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细胞衰老中的极性:氧化还原调节和营养的作用。

Cellular polarity in aging: role of redox regulation and nutrition.

机构信息

Departamento de Química e Bioquímica, Centro de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, Lisbon, Portugal.

出版信息

Genes Nutr. 2014 Jan;9(1):371. doi: 10.1007/s12263-013-0371-5. Epub 2013 Dec 4.

Abstract

Cellular polarity concerns the spatial asymmetric organization of cellular components and structures. Such organization is important not only for biological behavior at the individual cell level, but also for the 3D organization of tissues and organs in living organisms. Processes like cell migration and motility, asymmetric inheritance, and spatial organization of daughter cells in tissues are all dependent of cell polarity. Many of these processes are compromised during aging and cellular senescence. For example, permeability epithelium barriers are leakier during aging; elderly people have impaired vascular function and increased frequency of cancer, and asymmetrical inheritance is compromised in senescent cells, including stem cells. Here, we review the cellular regulation of polarity, as well as the signaling mechanisms and respective redox regulation of the pathways involved in defining cellular polarity. Emphasis will be put on the role of cytoskeleton and the AMP-activated protein kinase pathway. We also discuss how nutrients can affect polarity-dependent processes, both by direct exposure of the gastrointestinal epithelium to nutrients and by indirect effects elicited by the metabolism of nutrients, such as activation of antioxidant response and phase-II detoxification enzymes through the transcription factor nuclear factor (erythroid-derived 2)-like 2 (Nrf2). In summary, cellular polarity emerges as a key process whose redox deregulation is hypothesized to have a central role in aging and cellular senescence.

摘要

细胞极性涉及细胞成分和结构的空间不对称组织。这种组织不仅对单个细胞水平的生物学行为很重要,而且对生物体内组织和器官的 3D 组织也很重要。细胞迁移和运动、不对称遗传以及组织中细胞的空间组织等过程都依赖于细胞极性。许多这些过程在衰老和细胞衰老过程中受到损害。例如,通透性上皮屏障在衰老过程中变得更加渗漏;老年人的血管功能受损,癌症发病率增加,衰老细胞中的不对称遗传受到损害,包括干细胞。在这里,我们综述了极性的细胞调节,以及参与定义细胞极性的信号通路及其各自的氧化还原调节。重点将放在细胞骨架和 AMP 激活的蛋白激酶途径上。我们还讨论了营养物质如何通过直接暴露于胃肠道上皮细胞以及通过营养物质代谢引起的间接作用(例如通过转录因子核因子(红细胞衍生 2)样 2(Nrf2)激活抗氧化反应和 II 期解毒酶)来影响依赖极性的过程。总之,细胞极性是一个关键过程,其氧化还原失调被假设在衰老和细胞衰老中起核心作用。

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