Department of Ophthalmology and Visual Sciences, University of Louisville School of Medicine, 301 E Muhammad Ali Blvd, Louisville, Kentucky 40202, USA; Department of Ophthalmology, Beijing Tongren Hospital, Capital Medical University, Beijing 100005, China.
Department of Ophthalmology and Visual Sciences, University of Louisville School of Medicine, 301 E Muhammad Ali Blvd, Louisville, Kentucky 40202, USA; Department of Ophthalmology, Second Affiliated Hospital of Xiangya Medical School, Central South University, Changsha, China.
EBioMedicine. 2020 Feb;52:102618. doi: 10.1016/j.ebiom.2019.102618. Epub 2020 Jan 24.
The retinal pigment epithelium (RPE) has the potential to regenerate the entire neuroretina upon retinal injury in amphibians. In contrast, this regenerative capacity has been lost in mammals. The reprogramming of differentiated somatic cells into induced pluripotent stem cells (iPSCs) by viral transduction of exogenous stem cell factors has triggered a revolution in regenerative medicine. However, the risks of potential mutation(s) caused by random viral vector insertion in host genomes and tumor formation in recipients hamper its clinical application. One alternative is to immortalize adult stem cells with limited potential or to partially reprogram differentiated somatic cells into progenitor-like cells through non-integration protocols.
Sphere-induced RPE stem cells (iRPESCs) were generated from adult mouse RPE cells. Their stem cell functionality was studied in a mouse model of retinal degeneration. The molecular mechanism underlying the sphere-induced reprogramming was investigated using microarray and loss-of-function approaches.
We provide evidence that our sphere-induced reprogramming protocol can immortalize and transform mouse RPE cells into iRPESCs with dual potential to differentiate into cells that express either RPE or photoreceptor markers both in vitro and in vivo. When subretinally transplanted into mice with retinal degeneration, iRPESCs can integrate to the RPE and neuroretina, thereby delaying retinal degeneration in the model animals. Our molecular analyses indicate that the Hippo signaling pathway is important in iRPESC reprogramming.
The Hippo factor Yap1 is activated in the nuclei of cells at the borders of spheres. The factors Zeb1 and P300 downstream of the Hippo pathway are shown to bind to the promoters of the stemness genes Oct4, Klf4 and Sox2, thereby likely transactivate them to reprogram RPE cells into iRPESCs. FUND: National Natural Science Foundation of China and the National Institute of Health USA.
在两栖动物的视网膜损伤后,视网膜色素上皮 (RPE) 具有再生整个神经视网膜的潜力。相比之下,这种再生能力在哺乳动物中已经丧失。通过病毒转导外源性干细胞因子将分化的体细胞重编程为诱导多能干细胞 (iPSC) 引发了再生医学的革命。然而,由于随机病毒载体在宿主基因组中的插入而导致的潜在突变 (s) 的风险以及受者中肿瘤的形成,阻碍了其临床应用。一种替代方法是通过非整合方案使具有有限潜力的成体干细胞永生化,或部分重编程分化的体细胞为祖细胞样细胞。
从成年小鼠 RPE 细胞中生成球体诱导的 RPE 干细胞 (iRPESC)。在视网膜变性的小鼠模型中研究了它们的干细胞功能。使用微阵列和功能丧失方法研究了球体诱导重编程的分子机制。
我们提供的证据表明,我们的球体诱导重编程方案可以使小鼠 RPE 细胞永生化并转化为 iRPESC,这些细胞具有双重潜力,可以在体外和体内分化为表达 RPE 或光感受器标记物的细胞。当将其移植到患有视网膜变性的小鼠的视网膜下时,iRPESC 可以整合到 RPE 和神经视网膜中,从而延迟模型动物的视网膜变性。我们的分子分析表明,Hippo 信号通路在 iRPESC 重编程中很重要。
Hippo 因子 yap1 在球体边界处的细胞核中被激活。Hippo 途径下游的因子 Zeb1 和 P300 被显示与干细胞基因 Oct4、Klf4 和 Sox2 的启动子结合,从而可能通过它们转激活它们将 RPE 细胞重编程为 iRPESC。
中国国家自然科学基金和美国国立卫生研究院。