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Human dental pulp stem cells have comparable abilities to umbilical cord mesenchymal stem/stromal cells in regulating inflammation and ameliorating hepatic fibrosis.

Authors :
Chen, Peixing
Lin, Yanchun
Lin, Wenbo
Li, Yun
Fu, Ting
Liu, Yuanyue
Guan, Tian
Xin, Man
Ye, Ling
Wang, Peiluan
Zeng, Haoyu
Yao, Kaitao
Source :
Human Cell; Jan2024, Vol. 37 Issue 1, p204-213, 10p
Publication Year :
2024

Abstract

Hepatic fibrosis, also called cirrhosis, have wide prevalence worldwide for long yeas. Recently, many treatments for liver cirrhosis made marked progress, especially the umbilical cord-derived mesenchymal stromal cells (UCMSC) therapy. However, limited recourses and potential immune-related issues become the obstacles on UCMSC popularization in clinic. Therefore, we took dental pulp stem cells (DPSCs) into the consideration, since autologous DPSCs can be easily obtained without any ethnic or immune-related issues that heterogenous UCMSCs could encounter. We systematically compared the effects of both cell types and found that DPSCs had similar results to UCMSCs in regulating inflammation and reversing hepatic fibrosis. In our study, co-culturing T cells and PBMSCs showed that DPSCs have the ability to inhibit the proliferation of inflammatory cells and downregulate relevant inflammatory factors. In vitro and in vivo sterility tests confirmed the bio-safety of DPSCs. Moreover, the 1 year-aged mouse model demonstrated that DPSCs successfully reversed hepatic fibrosis. Overall, DPSCs demonstrated comparable effectiveness to UCMSCs in regulating inflammation and reversing hepatic fibrosis, particularly in the aged mouse model that represents middle-aged and elderly humans. Since autologous DPSCs avoid potential immune-related issues that heterogenous UCMSCs could encounter, they may be a better choice for stem cell-related therapies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09147470
Volume :
37
Issue :
1
Database :
Complementary Index
Journal :
Human Cell
Publication Type :
Academic Journal
Accession number :
174578030
Full Text :
https://doi.org/10.1007/s13577-023-01004-3