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      Lymphatic vascular defects promoted by Prox1 haploinsufficiency cause adult-onset obesity.

      Nature genetics
      Alleles, Animals, Disease Models, Animal, Gene Deletion, Homeodomain Proteins, genetics, metabolism, Insulin, blood, Leptin, Lipid Metabolism, Lipids, analysis, Liver, Lymph, Lymphatic Abnormalities, complications, Lymphatic Vessels, abnormalities, physiopathology, Mice, Mice, Knockout, Obesity, Tumor Suppressor Proteins

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          Abstract

          Multiple organs cooperate to regulate appetite, metabolism, and glucose and fatty acid homeostasis. Here, we identified and characterized lymphatic vasculature dysfunction as a cause of adult-onset obesity. We found that functional inactivation of a single allele of the homeobox gene Prox1 led to adult-onset obesity due to abnormal lymph leakage from mispatterned and ruptured lymphatic vessels. Prox1 heterozygous mice are a new model for adult-onset obesity and lymphatic vascular disease.

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