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Isolation of Mammary Epithelial Cells from Three-dimensional Mixed-cell Spheroid Co-culture
Published on: April 30, 2012
Bovine mammary epithelial cells retain stem-like phenotype in long-term cultures
Diego Cravero, Cravero Diego1, Eugenio Martignani
1Department of Veterinary Science, University of Turin, Via Leonardo da Vinci 44, 10095 Grugliasco, TO, Italy.
Insights
Researchers successfully cultured bovine mammary stem cells in vitro, preserving their regenerative potential. This breakthrough aids in understanding mammary development and could advance lactation yield manipulation and regenerative medicine.
Area of Science:
- Stem cell biology
- Mammary gland development
- Regenerative medicine
Background:
- Adult stem cells in the bovine mammary gland possess regenerative potential.
- In vitro culture and expansion of these primitive cells is challenging.
- Understanding mammary stem cells can inform lactation yield manipulation and regenerative strategies.
Purpose of the Study:
- To investigate the possibility of in vitro maintenance and expansion of bovine mammary stem cells.
- To determine if defined culture conditions influence mammary epithelial cell subpopulations.
- To assess the regenerative capabilities of cultured cells.
Main Methods:
- Culture of bovine mammary epithelial cells under two defined conditions.
- Analysis of cell differentiation markers (CK18, CK14, Vimentin).
- In vivo transplantation of cultured cells into immunodeficient mice.
- Colony-Forming Cell (CFC) assays to assess progenitor content.
Main Results:
- Defined culture conditions induced different mammary epithelial cell subpopulations with varying marker expression (CK18, CK14).
- Vimentin expression increased significantly after 20 days of culture.
- Transplanted cells formed organized pseudo-alveoli expressing mammary markers (CK14, CK18, p63, EpCAM) and milk proteins.
- Colony-forming cell assays showed no substantial differences in progenitor content across conditions and time.
Conclusions:
- Long-term in vitro culture of a multipotent bovine mammary stem cell subpopulation with intrinsic regenerative potential is feasible.
- Cultured cells retain the ability to form functional mammary structures upon transplantation.
- This study provides a foundation for further research into bovine mammary stem cell biology and applications.
Abstract:
The detection and characterization of bovine mammary stem cells may give a better understanding of the cyclic characteristic of mammary gland development. In turn, this could potentially offer techniques to manipulate lactation yield and for regenerative medicine. We previously demonstrated that adult stem cells reside in the bovine mammary gland and possess an intrinsic regenerative potential. In vitro maintenance and expansion of this primitive population is a challenging task that could make easier the study of adult mammary stem cells. The aim of this study is to investigate this possibility. Different subpopulations of mammary epithelial cells emerge when they are cultured in two defined culture conditions. Specific cell differentiation markers as cytokeratin 18 (CK18) and cytokeratin 14 (CK14) were expressed with significant differences according to culture conditions. Vimentin, a well-known fibroblast marker was observed to increase significantly (P < 0.5) only after day 20. In both conditions, after prolonged culture (25 days) a subset of cells still retained regenerative capabilities. These cells were able to form organized pseudo-alveoli when transplanted in immunodeficient mice as shown by the expression of cytokeratin 14 (CK14), cytokeratin 18 (CK18), p63 (a mammary basal cell layer marker) and Epithelial Cell Adhesion Molecule (EpCAM). We also were able to observe the presence of milk proteins signal in these regenerated structures, which is a specific marker of functional mammary alveoli. Progenitor content was also analyzed in vitro through Colony-Forming Cell (CFC) assays with no substantial differences among culture conditions and time points. These results demonstrate that long-term culture of a multipotent cell subpopulation with intrinsic regenerative potential is possible.

