MFG-E8-dependent clearance of apoptotic cells, and autoimmunity caused by its failure.

Rikinari Hanayama, Kay Miyasaka, Michio Nakaya, Shigekazu Nagata
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引用次数: 70

Abstract

Apoptotic cells are swiftly engulfed by macrophages and immature dendritic cells. Inefficient clearance of apoptotic cells has been implicated as a cause of inflammation and autoimmune diseases. Milk fat globule-EGF factor 8 (MFG-E8) and developmental endothelial locus-1 (Del-1) are glycoproteins secreted from macrophages that pass apoptotic cells to phagocytes. MFG-E8, but not Del-1, is expressed in the tingible-body macrophages at the germinal centers of the second lymphoid tissues. MFG-E8-deficient mice carry many unengulfed apoptotic cells in the germinal centers of the spleen, and develop a lupus-like autoimmune disease. In this review, we discuss the importance of the MFG-E8-mediated clearance of apoptotic cells in the prevention of autoimmune diseases.
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mfg - e8依赖性凋亡细胞的清除,以及其失效引起的自身免疫。
凋亡细胞被巨噬细胞和未成熟的树突状细胞迅速吞噬。凋亡细胞的低效清除已被认为是炎症和自身免疫性疾病的原因之一。乳脂球egf因子8 (MFG-E8)和发育内皮细胞座-1 (Del-1)是巨噬细胞分泌的糖蛋白,可将凋亡细胞传递给吞噬细胞。MFG-E8在第二淋巴组织生发中心的可感触体巨噬细胞中表达,而不表达Del-1。mfg - e8缺陷小鼠在脾脏生发中心携带许多未吞噬的凋亡细胞,并发展为狼疮样自身免疫性疾病。在这篇综述中,我们讨论了mfg - e8介导的凋亡细胞清除在预防自身免疫性疾病中的重要性。
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