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溶酶体活性降低引起的自噬扰动正向调节细胞竞争。

Autophagic perturbation caused by reduced lysosomal activity positively regulates cell competition.

机构信息

Division of Cancer Biology, Research Institute for Biomedical Sciences, Tokyo University of Science, Noda, Japan.

出版信息

Autophagy. 2023 Jun;19(6):1874-1875. doi: 10.1080/15548627.2022.2140559. Epub 2022 Nov 1.

Abstract

Newly emerging transformed epithelial cells are recognized and apically removed by surrounding normal cells through a biological event termed "cell competition". However, little is known about the mechanisms underlying this process. In a recent study, we describe that RAS/RasV12-transformed cells surrounded by normal cells exhibit decreased lysosomal activity accompanied with accumulation of autophagosomes. Restoration of low lysosomal activity or inhibition of autophagosome formation significantly antagonizes apical extrusion of RAS cells, suggesting that non-degradable autophagosomes are required for cell competition. Notably, analysis of a cell competition mouse model demonstrates that macroautophagy/autophagy-ablated RAS cells are less readily eliminated by cell competition, and remaining transformed cells destroy ductal integrity, leading to chronic pancreatitis. Thus, our findings illuminate a critical role for non-degradable autophagosomes in cell competition and reveal a homeostasis-preserving role of autophagy upon emergence of transformed cells.

摘要

新出现的转化上皮细胞被周围正常细胞通过一种称为“细胞竞争”的生物学事件识别并从顶端去除。然而,目前对于这一过程的机制知之甚少。在最近的一项研究中,我们描述了被正常细胞包围的 RAS/RasV12 转化细胞表现出溶酶体活性降低,同时自噬体积累。恢复低溶酶体活性或抑制自噬体形成可显著拮抗 RAS 细胞的顶端挤出,表明不可降解的自噬体是细胞竞争所必需的。值得注意的是,对细胞竞争小鼠模型的分析表明,巨自噬/自噬缺失的 RAS 细胞不太容易被细胞竞争消除,而剩余的转化细胞破坏导管完整性,导致慢性胰腺炎。因此,我们的研究结果阐明了不可降解自噬体在细胞竞争中的关键作用,并揭示了自噬在转化细胞出现时对维持内稳态的作用。

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