Shay Jerry W, Wright Woodring E
Department of Cell Biology, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, Texas 75390-9039, USA.
Ann N Y Acad Sci. 2005 Dec;1057:479-91. doi: 10.1196/annals.1356.037.
Telomeres are repetitive DNA (TTAGGG) elements at the ends of chromosomes. Telomerase is a ribonucleoprotein complex that catalyzes the addition of telomeric sequences to the ends of chromosomes. The catalytic protein component of telomerase (hTERT) is expressed only in specific germ line cells, proliferative stem cells of renewal tissues, and cancer cells. The expression of hTERT in normal cells reconstitutes telomerase activity and circumvents the induction of senescence. Telomeres shorten with each cell division, eventually leading to senescence (aging), due to incomplete lagging DNA strand synthesis and end-processing events, and because telomerase activity is not detected in most somatic tissues. There are specific tissues and locations in which replicative senescence likely contributes to the decline in human physiological function with increased age and with chronic illnesses. While expressing hTERT in cells results in the maintenance of telomere length and greatly extended life span, blocking replicative aging systemically would be predicted to increase the potential for tumor formation. However, there are many situations in which the transient rejuvenation of cells could be beneficial. Ectopic expression of hTERT has been shown to immortalize human skin keratinocytes, dermal fibroblasts, muscle satellite (stem), and vascular endothelial, myometrial, retinal-pigmented, and breast epithelial cells. In addition, human bronchial, corneal and skin cells expressing hTERT can be used to form organotypic (3D) cultures (bioengineered tissues) that express differentiation-specific proteins, demonstrating that hTERT by itself does not alter normal physiology. The production of hTERT-engineered tissues offers the possibility of producing tissues to treat a variety of chronic diseases and age-related medical conditions that are due to telomere-based replicative senescence.
端粒是位于染色体末端的重复DNA(TTAGGG)元件。端粒酶是一种核糖核蛋白复合物,可催化端粒序列添加到染色体末端。端粒酶的催化蛋白成分(hTERT)仅在特定的生殖系细胞、更新组织的增殖干细胞和癌细胞中表达。hTERT在正常细胞中的表达可重建端粒酶活性并避免衰老的诱导。由于滞后DNA链合成不完全和末端加工事件,以及在大多数体细胞组织中未检测到端粒酶活性,端粒会随着每次细胞分裂而缩短,最终导致衰老(老化)。在特定的组织和部位,复制性衰老可能会随着年龄增长和慢性疾病导致人类生理功能下降。虽然在细胞中表达hTERT可维持端粒长度并大大延长寿命,但全身性阻断复制性衰老预计会增加肿瘤形成的可能性。然而,在许多情况下,细胞的短暂年轻化可能是有益的。hTERT的异位表达已被证明可使人类皮肤角质形成细胞、真皮成纤维细胞、肌肉卫星(干)细胞、血管内皮细胞、子宫肌层细胞、视网膜色素上皮细胞和乳腺上皮细胞永生化。此外,表达hTERT的人支气管、角膜和皮肤细胞可用于形成表达分化特异性蛋白的器官型(3D)培养物(生物工程组织),这表明hTERT本身不会改变正常生理功能。hTERT工程组织的产生为生产用于治疗各种慢性疾病和与年龄相关的医学病症(这些病症是由于基于端粒的复制性衰老引起的)的组织提供了可能性。