TY - JOUR
T1 - Direct cell-fate conversion of somatic cells
T2 - Toward regenerative medicine and industries
AU - Horisawa, Kenichi
AU - Suzuki, Atsushi
N1 - Funding Information:
This work was supported in part by the JSPS KAKENHI (Grant Numbers: JP16H01850, JP16K08592, JP18H05102, JP19H01177, and JP19H05267), the Core Research for Evolutional Science and Technology (CREST) Program of the Japan Agency for Medical Research and Development (AMED), the Program for Basic and Clinical Research on Hepatitis of AMED, the Practical Research Project for Rare/Intractable Diseases of AMED, the Research Center Network for Realization of Regenerative Medicine of AMED, the Takeda Science Foundation, the Uehara Memorial Foundation, and the Japan Intractable Diseases Research Foundation.
Publisher Copyright:
© 2020 The Japan Academy.
PY - 2020
Y1 - 2020
N2 - Cells of multicellular organisms have diverse characteristics despite having the same genetic identity. The distinctive phenotype of each cell is determined by molecular mechanisms such as epigenetic changes that occur throughout the lifetime of an individual. Recently, technologies that enable modification of the fate of somatic cells have been developed, and the number of studies using these technologies has increased drastically in the last decade. Various cell types, including neuronal cells, cardiomyocytes, and hepatocytes, have been generated using these technologies. Although most direct reprogramming methods employ forced transduction of a defined sets of transcription factors to reprogram cells in a manner similar to induced pluripotent cell technology, many other strategies, such as methods utilizing chemical compounds and microRNAs to change the fate of somatic cells, have also been developed. In this review, we summarize transcription factor-based reprogramming and various other reprogramming methods. Additionally, we describe the various industrial applications of direct reprogramming technologies.
AB - Cells of multicellular organisms have diverse characteristics despite having the same genetic identity. The distinctive phenotype of each cell is determined by molecular mechanisms such as epigenetic changes that occur throughout the lifetime of an individual. Recently, technologies that enable modification of the fate of somatic cells have been developed, and the number of studies using these technologies has increased drastically in the last decade. Various cell types, including neuronal cells, cardiomyocytes, and hepatocytes, have been generated using these technologies. Although most direct reprogramming methods employ forced transduction of a defined sets of transcription factors to reprogram cells in a manner similar to induced pluripotent cell technology, many other strategies, such as methods utilizing chemical compounds and microRNAs to change the fate of somatic cells, have also been developed. In this review, we summarize transcription factor-based reprogramming and various other reprogramming methods. Additionally, we describe the various industrial applications of direct reprogramming technologies.
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U2 - 10.2183/PJAB.96.012
DO - 10.2183/PJAB.96.012
M3 - Review article
C2 - 32281550
AN - SCOPUS:85083303302
SN - 0386-2208
VL - 96
SP - 131
EP - 158
JO - Proceedings of the Japan Academy Series B: Physical and Biological Sciences
JF - Proceedings of the Japan Academy Series B: Physical and Biological Sciences
IS - 4
ER -