• Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Impaired survival of peripheral T cells, disrupted NK/NKT cell development, and liver failure in mice lacking Gimap5.

The loss of Gimap5 (GTPase of the immune-associated protein 5) gene function is the underlying cause of lymphopenia and autoimmune diabetes in the BioBreeding (BB) rat. The in vivo function of murine gimap5 is largely unknown. We show that selective gene ablation of the mouse gimap5 gene impairs the final intrathymic maturation of CD8 and CD4 T cells and compromises the survival of postthymic CD4 and CD8 cells, replicating findings in the BB rat model. In addition, gimap5 deficiency imposes a block of natural killer (NK)- and NKT-cell differentiation. Development of NK/NKT cells is restored on transfer of gimap5(-/-) bone marrow into a wild-type environment. Mice lacking gimap5 have a median survival of 15 weeks, exhibit chronic hepatic hematopoiesis, and in later stages show pronounced hepatocyte apoptosis, leading to liver failure. This pathology persists in a Rag2-deficient background in the absence of mature B, T, or NK cells and cannot be adoptively transferred by transplanting gimap5(-/-) bone marrow into wild-type recipients. We conclude that mouse gimap5 is necessary for the survival of peripheral T cells, NK/NKT-cell development, and the maintenance of normal liver function. These functions involve cell-intrinsic as well as cell-extrinsic mechanisms.

Pubmed ID: 18796632

Authors

  • Schulteis RD
  • Chu H
  • Dai X
  • Chen Y
  • Edwards B
  • Haribhai D
  • Williams CB
  • Malarkannan S
  • Hessner MJ
  • Glisic-Milosavljevic S
  • Jana S
  • Kerschen EJ
  • Ghosh S
  • Wang D
  • Kwitek AE
  • Lernmark A
  • Gorski J
  • Weiler H

Journal

Blood

Publication Data

December 15, 2008

Associated Grants

  • Agency: NIAID NIH HHS, Id: AI42380-04
  • Agency: NHLBI NIH HHS, Id: HL073284
  • Agency: NIAID NIH HHS, Id: P01 AI042380
  • Agency: NIAID NIH HHS, Id: P01 AI042380-090006
  • Agency: NIAID NIH HHS, Id: P01 AI042380-100006
  • Agency: NIAID NIH HHS, Id: P01 AI042380-110006
  • Agency: NIAID NIH HHS, Id: P01 AI042380-120006
  • Agency: NIAID NIH HHS, Id: P01 AI042380-130006
  • Agency: NIAID NIH HHS, Id: R01 AI073731
  • Agency: PHS HHS, Id: R01A1064826-01
  • Agency: NIAID NIH HHS, Id: R01AI47154
  • Agency: NIBIB NIH HHS, Id: R01EB001421

Mesh Terms

  • Animals
  • CD4-Positive T-Lymphocytes
  • CD8-Positive T-Lymphocytes
  • Cell Differentiation
  • Cell Survival
  • GTP Phosphohydrolases
  • GTP-Binding Proteins
  • Liver Failure
  • Mice
  • Mice, Mutant Strains
  • Natural Killer T-Cells
  • T-Lymphocytes