Repository of Research and Investigative Information

Repository of Research and Investigative Information

Baqiyatallah University of Medical Sciences

Autophagy-Modulated Human Bone Marrow-Derived Mesenchymal Stem Cells Accelerate Liver Restoration in Mouse Models of Acute Liver Failure

(2016) Autophagy-Modulated Human Bone Marrow-Derived Mesenchymal Stem Cells Accelerate Liver Restoration in Mouse Models of Acute Liver Failure. Iran Biomed J. pp. 135-44. ISSN 1028-852x

[img] Text
Autophagy-Modulated Human Bone Marrow-Derived Mesenchymal Stem Cells Accelerate Liver Restoration in Mouse Models of Acute Liver Failure..pdf

Download (1MB)

Official URL: http://www.ncbi.nlm.nih.gov/pubmed/26899739

Abstract

BACKGROUND: Mesenchymal stem cells (MSCs) have been recently received increasing attention for cell-based therapy, especially in regenerative medicine. However, the low survival rate of these cells restricts their therapeutic applications. It is hypothesized that autophagy might play an important role in cellular homeostasis and survival. This study aims to investigate the regenerative potentials of autophagy-modulated MSCs for the treatment of acute liver failure (ALF) in mice. METHODS: ALF was induced in mice by intraperitoneal injection of 1.5 ml/kg carbon tetrachloride. Mice were intravenously infused with MSCs, which were suppressed in their autophagy pathway. Blood and liver samples were collected at different intervals (24, 48 and 72 h) after the transplantation of MSCs. Both the liver enzymes and tissue necrosis levels were evaluated using biochemical and histopathological assessments. The survival rate of the transplanted mice was also recorded during one week. RESULTS: Biochemical and pathological results indicated that 1.5 ml/kg carbon tetrachloride induces ALF in mice. A significant reduction of liver enzymes and necrosis score were observed in autophagy-modulated MSC-transplanted mice compared to sham (with no cell therapy) after 24 h. After 72 h, liver enzymes reached their normal levels in mice transplanted with autophagy-suppressed MSCs. Interestingly, normal histology without necrosis was also observed. CONCLUSION: Autophagy suppression in MSCs ameliorates their liver regeneration potentials due to paracrine effects and might be suggested as a new strategy for the improvement of cell therapy in ALF.

Item Type: Article
Keywords: Animals Autophagy/*physiology Autophagy-Related Protein 7/metabolism Bone Marrow Cells/metabolism Carbon Tetrachloride/toxicity Cell Differentiation Cell Proliferation Cell Survival Cell- and Tissue-Based Therapy/*methods Disease Models, Animal Humans Liver/enzymology/pathology Liver Failure, Acute/pathology/*therapy Liver Regeneration/*physiology *Mesenchymal Stem Cell Transplantation Mesenchymal Stem Cells/*metabolism Mice *Acute liver failure *Autophagy *Mesenchymal stem cells
Divisions:
Page Range: pp. 135-44
Journal or Publication Title: Iran Biomed J
Journal Index: Pubmed
Volume: 20
Number: 3
Identification Number: https://doi.org/10.7508/ibj.2016.03.002
ISSN: 1028-852x
Depositing User: مهندس مهدی شریفی
URI: http://eprints.bmsu.ac.ir/id/eprint/1673

Actions (login required)

View Item View Item