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Efferocytosis and autoimmune disease

机译:泡腾病和自身免疫性疾病

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摘要

An enormous number of cells in the body die by apoptosis during development and under homeostasis. Apoptotic cells are swiftly engulfed by macrophages and digested into units. This removal of apoptotic cells is called ‘efferocytosis’. For efferocytosis, macrophages recognize phosphatidylserine (PtdSer) exposed on the cell surface as an ‘eat me’ signal. In healthy cells, PtdSer is exclusively localized to the inner leaflet of the plasma membrane by the action of flippases. When cells undergo apoptosis, caspase cleaves flippases to inactivate them, while it cleaves pro-scramblases to active scramblases, which quickly translocate PtdSer to the cell surface. The PtdSer is then recognized by PtdSer-binding proteins or by PtdSer receptors on macrophages, which subsequently engulf the apoptotic cells. When efferocytosis fails, apoptotic cells can rupture, releasing cellular materials that can evoke an autoimmune response. Thus, a defect in the PtdSer-exposing or PtdSer-recognizing processes triggers autoimmunity, leading to a systemic lupus erythematosus-type autoimmune disease.
机译:体内大量细胞在发育过程中和体内稳态下因凋亡而死亡。凋亡细胞被巨噬细胞迅速吞噬并消化成单位。凋亡细胞的这种去除称为“胞吞”。为了进行胞吞作用,巨噬细胞将暴露在细胞表面的磷脂酰丝氨酸(PtdSer)识别为“吞噬我”信号。在健康细胞中,PtdSer通过翻转酶的作用专门定位于质膜的内部小叶。当细胞发生凋亡时,半胱天冬酶裂解蛋白酶使它们失活,而裂解前顺式蛋白酶变成活性顺式蛋白酶,后者迅速将PtdSer转运到细胞表面。然后,PtdSer结合蛋白或巨噬细胞上的PtdSer受体识别PtdSer,随后吞噬凋亡细胞。当胞吐作用失败时,凋亡细胞会破裂,释放出可引起自身免疫反应的细胞物质。因此,暴露于PtdSer或识别PtdSer的过程中的缺陷会触发自身免疫,从而导致系统性红斑狼疮型自身免疫疾病。

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