...
首页> 外文期刊>Autophagy >The variability of autophagy and cell death susceptibility Unanswered questions
【24h】

The variability of autophagy and cell death susceptibility Unanswered questions

机译:自噬和细胞死亡易感性的变异性

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Impaired autophagic machinery is implicated in a number of diseases such as heart disease, neurodegeneration and cancer. A common denominator in these pathologies is a dys-regulation of autophagy that has been linked to a change in susceptibility to cell death. Although we have progressed in understanding the molecular machinery and regulation of the autophagic pathway, many unanswered questions remain. How does the metabolic contribution of autophagy connect with the cell's history and how does its current autophagic flux affect metabolic status and susceptibility to undergo cell death? How does autophagic flux operate to switch metabolic direction and what are the underlying mechanisms in metabolite and energetic sensing, metabolite substrate provision and metabolic integration during the cellular stress response? In this article we focus on unresolved questions that address issues around the role of autophagy in sensing the energetic environment and its role in actively generating metabolite substrates. We attempt to provide answers by explaining how and when a change in autophagic pathway activity such as primary stress response is able to affect cell viability and when not. By addressing the dynamic metabolic relationship between autophagy, apoptosis and necrosis we provide a new perspective on the parameters that connect autophagic activity, severity of injury and cellular history in a logical manner. Last, by evaluating the cell's condition and autophagic activity in a clear context of regulatory parameters in the intra- and extracellular environment, this review provides new concepts that set autophagy into an energetic feedback loop, that may assist in our understanding of autophagy in maintaining healthy cells or when it controls the threshold between cell death and cell survival.
机译:自噬机制受损涉及多种疾病,例如心脏病,神经退行性疾病和癌症。这些病理学的共同点是自噬的异常调节,与细胞死亡敏感性的变化有关。尽管我们在了解分子机制和自噬途径调控方面取得了进步,但仍有许多未解决的问题。自噬的代谢贡献如何与细胞历史联系起来,其当前的自噬通量如何影响代谢状态和发生细胞死亡的易感性?自噬通量如何操作以改变代谢方向,以及在细胞应激反应期间代谢物和能量感应,代谢物底物供应和代谢整合的潜在机制是什么?在本文中,我们重点关注尚未解决的问题,这些问题涉及自噬在感知高能环境中的作用及其在主动生成代谢物底物方面的作用。我们试图通过解释自噬通路活性的变化(如初级应激反应)如何以及何时能够影响细胞活力,何时不影响细胞活力来提供答案。通过解决自噬,细胞凋亡和坏死之间的动态代谢关系,我们以逻辑方式为连接自噬活性,损伤严重程度和细胞历史的参数提供了新的视角。最后,通过在细胞内和细胞外环境中清晰的调节参数背景下评估细胞的状况和自噬活性,本综述提供了将自噬设置为能量反馈回路的新概念,这可能有助于我们了解自噬以维持健康细胞或何时控制细胞死亡和细胞存活之间的阈值。

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