Contribution of DOCK11 to the Expansion of Antigen-Specific Populations among Germinal Center B Cells

Akihiko Sakamoto, Mitsuo Maruyama

doi:10.4049/immunohorizons.2000048

<jats:title>Abstract</jats:title> <jats:p>Germinal centers (GCs) are a structure in which B cell populations are clonally expanded, depending on their affinities to Ag. Although we previously isolated a characteristic protein called dedicator of cytokinesis 11 (DOCK11) from GC B cells, limited information is available on the roles of DOCK11 in GC B cells. In this study, we demonstrate that DOCK11 may contribute to the expansion of Ag-specific populations among GC B cells upon immunization of mice. The lack of DOCK11 in B cells resulted in the lower frequency of Ag-specific GC B cells along with enhanced apoptosis upon immunization. Under competitive conditions, DOCK11-deficient B cells were dramatically prevented from participating in GCs, in contrast to DOCK11-sufficient B cells. However, minor impacts of the DOCK11 deficiency were identified on somatic hypermutations. Mechanistically, the DOCK11 deficiency resulted in the suppression of B cell–intrinsic signaling in vitro and in vivo. Although DOCK11 expression by B cells was required for the induction of T follicular helper cells at the early stages of immune responses, minor impacts were identified on the expansion of Ag-specific populations among GC B cells. Thus, DOCK11 appears to contribute to the expansion of Ag-specific populations among GC B cells through the stimulation of B cell–intrinsic signaling.</jats:p>

Contribution of DOCK11 to the Expansion of Antigen-Specific Populations among Germinal Center B Cells

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