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巨噬细胞和最近发现的细胞死亡形式。

Macrophages and recently identified forms of cell death.

机构信息

1Laboratory of Nephrology, IIS-Fundación Jiménez Díaz, Universidad Autónoma de Madrid and Fundación Renal Iñigo Alvarez de Toledo, Madrid, Spain.

出版信息

Int Rev Immunol. 2014 Jan;33(1):9-22. doi: 10.3109/08830185.2013.771183. Epub 2013 Jun 26.

DOI:10.3109/08830185.2013.771183
PMID:23802146
Abstract

Recent advances in cell death biology have uncovered an ever increasing range of cell death forms. Macrophages have a bidirectional relationship with cell death that modulates the immune response. Thus, macrophages engulf apoptotic cells and secrete cytokines that may promote cell death in parenchymal cells. Furthermore, the presence of apoptotic or necrotic dead cells in the microenvironment elicits differential macrophage responses. Apoptotic cells elicit anti-inflammatory responses in macrophages. By contrast macrophages may undergo a proinflammatory form of cell death (pyroptosis) in response to damage-associated molecular patterns (DAMPs) released from necrotic cells and also in response to pathogen-associated molecular patterns (PAMPs). Pyroptosis is a recently identified form of cell death that occurs predominantly in subsets of inflammatory macrophages and is associated to the release of interleukin-1β (IL-1β) and IL-18. Deregulation of these processes may result in disease. Thus, failure of macrophages to engulf apoptotic cells may be a source of autoantigens in autoimmune diseases, excessive macrophage release of proapoptotic factors or sterile pyroptosis may contribute to tissue injury and failure of pathogen-induced pyroptosis may contribute to pathogen survival. Ongoing research is exploring the therapeutic opportunities resulting this new knowledge.

摘要

细胞死亡生物学的最新进展揭示了越来越多的细胞死亡形式。巨噬细胞与细胞死亡呈双向关系,调节免疫反应。因此,巨噬细胞吞噬凋亡细胞并分泌细胞因子,可能促进实质细胞的细胞死亡。此外,微环境中凋亡或坏死的死细胞的存在会引起巨噬细胞的不同反应。凋亡细胞在巨噬细胞中引发抗炎反应。相比之下,巨噬细胞可能会对来自坏死细胞释放的损伤相关分子模式 (DAMP) 以及病原体相关分子模式 (PAMP) 发生促炎形式的细胞死亡 (细胞焦亡)。细胞焦亡是一种最近发现的细胞死亡形式,主要发生在炎症巨噬细胞亚群中,并与白细胞介素-1β (IL-1β) 和白细胞介素-18 的释放有关。这些过程的失调可能导致疾病。因此,巨噬细胞不能吞噬凋亡细胞可能是自身免疫疾病中自身抗原的来源,巨噬细胞过度释放促凋亡因子或无菌性细胞焦亡可能导致组织损伤,病原体诱导的细胞焦亡失败可能导致病原体存活。正在进行的研究正在探索这一新知识带来的治疗机会。

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