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

AR Albright, J Kabat, M Li, F Raso, A Reboldi… - Journal of Experimental …, 2019 - rupress.org
AR Albright, J Kabat, M Li, F Raso, A Reboldi, JR Muppidi
Journal of Experimental Medicine, 2019rupress.org
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 …
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.
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