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典型衰老生物标志物的强度整合了细胞周期退出的持续时间。

The intensities of canonical senescence biomarkers integrate the duration of cell-cycle withdrawal.

机构信息

Department of Biochemistry, University of Colorado, Boulder, CO, 80303, USA.

BioFrontiers Institute, University of Colorado, Boulder, CO, 80303, USA.

出版信息

Nat Commun. 2023 Jul 27;14(1):4527. doi: 10.1038/s41467-023-40132-0.

Abstract

Senescence, a state of irreversible cell-cycle withdrawal, is difficult to distinguish from quiescence, a state of reversible cell-cycle withdrawal. This difficulty arises because quiescent and senescent cells are defined by overlapping biomarkers, raising the question of whether these states are truly distinct. To address this, we use single-cell time-lapse imaging to distinguish slow-cycling cells that spend long periods in quiescence from cells that never cycle after recovery from senescence-inducing treatments, followed by staining for various senescence biomarkers. We find that the staining intensity of multiple senescence biomarkers is graded rather than binary and reflects the duration of cell-cycle withdrawal, rather than senescence per se. Together, our data show that quiescent and apparent senescent cells are nearly molecularly indistinguishable from each other at a snapshot in time. This suggests that cell-cycle withdrawal itself is graded rather than binary, where the intensities of senescence biomarkers integrate the duration of past cell-cycle withdrawal.

摘要

衰老,一种不可逆的细胞周期退出状态,很难与静止期(一种可逆的细胞周期退出状态)区分开来。这种困难产生的原因是静止期和衰老期细胞是通过重叠的生物标志物来定义的,这就提出了这样一个问题:这些状态是否真的不同。为了解决这个问题,我们使用单细胞延时成像来区分那些在静止期长时间缓慢循环的细胞和那些在从衰老诱导处理中恢复后从未循环的细胞,然后用各种衰老生物标志物进行染色。我们发现,多个衰老生物标志物的染色强度是分级的,而不是二元的,它反映了细胞周期退出的持续时间,而不是衰老本身。总的来说,我们的数据表明,在时间的一个快照中,静止期和明显的衰老期细胞在分子水平上几乎无法区分。这表明细胞周期退出本身是分级的,而不是二元的,衰老生物标志物的强度整合了过去细胞周期退出的持续时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01b6/10374620/8ac5cdf0e301/41467_2023_40132_Fig1_HTML.jpg

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