Cargando…

A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells

We have been developing a therapy for liver cirrhosis using cultured autologous bone marrow–derived mesenchymal stem cells (BMSCs). Before human clinical trials can be considered, the safety and efficacy of BMSC infusion in medium to large animals must be confirmed; thus, we developed a canine liver...

Descripción completa

Detalles Bibliográficos
Autores principales: Matsuda, Takashi, Takami, Taro, Sasaki, Ryo, Nishimura, Tatsuro, Aibe, Yuki, Paredes, Bruno Diaz, Quintanilha, Luiz Fernando, Matsumoto, Toshihiko, Ishikawa, Tsuyoshi, Yamamoto, Naoki, Tani, Kenji, Terai, Shuji, Taura, Yasuho, Sakaida, Isao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5721436/
https://www.ncbi.nlm.nih.gov/pubmed/29404486
http://dx.doi.org/10.1002/hep4.1071
_version_ 1783284806227853312
author Matsuda, Takashi
Takami, Taro
Sasaki, Ryo
Nishimura, Tatsuro
Aibe, Yuki
Paredes, Bruno Diaz
Quintanilha, Luiz Fernando
Matsumoto, Toshihiko
Ishikawa, Tsuyoshi
Yamamoto, Naoki
Tani, Kenji
Terai, Shuji
Taura, Yasuho
Sakaida, Isao
author_facet Matsuda, Takashi
Takami, Taro
Sasaki, Ryo
Nishimura, Tatsuro
Aibe, Yuki
Paredes, Bruno Diaz
Quintanilha, Luiz Fernando
Matsumoto, Toshihiko
Ishikawa, Tsuyoshi
Yamamoto, Naoki
Tani, Kenji
Terai, Shuji
Taura, Yasuho
Sakaida, Isao
author_sort Matsuda, Takashi
collection PubMed
description We have been developing a therapy for liver cirrhosis using cultured autologous bone marrow–derived mesenchymal stem cells (BMSCs). Before human clinical trials can be considered, the safety and efficacy of BMSC infusion in medium to large animals must be confirmed; thus, we developed a canine liver fibrosis model. A small amount of bone marrow fluid was aspirated from the canine humerus to assess the characteristics of BMSCs. We implanted a venous catheter in the stomach and a subcutaneous infusion port in the back of the neck of each canine. Repeated injection of CCl(4) through the catheter was performed to induce liver cirrhosis. After 10 weeks of CCl(4) injection, eight canines were equally divided into two groups: no cell infusion (control group) and autologous BMSC infusion through the peripheral vein (BMSC group). A variety of assays were carried out before and 4 weeks after the infusion. The area of liver fibrosis stained with sirius red was significantly reduced in the BMSC group 4 weeks after BMSC infusion, consistent with a significantly shortened half‐life of indocyanine green and improved liver function. Conclusion: We established a useful canine liver fibrosis model and confirmed that cultured autologous BMSC infusion improved liver fibrosis without adverse effects. (Hepatology Communications 2017;1:691–703)
format Online
Article
Text
id pubmed-5721436
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-57214362018-02-05 A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells Matsuda, Takashi Takami, Taro Sasaki, Ryo Nishimura, Tatsuro Aibe, Yuki Paredes, Bruno Diaz Quintanilha, Luiz Fernando Matsumoto, Toshihiko Ishikawa, Tsuyoshi Yamamoto, Naoki Tani, Kenji Terai, Shuji Taura, Yasuho Sakaida, Isao Hepatol Commun Original Articles We have been developing a therapy for liver cirrhosis using cultured autologous bone marrow–derived mesenchymal stem cells (BMSCs). Before human clinical trials can be considered, the safety and efficacy of BMSC infusion in medium to large animals must be confirmed; thus, we developed a canine liver fibrosis model. A small amount of bone marrow fluid was aspirated from the canine humerus to assess the characteristics of BMSCs. We implanted a venous catheter in the stomach and a subcutaneous infusion port in the back of the neck of each canine. Repeated injection of CCl(4) through the catheter was performed to induce liver cirrhosis. After 10 weeks of CCl(4) injection, eight canines were equally divided into two groups: no cell infusion (control group) and autologous BMSC infusion through the peripheral vein (BMSC group). A variety of assays were carried out before and 4 weeks after the infusion. The area of liver fibrosis stained with sirius red was significantly reduced in the BMSC group 4 weeks after BMSC infusion, consistent with a significantly shortened half‐life of indocyanine green and improved liver function. Conclusion: We established a useful canine liver fibrosis model and confirmed that cultured autologous BMSC infusion improved liver fibrosis without adverse effects. (Hepatology Communications 2017;1:691–703) John Wiley and Sons Inc. 2017-07-17 /pmc/articles/PMC5721436/ /pubmed/29404486 http://dx.doi.org/10.1002/hep4.1071 Text en © 2017 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Matsuda, Takashi
Takami, Taro
Sasaki, Ryo
Nishimura, Tatsuro
Aibe, Yuki
Paredes, Bruno Diaz
Quintanilha, Luiz Fernando
Matsumoto, Toshihiko
Ishikawa, Tsuyoshi
Yamamoto, Naoki
Tani, Kenji
Terai, Shuji
Taura, Yasuho
Sakaida, Isao
A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells
title A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells
title_full A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells
title_fullStr A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells
title_full_unstemmed A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells
title_short A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells
title_sort canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5721436/
https://www.ncbi.nlm.nih.gov/pubmed/29404486
http://dx.doi.org/10.1002/hep4.1071
work_keys_str_mv AT matsudatakashi acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT takamitaro acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT sasakiryo acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT nishimuratatsuro acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT aibeyuki acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT paredesbrunodiaz acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT quintanilhaluizfernando acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT matsumototoshihiko acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT ishikawatsuyoshi acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT yamamotonaoki acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT tanikenji acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT teraishuji acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT taurayasuho acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT sakaidaisao acanineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT matsudatakashi canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT takamitaro canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT sasakiryo canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT nishimuratatsuro canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT aibeyuki canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT paredesbrunodiaz canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT quintanilhaluizfernando canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT matsumototoshihiko canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT ishikawatsuyoshi canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT yamamotonaoki canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT tanikenji canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT teraishuji canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT taurayasuho canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells
AT sakaidaisao canineliverfibrosismodeltodevelopatherapyforlivercirrhosisusingculturedbonemarrowderivedcells