| Literature DB >> 27502165 |
Azahara-María García-Serna1, María-José Alcaraz-García1, Natalia Ruiz-Lafuente1, Silvia Sebastián-Ruiz1, Carlos-Manuel Martínez2, María-Rosa Moya-Quiles1, Alfredo Minguela1, Ana-María García-Alonso1, Elena Martín-Orozco3, Antonio Parrado4.
Abstract
Dock10, a guanine nucleotide exchange factor for the Rho GTPases Rac1 and Cdc42, affects cell morphology, membrane protrusive activity, and cell movement. Dock10 is prominently expressed in lymphoid tissue and upregulated by IL-4 in B cells. To investigate the physiological role of Dock10, WT mice and Dock10 KO mice were used. KO mice showed decreased numbers of B cells in spleen, both follicular B cells and marginal zone B cells, and in peripheral blood, but not in bone marrow. The antiapoptotic effect of IL-4 in vitro, the migratory response to CXCL13 or CCL21 in vitro, and the whole genome expression profile were intact in spleen B cells from KO mice. CD23, the low-affinity receptor for immunoglobulin E, was overexpressed on follicular B cells from KO mice, suggesting that Dock10 negatively regulates membrane CD23 expression. Negative regulation of CD23 expression by Dock10 could play a role in B cell maturation and function.Entities:
Keywords: B cell; CD23; Cdc42 GTPase; Dock10; Fc epsilon receptor II (Fcer2); Guanine nucleotide exchange factor (GEF); Rac GTPase
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Year: 2016 PMID: 27502165 DOI: 10.1016/j.imbio.2016.07.015
Source DB: PubMed Journal: Immunobiology ISSN: 0171-2985 Impact factor: 3.144