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Updated: May 26, 2026

Isolation, In Vitro Expansion, and Characterization of Mesenchymal Stem Cells from Mouse Epididymal Adipose Tissue
Published on: January 12, 2024
Bone marrow- and subcutaneous adipose tissue-derived mesenchymal stem cells: differences and similarities
Renata I Dmitrieva1, Izida R Minullina, Anna A Bilibina
1Institute of Haematology, V.A. Almazov Federal Heart, Blood and Endocrinology Centre, St. Petersburg, Russia. renata.i.dmitrieva@gmail.com
Mesenchymal stem cells (MSCs) from bone marrow (BM) and adipose tissue (Ad) show similar early-passage characteristics but differ in CD146+ cell abundance and senescence. Adipose-derived MSCs (Ad-MSCs) exhibit prolonged in vitro expansion potential compared to BM-MSCs.
Area of Science:
- Regenerative Medicine
- Stem Cell Biology
- Tissue Engineering
Background:
- Mesenchymal stem cells (MSCs) are crucial for therapeutic applications.
- Bone marrow (BM) and adipose tissue (Ad) are primary MSC sources.
- Comparative functional analysis of MSCs from different tissues is limited.
Purpose of the Study:
- To compare functional properties of MSCs from BM and Ad in adult donors.
- To evaluate immunophenotype, secretion profiles, and differentiation potential.
- To assess senescence onset and proliferative capacity.
Main Methods:
- Cultured MSCs from 43 adult donors (BM-MSC and Ad-MSC).
- Assessed immunophenotype, growth factors (VEGF, SDF1, MCP1, IL6, TGFβ1) secretion.
- Quantified colony-forming units (CFU-F, CFU-Ad, CFU-Ost) and senescence onset.
Main Results:
- Early-passage BM-MSCs and Ad-MSCs showed comparable proliferation, clonogenicity, and differentiation.
- Significant differences observed in CD146+ cell abundance (higher in BM-MSC) and growth factor secretion.
- BM-MSCs senesced earlier (P3-4) than Ad-MSCs (P6-8).
Conclusions:
- MSC properties vary significantly based on tissue source (BM vs. Ad).
- Ad-MSCs demonstrate a greater in vitro expansion potential and delayed senescence.
- Tissue-specific MSC characteristics must guide clinical application protocol development.
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