The microanatomic segregation of selection by apoptosis in the germinal center

Science. 2017 Oct 13;358(6360):eaao2602. doi: 10.1126/science.aao2602. Epub 2017 Sep 21.

Abstract

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / genetics
  • Antibodies, Monoclonal / metabolism
  • Apoptosis / genetics
  • Apoptosis / immunology*
  • B-Lymphocytes / cytology*
  • B-Lymphocytes / enzymology
  • B-Lymphocytes / immunology
  • Cell Division*
  • Cytidine Deaminase / metabolism
  • Germinal Center / cytology*
  • Germinal Center / enzymology
  • Germinal Center / immunology
  • Immunoglobulin Class Switching
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Receptors, Antigen, B-Cell / genetics
  • Receptors, Antigen, B-Cell / metabolism

Substances

  • Antibodies, Monoclonal
  • Receptors, Antigen, B-Cell
  • AICDA (activation-induced cytidine deaminase)
  • Cytidine Deaminase