AI Article Synopsis

  • Mesenchymal stem cells (MSCs) from adipose tissue (AT) and umbilical cord (UC) were compared for their growth characteristics and potential in treating liver fibrosis, focusing on their optimal sources for therapy.
  • The study found that AT-MSCs had a shorter doubling time and higher cellular yield compared to UC-MSCs, making them more efficient for therapeutic use.
  • Both types of MSCs reduced liver fibrosis and improved liver function in a rat model, but AT-MSCs offer advantages for quick clinical applications due to their superior expansion characteristics.

Article Abstract

Background/aims: Mesenchymal stem cells (MSCs) are potential alternatives for liver fibrosis treatment; however, their optimal sources remain uncertain. This study compares the ex-vivo expansion characteristics of MSCs obtained from adipose tissue (AT) and umbilical cord (UC) and assesses their therapeutic potential for liver fibrosis treatment.

Methods: Since MSCs from early to mid-passage numbers (P2-P6) are preferable for cellular therapy, we investigated the growth kinetics of AT-MSCs and UC-MSCs up to P6 and evaluated their therapeutic effects in a rat model of liver fibrosis induced by diethylnitrosamine.

Results: Results from the expansion studies demonstrated that both cell types exhibited bona fide characteristics of MSCs, including surface antigens, pluripotent gene expression, and differentiation potential. However, AT-MSCs demonstrated a shorter doubling time (58.2 ± 7.3 vs. 82.3 ± 4.3 h;  < 0.01) and a higher population doubling level (10.1 ± 0.7 vs. 8.2 ± 0.3;  < 0.01) compared to UC-MSCs, resulting in more cellular yield (230 ± 9.0 vs. 175 ± 13.2 million) in less time. Animal studies demonstrated that both MSC types significantly reduced liver fibrosis ( < 0.05 vs. the control group) while also improving liver function and downregulating fibrosis-associated gene expression.

Conclusion: AT-MSCs and UC-MSCs effectively reduce liver fibrosis. However, adipose cultures display an advantage by yielding a higher number of MSCs in a shorter duration, rendering them a viable choice for scenarios requiring immediate single-dose administration, often encountered in clinical settings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10912848PMC
http://dx.doi.org/10.1016/j.jceh.2024.101364DOI Listing

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