The microanatomic segregation of selection by apoptosis in the germinal center

Author:

Mayer Christian T.1ORCID,Gazumyan Anna1ORCID,Kara Ervin E.1ORCID,Gitlin Alexander D.1,Golijanin Jovana1,Viant Charlotte1ORCID,Pai Joy1ORCID,Oliveira Thiago Y.1ORCID,Wang Qiao1,Escolano Amelia1,Medina-Ramirez Max2,Sanders Rogier W.23,Nussenzweig Michel C.14ORCID

Affiliation:

1. Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.

2. Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, Netherlands.

3. Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10065, USA.

4. Howard Hughes Medical Institute (HHMI), The Rockefeller University, New York, NY 10065, USA.

Abstract

Light- and dark-zone death dynamics Germinal centers (GCs) are areas within lymphoid organs where mature B cells expand and differentiate during normal immune responses. GCs are separated into two anatomic compartments: the dark zone, where B cells divide and undergo somatic hypermutation, and the light zone, where they are selected for affinity-enhancing mutations after interacting with T follicular helper cells. Mayer et al. studied apoptosis reporter mice and found that both GC zones experience very high rates of apoptosis (see the Perspective by Bryant and Hodgkin). However, the underlying mechanisms were distinct and microanatomically segregated. Light-zo ne B cells underwent apoptosis by default unless they were rescued by positive selection. In contrast, apoptotic dark-zone B cells were highly enriched among cells with genes damaged by random antibody-gene mutations. Science , this issue p. eaao2602 ; see also p. 171

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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