High Expression Level of PPARγ in CD24 Knockout Mice and Gender-Specific Metabolic Changes: A Model of Insulin-Sensitive Obesity

• Published in: Journal of personalized medicine 2021-01, Vol.11 (1), p.50
• Main Authors: Shapira, Shiran, Kazanov, Dina, Dankner, Rachel, Fishman, Sigal, Stern, Naftali, Arber, Nadir
• Format: Article
• Language: English
• Subjects: Adipocytes; Adipogenesis; Body weight; Cancer; Cell differentiation; Diabetes; Diabetes mellitus; Diet; Fatty acids; Food; Gender; Gender differences; Genotype & phenotype; Glucose; Homeostasis; Insulin; Insulin resistance; Lipid metabolism; Lipids; Metabolism; Next-generation sequencing; Obesity; Peptides; Precision medicine; Risk factors; rRNA 16S; Stem cells; Thermal stability; Tumors
• ISSN: 2075-4426; 2075-4426
• DOI: 10.3390/jpm11010050

The heat-stable HSA/CD24 gene encodes a protein that shows high expression levels in adipocyte precursor cells but low levels in terminally differentiated adipocytes. Its high expression in many types of human cancer suggests an association between cancer, diabetes, and obesity, which is currently unclear. In addition, peroxisome proliferator-activated receptor gamma (PPARγ) is a regulator of adipogenesis that plays a role in insulin sensitivity, lipid metabolism, and adipokine expression in adipocytes. To assess gender-dependent changes in CD24 KO and its association with PPARγ expression. WT and CD24 KO mice were monitored from birth up to 12 months, and various physiological and molecular characteristics were analysed. Mean body weight and adipose mass were higher in KO mice than in WT mice. Male, but not female, KO mice showed increased insulin sensitivity, glucose uptake, adipocyte size, and PPARγ expression than WT mice. In addition, enteric bacterial populations, assessed through high-throughput sequencing of stool 16S rRNA genes, were significantly different between male KO and WT mice. CD24 may negatively regulate PPARγ expression in male mice. Furthermore, the association between the CD24 and insulin sensitivity suggests a possible mechanism for diabetes as a cancer risk factor. Finally, CD24 KO male mice may serve as a model of obesity and insulin hyper-sensitivity.