The anti-fibrotic effect of human fetal skin-derived stem cell secretome on the liver fibrosis.


Journal

Stem cell research & therapy
ISSN: 1757-6512
Titre abrégé: Stem Cell Res Ther
Pays: England
ID NLM: 101527581

Informations de publication

Date de publication:
03 09 2020
Historique:
received: 30 06 2020
accepted: 18 08 2020
revised: 05 08 2020
entrez: 5 9 2020
pubmed: 5 9 2020
medline: 22 6 2021
Statut: epublish

Résumé

Liver fibrosis resulting from chronic liver injury is one of the major causes of mortality worldwide. Stem cell-secreted secretome has been evaluated for overcoming the limitations of cell-based therapy in hepatic disease, while maintaining its advantages. In this study, we investigated the effect of human fetal skin-derived stem cell (hFSSC) secretome in the treatment of liver fibrosis. To determine the therapeutic potential of the hFSSC secretome in liver fibrosis, we established the CCl Our results showed that hFSSC secretome effectively reduced collagen content in liver, improved the liver function and promoted liver regeneration. Interestingly, we also found that hFSSC secretome reduced liver fibrosis through suppressing the epithelial-mesenchymal transition (EMT) process. In addition, we found that hFSSC secretome inhibited the TGF-β1, Smad2, Smad3, and Collagen I expression, however, increased the Smad7 expression. In conclusions, our results suggest that hFSSC secretome treatment could reduce CCl

Sections du résumé

BACKGROUND
Liver fibrosis resulting from chronic liver injury is one of the major causes of mortality worldwide. Stem cell-secreted secretome has been evaluated for overcoming the limitations of cell-based therapy in hepatic disease, while maintaining its advantages.
METHODS
In this study, we investigated the effect of human fetal skin-derived stem cell (hFSSC) secretome in the treatment of liver fibrosis. To determine the therapeutic potential of the hFSSC secretome in liver fibrosis, we established the CCl
RESULTS
Our results showed that hFSSC secretome effectively reduced collagen content in liver, improved the liver function and promoted liver regeneration. Interestingly, we also found that hFSSC secretome reduced liver fibrosis through suppressing the epithelial-mesenchymal transition (EMT) process. In addition, we found that hFSSC secretome inhibited the TGF-β1, Smad2, Smad3, and Collagen I expression, however, increased the Smad7 expression.
CONCLUSIONS
In conclusions, our results suggest that hFSSC secretome treatment could reduce CCl

Identifiants

pubmed: 32883340
doi: 10.1186/s13287-020-01891-5
pii: 10.1186/s13287-020-01891-5
pmc: PMC7650526
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

379

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Auteurs

Xia Yao (X)

Department of Anesthesiology, The Affiliated Hospital of Changchun University of Chinese Medicine, 1478 Gongnong Road, Changchun, 130021, Jilin, China.

Jing Wang (J)

Department of Gynecology, The Affiliated Hospital of Changchun University of Chinese Medicine, 1478 Gongnong Road, Changchun, 130021, Jilin, China.

Jiajing Zhu (J)

Department of Radiology, The Third Hospital of Jilin University, 126 Xiantai St., Changchun, 130033, Jilin, China.

Xiaoli Rong (X)

Department of Clinical Laboratory, The Affiliated Hospital of Changchun University of Chinese Medicine, 1478 Gongnong Road, Changchun, 130021, Jilin, China. rongxl16@mails.jlu.edu.cn.
Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA. rongxl16@mails.jlu.edu.cn.

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