Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases
Abstract The liver, the largest organ with multiple synthetic and secretory functions in mammals, consists of hepatocytes, cholangiocytes, hepatic stellate cells (HSCs), sinusoidal endothelial cells, Kupffer cells (KCs), and immune cells, among others. Various causative factors, including viral infe...
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doaj-b0bb20371bbc401398e771d293aea5f92020-11-25T02:14:05ZengBMCStem Cell Research & Therapy1757-65122019-07-0110111310.1186/s13287-019-1310-1Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseasesChenxia Hu0Lingfei Zhao1Lanjuan Li2Kidney Disease Center, First Affiliated Hospital, College of Medicine, Zhejiang University; Key Laboratory of Kidney Disease Prevention and Control Technology, Institute of Nephrology, Zhejiang UniversityKidney Disease Center, First Affiliated Hospital, College of Medicine, Zhejiang University; Key Laboratory of Kidney Disease Prevention and Control Technology, Institute of Nephrology, Zhejiang UniversityKidney Disease Center, First Affiliated Hospital, College of Medicine, Zhejiang University; Key Laboratory of Kidney Disease Prevention and Control Technology, Institute of Nephrology, Zhejiang UniversityAbstract The liver, the largest organ with multiple synthetic and secretory functions in mammals, consists of hepatocytes, cholangiocytes, hepatic stellate cells (HSCs), sinusoidal endothelial cells, Kupffer cells (KCs), and immune cells, among others. Various causative factors, including viral infection, toxins, autoimmune defects, and genetic disorders, can impair liver function and result in chronic liver disease or acute liver failure. Mesenchymal stem cells (MSCs) from various tissues have emerged as a potential candidate for cell transplantation to promote liver regeneration. Adipose-derived MSCs (ADMSCs) with high multi-lineage potential and self-renewal capacity have attracted great attention as a promising means of liver regeneration. The abundance source and minimally invasive procedure required to obtain ADMSCs makes them superior to bone marrow-derived MSCs (BMMSCs). In this review, we comprehensively analyze landmark studies that address the isolation, proliferation, and hepatogenic differentiation of ADMSCs and summarize the therapeutic effects of ADMSCs in animal models of liver diseases. We also discuss key points related to improving the hepatic differentiation of ADMSCs via exposure of the cells to cytokines and growth factors (GFs), extracellular matrix (ECM), and various physical parameters in in vitro culture. The optimization of culturing methods and of the transplantation route will contribute to the further application of ADMSCs in liver regeneration and help improve the survival rate of patients with liver diseases. To this end, ADMSCs provide a potential strategy in the field of liver regeneration for treating acute or chronic liver injury, thus ensuring the availability of ADMSCs for research, trial, and clinical applications in various liver diseases in the future.http://link.springer.com/article/10.1186/s13287-019-1310-1 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chenxia Hu Lingfei Zhao Lanjuan Li |
spellingShingle |
Chenxia Hu Lingfei Zhao Lanjuan Li Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases Stem Cell Research & Therapy |
author_facet |
Chenxia Hu Lingfei Zhao Lanjuan Li |
author_sort |
Chenxia Hu |
title |
Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases |
title_short |
Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases |
title_full |
Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases |
title_fullStr |
Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases |
title_full_unstemmed |
Current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases |
title_sort |
current understanding of adipose-derived mesenchymal stem cell-based therapies in liver diseases |
publisher |
BMC |
series |
Stem Cell Research & Therapy |
issn |
1757-6512 |
publishDate |
2019-07-01 |
description |
Abstract The liver, the largest organ with multiple synthetic and secretory functions in mammals, consists of hepatocytes, cholangiocytes, hepatic stellate cells (HSCs), sinusoidal endothelial cells, Kupffer cells (KCs), and immune cells, among others. Various causative factors, including viral infection, toxins, autoimmune defects, and genetic disorders, can impair liver function and result in chronic liver disease or acute liver failure. Mesenchymal stem cells (MSCs) from various tissues have emerged as a potential candidate for cell transplantation to promote liver regeneration. Adipose-derived MSCs (ADMSCs) with high multi-lineage potential and self-renewal capacity have attracted great attention as a promising means of liver regeneration. The abundance source and minimally invasive procedure required to obtain ADMSCs makes them superior to bone marrow-derived MSCs (BMMSCs). In this review, we comprehensively analyze landmark studies that address the isolation, proliferation, and hepatogenic differentiation of ADMSCs and summarize the therapeutic effects of ADMSCs in animal models of liver diseases. We also discuss key points related to improving the hepatic differentiation of ADMSCs via exposure of the cells to cytokines and growth factors (GFs), extracellular matrix (ECM), and various physical parameters in in vitro culture. The optimization of culturing methods and of the transplantation route will contribute to the further application of ADMSCs in liver regeneration and help improve the survival rate of patients with liver diseases. To this end, ADMSCs provide a potential strategy in the field of liver regeneration for treating acute or chronic liver injury, thus ensuring the availability of ADMSCs for research, trial, and clinical applications in various liver diseases in the future. |
url |
http://link.springer.com/article/10.1186/s13287-019-1310-1 |
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