Germinal Center Dynamics Revealed by Multiphoton Microscopy with a Photoactivatable Fluorescent Reporter
Author(s) -
Gabriel D. Victora,
Tanja A. Schwickert,
David Fooksman,
Alice O. Kamphorst,
Michael MeyerHermann,
Michael L. Dustin,
Michel C. Nussenzweig
Publication year - 2010
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2010.10.032
Subject(s) - biology , fluorescence , germinal center , fluorescence microscope , dynamics (music) , center (category theory) , microscopy , multiphoton fluorescence microscope , fluorescent protein , fluorescent labelling , green fluorescent protein , biophysics , microbiology and biotechnology , optics , genetics , physics , antibody , crystallography , chemistry , acoustics , b cell , gene
The germinal center (GC) reaction produces high-affinity antibodies by random mutation and selective clonal expansion of B cells with high-affinity receptors. The mechanism by which B cells are selected remains unclear, as does the role of the two anatomically defined areas of the GC, light zone (LZ) and dark zone (DZ). We combined a transgenic photoactivatable fluorescent protein tracer with multiphoton laser-scanning microscopy and flow cytometry to examine anatomically defined LZ and DZ B cells and GC selection. We find that B cell division is restricted to the DZ, with a net vector of B cell movement from the DZ to the LZ. The decision to return to the DZ and undergo clonal expansion is controlled by T helper cells in the GC LZ, which discern between LZ B cells based on the amount of antigen captured and presented. Thus, T cell help, and not direct competition for antigen, is the limiting factor in GC selection.
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