• 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

低剂量X射线诱导人胚胎细胞寿命延长过程中的端粒酶活性、端粒长度和染色体畸变

Telomerase activity, telomere length, and chromosome aberrations in the extension of life span of human embryo cells induced by low-dose X-rays.

作者信息

Yang Z, Kodama S, Suzuki K, Watanabe M

机构信息

Department of Health Sciences, School of Pharmaceutical Sciences, Nagasaki University, Japan.

出版信息

J Radiat Res. 1998 Mar;39(1):35-51. doi: 10.1269/jrr.39.35.

DOI:10.1269/jrr.39.35
PMID:9610031
Abstract

We examined whether the shortening of telomere structure is related to in vitro cellular aging after multiple low-dose irradiation. We used three strains of HE cells (HE23, HE31, and HE40) exhibiting different levels of telomerase activity and irradiated these cells twice a week with a dose of 2 cGy or 4 cGy of X-rays until they senesced. The cells were in total exposed to doses of 52-208 cGy of X-rays. Only the HE31 cells, which had no telomerase activity, experienced an increase in the number of cell divisions, reaching a maximum of 120-124% of the non-irradiated controls. However, in two strains which did exhibit telomerase activity in an early passage in culture, no extension of cell life span was found. Telomerase-positive cells completely lost all telomerase activity when the cells were subcultured several times without irradiation. In the HE31 cells where the life span was extended, the ratio of cell having a long telomere was higher than those of the other two cells (HE23 and HE40). Cytogenetic analysis revealed that the life span extension due to multiple low-dose irradiation which was observed in HE31 cells did not correlate with specific chromosome alterations. Our results suggest that the telomerase activity remaining in the cells at an early passage does not correlate with the extension of life span in vitro by X-irradiation. The factor other than telomerase activity may play an important role in the regulation of telomere length and the extension of life span.

摘要

我们研究了多次低剂量照射后端粒结构缩短是否与体外细胞衰老相关。我们使用了三株端粒酶活性水平不同的HE细胞(HE23、HE31和HE40),每周用2 cGy或4 cGy的X射线对这些细胞照射两次,直至它们衰老。细胞总共接受了52 - 208 cGy的X射线照射。只有没有端粒酶活性的HE31细胞经历了细胞分裂次数的增加,达到未照射对照的120 - 124%的最大值。然而,在培养早期传代时确实表现出端粒酶活性的两株细胞中,未发现细胞寿命延长。当细胞在未照射的情况下传代几次时,端粒酶阳性细胞完全丧失了所有端粒酶活性。在寿命延长的HE细胞中,具有长端粒的细胞比例高于其他两株细胞(HE23和HE40)。细胞遗传学分析表明,在HE31细胞中观察到的多次低剂量照射导致的寿命延长与特定的染色体改变无关。我们的结果表明,早期传代时细胞中残留的端粒酶活性与X射线照射导致的体外寿命延长无关。除端粒酶活性外的其他因素可能在端粒长度调节和寿命延长中起重要作用。

相似文献

1
Telomerase activity, telomere length, and chromosome aberrations in the extension of life span of human embryo cells induced by low-dose X-rays.低剂量X射线诱导人胚胎细胞寿命延长过程中的端粒酶活性、端粒长度和染色体畸变
J Radiat Res. 1998 Mar;39(1):35-51. doi: 10.1269/jrr.39.35.
2
Extension of in vitro life-span of gamma-irradiated human embryo cells accompanied by chromosome instability.γ射线照射的人胚胎细胞体外寿命的延长伴随着染色体不稳定。
J Radiat Res. 1998 Sep;39(3):203-13. doi: 10.1269/jrr.39.203.
3
Culture condition-dependent senescence-like growth arrest and immortalization in rodent embryo cells.啮齿动物胚胎细胞中依赖培养条件的衰老样生长停滞和永生化
Radiat Res. 2001 Jan;155(1 Pt 2):254-262. doi: 10.1667/0033-7587(2001)155[0254:ccdslg]2.0.co;2.
4
Induction of telomerase activity by in vivo X-irradiation of mouse splenocytes and its possible role in chromosome healing.小鼠脾细胞体内X射线照射诱导端粒酶活性及其在染色体修复中的可能作用。
Mutat Res. 1998 Aug 3;404(1-2):205-14. doi: 10.1016/s0027-5107(98)00115-8.
5
Telomerase activity and telomere length in Daphnia.水蚤中的端粒酶活性与端粒长度
PLoS One. 2015 May 11;10(5):e0127196. doi: 10.1371/journal.pone.0127196. eCollection 2015.
6
Telomere shortening, telomerase expression, and chromosome instability in rat hepatic epithelial stem-like cells.大鼠肝上皮样干细胞中的端粒缩短、端粒酶表达及染色体不稳定性
Mol Carcinog. 1999 Mar;24(3):209-17. doi: 10.1002/(sici)1098-2744(199903)24:3<209::aid-mc7>3.0.co;2-f.
7
Analysis of genomic integrity and p53-dependent G1 checkpoint in telomerase-induced extended-life-span human fibroblasts.端粒酶诱导延长寿命的人成纤维细胞中基因组完整性及p53依赖的G1期检查点分析。
Mol Cell Biol. 1999 Mar;19(3):2373-9. doi: 10.1128/MCB.19.3.2373.
8
Telomere length and radiosensitivity in human fibroblast clones immortalized by ectopic telomerase expression.通过异位端粒酶表达永生化的人成纤维细胞克隆中的端粒长度与放射敏感性
Oncol Rep. 2008 Jun;19(6):1605-9.
9
Extension of cell life span using exogenous telomerase.使用外源性端粒酶延长细胞寿命。
Methods Mol Biol. 2007;371:151-65. doi: 10.1007/978-1-59745-361-5_12.
10
Immortal, telomerase-negative cell lines derived from a Li-Fraumeni syndrome patient exhibit telomere length variability and chromosomal and minisatellite instabilities.源自一名李-弗劳梅尼综合征患者的永生、端粒酶阴性细胞系表现出端粒长度变异性以及染色体和小卫星不稳定性。
Carcinogenesis. 2003 May;24(5):953-65. doi: 10.1093/carcin/bgg024.

引用本文的文献

1
Senescence in Post-Mitotic Cells: A Driver of Aging?有丝分裂后细胞衰老:衰老的驱动因素?
Antioxid Redox Signal. 2021 Feb 1;34(4):308-323. doi: 10.1089/ars.2020.8048. Epub 2020 Apr 27.
2
Dysregulation of gene expression in the artificial human trisomy cells of chromosome 8 associated with transformed cell phenotypes.人工人类 8 号染色体三体细胞中基因表达失调与转化细胞表型相关。
PLoS One. 2011;6(9):e25319. doi: 10.1371/journal.pone.0025319. Epub 2011 Sep 29.