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Published on: May 13, 2016
Nanofiber-expanded stem cells mitigate liver fibrosis: Experimental study
Neveen A Salem1, Hanaa H Ahmed2, Hadeer A Aglan2
1Department of Biochemistry, Faculty of Science, AlFaisalia, King Abdulaziz University, Jeddah, Saudi Arabia; Narcotics, Ergogenic Aids and Poisons Department, Medical Research Division, National Research Centre, Giza, Egypt.
Nanofiber scaffolds enhance mesenchymal stem cell (MSC) pretreatment, improving liver function and hepatic differentiation for liver fibrosis treatment. This strategy boosts cell homing and repopulation, offering a promising therapeutic approach.
Area of Science:
- Regenerative Medicine
- Stem Cell Biology
- Hepatology
Background:
- Liver fibrosis is a significant health concern.
- Mesenchymal stem cells (MSCs) show therapeutic potential but require optimization for hepatic differentiation.
- Pretreatment strategies are being explored to enhance MSC efficacy.
Purpose of the Study:
- To investigate the efficacy of a pretreatment strategy using nanofiber (NF) scaffolds and growth factors (GF) to enhance hepatic lineage divergence of bone marrow-derived MSCs (BMSCs).
- To evaluate the therapeutic potential of NF-expanded BMSCs in a liver fibrosis model.
Main Methods:
- BMSCs were expanded with or without NF scaffolds and treated with GF.
- Liver fibrosis was induced using thioacetamide (TA).
- NF-expanded BMSCs were transplanted and compared biochemically and histologically to control MSCs.
Main Results:
- NF expansion improved BMSC proliferation and characterization.
- Transplanted NF-MSCs significantly improved liver function, increasing hepatic HGF and Bcl-2, while decreasing fibronectin, TNF-α, and TGF-β1.
- NF-MSCs enhanced hepatic gene expression (HNF4α, FOXa2, CYP7a1) and suppressed fibrotic/progenitor markers (β-5-Tub, AFP).
Conclusions:
- Pretreatment with GF and NF scaffolds augments MSC homing, repopulation, and hepatic differentiation.
- This NF-based pretreatment strategy is a promising approach for treating liver fibrosis.

