Skip Navigation


International Immunology Advance Access originally published online on May 19, 2009
International Immunology 2009 21(6):715-725; doi:10.1093/intimm/dxp043
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
21/6/715    most recent
dxp043v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Huntington, N. D.
Right arrow Articles by Alves, N. L.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Huntington, N. D.
Right arrow Articles by Alves, N. L.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?


© The Japanese Society for Immunology. 2009. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Loss of the pro-apoptotic BH3-only Bcl-2 family member Bim sustains B lymphopoiesis in the absence of IL-7

Nicholas D. Huntington1,2, Verena Labi3, Ana Cumano2,4, Paulo Vieira2,4, Andreas Strasser5, Andreas Villunger3, James P. Di Santo1,2 and Nuno L. Alves1,2

1 Cytokines and Lymphoid Development Unit, Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris, France
2 Inserm U668, Paris, France
3 Division of Developmental Immunology, Department of Biocenter, Innsbruck Medical University, Innsbruck, Austria
4 Lymphocyte Development Unit, Institut Pasteur, Paris, France
5 Molecular Genetics of Cancer Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia

Correspondence to: N. L. Alves; E-mail: nalves{at}pasteur.fr

IL-7 is pivotal for B cell development. Proteins of the Bcl-2 family are essential regulators of lymphocyte survival. Particularly, the pro-apoptotic BH3-only members Bim and Puma mediate lymphocyte apoptosis provoked by cytokine deprivation. Herein, we addressed whether the absence of Bim or Puma within the hematopoietic compartment could bypass the requirement for IL-7-driven B cell development in adult mice. We found that deficiency of Bim, but not Puma, partially rescued B cell development in the absence of IL-7. The numbers of both sIgM and sIgM+ B cells were markedly increased in the bone marrow of recipients lacking IL-7 upon reconstitution with Bim-deficient hematopoietic progenitors, compared with their control or Puma-deficient counterparts. The augmentation of B cell lymphopoiesis in the absence of Bim was reflected in the mature peripheral compartment by an increase in both the number of immature and mature B cells in the spleen and in the circulating IgM levels. Bim-deficient B cells were also increased in IL-7-sufficient recipients suggesting that peripheral B cells homeostasis is governed by a Bim-dependent and IL-7-independent mechanism. Our data highlight the role of Bim as a key regulator of cell survival during B lymphocyte development in vivo.

Keywords: Bim, B lymphopoiesis, IL-7, Puma


Transmitting editor: D. Tarlinton

Received 12 January 2009, accepted 13 April 2009.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Immunol.Home page
A. J. Giles, T. P. Bender, and K. S. Ravichandran
The Adaptor Protein Shc Plays a Key Role during Early B Cell Development
J. Immunol., November 1, 2009; 183(9): 5468 - 5476.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.