Avdonin P P, Markitantova Iu V, Zinov'eva R D, Mitashov V I
Izv Akad Nauk Ser Biol. 2008 Jul-Aug(4):414-21.
Molecular-genetic mechanisms of regeneration of adult newt (Pleurodeles waltl) retina were studied. For the first time, a comparative analysis of the expression of regulatory genes Pax6, Otx2, and Six3 and Fgf2 genes encoding signal molecules was performed in the native retinal pigment epithelium (RPE) and retina and at successive stages of retina regeneration. Cell differentiation types were determined using genetic markers of cell differentiation in the RPE (RPE65) and the retina (betaII-tubulin and Rho). Activation of the expression of neurospecific genes Pax6 and Six3 and the growth factor gene Fgf2 and suppression of activation of the regulatory gene Otx2 and the RPE65 were observed at the stage of multipotent neuroblast formation in the regenerating retina. The expression of genes Pax6, Six3, and Fgf2 was retained at a later stage of retina regeneration at which the expression of retinal differentiation markers, the genes encoding betaII-tubulin (betaII-tubulin) and rhodopsin (Rho), was also detected. We assume that the above regulatory genes are multifunctional and control not only transdifferentiation of RPE cells (the key stage of retina regeneration) but also differentiation of regenerating retina cells. The results of this study, demonstrating coexpression of Pax6, Six3, Fgf2, betaII-tubulin, and Rho genes, provide indirect evidence for the interaction of regulatory and specific genes during retina regeneration.
对成年蝾螈(Pleurodeles waltl)视网膜再生的分子遗传机制进行了研究。首次在天然视网膜色素上皮(RPE)和视网膜以及视网膜再生的连续阶段,对调控基因Pax6、Otx2和Six3以及编码信号分子的Fgf2基因的表达进行了比较分析。使用RPE(RPE65)和视网膜(βII-微管蛋白和视紫红质)中细胞分化的遗传标记来确定细胞分化类型。在再生视网膜中多能成神经细胞形成阶段,观察到神经特异性基因Pax6和Six3以及生长因子基因Fgf2的表达激活,以及调控基因Otx2和RPE65激活的抑制。在视网膜再生的后期阶段,Pax6、Six3和Fgf2基因的表达得以保留,此时还检测到了视网膜分化标记物、编码βII-微管蛋白(βII-微管蛋白)和视紫红质(Rho)的基因的表达。我们假设上述调控基因具有多种功能,不仅控制RPE细胞的转分化(视网膜再生的关键阶段),还控制再生视网膜细胞的分化。这项研究的结果表明Pax6、Six3、Fgf2、βII-微管蛋白和Rho基因的共表达,为视网膜再生过程中调控基因和特异性基因的相互作用提供了间接证据。