• 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 Aug 14;104(2):207-11. doi: 10.1016/s0047-6374(98)00087-6.

DOI:10.1016/s0047-6374(98)00087-6
PMID:9792198
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。一个被认为能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的标志物,无论该静止期是可逆的还是不可逆的。其他标志物表明,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”这个术语是用词不当,应该仅在操作层面使用。

相似文献

1
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.
2
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.
3
Accumulation of senescent cells in mitotic tissue of aging primates.衰老灵长类有丝分裂组织中衰老细胞的积累。
Mech Ageing Dev. 2007 Jan;128(1):36-44. doi: 10.1016/j.mad.2006.11.008. Epub 2006 Nov 20.
4
Senescence-like phenotype in post-mitotic cells of mice entering middle age.中年期小鼠有丝分裂后细胞出现衰老样表型。
Aging (Albany NY). 2020 Aug 5;12(14):13979-13990. doi: 10.18632/aging.103637.
5
The implications of the 'hayflick limit' for aging of the organism have been misunderstood by many gerontologists.
Gerontology. 1995;41(2):94-7. doi: 10.1159/000213669.
6
Replicative senescence and oxidant-induced premature senescence. Beyond the control of cell cycle checkpoints.复制性衰老与氧化应激诱导的早衰。超越细胞周期检查点的控制。
Ann N Y Acad Sci. 2000 Jun;908:111-25. doi: 10.1111/j.1749-6632.2000.tb06640.x.
7
Replicative senescence of human fibroblast-like cells in culture.培养的人成纤维细胞样细胞的复制性衰老
Physiol Rev. 1993 Jul;73(3):617-38. doi: 10.1152/physrev.1993.73.3.617.
8
Biomarkers to identify and isolate senescent cells.鉴定和分离衰老细胞的生物标志物。
Ageing Res Rev. 2016 Aug;29:1-12. doi: 10.1016/j.arr.2016.05.003. Epub 2016 May 20.
9
Senescence Phenotypes Induced by Ras in Primary Cells.原代细胞中由Ras诱导的衰老表型。
Methods Mol Biol. 2017;1534:17-30. doi: 10.1007/978-1-4939-6670-7_2.
10
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.

引用本文的文献

1
The role of TGFBI in mesothelioma and breast cancer: association with tumor suppression.TGFBI 在间皮瘤和乳腺癌中的作用:与肿瘤抑制的关联。
BMC Cancer. 2012 Jun 13;12:239. doi: 10.1186/1471-2407-12-239.