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干细胞中的端粒与端粒酶:与衰老及疾病的相关性

Telomere and telomerase in stem cells: relevance in ageing and disease.

作者信息

Choudhary Bibha, Karande Anjali A, Raghavan Sathees C

机构信息

Department of Biochemistry, Indian Institute of Science, Bangalore, India.

出版信息

Front Biosci (Schol Ed). 2012 Jan 1;4(1):16-30. doi: 10.2741/248.

Abstract

Telomeres, at the end of chromosomes provide genomic stability. During embryonic development, telomerase, a reverse transcriptase elongates the ends of the DNA. In somatic cells, the activity of telomerase decreases after birth leading to shortening of telomere with cell division, which thereby triggers senescence. In embryonic stem cells and germ cells, telomere length is maintained. In adults, the tissue specific stem cells have telomerase activity, but it is not enough to maintain the length of telomere. The stem cells also undergo the process of ageing but it is delayed as compared to the somatic cells. Studies on the genetic disorder, dyskeratosis congenital, caused by mutations in the human telomerase, reiterate the importance of telomere maintenance in human stem cells. This review covers the role of telomere and telomerase in stem cells and their relevance in disease and ageing.

摘要

染色体末端的端粒可提供基因组稳定性。在胚胎发育过程中,端粒酶(一种逆转录酶)会延长DNA的末端。在体细胞中,端粒酶的活性在出生后降低,导致端粒随着细胞分裂而缩短,从而引发细胞衰老。在胚胎干细胞和生殖细胞中,端粒长度得以维持。在成年人中,组织特异性干细胞具有端粒酶活性,但不足以维持端粒长度。干细胞也会经历衰老过程,但与体细胞相比有所延迟。对由人类端粒酶突变引起的遗传性疾病先天性角化不良的研究,重申了端粒维持在人类干细胞中的重要性。本综述涵盖了端粒和端粒酶在干细胞中的作用及其与疾病和衰老的相关性。

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