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Norway

PMID:15353487  

Combined adipocyte-macrophage fatty acid-binding protein deficiency improves metabolism, atherosclerosis, and survival in apolipoprotein E-deficient mice.

Jeffrey B Boord | Kazuhisa Maeda | Liza Makowski | Vladimir R Babaev | Sergio Fazio | MacRae F Linton | Gökhan S Hotamisligil
Circulation | 2004

The adipocyte fatty acid-binding protein (FABP) aP2 is expressed by adipocytes and macrophages and modulates insulin resistance, glucose and lipid metabolism, and atherosclerosis. Insulin sensitivity is improved in obese but not in lean aP2-deficient mice. A second fatty acid-binding protein, mal1, also is expressed in adipocytes and macrophages, and mal1 deficiency produces similar effects on insulin resistance. We tested the hypothesis that combined aP2 and mal1 deficiency would produce synergistic effects on metabolism and reduce atherosclerosis in apolipoprotein E-deficient (apoE-/-) mice.

Pubmed ID: 15353487

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: F32 HL075970
  • Agency: NIEHS NIH HHS, United States
    Id: 5 T32 ES07155-17
  • Agency: NIDDK NIH HHS, United States
    Id: DK59637-01
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL065405
  • Agency: NHLBI NIH HHS, United States
    Id: HL-65405-01
  • Agency: NIEHS NIH HHS, United States
    Id: T32 ES007155
  • Agency: NIDDK NIH HHS, United States
    Id: U24 DK059637

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National Mouse Metabolic Phenotyping Centers (tool)

RRID:SCR_008997

The mission is to advance medical and biological research by providing the scientific community with standardized, high quality metabolic and physiologic phenotyping services for mouse models of diabetes, diabetic complications, obesity and related disorders.

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