Haraldsson M Katarina, Louis-Dit-Sully Christine A, Lawson Brian R, Sternik Gabriel, Santiago-Raber Marie-Laure, Gascoigne Nicholas R J, Theofilopoulos Argyrios N, Kono Dwight H
Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Immunity. 2008 Jan;28(1):40-51. doi: 10.1016/j.immuni.2007.11.023.
Here, we show that a lupus-suppressing locus is caused by a nonsense mutation of the filamentous actin-inhibiting Coronin-1A gene. This mutation was associated with developmental and functional alterations in T cells including reduced migration, survival, activation, and Ca2+ flux. T-dependent humoral responses were impaired, but no intrinsic B cell defects were detected. By transfer of T cells, it was shown that suppression of autoimmunity could be accounted for by the presence of the Coro1a(Lmb3) mutation in T cells. Our results demonstrate that Coronin-1A is required for the development of systemic lupus and identify actin-cytoskeleton regulatory proteins as potential targets for modulating autoimmune diseases.
在此,我们表明一个狼疮抑制基因座是由丝状肌动蛋白抑制蛋白冠蛋白-1A基因的无义突变引起的。该突变与T细胞的发育和功能改变有关,包括迁移、存活、激活和Ca2+通量降低。T细胞依赖性体液反应受损,但未检测到内在的B细胞缺陷。通过T细胞转移,表明T细胞中存在Coro1a(Lmb3)突变可解释自身免疫的抑制。我们的结果表明,冠蛋白-1A是系统性红斑狼疮发展所必需的,并确定肌动蛋白细胞骨架调节蛋白是调节自身免疫性疾病的潜在靶点。