Cell circuits between B cell progenitors and IL-7+ mesenchymal progenitor cells control B cell development

Author:

Fistonich Chris1,Zehentmeier Sandra1,Bednarski Jeffrey J.2,Miao Runfeng1,Schjerven Hilde3ORCID,Sleckman Barry P.4ORCID,Pereira João P.1ORCID

Affiliation:

1. Department of Immunobiology, Yale University School of Medicine, Yale University, New Haven, CT

2. Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO

3. Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA

4. Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY

Abstract

B cell progenitors require paracrine signals such as interleukin-7 (IL-7) provided by bone marrow stromal cells for proliferation and survival. Yet, how B cells regulate access to these signals in vivo remains unclear. Here we show that proB and IL-7+ cells form a cell circuit wired by IL-7R signaling, which controls CXCR4 and focal adhesion kinase (FAK) expression and restricts proB cell movement due to increased adhesion to IL-7+CXCL12Hi cells. PreBCR signaling breaks this circuit by switching the preB cell behavior into a fast-moving and lower-adhesion state via increased CXCR4 and reduced FAK/α4β1 expression. This behavioral change reduces preB cell exposure to IL-7, thereby attenuating IL-7R signaling in vivo. Remarkably, IL-7 production is downregulated by signals provided by preB cells with unrepaired double-stranded DNA breaks and by preB acute lymphoblastic leukemic cells. Combined, these studies revealed that distinct cell circuits control the quality and homeostasis of B cell progenitors.

Funder

National Institutes of Health

German Research Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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