Remez Liv Aleen, Onishi Akishi, Menuchin-Lasowski Yotam, Biran Assaf, Blackshaw Seth, Wahlin Karl J, Zack Donlad J, Ashery-Padan Ruth
Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel-Aviv University, Tel Aviv, Israel.
Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Dev Biol. 2017 Dec 1;432(1):140-150. doi: 10.1016/j.ydbio.2017.09.030. Epub 2017 Oct 7.
In the developing retina, as in other regions of the CNS, neural progenitors give rise to individual cell types during discrete temporal windows. Pax6 is expressed in retinal progenitor cells (RPCs) throughout the course of retinogenesis, and has been shown to be required during early retinogenesis for generation of most early-born cell types. In this study, we examined the function of Pax6 in postnatal mouse retinal development. We found that Pax6 is essential for the generation of late-born interneurons, while inhibiting photoreceptor differentiation. Generation of bipolar interneurons requires Pax6 expression in RPCs, while Pax6 is required for the generation of glycinergic, but not for GABAergic or non-GABAergic-non-glycinergic (nGnG) amacrine cell subtypes. In contrast, overexpression of either full-length Pax6 or its 5a isoform in RPCs induces formation of cells with nGnG amacrine features, and suppresses generation of other inner retinal cell types. Moreover, overexpression of both Pax6 variants prevents photoreceptor differentiation, most likely by inhibiting Crx expression. Taken together, these data show that Pax6 acts in RPCs to control differentiation of multiple late-born neuronal cell types.
在发育中的视网膜中,与中枢神经系统的其他区域一样,神经祖细胞在离散的时间窗口内产生不同的细胞类型。在整个视网膜发生过程中,Pax6在视网膜祖细胞(RPCs)中表达,并且已表明在早期视网膜发生过程中,Pax6是生成大多数早期产生的细胞类型所必需的。在本研究中,我们研究了Pax6在出生后小鼠视网膜发育中的功能。我们发现,Pax6对于晚期产生的中间神经元的生成至关重要,同时抑制光感受器分化。双极中间神经元的生成需要RPCs中Pax6的表达,而甘氨酸能无长突细胞亚型的生成需要Pax6,但GABA能或非GABA能 - 非甘氨酸能(nGnG)无长突细胞亚型的生成则不需要Pax6。相反,在RPCs中全长Pax6或其5a亚型的过表达会诱导形成具有nGnG无长突细胞特征的细胞,并抑制其他视网膜内层细胞类型的生成。此外,两种Pax6变体的过表达很可能通过抑制Crx表达来阻止光感受器分化。综上所述,这些数据表明Pax6在RPCs中发挥作用,以控制多种晚期产生的神经元细胞类型的分化。