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Regulation of telomerase activity in immortal cell lines.永生化细胞系中端粒酶活性的调控。
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Changes in telomerase activity and telomere length during human T lymphocyte senescence.人T淋巴细胞衰老过程中端粒酶活性和端粒长度的变化。
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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。
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Differentiation of immortal cells inhibits telomerase activity.永生细胞的分化会抑制端粒酶活性。
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Telomerase activity in hybrids between telomerase-negative and telomerase-positive immortal human cells is repressed in the different complementation groups but not in the same complementation group of immortality.端粒酶阴性和端粒酶阳性的永生人类细胞之间的杂交细胞中的端粒酶活性在不同的互补组中受到抑制,但在相同的永生互补组中则不受抑制。
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本文引用的文献

1
Aging and cancer: are telomeres and telomerase the connection?衰老与癌症:端粒和端粒酶是其中的关联所在吗?
Mol Med Today. 1995 Nov;1(8):378-84. doi: 10.1016/s1357-4310(95)93872-9.
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Differential expression of telomerase activity in hematopoietic progenitors from adult human bone marrow.成人骨髓造血祖细胞中端粒酶活性的差异表达。
Stem Cells. 1996 Mar;14(2):239-48. doi: 10.1002/stem.140239.
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Telomerase activity in human germline and embryonic tissues and cells.人类生殖系及胚胎组织和细胞中的端粒酶活性。
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Differentiation of immortal cells inhibits telomerase activity.永生细胞的分化会抑制端粒酶活性。
Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12343-6. doi: 10.1073/pnas.92.26.12343.
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Saccharomyces telomeres acquire single-strand TG1-3 tails late in S phase.酿酒酵母端粒在S期后期获得单链TG1-3尾。
Cell. 1993 Jan 15;72(1):51-60. doi: 10.1016/0092-8674(93)90049-v.
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Hepatocyte growth factor (HGF) receptor expression is inducible and is part of the delayed-early response to HGF.
J Biol Chem. 1994 Apr 29;269(17):12846-51.
7
Differential induction of Pax genes by NGF and BDNF in cerebellar primary cultures.在小脑原代培养物中,神经生长因子(NGF)和脑源性神经营养因子(BDNF)对Pax基因的差异诱导作用。
J Cell Biol. 1994 Apr;125(2):417-25. doi: 10.1083/jcb.125.2.417.
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Telomerase activity in human ovarian carcinoma.人卵巢癌中的端粒酶活性
Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):2900-4. doi: 10.1073/pnas.91.8.2900.
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Telomerase activity in germline and embryonic cells of Xenopus.非洲爪蟾生殖细胞和胚胎细胞中的端粒酶活性
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Mammalian telomere dynamics: healing, fragmentation shortening and stabilization.哺乳动物端粒动力学:修复、片段化、缩短与稳定
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永生化细胞系中端粒酶活性的调控。

Regulation of telomerase activity in immortal cell lines.

作者信息

Holt S E, Wright W E, Shay J W

机构信息

Department of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235-9039, USA.

出版信息

Mol Cell Biol. 1996 Jun;16(6):2932-9. doi: 10.1128/MCB.16.6.2932.

DOI:10.1128/MCB.16.6.2932
PMID:8649404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC231287/
Abstract

Telomerase is a ribonucleoprotein whose activity has been detected in germ line cells, immortal cells, and most cancer cells. Except in stem cells, which have a low level of telomerase activity, its activity is absent from normal somatic tissues. Understanding the regulation of telomerase activity is critical for the development of potential tools for the diagnosis and treatment of cancer. Using the telomeric repeat amplification protocol, we found that immortal, telomerase-positive, pseudodiploid human cells (HT1080 and HL60 cells) sorted by flow repressed in quiescent cells. This was true whether quiescence was induced by contact inhibition (NIH 3T3 mouse cells), growth factor removal (bromodeoxyuridine-blocked mouse myoblasts), reexpression of cellular senescence (the reversibly immortalized IDH4 cells), or irreversible cell differentiation (HL60 promyelocytic leukemia cells and C2C12 mouse myoblasts). Taken together, these results indicate that telomerase is active throughout the cell in dividing, immortal cells but that its activity is repressed in cells that exit the cell cycle. This suggests that quiescent stem cells that have the potential to express telomerase may remain unaffected by potential antitelomerase cancer therapies.

摘要

端粒酶是一种核糖核蛋白,其活性已在生殖系细胞、永生化细胞和大多数癌细胞中被检测到。除了在具有低水平端粒酶活性的干细胞中,正常体细胞组织中不存在其活性。了解端粒酶活性的调节对于开发癌症诊断和治疗的潜在工具至关重要。使用端粒重复序列扩增协议,我们发现通过流式细胞术分选的永生化、端粒酶阳性、假二倍体人类细胞(HT1080和HL60细胞)在静止细胞中受到抑制。无论静止是由接触抑制(NIH 3T3小鼠细胞)、生长因子去除(溴脱氧尿苷阻断的小鼠成肌细胞)、细胞衰老的重新表达(可逆性永生化的IDH4细胞)还是不可逆的细胞分化(HL60早幼粒细胞白血病细胞和C2C12小鼠成肌细胞)诱导,都是如此。综上所述,这些结果表明端粒酶在分裂的永生化细胞的整个细胞中是活跃的,但在退出细胞周期的细胞中其活性受到抑制。这表明有可能表达端粒酶的静止干细胞可能不受潜在的抗端粒酶癌症治疗的影响。