“…Over the past decade, achievements in direct reprogramming have provided genuine opportunities to generate unlimited and lineage-specific human NSCs. The ectopic expression of defined transcription factors with or without small molecules has successfully converted human somatic cells, including fibroblasts (Kumar et al, 2012;Lu et al, 2013;Ring et al, 2012;Zhu et al, urine cells et al, 2014), mononuclear cells from both cord blood (Bruzos-Cidon et al, 2016;Liao et al, 2015;Tang et al, 2016) and adult peripheral blood (Dowey et al, 2012;Zhang et al, 2019), into iNSCs. The iNSCs have been shown to capture the key features of adult NSCs in the human brain, indicating that they might possess a therapeutic potential that rivals adult NSCs.…”