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      Age-related adipose tissue mRNA expression of ADD1/SREBP1, PPARgamma, lipoprotein lipase, and GLUT4 glucose transporter in rhesus monkeys.

      The Journals of Gerontology Series A: Biological Sciences and Medical Sciences
      Adipocytes, cytology, Adipose Tissue, metabolism, Aging, genetics, Animals, Body Weight, CCAAT-Enhancer-Binding Proteins, Cell Differentiation, Complement Factor D, DNA-Binding Proteins, Down-Regulation, Enhancer Elements, Genetic, Gene Expression Regulation, Glucose Transporter Type 4, Insulin, blood, Leucine Zippers, Lipoprotein Lipase, Macaca mulatta, Monosaccharide Transport Proteins, Muscle Proteins, Nuclear Proteins, RNA, Messenger, Receptors, Cytoplasmic and Nuclear, Serine Endopeptidases, Sterol Regulatory Element Binding Protein 1, Transcription Factors, Zinc Fingers

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          Abstract

          Aging has been shown to have an effect on the capacity to differentiate preadipocytes and on the expression of some genes expressed in adipose tissue. The mRNA levels of adipocyte differentiation-related genes were examined in rhesus monkeys (Macaca Mulatta) ranging in age from 7 to 30 years. The effect of aging on the expression of peroxisome proliferator activated receptor gamma (PPARgamma), adipocyte determination- and differentiation-dependent factor 1/sterol regulatory element binding protein 1 (ADD1/SREBP1), CCAAT/enhancer binding protein alpha (C/EBPalpha), lipoprotein lipase (LPL), GLUT4 glucose transporter, and adipsin were examined by slot blot analysis. Significant inverse correlations were observed between age and the mRNA levels of PPARgamma, ADD1/SREBP1, LPL, and GLUT4. The coordinate downregulation of these genes may be linked to the declining fat mass of senescent animals. There was no correlation between age and the mRNA levels of adipsin. The mRNA levels of these genes were not correlated to body weight orfasting plasma insulin. These findings indicate that aging may have an effect on the adipocyte differentiation program and this effect appears to be gene specific.

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