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2021, Progress in Retinal and Eye ResearchCitation Excerpt :A common theme in non-mammalian systems that possess the capacity to regenerate lost or damaged tissues is the reprogramming of differentiated cells to a progenitor-like state, which then proliferate and regenerate lost tissue (Tai et al., 2020; Fang et al., 2018). Reprogramming refers to the process through which a differentiated somatic cell is converted into a multipotent or pluripotent state, so called induced pluripotent stem cells (iPSCs) (Gurdon, 1962; Takahashi and Yamanaka, 2006), or converted directly into an unrelated terminally differentiated cell type (reviewed in Srivastava and DeWitt, 2016; Fang et al., 2018). The reprogramming process has been studied extensively in many cell types and organs (reviewed Chen et al., 2020), including the retina, where Müller glia of zebrafish and Xenopus are able to regenerate damaged retinal neurons (reviewed in Lahne et al., 2020; Garcia-Garcia et al., 2020).
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2014, Drug Discovery TodayCitation Excerpt :However, because in vitro and in vivo cellular reprogramming results can differ, genetically engineered animal model organisms have gained popularity as a useful tool in regenerative medicine [2]. Indeed the first evidence that somatic cells can be reprogrammed was obtained following successful nuclear transfer in frogs [3]. Likewise, direct cell type conversions can be accomplished in vivo in the model nematode Caenorhabditis elegans, via the application of chemical compounds as well as the overexpression of defined factors [4].