Your browser doesn't support javascript.
loading
<Editors' Choice> Mesenchymal stem/stromal cells generated from induced pluripotent stem cells are highly resistant to senescence.
Aoi, Tomonori; Tanaka, Akihito; Furuhashi, Kazuhiro; Ikeya, Makoto; Shimizu, Asuka; Arioka, Yuko; Kushima, Itaru; Ozaki, Norio; Maruyama, Shoichi.
Afiliação
  • Aoi T; Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Tanaka A; Department of Nephrology, Nagoya University Hospital, Nagoya, Japan.
  • Furuhashi K; Department of Nephrology, Nagoya University Hospital, Nagoya, Japan.
  • Ikeya M; Institute for Advanced Research, Nagoya University, Nagoya, Japan.
  • Shimizu A; Department of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
  • Arioka Y; Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Kushima I; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Ozaki N; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Maruyama S; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nagoya J Med Sci ; 85(4): 682-690, 2023 Nov.
Article em En | MEDLINE | ID: mdl-38155616
ABSTRACT
The use of mesenchymal stem/stromal cells (MSCs) has attracted attention in the field of regenerative medicine based on their anti-inflammatory and tissue repair-promoting effects. Bone marrow is widely used as a source of MSCs; however, the performance of bone marrow (BM)-MSCs deteriorates as the cells age along with cell passaging. Recently, it has been reported that MSCs can be generated from induced pluripotent stem cells (iPSCs), which is expected to represent a new source of MSCs. However, few studies have investigated aging in iPSC-derived MSCs (iMSCs) and their functions. In this study, we investigated whether iMSCs overcome cellular senescence compared to that in BM-MSCs. Cellular senescence was quantitatively evaluated by staining iMSCs and BM-MSCs with fluorescein di-ß-D-galactopyranoside (FDG) and following flow cytometer analysis. The hepatocyte growth factor (HGF) concentration in the culture supernatant was also measured as a factor in the therapeutic efficacy of nephritis. The iMSCs did not reach their proliferation limit and their morphology did not change even after 10 passages. The FDG positivity of BM-MSCs increased with passaging, whereas that in iMSCs did not increase. The HGF concentration increased with passaging in iMSCs. In conclusion, our results suggest that iMSCs may be less susceptible to senescence than BM-MSCs and may be used in clinical applications.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article