TGFβ signaling in germinal center B cells promotes the transition from light zone to dark zone

Author:

Albright Anne R.1,Kabat Juraj2,Li Moyi1,Raso Fiona3ORCID,Reboldi Andrea3,Muppidi Jagan R.1ORCID

Affiliation:

1. Lymphoid Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD

2. Biological Imaging Section, Research Technologies Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD

3. Department of Pathology, University of Massachusetts Medical School, Worcester, MA

Abstract

B cells in germinal centers (GCs) cycle between light zone (LZ) and dark zone (DZ). The cues in the GC microenvironment that regulate the transition from LZ to DZ have not been well characterized. In Peyer’s patches (PPs), transforming growth factor-β (TGFβ) promotes IgA induction in activated B cells that can then differentiate into GC B cells. We show here that TGFβ signaling occurs in B cells in GCs and is distinct from signaling that occurs in activated B cells in PPs. Whereas in activated B cells TGFβ signaling is required for IgA induction, in the GC it was instead required for the transition from LZ to DZ. In the absence of TGFβ signaling, there was an accumulation of LZ GC B cells and reduced antibody affinity maturation likely due to reduced activation of Foxo1. This work identifies TGFβ as a microenvironmental cue that is critical for GC homeostasis and function.

Funder

National Institutes of Health

Center for Cancer Research

National Cancer Institute

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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