FABP7 Regulates Acetyl-CoA Metabolism Through the Interaction with ACLY in the Nucleus of Astrocytes.
Yoshiteru KagawaBanlanjo Abdulaziz UmaruHiroki ShimaRyo ItoRyo ZamaAriful IslamShin-Ichiro KannoAkira YasuiShun SatoKosuke JozakiSubrata Kumar ShilHirofumi MiyazakiShuhei KobayashiYui YamamotoHiroshi KogoChie Shimamoto-MitsuyamaAkira SugawaraNorihiro SuginoMasayuki KanamoriTeiji TominagaTakeo YoshikawaKohji FukunagaKazuhiko IgarashiYuji OwadaPublished in: Molecular neurobiology (2020)
Fatty acid binding protein 7 (FABP7) is an intracellular fatty acid chaperon that is highly expressed in astrocytes, oligodendrocyte-precursor cells, and malignant glioma. Previously, we reported that FABP7 regulates the response to extracellular stimuli by controlling the expression of caveolin-1, an important component of lipid raft. Here, we explored the detailed mechanisms underlying FABP7 regulation of caveolin-1 expression using primary cultured FABP7-KO astrocytes as a model of loss of function and NIH-3T3 cells as a model of gain of function. We discovered that FABP7 interacts with ATP-citrate lyase (ACLY) and is important for acetyl-CoA metabolism in the nucleus. This interaction leads to epigenetic regulation of several genes, including caveolin-1. Our novel findings suggest that FABP7-ACLY modulation of nuclear acetyl-CoA has more influence on histone acetylation than cytoplasmic acetyl-CoA. The changes to histone structure may modify caveolae-related cell activity in astrocytes and tumors, including malignant glioma.