Abstract
In the present manuscript, the methods required to generate purified cultures of mature adipocytes, as well as stromal vascular cells, from the same isolation are detailed. Also, we describe the in vitro conditions for the dedifferentiation of the isolated mature adipocytes. These two types of cells may be used to reevaluate differences between presently available cellular models for lipogenesis/lipolysis and might provide a new cellular physiological system for studies utilizing the proliferative progeny from mature adipocyte dedifferentiation. Alternative possibilities to the dedifferentiation phenomenon are proposed, as this new area of research is novel.
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Abbreviations
- DMEM:
-
Dulbecco’s modified Eagle medium
- DMEM/F12:
-
1:1 ratio; Dulbecco’s modified Eagle medium + Ham’s F12
- FBS:
-
fetal bovine serum
- HBSS:
-
Hank’s balanced salt solution
- HS:
-
horse serum
- PBS:
-
phosphate buffered saline, pH 7.08
- PSG:
-
pigskin gelatin
- SC:
-
satellite cell
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Fernyhough, M.E., Vierck, J.L., Hausman, G.J. et al. Primary Adipocyte Culture: Adipocyte Purification Methods May Lead to a New Understanding of Adipose Tissue Growth and Development. Cytotechnology 46, 163–172 (2004). https://doi.org/10.1007/s10616-005-2602-0
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DOI: https://doi.org/10.1007/s10616-005-2602-0