Key result
Pharmacological cocktails induced significant upregulation of thermogenic and adipogenic markers in murine and human adipose-derived SVF after six days of in vitro differentiation.
The described in vitro system offers a practical platform to study adipogenesis and thermogenic regulation using murine and human adipose-derived SVF.
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May advance in vitro thermogenic adipocyte models; leaves open clinical translation to metabolic therapies.
Adipose cells vary functionally, with white adipocytes storing energy and brown/beige adipocytes generating heat. Mouse and human subcutaneous white adipose tissue (WAT)-derived stromal vascular fraction (SVF) provides mesenchymal stem cells (MSCs) that can be differentiated into thermogenic adipocytes using pharmacological cocktails. After six days of browning induction, these cells exhibited significant upregulation of thermogenic markers (UCP1, Cidea, Dio2, PRDM16) along with adipogenic genes (PPARγ, aP2), showing enhanced thermogenic potential. This in vitro system offers a practical platform to study adipogenesis and thermogenic regulation.
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Yadav et al. (2025) studied Adipocyte differentiation. Pharmacological cocktails was evaluated on Upregulation of thermogenic markers (UCP1, Cidea, Dio2, PRDM16) and adipogenic genes (PPARγ, aP2). Pharmacological cocktails induced significant upregulation of thermogenic and adipogenic markers in murine and human adipose-derived SVF after six days of in vitro differentiation.
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