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Abstract 


The gene product of the recently cloned mouse obese gene (ob) is important in regulating adipose tissue mass. ob RNA is expressed specifically by mouse adipocytes in vivo in each of several different fat cell depots, including brown fat. ob RNA is also expressed in cultured 3T3-442A preadipocyte cells that have been induced to differentiate. Mice with lesions of the hypothalamus, as well as mice mutant at the db locus, express a 20-fold higher level of ob RNA in adipose tissue. These data suggest that both the db gene and the hypothalamus are downstream of the ob gene in the pathway that regulates adipose tissue mass and are consistent with previous experiments suggesting that the db locus encodes the ob receptor. In db/db and lesioned mice, quantitative differences in expression level of ob RNA correlated with adipocyte lipid content. The molecules that regulate expression level of the ob gene in adipocytes probably are important in determining body weight, as are the molecules that mediate the effects of ob at its site of action.

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Proc Natl Acad Sci U S A. 1995 Jul 18; 92(15): 6957–6960.
PMCID: PMC41450
PMID: 7624352

Increased expression in adipocytes of ob RNA in mice with lesions of the hypothalamus and with mutations at the db locus.

Abstract

The gene product of the recently cloned mouse obese gene (ob) is important in regulating adipose tissue mass. ob RNA is expressed specifically by mouse adipocytes in vivo in each of several different fat cell depots, including brown fat. ob RNA is also expressed in cultured 3T3-442A preadipocyte cells that have been induced to differentiate. Mice with lesions of the hypothalamus, as well as mice mutant at the db locus, express a 20-fold higher level of ob RNA in adipose tissue. These data suggest that both the db gene and the hypothalamus are downstream of the ob gene in the pathway that regulates adipose tissue mass and are consistent with previous experiments suggesting that the db locus encodes the ob receptor. In db/db and lesioned mice, quantitative differences in expression level of ob RNA correlated with adipocyte lipid content. The molecules that regulate expression level of the ob gene in adipocytes probably are important in determining body weight, as are the molecules that mediate the effects of ob at its site of action.

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Selected References

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  • Liebelt RA, Nicholson N, Ichinoe S. Regulatory influences of adipose tissue on food intake and body weight. Ann N Y Acad Sci. 1965 Oct 8;131(1):559–582. [Abstract] [Google Scholar]
  • Zhang Y, Proenca R, Maffei M, Barone M, Leopold L, Friedman JM. Positional cloning of the mouse obese gene and its human homologue. Nature. 1994 Dec 1;372(6505):425–432. [Abstract] [Google Scholar]
  • Ashwell M, Meade CJ, Medawar P, Sowter C. Adipose tissue: contributions of nature and nurture to the obesity of an obese mutant mouse (ob/ob). Proc R Soc Lond B Biol Sci. 1977 Jan 14;195(1120):343–353. [Abstract] [Google Scholar]
  • Ashwell M, Meade CJ. Obesity: do fat cells from genetically obese mice (C57BL/6J ob/ob) have an innate capacity for increased fat storage? Diabetologia. 1978 Dec;15(6):465–470. [Abstract] [Google Scholar]
  • Richardson RL, Wright JT, Kim JW, Hausman GJ. Expression of transforming growth factor-beta (TGF-beta 1) and insulin-like growth factor II (IGF-II) messenger RNA in the developing subcutaneous tissue (SQ) of the fetal pig. Growth Dev Aging. 1992 Fall;56(3):149–157. [Abstract] [Google Scholar]
  • Schaeren-Wiemers N, Gerfin-Moser A. A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes. Histochemistry. 1993 Dec;100(6):431–440. [Abstract] [Google Scholar]
  • RODBELL M. METABOLISM OF ISOLATED FAT CELLS. I. EFFECTS OF HORMONES ON GLUCOSE METABOLISM AND LIPOLYSIS. J Biol Chem. 1964 Feb;239:375–380. [Abstract] [Google Scholar]
  • Dani C, Bertrand B, Bardon S, Doglio A, Amri E, Grimaldi P. Regulation of gene expression by insulin in adipose cells: opposite effects on adipsin and glycerophosphate dehydrogenase genes. Mol Cell Endocrinol. 1989 May;63(1-2):199–208. [Abstract] [Google Scholar]
  • Bahary N, Leibel RL, Joseph L, Friedman JM. Molecular mapping of the mouse db mutation. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8642–8646. [Europe PMC free article] [Abstract] [Google Scholar]
  • Dani C, Doglio A, Amri EZ, Bardon S, Fort P, Bertrand B, Grimaldi P, Ailhaud G. Cloning and regulation of a mRNA specifically expressed in the preadipose state. J Biol Chem. 1989 Jun 15;264(17):10119–10125. [Abstract] [Google Scholar]
  • Johnson PR, Hirsch J. Cellularity of adipose depots in six strains of genetically obese mice. J Lipid Res. 1972 Jan;13(1):2–11. [Abstract] [Google Scholar]
  • Baura GD, Foster DM, Porte D, Jr, Kahn SE, Bergman RN, Cobelli C, Schwartz MW. Saturable transport of insulin from plasma into the central nervous system of dogs in vivo. A mechanism for regulated insulin delivery to the brain. J Clin Invest. 1993 Oct;92(4):1824–1830. [Europe PMC free article] [Abstract] [Google Scholar]
  • Pardridge WM. Receptor-mediated peptide transport through the blood-brain barrier. Endocr Rev. 1986 Aug;7(3):314–330. [Abstract] [Google Scholar]
  • Faust IM, Johnson PR, Stern JS, Hirsch J. Diet-induced adipocyte number increase in adult rats: a new model of obesity. Am J Physiol. 1978 Sep;235(3):E279–E286. [Abstract] [Google Scholar]
  • Faust IM, Johnson PR, Hirsch J. Surgical removal of adipose tissue alters feeding behavior and the development of obesity in rats. Science. 1977 Jul 22;197(4301):393–396. [Abstract] [Google Scholar]
  • Jacobsson A, Stadler U, Glotzer MA, Kozak LP. Mitochondrial uncoupling protein from mouse brown fat. Molecular cloning, genetic mapping, and mRNA expression. J Biol Chem. 1985 Dec 25;260(30):16250–16254. [Abstract] [Google Scholar]
  • Bray GA, Campfield LA. Metabolic factors in the control of energy stores. Metabolism. 1975 Jan;24(1):99–117. [Abstract] [Google Scholar]
  • HERVEY GR. The effects of lesions in the hypothalamus in parabiotic rats. J Physiol. 1959 Mar 3;145(2):336–352. [Abstract] [Google Scholar]
  • Coleman DL. Obese and diabetes: two mutant genes causing diabetes-obesity syndromes in mice. Diabetologia. 1978 Mar;14(3):141–148. [Abstract] [Google Scholar]
  • Debons AF, Krimsky I, Maayan ML, Fani K, Jemenez FA. Gold thioglucose obesity syndrome. Fed Proc. 1977 Feb;36(2):143–147. [Abstract] [Google Scholar]
  • Johnson AK, Gross PM. Sensory circumventricular organs and brain homeostatic pathways. FASEB J. 1993 May;7(8):678–686. [Abstract] [Google Scholar]

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