老化皮肤的衰老:mTORC1 和溶酶体的新焦点。

Phineas Smith, Bernadette Carroll
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引用次数: 0

摘要

衰老被定义为组织功能和再生能力的逐渐丧失,是由内在因素(即损伤的自然积累)和外在因素(即环境压力造成的损伤)造成的。简而言之,细胞衰老是一种不可逆转的细胞周期退出,主要是对紫外线(UV)照射和氧化应激等过度细胞损伤的反应。在本综述中,我们将重点关注皮肤这一器官,它是抵御伤害、损伤和感染的重要保护屏障。我们将探讨细胞衰老的存在及其对皮肤老化所起作用的证据。我们将讨论驱动皮肤衰老的已知分子机制,重点关注生长调节因子--雷帕霉素靶复合物 1(mTORC1)--的失调。我们探讨了失调的 mTORC1 与溶酶体之间的相互作用,以及它们是如何导致衰老表型的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Senescence in the ageing skin: a new focus on mTORC1 and the lysosome.

Ageing is defined as the progressive loss of tissue function and regenerative capacity and is caused by both intrinsic factors i.e. the natural accumulation of damage, and extrinsic factors i.e. damage from environmental stressors. Cellular senescence, in brief, is an irreversible exit from the cell cycle that occurs primarily in response to excessive cellular damage, such as from ultraviolet (UV) exposure and oxidative stress, and it has been comprehensively demonstrated to contribute to tissue and organismal ageing. In this review, we will focus on the skin, an organ which acts as an essential protective barrier against injury, insults, and infection. We will explore the evidence for the existence and contribution of cellular senescence to skin ageing. We discuss the known molecular mechanisms driving senescence in the skin, with a focus on the dysregulation of the master growth regulator, mechanistic Target of Rapamycin Complex 1 (mTORC1). We explore the interplay of dysregulated mTORC1 with lysosomes and how they contribute to senescence phenotypes.

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