Stem Cell Factor/pharmacology
Chemicals
Carrier Proteins Growth Substances Membrane Proteins Phospholipid Transfer Proteins Stem Cell Factor Granulocyte-Macrophage Colony-Stimulating Factor Ca(2+) Mg(2+)-ATPase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zhou Quansheng
Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
Zhao Ji
Wiedmer Therese
Sims Peter J
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2002-06-01
Pages
4030-8
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NHLBI NIH HHS · HL36946 · United States
NHLBI NIH HHS · HL61200 · United States
NHLBI NIH HHS · HL63819 · United States
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