Autocrine Secretion of Interferon γ Negatively Regulates Homing of Immature B Cells

Author:

Flaishon Liat12,Hershkoviz Rami1,Lantner Frida1,Lider Ofer1,Alon Ronen1,Levo Yoram2,Flavell Richard A.3,Shachar Idit1

Affiliation:

1. Department of Immunology, The Weizmann Institute of Science, Rehovot 76100, Israel

2. Sourasky Medical Center, Tel-Aviv 64239, Israel

3. Howard Hughes Medical Institute, Section of Immunobiology, Yale School of Medicine, New Haven, Connecticut 06510

Abstract

The mechanism by which immature B cells are sequestered from encountering foreign antigens present in lymph nodes or sites of inflammation, before their final maturation in the spleen, has not been elucidated. We show here that immature B cells fail to home to the lymph nodes. These cells can actively exclude themselves from antigen-enriched sites by downregulating their integrin-mediated adhesion to the extracellular matrix protein, fibronectin. This inhibition is mediated by interferon γ secretion. Perturbation of interferon γ activity in vivo leads to the homing of immature B cells to the lymph nodes. This is the first example of autocrine regulation of immune cell migration to sites of foreign antigen presentation.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Reference23 articles.

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3. Newly produced virgin B cells migrate to secondary lymphoid organs but their capacity to enter follicles is restricted;Lortan;Eur. J. Immunol.,1987

4. Resolution and characterization of pro-B and pre–pro-B cell stages in normal mouse bone marrow;Hardy;J. Exp. Med.,1991

5. Lymphocyte population kinetics during the development of the immune system. B cell persistence and life-span can be determined by the host environment;Thomas-Vaslin;Int. Immunol.,1989

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