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Pennington Biomedical Research Center, Baton Rouge 70808; and Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803
Agouti is a
secreted paracrine factor that regulates pigmentation in hair follicle
melanocytes. Several dominant mutations cause ectopic expression of
agouti, resulting in a phenotype characterized by yellow
fur, adult-onset obesity and diabetes, increased linear growth and
skeletal mass, and increased susceptibility to tumors. Humans also
produce agouti protein, but the highest levels of agouti in humans are
found in adipose tissue. To mimic the human agouti
expression pattern in mice, transgenic mice (aP2-agouti) that express
agouti in adipose tissue were generated. The transgenic mice develop a mild form of obesity, and they are sensitized to the
action of insulin. We correlated the levels of specific regulators of
insulin signaling and adipocyte differentiation with these phenotypic
changes in adipose tissue. Signal transducers and activators of
transcription (STAT)1, STAT3, and peroxisome proliferator-activated receptor (PPAR)-
protein levels were elevated in the transgenic mice. Treatment of mature 3T3-L1 adipocytes recapitulated these effects. These data demonstrate that agouti has potent effects on
adipose tissue. We hypothesize that agouti increases adiposity and
promotes insulin sensitivity by acting directly on adipocytes via
PPAR-
.
adipose tissue; signal transducers and activators of transcription; peroxisome proliferator-activated receptor; melanocortins
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