Krause S, Kuckelkorn U, Dörner T, Burmester G-R, Feist E, Kloetzel P-M
Laboratory of Molecular Myology, Department of Neurology, Friedrich-Baur-Institute, Ludwig-Maximilians University, Marchioninistrasse 17, 81377 Munich, Germany.
Ann Rheum Dis. 2006 Aug;65(8):1021-7. doi: 10.1136/ard.2005.045930. Epub 2006 Jan 13.
The proteasome system has a pivotal role in the control of the immune response, which suggests that it might be involved in the pathogenesis of autoimmune disorders.
To investigate the expression profile of selected proteasomal genes in human peripheral blood mononuclear cells in patients with a variety of autoimmune diseases compared with healthy subjects.
Real time quantitative RT-PCR was used to analyse the mRNA expression pattern of the proteasome activator subunits PA28alpha and PA28beta and of constitutive proteasome and interferon-gamma-inducible immunoproteasome subunits in peripheral blood mononuclear cells. Simultaneously, protein expression of selected proteasome subunits was quantified by immunoblotting.
Under systemic inflammatory conditions the proteasome subunits LMP2 (beta1i), LMP7 (beta5i), MECL1 (beta2i), and PA28alpha were expressed abundantly at the protein level in the vast majority of systemic autoimmune disorders. However, simultaneous mRNA and protein quantification showed a characteristic proteasome expression signature in primary Sjögren's syndrome. At the transcript level, the interferon-gamma-responsive subunits LMP2 (beta1i), MECL1 (beta2i), and the proteasome activator subunit PA28alpha were markedly up regulated. In contrast, LMP2 (beta1i) deficiency was evident at the protein level, indicating deregulation of proteasome expression in Sjögren's syndrome.
These data provide evidence for a regulatory defect in the proteasome system in human autoimmune disorders, pointing to a unique role for LMP2 (beta1i) in the pathogenesis of primary Sjögren's syndrome.
蛋白酶体系统在免疫反应的调控中起关键作用,这表明它可能参与自身免疫性疾病的发病机制。
研究多种自身免疫性疾病患者与健康受试者相比,人外周血单个核细胞中选定蛋白酶体基因的表达谱。
采用实时定量逆转录聚合酶链反应分析外周血单个核细胞中蛋白酶体激活亚基PA28α和PA28β、组成型蛋白酶体及干扰素-γ诱导的免疫蛋白酶体亚基的mRNA表达模式。同时,通过免疫印迹法定量选定蛋白酶体亚基的蛋白表达。
在全身炎症条件下,蛋白酶体亚基LMP2(β1i)、LMP7(β5i)、MECL1(β2i)和PA28α在绝大多数全身自身免疫性疾病的蛋白水平上大量表达。然而,同时进行的mRNA和蛋白定量显示原发性干燥综合征具有特征性的蛋白酶体表达特征。在转录水平上,干扰素-γ反应性亚基LMP2(β1i)、MECL1(β2i)和蛋白酶体激活亚基PA28α明显上调。相反,在蛋白水平上LMP2(β1i)缺乏明显,表明干燥综合征中蛋白酶体表达失调。
这些数据为人类自身免疫性疾病中蛋白酶体系统的调节缺陷提供了证据,表明LMP2(β1i)在原发性干燥综合征发病机制中具有独特作用。