The microanatomic segregation of selection by apoptosis in the germinal center
Author(s) -
Christian T. Mayer,
Anna Gazumyan,
Ervin E. Kara,
Alexander D. Gitlin,
Jovana Golijanin,
Charlotte Viant,
Joy A. Pai,
Thiago Y. Oliveira,
Qiao Wang,
Amelia Escolano,
Max Medina-Ramírez,
Rogier W. Sanders,
Michel C. Nussenzweig
Publication year - 2017
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aao2602
Subject(s) - germinal center , selection (genetic algorithm) , center (category theory) , biology , evolutionary biology , genetics , computer science , artificial intelligence , chemistry , b cell , antibody , crystallography
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 deaminas
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