Zhao Xiao-Feng, Wan Jin, Powell Curtis, Ramachandran Rajesh, Myers Martin G, Goldman Daniel
Molecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109, USA; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI 48109, USA.
Cell Rep. 2014 Oct 9;9(1):272-284. doi: 10.1016/j.celrep.2014.08.047. Epub 2014 Sep 25.
Unlike mammals, zebrafish can regenerate a damaged retina. This remarkable regenerative response is mediated by Müller glia (MG) that undergo a reprogramming event that drives their proliferation and the generation of multipotent progenitors for retinal repair. The mechanisms that drive MG reprogramming are poorly understood. Here, we report that Leptin and Gp130-coupled receptors, acting via a Jak/Stat signaling pathway, stimulate MG reprogramming and progenitor formation in the injured retina. Importantly, we find that ascl1a gene expression, which drives MG reprogramming in fish and mammals, is regulated in a Jak/Stat-dependent manner and requires consensus Stat-binding sites for injury-dependent activation. Finally, we identify cytokines that are induced by retinal injury and exhibit a remarkable synergy in their ability to activate Jak/Stat signaling and MG reprogramming in the uninjured retina. Our study not only furthers our understanding of retina regeneration in zebrafish but also suggests new strategies for awakening retina regeneration in mammals.
与哺乳动物不同,斑马鱼能够再生受损的视网膜。这种显著的再生反应是由米勒胶质细胞(MG)介导的,这些细胞会经历一种重编程事件,该事件驱动它们增殖并产生用于视网膜修复的多能祖细胞。驱动MG重编程的机制目前还知之甚少。在这里,我们报告瘦素和与Gp130偶联的受体通过Jak/Stat信号通路发挥作用,刺激受损视网膜中的MG重编程和祖细胞形成。重要的是,我们发现驱动鱼类和哺乳动物中MG重编程的ascl1a基因表达是以Jak/Stat依赖的方式调控的,并且需要共有Stat结合位点来进行损伤依赖性激活。最后,我们鉴定出视网膜损伤诱导的细胞因子,它们在激活未受损视网膜中的Jak/Stat信号和MG重编程的能力方面表现出显著的协同作用。我们的研究不仅加深了我们对斑马鱼视网膜再生的理解,还为唤醒哺乳动物的视网膜再生提出了新策略。