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Naonobu Nishino, Yoshikazu Tamori, Sanshiro Tateya, Takayuki Kawaguchi, Tetsuro Shibakusa, Wataru Mizunoya, Kazuo Inoue, Riko Kitazawa, Sohei Kitazawa, Yasushi Matsuki, Ryuji Hiramatsu, Satoru Masubuchi, Asako Omachi, Kazuhiro Kimura, Masayuki Saito, Taku Amo, Shigeo Ohta, Tomohiro Yamaguchi, Takashi Osumi, Jinglei Cheng, Toyoshi Fujimoto, Harumi Nakao, Kazuki Nakao, Atsu Aiba, Hitoshi Okamura, Tohru Fushiki, Masato Kasuga
Published in Volume 118, Issue 8
J Clin Invest. 2008; 118(8):2808–2821 doi:10.1172/JCI34090
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Figure 4
Mitochondrion-related gene expression and metabolic rate in WAT of FSP27-knockout mice.

(A and B) Quantitative RT-PCR analysis of the expression of genes related to mitochondrial biogenesis (A) or to FFA oxidation (B) in WAT and BAT of 20-week-old wild-type and FSP27-KO mice. Data were normalized by the amount of 36B4 mRNA and expressed relative to the corresponding value for WAT of wild-type mice; data are mean ± SEM (n = 4). *P < 0.05, **P < 0.01, ***P < 0.001 versus the corresponding value for wild-type mice. (C) Northern blot analysis of mRNAs for COXI, COXII, COXIV, and UCP1 in WAT and BAT of 14-week-old wild-type and FSP27-KO mice. (D) Oxygen consumption by adipocytes isolated from inguinal WAT (IWAT; left panel) or interscapular BAT (right panel) of wild-type and FSP27-KO mice. Arrows indicate the addition of the β3-adrenergic agonist CL316,243 or vehicle (Ca2+- and Mg2+-free PBS). Data are mean ± SEM of values from 4 independent experiments. (E and F) Glucose (E) and oleic acid (F) oxidation in adipocytes isolated from epididymal WAT or interscapular BAT of wild-type and FSP27-KO mice. Data are expressed relative to the corresponding value for WAT of wild-type mice and are mean ± SEM of values from 4 WT or 3 KO independent experiments. P < 0.05, ††P < 0.01 versus the corresponding value for wild-type cells.