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多系统疾病中的噬作用(综述)。

Efferocytosis in multisystem diseases (Review).

机构信息

Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200032, P.R. China.

出版信息

Mol Med Rep. 2022 Jan;25(1). doi: 10.3892/mmr.2021.12529. Epub 2021 Nov 15.

Abstract

Efferocytosis, the phagocytosis of apoptotic cells performed by both specialized phagocytes (such as macrophages) and non‑specialized phagocytes (such as epithelial cells), is involved in tissue repair and homeostasis. Effective efferocytosis prevents secondary necrosis, terminates inflammatory responses, promotes self‑tolerance and activates pro‑resolving pathways to maintain homeostasis. When efferocytosis is impaired, apoptotic cells that could not be cleared in time aggregate, resulting in the necrosis of apoptotic cells and release of pro‑inflammatory factors. In addition, defective efferocytosis inhibits the intracellular cholesterol reverse transportation pathways, which may lead to atherosclerosis, lung damage, non‑alcoholic fatty liver disease and neurodegenerative diseases. The uncleared apoptotic cells can also release autoantigens, which can cause autoimmune diseases. Cancer cells escape from phagocytosis via efferocytosis. Therefore, new treatment strategies for diseases related to defective efferocytosis are proposed. This review illustrated the mechanisms of efferocytosis in multisystem diseases and organismal homeostasis and the pathophysiological consequences of defective efferocytosis. Several drugs and treatments available to enhance efferocytosis are also mentioned in the review, serving as new evidence for clinical application.

摘要

噬作用,即凋亡细胞被专业吞噬细胞(如巨噬细胞)和非专业吞噬细胞(如上皮细胞)吞噬的过程,参与组织修复和内稳态的维持。有效的噬作用可防止继发性坏死、终止炎症反应、促进自身耐受,并激活促解决途径以维持内稳态。当噬作用受损时,不能及时清除的凋亡细胞聚集,导致凋亡细胞坏死并释放促炎因子。此外,噬作用缺陷抑制细胞内胆固醇逆向转运途径,可能导致动脉粥样硬化、肺损伤、非酒精性脂肪肝和神经退行性疾病。未清除的凋亡细胞还可以释放自身抗原,从而导致自身免疫性疾病。癌细胞通过噬作用逃避吞噬。因此,提出了针对与噬作用缺陷相关疾病的新治疗策略。本文综述了噬作用在多系统疾病和机体稳态中的机制以及噬作用缺陷的病理生理后果。还提到了几种可增强噬作用的药物和治疗方法,为临床应用提供了新的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc4e/8600411/49964b9de212/mmr-25-01-12529-g00.jpg

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