ATG5 非自噬调节小鼠胚胎干细胞的炎症和分化。

Autophagy Pub Date : 2024-08-01 Epub Date: 2024-03-22 DOI:10.1080/15548627.2024.2330042
Sheng Li, Bo-Wen Zhang, Qian-Qian Lou, Yue Liu, Zi-Juan Wei, Jing Huang, Kun-Hou Yao, Qian-Ru Xu, Juan Fan, Yan Xi, Lu Yang, Su Chen
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引用次数: 0

摘要

胚胎干细胞(ESCs)具有无限增殖(自我更新)和分化成不同细胞类型(多能性)的能力,对细胞因子或病原体的炎症反应减弱,这被认为是 ESCs 与体细胞相比的一个独特特征。然而,其潜在的分子机制仍不清楚,炎症减弱状态是否参与了 ESC 的分化也完全未知。我们最近的研究表明,大自噬/自噬相关蛋白ATG5通过促进BTRC/β-TrCP1的降解和进一步下调NFKB/NF-κB信号,抑制了小鼠ESCs(MmESCs)的炎症反应。此外,MmESCs 的分化还需要炎症减弱状态的维持。总之,ATG5 是调节 MmESCs 炎症反应和分化的关键调节因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ATG5 nonautophagically regulates inflammation and differentiation in mouse embryonic stem cells.

Embryonic stem cells (ESCs), with abilities of infinite proliferation (self-renewal) and to differentiate into distinct cell types (pluripotency), show attenuated inflammatory response against cytokines or pathogens, which is recognized as a unique characteristic of ESCs compared with somatic cells. However, the underlying molecular mechanisms remain unclear, and whether the attenuated inflammatory state is involved in ESC differentiation is completely unknown. Our recent study demonstrated that macroautophagy/autophagy-related protein ATG5 inhibits the inflammatory response of mouse ESCs (MmESCs) by promoting the degradation of BTRC/β-TrCP1 and further the downregulation of NFKB/NF-κB signaling. In addition, maintenance of an attenuated inflammation status in MmESCs is required for their differentiation. In conclusion, ATG5 is a key regulator for the regulation of inflammatory response and differentiation of MmESCs.

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