Regulation of memory B-cell survival by the BH3-only protein Puma

Author:

Clybouw Cyril1234,Fischer Silke34,Auffredou Marie Thérèse12,Hugues Patricia25,Alexia Catherine12,Bouillet Philippe34,Raphael Martine25,Leca Gérald12,Strasser Andreas34,Tarlinton David M.34,Vazquez Aimé12

Affiliation:

1. Inserm Unité Mixte de Recherche (UMR)-S 1014, Villejuif, France;

2. Université Paris-Sud, Paris, France;

3. The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia;

4. Department of Medical Biology, Melbourne University, Melbourne, Australia; and

5. Inserm UMR-S 802 and Assistance Publique–Hôpitanx de Paris Hopital Bicêtre, Paris, France

Abstract

Abstract Apoptosis is crucial for immune system homeostasis, including selection and survival of long-lived antibody-forming cells and memory cells. The interactions between proapoptotic and pro-survival proteins of the Bcl-2 family are critical for this process. In this report, we show that expression of the proapoptotic BH3-only Bcl-2 family member Puma was selectively up-regulated on in vitro activation with antigens or mitogens of both human and mouse B cells. Puma expression coincided in vivo, with the prosurvival Bcl-2 family member Mcl-1 within the germinal centers and its expression correlates with the germinal center like phenotype of Burkitt lymphoma. Experiments performed in Puma-deficient mice revealed that Puma is essential for apoptosis of mitogen-activated B cells in vitro and for the control of memory B-cell survival. In conclusion, using both human and murine models, our data show that Puma has a major role in the T cell– dependent B-cell immune response. These data demonstrate that Puma is a major regulator of memory B lymphocyte survival and therefore a key molecule in the control of the immune response.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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