Direct Neuronal Reprogramming of Common Marmoset Fibroblasts by ASCL1, microRNA-9/9, and microRNA-124 Overexpression

• Published in: Cells (Basel, Switzerland) Switzerland), 2020-12, Vol.10 (1), p.6
• Main Authors: Nemoto, Akisa, Kobayashi, Reona, Yoshimatsu, Sho, Sato, Yuta, Kondo, Takahiro, Yoo, Andrew S, Shiozawa, Seiji, Okano, Hideyuki
• Format: Article
• Language: English
• Subjects: Animals; ASCL1; Basic Helix-Loop-Helix Transcription Factors - metabolism; Callithrix; Cells, Cultured; Cellular Reprogramming; common marmoset; direct reprogramming; Disease Models, Animal; Fibroblasts; induced neuron (iN); microRNA-124; microRNA-9/9; MicroRNAs; Nervous System Diseases - metabolism; Neurons - metabolism
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells10010006

The common marmoset ( ) has attracted considerable attention, especially in the biomedical science and neuroscience research fields, because of its potential to recapitulate the complex and multidimensional phenotypes of human diseases, and several neurodegenerative transgenic models have been reported. However, there remain several issues as (i) it takes years to generate late-onset disease models, and (ii) the onset age and severity of phenotypes can vary among individuals due to differences in genetic background. In the present study, we established an efficient and rapid direct neuronal induction method (induced neurons; iNs) from embryonic and adult marmoset fibroblasts to investigate cellular-level phenotypes in the marmoset brain in vitro. We overexpressed reprogramming effectors, i.e., microRNA-9/9*, microRNA-124, and Achaete-Scute family bHLH transcription factor 1, in fibroblasts with a small molecule cocktail that facilitates neuronal induction. The resultant iNs from embryonic and adult marmoset fibroblasts showed neuronal characteristics within two weeks, including neuron-specific gene expression and spontaneous neuronal activity. As directly reprogrammed neurons have been shown to model neurodegenerative disorders, the neuronal reprogramming of marmoset fibroblasts may offer new tools for investigating neurological phenotypes associated with disease progression in non-human primate neurological disease models.