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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |