Abstract
Common variants of human fat mass- and obesity-associated gene Fto have been linked with higher body mass index, but the biological explanation for the link has remained obscure. Recent findings suggest that these variants affect the homeobox protein IRX3. Here we report that FTO has a role in white adipose tissue which modifies its response to high-fat feeding. Wild type and Fto-deficient mice were exposed to standard or high-fat diet for 16 weeks after which metabolism, behavior and white adipose tissue morphology were analyzed together with adipokine levels and relative expression of genes regulating white adipose tissue adipogenesis and Irx3. Our results indicate that Fto deficiency increases the expression of genes related to adipogenesis preventing adipocytes from becoming hypertrophic after high-fat diet. In addition, we report a novel finding of increased Irx3 expression in Fto-deficient mice after high-fat feeding indicating a complex link between FTO, IRX3 and fat metabolism.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adipogenesis
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Adipokines / metabolism
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Adiponectin / biosynthesis
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Adipose Tissue, White / metabolism*
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Adipose Tissue, White / pathology
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Alpha-Ketoglutarate-Dependent Dioxygenase FTO
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Animals
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Diet, High-Fat*
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Embryonic Stem Cells / cytology
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Embryonic Stem Cells / metabolism
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Energy Metabolism
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Glucose Transporter Type 4 / metabolism
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Homeodomain Proteins / metabolism
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Leptin / biosynthesis
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Mice
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Mice, Inbred C57BL
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Mice, Knockout
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Mixed Function Oxygenases / deficiency
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Mixed Function Oxygenases / genetics
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Mixed Function Oxygenases / metabolism*
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Obesity / metabolism
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Obesity / pathology
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Oxo-Acid-Lyases / deficiency
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Oxo-Acid-Lyases / genetics
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Oxo-Acid-Lyases / metabolism*
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Transcription Factors / metabolism
Substances
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Adipokines
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Adiponectin
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Glucose Transporter Type 4
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Homeodomain Proteins
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Irx3 protein, mouse
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Leptin
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Slc2a4 protein, mouse
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Transcription Factors
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Mixed Function Oxygenases
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FTO protein, mouse
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Alpha-Ketoglutarate-Dependent Dioxygenase FTO
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Oxo-Acid-Lyases