Targeted disruption of peroxisomal proliferator-activated receptor β (δ) results in distinct gender differences in mouse brain phospholipid and esterified FA levels

摘要

The peroxisomal proliferator-activated receptor β (δ) (PPARβ) is a nuclear hormone receptor that is ubiquitously expressed and that regulates the transcription of genes involved in lipid metabolism. A homozygous PPARβ-null mouse has been developed in which the ligand-binding domain of the PPARβ receptor is disrupted. Analysis of brains from these animals shows that female null mice have 24 and 17% increases in plasmenylethanolamine and phosphatidylserine and a 9% decrease in the level of phosphatidylinositol when compared to controls. The phospholipid changes found in female null mice were associated with increased levels of esterified 18∶1n−9, 20∶1n−9, 20∶4n−6, and 22∶5n−3 FA in plasmenylethanolamine, 20∶1n−9 in phosphatidylinositol, and 18∶0, 18∶1n−9, 18∶3n−6, 20∶1n−9, and 20∶4n−6 in phosphatidylserine. Increased levels of esterified 18∶1n−9, 18∶2n−6, 18∶3n−6, and 20∶1n−9 were also found in the phosphatidylethanolamine fraction despite its cellular content remaining unchanged. Brain phospholipid content in male PPARβ-null mice did not differ from controls, but increased levels of 20∶1n−9 in the phosphatidylinositol and 18∶1n−9 in the phosphatidylserine fractions were observed. No changes were found in the content of brain cholesterol, TAG, and FFA in either female or male PPARβ-null mice. These data suggest that PPARβ is involved in maintaining FA and phospholipid levels in adult female mouse brain and provide strong evidence that suggests a role for PPARβ in brain peroxisomal acyl-CoA utilization.