T细胞的端粒生物学:它们寿命之路上的一个重要刹车?

Alexander Röth , Gabriela M. Baerlocher
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引用次数: 0

摘要

端粒和端粒酶在调节人体细胞的寿命中起着至关重要的作用。端粒随着细胞分裂和其他原因而逐渐缩短,最终导致细胞衰老和凋亡。与大多数人类体细胞不同,T细胞和某些B细胞在激活或刺激时表达端粒酶复合物,这在一定程度上补偿了端粒的损耗。端粒酶的再激活很可能是为了延长某些T细胞和B细胞的寿命,以便在大量细胞扩张的情况下充分实现免疫反应。然而,端粒酶的病理或异常再激活是癌细胞的标志之一,似乎是T细胞和b细胞肿瘤发生的关键因素之一。在正常和恶性的T细胞和B细胞中,端粒/端粒酶复合物的操纵是非常有吸引力的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Telomere Biology in T Cells: An Important Brake on the Road of Their Life Span?

Telomeres and telomerase play an essential role in the regulation of the life span of human cells. Telomeres shorten progressively with each cell division, as well as in response to other causes, eventually leading to cell senescence and apoptosis. In contrast to most human somatic cells, T cells and certain B cells express the telomerase complex upon activation or stimulation, which compensates for telomere attrition to some degree. Telomerase reactivation has most likely evolved to extend the life span of certain T cells and B cells in order to adequately fulfill immune responses despite massive cellular expansion. Pathologic or abnormal reactivation of telomerase, however, is one of the hallmarks of cancer cells, and seems to be one of the key elements for developing T- and B-cell neoplasias. Manipulation of the telomere/telomerase complex in both normal and malignant T and B cells is highly attractive for therapeutic strategies.

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