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Induction of Retinal Progenitors and Neurons from Mammalian Müller Glia under Defined Conditions

机译:在限定条件下从哺乳动物穆勒胶质细胞诱导视网膜祖细胞和神经元

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摘要

Vision impairment caused by loss of retinal neurons affects millions of people worldwide, and currently, there is no effective treatment. Müller glia of mammalian retina may represent an under-recognized and potential source for regeneration of a wide range of retinal cell types, including retinal ganglion cells and photoreceptors. Here, we demonstrated that mouse Müller glia cells have the capacity to be reprogrammed into the retinal neuronal cell fate and are competent to give rise to photoreceptors under a defined culture condition. Inactivation of p53 released proliferation restriction of Müller glia and significantly enhanced the induction of retinal progenitor from Müller glia in culture. Moreover, following the ocular transplantation, the Müller glia-derived progenitors were differentiated toward the fates of photoreceptors and retinal ganglion cells. Together, these results demonstrate the feasibility of using Müller glia as a potential source for retinal repair and regeneration.
机译:视网膜神经元丧失引起的视力障碍影响全球数以百万计的人,目前尚无有效的治疗方法。哺乳动物视网膜的Müller胶质细胞可能代表了人们认识不足的潜在来源,可再生多种视网膜细胞类型,包括视网膜神经节细胞和感光细胞。在这里,我们证明了小鼠Müller胶质细胞具有重编程进入视网膜神经元细胞命运的能力,并且能够在定义的培养条件下产生光感受器。 p53的失活释放了Müller胶质细胞的增殖限制,并显着增强了文化中Müller胶质细胞对视网膜祖细胞的诱导。此外,眼移植后,Müller胶质细胞衍生的祖细胞向感光细胞和视网膜神经节细胞的命运分化。总之,这些结果证明了使用Müller胶质细胞作为视网膜修复和再生的潜在来源的可行性。

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