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坏死细胞是如何被它们的捕食者识别的?

How are necrotic cells recognized by their predators?

作者信息

Li Zao, Zhou Zheng

机构信息

Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine , Houston, TX, USA.

出版信息

Worm. 2015 Nov 30;5(1):e1120400. doi: 10.1080/21624054.2015.1120400. eCollection 2016 Jan-Mar.

Abstract

Necrosis is a type of cell death often caused by cell injury and is linked to human diseases including neuron degeneration, stroke, and cancer. Cells undergoing necrosis are engulfed and degraded by engulfing cells, their predators. The mechanisms by which necrotic cells are recognized and removed remain elusive. Here we comment on our recent findings that reveal new molecular mechanisms of necrotic-cell recognition. Through studying the C. elegans touch neurons undergoing excitotoxic necrosis, we identified a receptor/ligand pair that enables engulfing cells to recognize necrotic neurons. The phagocytic receptor CED-1 is activated through interaction with its ligand phosphatidylserine (PS), exposed on the surface of necrotic cells. Furthermore, against the common belief that necrotic cells have ruptured plasma membrane, we found that necrotic C. elegans touch neurons actively present PS on their outer surfaces while maintaining plasma membrane integrity. We further identified 2 mechanisms governing the presentation of PS, one of which is shared with cells undergoing apoptosis, a "cell suicide" event, whereas the other is unique to necrotic neurons. The influx of Ca(2+), a key necrosis-triggering factor, is implicated in activating a neuronal PS-scramblase for PS exposure. We propose that the mechanisms controlling PS-exposure and necrotic-cell recognition by engulfing cells are likely conserved from worms to humans.

摘要

坏死是一种常由细胞损伤引起的细胞死亡类型,与包括神经元退化、中风和癌症在内的人类疾病相关。正在经历坏死的细胞会被吞噬细胞(它们的捕食者)吞噬并降解。坏死细胞被识别和清除的机制仍然不清楚。在此,我们对我们最近的发现进行评论,这些发现揭示了坏死细胞识别的新分子机制。通过研究经历兴奋性毒性坏死的秀丽隐杆线虫触觉神经元,我们鉴定出一对受体/配体,它能使吞噬细胞识别坏死神经元。吞噬受体CED-1通过与其配体磷脂酰丝氨酸(PS)相互作用而被激活,PS暴露在坏死细胞表面。此外,与坏死细胞具有破裂质膜的普遍观点相反,我们发现坏死的秀丽隐杆线虫触觉神经元在保持质膜完整性的同时,会在其外表面主动呈现PS。我们进一步确定了两种控制PS呈现的机制,其中一种与经历凋亡(一种“细胞自杀”事件)的细胞相同,而另一种是坏死神经元所特有的。Ca(2+)(一种关键的坏死触发因子)的内流与激活一种神经元PS翻转酶以暴露PS有关。我们提出,控制PS暴露以及吞噬细胞对坏死细胞识别的机制可能从线虫到人类都是保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e27/4805362/e55cdd7dfb94/kwrm-05-01-1120400-g001.jpg

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