Sakami Sanae, Etter Paige, Reh Thomas A
Department of Biological Structure, 357420 Health Science Center, University of Washington, School of Medicine, Seattle, WA 98195, USA.
Mech Dev. 2008 Jan-Feb;125(1-2):106-16. doi: 10.1016/j.mod.2007.10.001. Epub 2007 Oct 10.
Regeneration of the retina in amphibians is initiated by the transdifferentiation of the retinal pigmented epithelium (RPE) into neural progenitors. A similar process occurs in the early embryonic chick, but the RPE soon loses this ability. The factors that limit the competence of RPE cells to regenerate neural retina are not understood; however, factors normally involved in the development of the eye (i.e. FGF and Pax6) have also been implicated in transdifferentiation. Therefore, we tested whether activin, a TGFbeta family signaling protein shown to be important in RPE development, contributes to the loss in competence of the RPE to regenerate retina. We have found that addition of activin blocks regeneration from the RPE, even during stages when the cells are competent. Conversely, a small molecule inhibitor of the activin/TGFbeta/nodal receptors can delay, and even reverse, the developmental restriction in FGF-stimulated neural retinal regeneration.
两栖动物视网膜的再生由视网膜色素上皮(RPE)向神经祖细胞的转分化启动。类似的过程发生在早期胚胎期的鸡中,但RPE很快就会失去这种能力。限制RPE细胞再生神经视网膜能力的因素尚不清楚;然而,通常参与眼睛发育的因素(即FGF和Pax6)也与转分化有关。因此,我们测试了激活素(一种在RPE发育中显示出重要作用的TGFβ家族信号蛋白)是否导致RPE再生视网膜能力的丧失。我们发现,添加激活素会阻止RPE的再生,即使在细胞具有再生能力的阶段也是如此。相反,激活素/TGFβ/节点受体的小分子抑制剂可以延迟甚至逆转FGF刺激的神经视网膜再生中的发育限制。