Efficacy of Autologous Skeletal Myoblast Cell Sheet Transplantation for Liver Regeneration in Liver Failure.


Journal

Transplantation
ISSN: 1534-6080
Titre abrégé: Transplantation
Pays: United States
ID NLM: 0132144

Informations de publication

Date de publication:
01 08 2023
Historique:
medline: 24 7 2023
pubmed: 14 4 2023
entrez: 13 4 2023
Statut: ppublish

Résumé

No effective therapies have yet been established for liver regeneration in liver failure. Autologous skeletal myoblast cell sheet transplantation has been proven to improve cardiac function in patients with heart failure, and one of the mechanisms has been reported to be a paracrine effect by various growth factors associated with liver regeneration. Therefore, the present study focused on the effect of myoblast cells on liver regeneration in vitro and in vivo. We assessed the effect of myoblast cells on the cells comprising the liver in vitro in association with liver regeneration. In addition, we examined in vivo effect of skeletal myoblast cell sheet transplantation in C57/BL/6 mouse models of liver failure, such as liver fibrosis induced by thioacetamide and hepatectomy. In vitro, the myoblast cells exhibited a capacity to promote the proliferation of hepatic epithelial cells and the angiogenesis of liver sinusoidal endothelial cells, and suppress the activation of hepatic stellate cells. In vivo, sheet transplantation significantly suppressed liver fibrosis in the induced liver fibrosis model and accelerated liver regeneration in the hepatectomy model. Autologous skeletal myoblast cell sheet transplantation significantly improved the liver failure in the in vitro and in vivo models. Sheet transplantation is expected to have the potential to be a clinically therapeutic option for liver regeneration in liver failure.

Sections du résumé

BACKGROUND
No effective therapies have yet been established for liver regeneration in liver failure. Autologous skeletal myoblast cell sheet transplantation has been proven to improve cardiac function in patients with heart failure, and one of the mechanisms has been reported to be a paracrine effect by various growth factors associated with liver regeneration. Therefore, the present study focused on the effect of myoblast cells on liver regeneration in vitro and in vivo.
METHODS
We assessed the effect of myoblast cells on the cells comprising the liver in vitro in association with liver regeneration. In addition, we examined in vivo effect of skeletal myoblast cell sheet transplantation in C57/BL/6 mouse models of liver failure, such as liver fibrosis induced by thioacetamide and hepatectomy.
RESULTS
In vitro, the myoblast cells exhibited a capacity to promote the proliferation of hepatic epithelial cells and the angiogenesis of liver sinusoidal endothelial cells, and suppress the activation of hepatic stellate cells. In vivo, sheet transplantation significantly suppressed liver fibrosis in the induced liver fibrosis model and accelerated liver regeneration in the hepatectomy model.
CONCLUSIONS
Autologous skeletal myoblast cell sheet transplantation significantly improved the liver failure in the in vitro and in vivo models. Sheet transplantation is expected to have the potential to be a clinically therapeutic option for liver regeneration in liver failure.

Identifiants

pubmed: 37046371
doi: 10.1097/TP.0000000000004567
pii: 00007890-202308000-00017
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e190-e200

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors declare no funding or conflicts of interest.

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Auteurs

Keisuke Toya (K)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Yoshito Tomimaru (Y)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Shogo Kobayashi (S)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Akima Harada (A)

Department of Cardiovascular Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Kazuki Sasaki (K)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Yoshifumi Iwagami (Y)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Daisaku Yamada (D)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Takehiro Noda (T)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Hidenori Takahashi (H)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Takeshi Kado (T)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Hiroki Imamura (H)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Shohei Takaichi (S)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Ryota Chijimatsu (R)

Center for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama, Japan.

Tadafumi Asaoka (T)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Masahiro Tanemura (M)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Shigeru Miyagawa (S)

Department of Cardiovascular Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Yuichiro Doki (Y)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

Hidetoshi Eguchi (H)

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

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