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Rosiglitazone and a ?3-Adrenoceptor Agonist Are Both Required for Functional Browning of White Adipocytes in Culture.

ABSTRACT: The recruitment of brite (or beige) adipocytes has been advocated as a means to combat obesity, due to their ability to phenotypically resemble brown adipocytes (BA). Lineage studies indicate that brite adipocytes are formed by differentiation of precursor cells or by direct conversion of existing white adipocytes, depending on the adipose depot examined. We have systematically compared the gene expression profile and a functional output (oxygen consumption) in mouse adipocytes cultured from two contrasting depots, namely interscapular brown adipose tissue, and inguinal white adipose tissue (iWAT), following treatment with a known browning agent, the peroxisome proliferator-activated receptor (PPAR?) activator rosiglitazone. Prototypical BA readily express uncoupling protein (UCP)1, and upstream regulators including the ?3-adrenoceptor and transcription factors involved in energy homeostasis. Adipocytes from inguinal WAT display maximal UCP1 expression and mitochondrial uncoupling only when treated with a combination of the PPAR? activator rosiglitazone and a ?3-adrenoceptor agonist. In conclusion, brite adipocytes are fully activated only when a browning agent (rosiglitazone) and a thermogenic agent (?3-adrenoceptor agonist) are added in combination. The presence of rosiglitazone throughout the 7-day culture period partially masks the effects of ?3-adrenoceptor signaling in inguinal white adipocyte cultures, whereas including rosiglitazone only for the first 3?days promotes robust ?3-adrenoceptor expression and provides an improved window for detection of ?3-adrenoceptor responses.

PROVIDER: S-EPMC5992408 | BioStudies |

REPOSITORIES: biostudies

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