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Chaperones and Beyond as Key Players in Pluripotency Maintenance

机译:伴侣和超越者在多能性维持中起关键作用

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摘要

Pluripotency is orchestrated by distinct players and chaperones and their partners have emerged as pivotal molecules in proteostasis control to maintain stemness. The proteostasis network consists of diverse interconnected pathways that function dynamically according to the needs of the cell to quality control and maintain protein homeostasis. The proteostasis machinery of pluripotent stem cells (PSCs) is finely adjusted in response to distinct stimuli during cell fate commitment to determine successful organism development. Growing evidence has shown different classes of chaperones regulating crucial cellular processes in PSCs. Histones chaperones promote proper nucleosome assembly and modulate the epigenetic regulation of factors involved in PSCs’ rapid turnover from pluripotency to differentiation. The life cycle of pluripotency proteins from synthesis and folding, transport and degradation is finely regulated by chaperones and co-factors either to maintain the stemness status or to cell fate commitment. Here, we summarize current knowledge of the chaperone network that govern stemness and present the versatile role of chaperones in stem cells resilience. Elucidation of the intricate regulation of pluripotency, dissecting in detail molecular determinants and drivers, is fundamental to understanding the properties of stem cells in order to provide a reliable foundation for biomedical research and regenerative medicine.
机译:多能性是由不同的参与者和伴侣精心策划的,并且伴侣已作为蛋白质稳定控制中的关键分子而出现,以维持干性。蛋白质稳态网络由多种相互连接的途径组成,这些途径根据细胞对质量控制和维持蛋白质稳态的需求而动态发挥作用。对多能干细胞(PSC)的蛋白质稳定机制进行了微调,以响应细胞命运承诺期间的独特刺激,从而确定成功的生物体发育。越来越多的证据表明,不同种类的伴侣分子可调节PSC中的关键细胞过程。组蛋白伴侣可以促进核小体的正确装配,并调节与多能干细胞从多能性到分化的快速转换有关的因素的表观遗传学调控。伴侣和辅助因子对来自合成,折叠,转运和降解的全能蛋白的生命周期进行了精细调节,以维持干状态或细胞命运。在这里,我们总结了支配干性的分子伴侣网络的当前知识,并介绍了分子伴侣在干细胞弹性中的多种作用。阐明多能性的复杂调节,详细剖析分子决定因素和驱动因素,是理解干细胞特性的基础,从而为生物医学研究和再生医学提供可靠的基础。

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