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Updated: Feb 16, 2026

Derivation and Differentiation of Canine Ovarian Mesenchymal Stem Cells
Published on: December 16, 2018
Stem cell factor supports migration in canine mesenchymal stem cells.
Nathaly Enciso1, Luciana L K Ostronoff1, Guillermo Mejías1
1Departamento de Bioquímica y Biología Molecular, Facultad de Veterinaria, Universidad Complutense de Madrid, Avda. Puerta de Hierro s/n, 28040, Madrid, Spain.
This study compares mesenchymal stem cells (MSCs) from bone marrow and adipose tissue in dogs, finding similarities in markers and gene expression. Stem Cell Factor (SCF) did not impact MSC proliferation but increased metalloproteinase secretion in adipose-derived MSCs.
Area of Science:
- Veterinary Science
- Regenerative Medicine
- Cell Biology
Background:
- Adult mesenchymal stem cells (MSCs) are multipotent cells crucial for regenerative medicine.
- MSCs are found in various tissues, including bone marrow (BMMSC) and adipose tissue (ASC).
- Understanding MSC characteristics from different sources is vital for therapeutic applications.
Purpose of the Study:
- To compare proliferation, surface markers, and gene expression of BMMSCs and ASCs in dogs.
- To investigate the effect of Stem Cell Factor (SCF) on MSC proliferation and metalloproteinase secretion.
Main Methods:
- Comparative analysis of BMMSCs and ASCs from healthy dogs.
- Flow cytometry for surface marker identification (CD90, CD34, CD45, MCH-II).
- RT-PCR for gene expression (OCT4, SOX9, RUNX2, PPARG) and zymography for metalloproteinases (MMP-2, MMP-9).
Main Results:
- BMMSCs and ASCs exhibited morphological and immunological similarities.
- Both cell types expressed CD90 and lacked CD34, CD45, and MCH-II markers.
- SCF did not influence MSC proliferation but upregulated MMP-2 and MMP-9 secretion in ASCs.
Conclusions:
- Canine BMMSCs and ASCs share significant characteristics, suggesting potential for regenerative medicine.
- Metalloproteinases (MMP-2, MMP-9) may play a key role in MSC migration, particularly in ASCs.
- SCF's role in modulating ASC metalloproteinase secretion warrants further investigation for therapeutic strategies.
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