Published August 8, 2008 | Version v1
Journal article

Essential roles of mgcRacGAP in multilineage differentiation and survival of murine hematopoietic cells

  • 1. Department of Molecular Genetics, Institute for Liver Research, Kansai Medical University (Japan)
  • 2. Laboratory for Lymphocyte Differentiation, RIKEN Research Center for Allergy and Immunology, Suehiro-cho 1-7-22, Tsurumi-ku, Yokohama, Kanagawa 230-0045 (Japan)

Description

MgcRacGAP, a negative regulator for Rho family GTPases, has been shown to play important roles in cytokinesis using several cell lines. However, the physiological role of mgcRacGAP in multilineage hematopoietic development remains unclear. Here, we conditionally ablated mgcRacGAP in vivo to clarify this issue. As the result, we found that normal hematopoietic development including proliferation and survival requires mgcRacGAP. We also found that depletion of mgcRacGAP in hematopoietic cells results in a marked decrease in c-Kit+Sca-1+Lin- cells, suggesting that mgcRacGAP is required for the maintenance of the hematopoietic stem cells. In addition, B cells in which mgcRacGAP had been selectively ablated showed proliferation failure and fell into apoptosis. Taken together, mgcRacGAP is now shown to play a indispensable role in the development of hematopoietic cells in vivo

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2008.05.170

Additional details

Identifiers

DOI
10.1016/j.bbrc.2008.05.170;
PII
S0006-291X(08)01119-4;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
372
Journal Issue
4
Journal Page Range
p. 941-946
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
40023728
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
APOPTOSIS; CELL DIVISION; CELL PROLIFERATION; FAILURES; IN VIVO; STEM CELLS
Descriptors DEC
ANIMAL CELLS; SOMATIC CELLS

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.