Shay J W, Wright W E
University of Texas Southwestern Medical Center, Department of Cell Biology, Dallas, TX 75390-9039, USA.
J Pathol. 2007 Jan;211(2):114-23. doi: 10.1002/path.2090.
Telomeres are repetitive DNA sequences at the ends of linear chromosomes. Telomerase, a cellular reverse transcriptase, helps maintain telomere length in human stem cells, reproductive cells and cancer cells by adding TTAGGG repeats onto the telomeres. However, most normal human cells do not express telomerase and thus each time a cell divides some telomeric sequences are lost. When telomeres in a subset of cells become short (unprotected), cells enter an irreversible growth arrest state called replicative senescence. Cells in senescence produce a different constellation of proteins compared to normal quiescent cells. This may lead to a change in the homeostatic environment in a tissue-specific manner. In most instances cells become senescent before they can become cancerous; thus, the initial growth arrest induced by short telomeres may be thought of as a potent anti-cancer protection mechanism. When cells can be adequately cultured until they reach telomere-based replicative senescence, introduction of the telomerase catalytic protein component (hTERT) into telomerase-silent cells is sufficient to restore telomerase activity and extend cellular lifespan. Cells with introduced telomerase are not cancer cells, since they have not accumulated the other changes needed to become cancerous. This indicates that telomerase-induced telomere length manipulations may have utility for tissue engineering and for dissecting the molecular mechanisms underlying genetic diseases, including cancer.
端粒是线性染色体末端的重复性DNA序列。端粒酶是一种细胞逆转录酶,通过在端粒上添加TTAGGG重复序列,帮助维持人类干细胞、生殖细胞和癌细胞中的端粒长度。然而,大多数正常人类细胞不表达端粒酶,因此每次细胞分裂时,一些端粒序列都会丢失。当一部分细胞中的端粒变短(无保护)时,细胞会进入一种不可逆的生长停滞状态,称为复制性衰老。与正常静止细胞相比,衰老细胞产生的蛋白质组合不同。这可能会以组织特异性的方式导致体内平衡环境的改变。在大多数情况下,细胞在癌变之前就会衰老;因此,由短端粒诱导的初始生长停滞可被视为一种强大的抗癌保护机制。当细胞能够被充分培养直至达到基于端粒的复制性衰老时,将端粒酶催化蛋白成分(hTERT)引入不表达端粒酶的细胞中足以恢复端粒酶活性并延长细胞寿命。导入端粒酶的细胞不是癌细胞,因为它们尚未积累癌变所需的其他变化。这表明端粒酶诱导的端粒长度操纵可能在组织工程以及剖析包括癌症在内的遗传疾病的分子机制方面具有实用性。