Hematopoietic Cell Regulation by Rac1 and Rac2 Guanosine Triphosphatases

Author:

Gu Yi1234,Filippi Marie-Dominique1234,Cancelas Jose A.1234,Siefring Jamie E.1234,Williams Emily P.1234,Jasti Aparna C.1234,Harris Chad E.1234,Lee Andrew W.1234,Prabhakar Rethinasamy1234,Atkinson Simon J.1234,Kwiatkowski David J.1234,Williams David A.1234

Affiliation:

1. Division of Experimental Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

2. Hoxworth Blood Center, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.

3. Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.

4. Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.

Abstract

The Rho guanosine triphosphatases (GTPases) Rac1 and Rac2 are critical signaling regulators in mammalian cells. The deletion of both Rac1 and Rac2 murine alleles leads to a massive egress of hematopoietic stem/progenitor cells (HSC/Ps) into the blood from the marrow, whereas Rac1 –/– but not Rac2 –/– HSC/Ps fail to engraft in the bone marrow of irradiated recipient mice. In contrast, Rac2, but not Rac1, regulates superoxide production and directed migration in neutrophils, and in each cell type, the two GTPases play distinct roles in actin organization, cell survival, and proliferation. Thus, Rac1 and Rac2 regulate unique aspects of hematopoietic development and function.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference32 articles.

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5. Deficiency of the Hematopoietic Cell-Specific Rho Family GTPase Rac2 Is Characterized by Abnormalities in Neutrophil Function and Host Defense

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