Chen Min, Wang Yui-Hsi, Wang Yihong, Huang Li, Sandoval Hector, Liu Yong-Jun, Wang Jin
Department of Immunology, Baylor College of Medicine, Houston, TX 77030, USA.
Science. 2006 Feb 24;311(5764):1160-4. doi: 10.1126/science.1122545.
Apoptosis in the immune system is critical for maintaining self-tolerance and preventing autoimmunity. Nevertheless, inhibiting apoptosis in lymphocytes is not alone sufficient to break self-tolerance, suggesting the involvement of other cell types. We investigated whether apoptosis in dendritic cells (DCs) helps regulate self-tolerance by generating transgenic mice expressing the baculoviral caspase inhibitor, p35, in DCs (DC-p35). DC-p35 mice displayed defective DC apoptosis, resulting in their accumulation and, in turn, chronic lymphocyte activation and systemic autoimmune manifestations. The observation that a defect in DC apoptosis can independently lead to autoimmunity is consistent with a central role for these cells in maintaining immune self-tolerance.
免疫系统中的细胞凋亡对于维持自身耐受性和预防自身免疫至关重要。然而,仅抑制淋巴细胞中的细胞凋亡不足以打破自身耐受性,这表明其他细胞类型也参与其中。我们研究了树突状细胞(DCs)中的细胞凋亡是否通过生成在DCs中表达杆状病毒半胱天冬酶抑制剂p35的转基因小鼠(DC-p35)来帮助调节自身耐受性。DC-p35小鼠表现出DC凋亡缺陷,导致其积累,进而导致慢性淋巴细胞活化和全身性自身免疫表现。DC凋亡缺陷可独立导致自身免疫的观察结果与这些细胞在维持免疫自身耐受性中的核心作用一致。