Morrison S J, Prowse K R, Ho P, Weissman I L
Department of Pathology, Stanford University School of Medicine, California 94305, USA.
Immunity. 1996 Sep;5(3):207-16. doi: 10.1016/s1074-7613(00)80316-7.
It has been proposed that the biological clock underlying the limited division potential of eukaryotic cells is telomere length. We assayed telomerase activity in single cells of the hematopoietic and immune systems. We examined hematopoietic stem cells at four stages of differentiation, lineage-committed progenitors, and mature myeloid and lymphoid cells. The frequency of telomerase-expressing cells within each population was proportional to the frequency of cells thought to have self-renewal potential. Among bone marrow hematopoietic stem cells, 70% exhibited detectable telomerase activity. The telomerase-expressing somatic cells observed in this study are not thought to be immortal, and expression was not correlated with cell cycle distribution or differentiation state. This study demonstrates that the developmental characteristic most consistently associated with telomerase expression is self-renewal potential.
有人提出,真核细胞有限分裂潜能背后的生物钟是端粒长度。我们检测了造血和免疫系统单细胞中的端粒酶活性。我们研究了处于四个分化阶段的造血干细胞、定向祖细胞以及成熟的髓系和淋巴系细胞。每个群体中表达端粒酶的细胞频率与被认为具有自我更新潜能的细胞频率成正比。在骨髓造血干细胞中,70%表现出可检测到的端粒酶活性。本研究中观察到的表达端粒酶的体细胞不被认为是永生的,并且其表达与细胞周期分布或分化状态无关。这项研究表明,与端粒酶表达最始终相关的发育特征是自我更新潜能。