College of Veterinary Medicine, Jilin Agricultural University, Changchun, China.
Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Agricultural University, Changchun, China.
Antioxid Redox Signal. 2023 Mar;38(7-9):550-580. doi: 10.1089/ars.2022.0110. Epub 2022 Oct 12.
Autophagy is critical to cellular homeostasis. Emergence of the concept of regulated necrosis, such as necroptosis, ferroptosis, pyroptosis, and mitochondrial membrane-permeability transition (MPT)-derived necrosis, has revolutionized the research into necrosis. Both altered autophagy and regulated necrosis contribute to major human diseases. Recent studies reveal an intricate interplay between autophagy and regulated necrosis. Understanding the interplay at the molecular level will provide new insights into the pathophysiology of related diseases. Among the three forms of autophagy, macroautophagy is better studied for its crosstalk with regulated necrosis. Macroautophagy seemingly can either antagonize or promote regulated necrosis, depending upon the form of regulated necrosis, the type of cells or stimuli, and other cellular contexts. This review will critically analyze recent advances in the molecular mechanisms governing the intricate dialogues between macroautophagy and main forms of regulated necrosis. The dual roles of autophagy, either pro-survival or pro-death characteristics, intricate the mechanistic relationship between autophagy and regulated necrosis at molecular level in various pathological conditions. Meanwhile, key components of regulated necrosis are also involved in the regulation of autophagy, which further complicates the interrelationship. Resolving the controversies over causation between altered autophagy and a specific form of regulated necrosis requires approaches that are more definitive, where rigorous evaluation of autophagic flux and the development of more reliable and specific methods to quantify each form of necrosis will be essential. The relationship between chaperone-mediated autophagy or microautophagy and regulated necrosis remains largely unstudied. 38, 550-580.
自噬对于细胞内稳态至关重要。调节性细胞坏死概念的出现,如坏死性凋亡、铁死亡、细胞焦亡和线粒体膜通透性转换(MPT)源性坏死,彻底改变了对细胞坏死的研究。改变的自噬和调节性细胞坏死都导致了重大的人类疾病。最近的研究揭示了自噬和调节性细胞坏死之间的复杂相互作用。在分子水平上理解这种相互作用将为相关疾病的病理生理学提供新的见解。在三种自噬形式中,巨自噬因其与调节性细胞坏死的相互作用而得到了更好的研究。巨自噬似乎可以拮抗或促进调节性细胞坏死,这取决于调节性细胞坏死的形式、细胞类型或刺激物以及其他细胞环境。这篇综述将批判性地分析最近在调控巨自噬和主要调节性细胞坏死形式之间复杂对话的分子机制方面的进展。自噬的双重作用,即生存或死亡特征,使自噬和调节性细胞坏死在各种病理条件下的分子水平上的机制关系变得复杂。同时,调节性细胞坏死的关键组成部分也参与了自噬的调节,这进一步使它们之间的关系复杂化。在改变的自噬和特定形式的调节性细胞坏死之间的因果关系上存在争议,需要更明确的方法来解决,其中严格评估自噬流以及开发更可靠和特定的方法来量化每种形式的细胞坏死将是至关重要的。伴侣介导的自噬或微自噬与调节性细胞坏死之间的关系在很大程度上仍未得到研究。