• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

“细胞衰老”的标志物

Markers of 'cell senescence'.

作者信息

Macieira-Coelho A

机构信息

INSERM and University of Paris VI, Versailles, France.

出版信息

Mech Ageing Dev. 1998 Jun 1;103(1):105-9. doi: 10.1016/s0047-6374(98)00038-4.

DOI:10.1016/s0047-6374(98)00038-4
PMID:9681883
Abstract

In the current literature cells that have finished their proliferative life span in vitro and have reached a terminal post-mitotic state are called senescent cells. This definition originated from the belief that the irreversible non-dividing state has a relationship with aging of the organism. Attempts have been made to find markers of the so-called senescent cell in order to detect their presence in vivo in donors of different ages. One marker which was supposed to demonstrate an increase of post-mitotic cells with aging is a marker of a long resting phase whether reversible or irreversible. Other markers suggest that the postmitotic cell does not increase with aging of the organism, that it is irrelevant for aging, that it is found in an increased number in pathology, and that the term senescent cell is a misnomer that should be used only in an operational manner.

摘要

在当前文献中,那些在体外已完成其增殖寿命并达到终末有丝分裂后状态的细胞被称为衰老细胞。这一定义源于这样一种观点,即不可逆的非分裂状态与生物体的衰老有关。人们试图寻找所谓衰老细胞的标志物,以便在不同年龄供体的体内检测到它们的存在。一种被认为可证明有丝分裂后细胞随衰老而增加的标志物,是处于长静止期(无论可逆与否)的标志物。其他标志物则表明,有丝分裂后细胞并不会随着生物体的衰老而增加,它与衰老无关,在病理状态下数量会增加,并且衰老细胞这一术语是用词不当,仅应以操作性方式使用。

相似文献

1
Markers of 'cell senescence'.“细胞衰老”的标志物
Mech Ageing Dev. 1998 Jun 1;103(1):105-9. doi: 10.1016/s0047-6374(98)00038-4.
2
Markers of 'cell senescence'.“细胞衰老”的标志物
Mech Ageing Dev. 1998 Aug 14;104(2):207-11. doi: 10.1016/s0047-6374(98)00087-6.
3
Markers of cellular senescence. Telomere shortening as a marker of cellular senescence.细胞衰老的标志物。端粒缩短作为细胞衰老的标志物。
Aging (Albany NY). 2016 Jan;8(1):3-11. doi: 10.18632/aging.100871.
4
Do senescence markers correlate in vitro and in situ within individual human donors?衰老标志物在个体人类供体体内的体外和原位情况是否相关?
Aging (Albany NY). 2018 Feb 28;10(2):278-289. doi: 10.18632/aging.101389.
5
Telomere-based proliferative lifespan barriers in Werner-syndrome fibroblasts involve both p53-dependent and p53-independent mechanisms.沃纳综合征成纤维细胞中基于端粒的增殖寿命障碍涉及p53依赖和p53非依赖机制。
J Cell Sci. 2003 Apr 1;116(Pt 7):1349-57. doi: 10.1242/jcs.00331.
6
Does aging need its own program, or is the program of development quite sufficient for it? Stationary cell cultures as a tool to search for anti-aging factors.衰老需要自身特定的程序吗?还是发育程序对衰老而言已足够?以静止细胞培养作为寻找抗衰老因子的工具。
Curr Aging Sci. 2013 Feb;6(1):14-20. doi: 10.2174/18746098112059990009.
7
From the Hayflick mosaic to the mosaics of ageing. Role of stress-induced premature senescence in human ageing.从海弗利克细胞衰老模式到衰老的细胞衰老模式。应激诱导的早衰在人类衰老中的作用。
Int J Biochem Cell Biol. 2002 Nov;34(11):1415-29. doi: 10.1016/s1357-2725(02)00034-1.
8
Cellular senescence as a tumor-protection mechanism: the essential role of counting.细胞衰老作为一种肿瘤保护机制:计数的关键作用。
Curr Opin Genet Dev. 2001 Feb;11(1):98-103. doi: 10.1016/s0959-437x(00)00163-5.
9
Asymmetric distribution of DNA between daughter cells with final symmetry breaking during aging of human fibroblasts.
Prog Mol Subcell Biol. 2007;45:227-42. doi: 10.1007/978-3-540-69161-7_10.
10
Human fibroblasts in vitro senesce with a donor-specific telomere length.体外培养的人成纤维细胞会随着供体特异性端粒长度而衰老。
FEBS Lett. 2002 Apr 10;516(1-3):71-4. doi: 10.1016/s0014-5793(02)02504-8.