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Updated: Mar 29, 2026

Isolation and Expansion of Mesenchymal Stem/Stromal Cells Derived from Human Placenta Tissue
Published on: June 6, 2016
Placenta Mesenchymal Stem Cell Derived Exosomes Confer Plasticity on Fibroblasts
Masayuki Tooi1, Motohiro Komaki2, Chikako Morioka3
1Department of Periodontology, Graduate School of Medical and Dental Science, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan.
Human placenta mesenchymal stem cell-derived exosomes (PlaMSC-exo) promote fibroblast reprogramming. These exosomes enhance expression of stemness genes OCT4 and NANOG, influencing fibroblast differentiation into osteoblastic and adipocyte lineages.
Area of Science:
- Cell Biology
- Stem Cell Biology
- Regenerative Medicine
Background:
- Mesenchymal stem cell (MSC)-conditioned medium (MSC-CM) shows potential in wound healing.
- Exosomes mediate intercellular communication, but the specific function of MSC-derived exosomes (MSC-exo) is not fully understood.
- Investigating MSC-exo offers insights into paracrine signaling and potential therapeutic applications.
Purpose of the Study:
- To isolate and characterize human placenta MSC (PlaMSC)-derived exosomes (PlaMSC-exo).
- To examine the in vitro effects of PlaMSC-exo on normal adult human dermal fibroblasts (NHDF).
- To assess the influence of PlaMSC-exo on stemness gene expression and differentiation potential of fibroblasts.
Main Methods:
- Isolation of PlaMSCs from human term placenta via enzymatic digestion.
- Preparation of PlaMSC-exo from PlaMSC-CM using ultracentrifugation.
- Analysis of OCT4 and NANOG mRNA expression in NHDF using real-time PCR.
- Assessment of OCT4 transcription activity using Oct4-EGFP reporter fibroblasts.
- Evaluation of osteoblastic and adipocyte differentiation of NHDF using ALP, Alizarin red S, and oil red O staining.
Main Results:
- PlaMSC-exo treatment significantly upregulated OCT4 and NANOG mRNA expression in NHDF.
- PlaMSC-exo enhanced OCT4 transcription activity in fibroblasts.
- NHDF treated with PlaMSC-exo demonstrated enhanced osteoblastic and adipocyte differentiation potential.
Conclusions:
- PlaMSC-exo increase OCT4 and NANOG mRNA expression in fibroblasts, influencing their differentiation capacity.
- PlaMSC-exo promote fibroblast differentiation towards both osteoblastic and adipocyte lineages.
- These findings reveal a novel function of MSC-exo and suggest their potential for clinical applications.
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