首页> 外文期刊>Scientific reports. >Metabolomic Analysis of Mouse Embryonic Fibroblast Cells in Response to Autophagy Induced by Acute Starvation
【24h】

Metabolomic Analysis of Mouse Embryonic Fibroblast Cells in Response to Autophagy Induced by Acute Starvation

机译:小鼠胚胎成纤维细胞响应急性饥饿诱导的自噬的代谢组分分析

获取原文
获取外文期刊封面目录资料

摘要

Autophagy-related protein 7 (Atg7) is essential in the formation of the autophagophore and is indispensable for autophagy induction. Autophagy will exist in lower level or even be blocked in cells without Atg7. Even though the possible signaling pathways of Atg7 have been proposed, the metabolomic responses under acute starvation in cells with and without Atg7 have not been elucidated. This study therefore was designed and aimed to reveal the metabolomics of Atg7-dependent autophagy through metabolomic analysis of Atg7(-/-) mouse embryonic fibroblast cells (MEFs) and wild-type MEFs along with the starvation time. 30 significantly altered metabolites were identified in response to nutrient stress, which were mainly associated with amino acid, energy, carbohydrate, and lipid metabolism. For the wild-type MEFs, the induction of autophagy protected cell survival with some up-regulated lipids during the first two hours' starvation, while the subsequent apoptosis resulted in the decrease of cell viability after four hours' starvation. For the Atg7(-/-) MEFs, apoptosis perhaps led to the deactivation of tricarboxylic acid (TCA) cycle due to the lack of autophagy, which resulted in the immediate drop of cellular viability under starvation. These results contributed to the metabolomic study and provided new insights into the mechanism associated with Atg7-dependent autophagy.
机译:自噬相关的蛋白质7(ATG7)在自噬细胞的形成中是必不可少的,并且对自噬诱导是必不可少的。自噬在较低级别中将存在,甚至在没有ATG7的细胞中封锁。即使已经提出了ATG7的可能信号通路,也没有阐明具有和不含ATG7的细胞中的急性饥饿下的代谢物反应。因此,本研究的设计和旨在通过ATG7( - / - )小鼠胚胎成纤维细胞(MEF)和野生型MEF以及饥饿时间来揭示ATG7依赖性自噬的代谢组合。 30响应于营养应激的营养应激而鉴定出显着改变的代谢物,其主要与氨基酸,能量,碳水化合物和脂质代谢相关。对于野生型MEFS,在前两个小时的饥饿期间,在前调节的脂质中诱导自噬受体的细胞存活,而随后的细胞凋亡导致四小时饥饿后细胞活力降低。对于ATG7( - / - )MEFS,凋亡可能导致缺乏自噬引起的三羧酸(TCA)循环的失活,这导致饥饿下的细胞活力直接下降。这些结果导致代谢组合研究,并为与ATG7依赖性自噬相关的机制提供了新的见解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号