Improved Sendai viral system for reprogramming to naive pluripotency

Akira Kunitomi, Ryoko Hirohata, Vanessa Arreola, Mitsujiro Osawa, Tomoaki M. Kato, Masaki Nomura, Jitsutaro Kawaguchi, Hiroto Hara, Kohji Kusano, Yasuhiro Takashima, Kazutoshi Takahashi, Keiichi Fukuda, Naoko Takasu, Shinya Yamanaka

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

Naive human induced pluripotent stem cells (iPSCs) can be generated by reprogramming somatic cells with Sendai virus (SeV) vectors. However, only dermal fibroblasts have been successfully reprogrammed this way, and the process requires culture on feeder cells. Moreover, SeV vectors are highly persistent and inhibit subsequent differentiation of iPSCs. Here, we report a modified SeV vector system to generate transgene-free naive human iPSCs with superior differentiation potential. The modified method can be applied not only to fibroblasts but also to other somatic cell types. SeV vectors disappear quickly at early passages, and this approach enables the generation of naive iPSCs in a feeder-free culture. The naive iPSCs generated by this method show better differentiation to trilineage and extra-embryonic trophectoderm than those derived by conventional methods. This method can expand the application of iPSCs to research on early human development and regenerative medicine.

Original languageEnglish
Article number100317
JournalCell Reports Methods
Volume2
Issue number11
DOIs
Publication statusPublished - 2022 Nov 21

Keywords

  • LMYC
  • Sendai virus vector
  • extra-embryonic trophectoderm
  • feeder-free culture
  • hsa-microRNA-367
  • induced pluripotent stem cells
  • naive pluripotency
  • reprogramming
  • residual transgenes
  • temperature sensitivity

ASJC Scopus subject areas

  • Biotechnology
  • Biochemistry
  • Biochemistry, Genetics and Molecular Biology (miscellaneous)
  • Genetics
  • Radiology Nuclear Medicine and imaging
  • Computer Science Applications

Fingerprint

Dive into the research topics of 'Improved Sendai viral system for reprogramming to naive pluripotency'. Together they form a unique fingerprint.

Cite this