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p130和视网膜母细胞瘤蛋白在间充质干细胞短暂静止状态维持中的作用

p130 And pRb in the Maintenance of Transient Quiescence of Mesenchymal Stem Cells.

作者信息

Popov Boris, Petrov Nikolai, Ryabov Vladimir, Evsyukov Igor

机构信息

Institute of Cytology Russian Academy of Sciences, St. Petersburg 194064, Russia.

Children's Hospital, The Ohio State University, Columbus, OH 43205-2696, USA.

出版信息

Stem Cells Int. 2020 Sep 18;2020:8883436. doi: 10.1155/2020/8883436. eCollection 2020.

DOI:10.1155/2020/8883436
PMID:33014072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7519995/
Abstract

An effective regulation of quiescence plays a key role in the differentiation, plasticity, and prevention of stem cells from becoming malignant. The state of quiescence is being controlled by the pRb family proteins which show overlapping functions in cell cycle regulation; however, their roles in controlling the proliferation of mesenchymal stem cells (MSCs) remain to be understood. This study investigated the regulation of transient quiescence using growth curves, proliferation assay, the cytometric evaluation of cell cycle, Western blotting, and the electromobility gel shift assay (EMSA) on synchronized MSCs of the C3H10Т1/2 and control cells with different statuses of pRb proteins. It has been found that functional steady-state level of p130 but not pRb plays a critical role for entering, exiting, and maintenance of transient quiescence in multipotent mesenchymal stem cells.

摘要

静止状态的有效调节在干细胞的分化、可塑性以及防止其恶变方面起着关键作用。静止状态受pRb家族蛋白控制,这些蛋白在细胞周期调控中具有重叠功能;然而,它们在控制间充质干细胞(MSC)增殖方面的作用仍有待了解。本研究使用生长曲线、增殖测定、细胞周期的细胞计量学评估、蛋白质免疫印迹法以及对具有不同pRb蛋白状态的C3H10Т1/2同步化间充质干细胞和对照细胞进行的电泳迁移率凝胶位移分析(EMSA),研究了短暂静止的调节。研究发现,对于多能间充质干细胞进入、退出和维持短暂静止状态,起关键作用的是p130而非pRb的功能性稳态水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/ebbfcfb767a3/SCI2020-8883436.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/e91478cb35c4/SCI2020-8883436.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/bca297aa3625/SCI2020-8883436.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/578d5f0bb7d5/SCI2020-8883436.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/ebbfcfb767a3/SCI2020-8883436.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/e91478cb35c4/SCI2020-8883436.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/bca297aa3625/SCI2020-8883436.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/578d5f0bb7d5/SCI2020-8883436.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6568/7519995/ebbfcfb767a3/SCI2020-8883436.004.jpg

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本文引用的文献

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Timing of transcription during the cell cycle: Protein complexes binding to E2F, E2F/CLE, CDE/CHR, or CHR promoter elements define early and late cell cycle gene expression.细胞周期中的转录时机:与E2F、E2F/CLE、CDE/CHR或CHR启动子元件结合的蛋白质复合物决定了细胞周期早期和晚期基因的表达。
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Crosstalk between stem cell and cell cycle machineries.
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The retinoblastoma tumor suppressor and stem cell biology.视网膜母细胞瘤肿瘤抑制因子与干细胞生物学。
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Functional heterogeneity of mesenchymal stem cells: implications for cell therapy.间质干细胞的功能异质性:对细胞治疗的启示。
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Adipogenesis: from stem cell to adipocyte.脂肪生成:从干细胞到脂肪细胞。
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Disruption of repressive p130-DREAM complexes by human papillomavirus 16 E6/E7 oncoproteins is required for cell-cycle progression in cervical cancer cells.人乳头瘤病毒 16 型 E6/E7 癌蛋白破坏抑制性 p130-DREAM 复合物是宫颈癌细胞周期进展所必需的。
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