N-WASP is required for B-cell-mediated autoimmunity in Wiskott-Aldrich syndrome.
Data(s) |
2016
|
---|---|
Resumo |
Mutations of the Wiskott-Aldrich syndrome gene (WAS) are responsible for Wiskott-Aldrich syndrome (WAS), a disease characterized by thrombocytopenia, eczema, immunodeficiency, and autoimmunity. Mice with conditional deficiency of Was in B lymphocytes (B/WcKO) have revealed a critical role for WAS protein (WASP) expression in B lymphocytes in the maintenance of immune homeostasis. Neural WASP (N-WASP) is a broadly expressed homolog of WASP, and regulates B-cell signaling by modulating B-cell receptor (BCR) clustering and internalization. We have generated a double conditional mouse lacking both WASP and N-WASP selectively in B lymphocytes (B/DcKO). Compared with B/WcKO mice, B/DcKO mice showed defective B-lymphocyte proliferation and impaired antibody responses to T-cell-dependent antigens, associated with decreased autoantibody production and lack of autoimmune kidney disease. These results demonstrate that N-WASP expression in B lymphocytes is required for the development of autoimmunity of WAS and may represent a novel therapeutic target in WAS. |
Identificador |
http://serval.unil.ch/?id=serval:BIB_3AB2A62512A7 isbn:1528-0020 (Electronic) pmid:26468226 doi:10.1182/blood-2015-05-643817 isiid:000369285400011 |
Idioma(s) |
en |
Direitos |
info:eu-repo/semantics/openAccess |
Fonte |
Blood, vol. 127, no. 2, pp. 216-220 |
Tipo |
info:eu-repo/semantics/article article |