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基于 Ki67、RPS6 和β-半乳糖苷酶活性表达的分子算法鉴定的静止期、衰老期和细胞应激的不同阶段。

Different Stages of Quiescence, Senescence, and Cell Stress Identified by Molecular Algorithm Based on the Expression of Ki67, RPS6, and Beta-Galactosidase Activity.

机构信息

Department of Experimental Medicine, Luigi Vanvitelli Campania University, 80138 Naples, Italy.

Department of Precision Medicine, Luigi Vanvitelli Campania University, 80138 Naples, Italy.

出版信息

Int J Mol Sci. 2021 Mar 18;22(6):3102. doi: 10.3390/ijms22063102.


DOI:10.3390/ijms22063102
PMID:33803589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8002939/
Abstract

During their life span, cells have two possible states: a non-cycling, quiescent state (G0) and a cycling, activated state. Cells may enter a reversible G0 state of quiescence or, alternatively, they may undergo an irreversible G0 state. The latter may be a physiological differentiation or, following a stress event, a senescent status. Discrimination among the several G0 states represents a significant investigation, since quiescence, differentiation, and senescence are progressive phenomena with intermediate transitional stages. We used the expression of Ki67, RPS6, and beta-galactosidase to identify healthy cells that progressively enter and leave quiescence through G0-entry, G0 and G0-alert states. We then evaluated how cells may enter senescence following a genotoxic stressful event. We identified an initial stress stage with the expression of beta-galactosidase and Ki67 proliferation marker. Cells may recover from stress events or become senescent passing through early and late senescence states. Discrimination between quiescence and senescence was based on the expression of RPS6, a marker of active protein synthesis that is present in senescent cells but absent in quiescent cells. Even taking into account that fixed G0 states do not exist, our molecular algorithm may represent a method for identifying turning points of G0 transitional states that continuously change.

摘要

在其生命周期内,细胞有两种可能的状态:非循环、静止状态(G0)和循环、激活状态。细胞可能进入静止的可逆 G0 状态,或者,它们可能经历不可逆的 G0 状态。后者可能是生理分化,或者在应激事件后,是衰老状态。区分几种 G0 状态是一项重要的研究,因为静止、分化和衰老都是渐进的现象,具有中间过渡阶段。我们使用 Ki67、RPS6 和β-半乳糖苷酶的表达来识别通过 G0 进入、G0 和 G0-警报状态逐渐进入和离开静止的健康细胞。然后,我们评估了细胞在经历遗传毒性应激事件后如何进入衰老。我们通过β-半乳糖苷酶和 Ki67 增殖标志物的表达来鉴定初始应激阶段。细胞可以从应激事件中恢复,或者通过早期和晚期衰老状态而进入衰老。静止和衰老之间的区别基于 RPS6 的表达,RPS6 是一种活跃的蛋白质合成标志物,存在于衰老细胞中,但不存在于静止细胞中。即使考虑到固定的 G0 状态不存在,我们的分子算法也可能代表一种识别不断变化的 G0 过渡状态转折点的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/4c67335bc6f4/ijms-22-03102-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/50e2999e8f59/ijms-22-03102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/f94faba5d090/ijms-22-03102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/6203ddc5ac35/ijms-22-03102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/4c67335bc6f4/ijms-22-03102-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/50e2999e8f59/ijms-22-03102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/f94faba5d090/ijms-22-03102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/6203ddc5ac35/ijms-22-03102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/8002939/4c67335bc6f4/ijms-22-03102-g004.jpg

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本文引用的文献

[1]
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