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Pparγfl fl

Manufactured by Jackson ImmunoResearch

The PPARγfl/fl is a genetic construct that contains loxP sites flanking the PPAR gamma gene. This allows for the conditional deletion of the PPAR gamma gene in cells expressing Cre recombinase. The core function of this construct is to enable the study of the role of PPAR gamma in various cellular and biological processes.

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2 protocols using pparγfl fl

1

Adipocyte-specific Genetic Manipulations

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Adipoq-Cre, PPARγfl/fl, adiponectin–/–, and leptin–/– mice were purchased from The Jackson Laboratory. FF mice were generated by mating homozygous Lox-stop-Lox-ROSA-DTA mice (7 (link)) to those expressing Adipoq-Cre. Adipocyte-specific PPARγ deletion mice were generated by mating PPARγfl/fl mice with Adipoq-Cre (PPAR ADQ). Lox-stop-Lox-ROSA-DTA mice and PPARγfl/fl mice were used as control mice of FF mice and PPAR ADQ mice, respectively. C57BL/6 and Leptin+/– mice were used as control mice of adiponectin–/– and leptin–/– mice, respectively. Both FF and PPAR ADQ mice could not survive at room temperature after birth because of lack of BAT, so they were housed at thermoneutral condition (30°C) till weaning age (3 weeks old). All other mice were kept at 22°C on a 12-hour light/12-hour dark cycle. Although no sex differences existed in phenotype, female mice were exclusively used. Mice used in experiments were 8–16 weeks old.
For HFD-feeding studies, mice were fed with chow diet until age 8 weeks and thereafter were randomized into groups that were fed either chow diet or HFD (Research Diets Inc., catalog D12492) for 3 months. Metformin was purchased from MP Biomedicals and dissolved in mouse drinking water (2 g/L) (7 (link)). Fresh drinking water with Metformin was changed daily for 2 months.
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2

Conditional Genetic Manipulation of Mice

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All animals were maintained under the guidelines of the UT Southwestern Medical Center Animal Care and Use Committee according to NIH guidelines. Mice were housed in a 12:12 light:dark cycle and chow and water were provided ad libitum. C57/Bl6, PPARγfl/fl, and R26RRFP mice were obtained in the Jackson Laboratory. Dr. Eric Olson generously provided UCP1-CreERT2 and Ink4a/Arffl/fl mice. SMA-CreERT2 mice were generously provided by Dr. Pierre Chambon. SMA-rtTA mice were generously provided by Dr. Beverly Rothermel. Cre recombination was induced by administering tamoxifen dissolved in sunflower oil (Sigma, 100 mg/Kg interperitoneal injection) on 2 consecutive days. rtTA activation was induced by Doxycycline (0.5mg/ml in 1% sucrose) provided in the drinking water and protected from light, and it was changed every 2-3 days. For cold experiments mice were placed in a 6°C cold room or maintained at room temperature (23°C) for seven days.
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