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Merck

Mitofusin 2 in Mature Adipocytes Controls Adiposity and Body Weight.

Cell reports (2019-03-14)
Giacomo Mancini, Kevin Pirruccio, Xiaoyong Yang, Matthias Blรผher, Matthew Rodeheffer, Tamas L Horvath
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We found that exposure of adult animals to calorie-dense foods rapidly abolished expression of mitofusin 2 (Mfn2), a gene promoting mitochondrial fusion and mitochondrion-endoplasmic reticulum interactions, in white and brown fat. Mfn2 mRN was also robustly lower in obese human subjects compared with lean controls. Adipocyte-specific knockdown of Mfn2 in adult mice led to increased food intake, adiposity, and impaired glucose metabolism on standard chow as well as on a diet with high calorie content. The body weight and adiposity of mature adipocyte-specific Mfn2 knockout mice on a standard diet were similar to those of control mice on a high-fat diet. The transcriptional profile of the adipose tissue in adipocyte-specific Mfn2 knockout mice was consistent with adipocyte proliferation, increased lipogenesis at the tissue level, and decreased glucose utilization at the systemic level. These observations suggest a possible crucial role for mitochondrial dynamics in adipocytes in initiating systemic metabolic dysregulation.

MATERIALS
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Sigma-Aldrich
Goat Anti-Mouse IgG Antibody, HRP conjugate, Upstateยฎ, from goat
Sigma-Aldrich
Anti-phospho-Acetyl CoA Carboxylase (Ser79) Antibody, clone BK102, clone BK102, Upstateยฎ, from mouse
Sigma-Aldrich
Goat Anti-Rabbit IgG Antibody, HRP-conjugate, 1 mg/mL, Upstateยฎ
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Anti-acetyl CoA Carboxylase Antibody, clone 7D2.2, clone 7D2.2, from mouse
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Anti-GAPDH Antibody, from rabbit, purified by affinity chromatography
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Tamoxifen, ≥99%
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Anti-Mitofusin 2 antibody produced in rabbit, ~1 mg/mL, affinity isolated antibody, buffered aqueous solution