TY - JOUR
T1 - The microanatomic segregation of selection by apoptosis in the germinal center
AU - Mayer, Christian T.
AU - Gazumyan, Anna
AU - Kara, Ervin E.
AU - Gitlin, Alexander D.
AU - Golijanin, Jovana
AU - Viant, Charlotte
AU - Pai, Joy
AU - Oliveira, Thiago Y.
AU - Wang, Qiao
AU - Escolano, Amelia
AU - Medina-Ramirez, Max
AU - Sanders, Rogier W.
AU - Nussenzweig, Michel C.
PY - 2017
Y1 - 2017
N2 - B cells undergo rapid cell division and affinity maturation in anatomically distinct sites in lymphoid organs called germinal centers (GCs). Homeostasis is maintained in part by B cell apoptosis. However, the precise contribution of apoptosis to GC biology and selection is not well defined. We developed apoptosis-indicator mice and used them to visualize, purify, and characterize dying GC B cells. Apoptosis is prevalent in the GC, with up to half of all GC B cells dying every 6 hours. Moreover, programmed cell death is differentially regulated in the light zone and the dark zone: Light-zone B cells die by default if they are not positively selected, whereas dark-zone cells die when their antigen receptors are damaged by activation-induced cytidine deaminase
AB - B cells undergo rapid cell division and affinity maturation in anatomically distinct sites in lymphoid organs called germinal centers (GCs). Homeostasis is maintained in part by B cell apoptosis. However, the precise contribution of apoptosis to GC biology and selection is not well defined. We developed apoptosis-indicator mice and used them to visualize, purify, and characterize dying GC B cells. Apoptosis is prevalent in the GC, with up to half of all GC B cells dying every 6 hours. Moreover, programmed cell death is differentially regulated in the light zone and the dark zone: Light-zone B cells die by default if they are not positively selected, whereas dark-zone cells die when their antigen receptors are damaged by activation-induced cytidine deaminase
U2 - https://doi.org/10.1126/science.aao2602
DO - https://doi.org/10.1126/science.aao2602
M3 - Article
C2 - 28935768
VL - 358
SP - 193-+
JO - Science (New York, N.Y.)
JF - Science (New York, N.Y.)
SN - 0036-8075
IS - 6360
ER -