Lehrer M S, Sun T T, Lavker R M
Department of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
J Cell Sci. 1998 Oct;111 ( Pt 19):2867-75. doi: 10.1242/jcs.111.19.2867.
Using double labeling techniques, we studied the replication of corneal epithelial stem cells that reside exclusively in the limbal zone, and their progeny transit amplifying cells. We show that corneal epithelial stem cells can be induced to enter DNA synthesis by wounding and by TPA. We demonstrate the existence of a hierarchy of TA cells; those of peripheral cornea undergo at least two rounds of DNA synthesis before they become post-mitotic, whereas those of central cornea are capable of only one round of division. However, the cell cycle time of these TA cells can be shortened and the number of times these TA cells can replicate is increased in response to wounding. These results thus demonstrate three strategies of epithelial repair: (i) stem cell replication, (ii) the unleashing of additional rounds of cell proliferation that remain as an untapped reserve under normal circumstances, and (iii) enhancement of TA cell proliferation via a shortening of the cycling time.
我们运用双重标记技术,研究了仅存在于角膜缘区域的角膜上皮干细胞及其子代过渡增殖细胞的复制情况。我们发现,角膜上皮干细胞可因创伤和佛波酯(TPA)诱导而进入DNA合成阶段。我们证实了过渡增殖细胞存在层级结构;周边角膜的过渡增殖细胞在进入有丝分裂后期前至少经历两轮DNA合成,而中央角膜的过渡增殖细胞仅能进行一轮分裂。然而,这些过渡增殖细胞的细胞周期时间可因创伤而缩短,其可复制的次数也会增加。因此,这些结果证明了上皮修复的三种策略:(i)干细胞复制;(ii)释放额外的细胞增殖轮次,这些增殖轮次在正常情况下作为未被利用的储备;(iii)通过缩短细胞周期时间增强过渡增殖细胞的增殖。