Centrocyte
B cell with a cleaved nucleus derived from centroblasts
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Through Antibody
Development
The dark zone of germinal centers contain proliferating centroblasts. Once these centroblasts are stimulated, they no longer divide, and proceed to move to the light zone of germinal centers. In the light zone, T follicular helper cells mediate centrocyte selection through CD40L and provide them with pro-survival signals. The centrocytes then compete for T follicular helper cell and dendritic cell help, allowing for selectivity towards centrocytes that bind to antigen with higher affinity. Centrocytes with high affinity are allowed to exit the germinal center as memory B cells or long-lived plasma cells, while other selected centrocytes are allowed to reenter the cell cycle by T cells. The remaining centrocytes undergo apoptosis or return to the centroblast pool for further somatic hypermutation. Centrocytes that do not recognize antigen properly due to an altered B cell receptor will undergo apoptosis.

