摘要：SummaryPolyunsaturated fatty acids (PUFAs), such as docosahexaenoic acid (DHA) and arachidonic acid (ARA), play fundamental roles in mammalian physiology. Although PUFA imbalance causes various disorders, mechanisms of the regulation of their systemic levels are poorly understood. Here, we report that hepatic DHA-containing phospholipids (DHA-PLs) determine the systemic levels of PUFAs through the SREBP1-mediated transcriptional program. We demonstrated that liver-specific deletion ofAgpat3leads to a decrease of DHA-PLs and a compensatory increase of ARA-PLs not only in the liver but also in other tissues including the brain. Together with recent findings that plasma lysophosphatidylcholine (lysoPC) is the major source of brain DHA, our results indicate that hepatic AGPAT3 contributes to brain DHA accumulation by supplying DHA-PLs as precursors of DHA-lysoPC. Furthermore, dietary fish oil-mediated suppression of hepatic PUFA biosynthetic program was blunted in liver-specificAgpat3deletion. Our findings highlight the central role of hepatic DHA-PLs as the molecular rheostat for systemic homeostasis of PUFAs.Graphical AbstractDisplay OmittedHighlights•DHA-PLs' deficiency leads to liver-specific induction of PUFA biosynthetic genes•AGPAT3-produced DHA-PLs in the liver are the partial source of DHA in the brain•SREBP1 upregulates PUFA biosynthetic genes in response to hepatic DHA-PLs' deficiency•Dietary DHA suppresses hepatic PUFA biosynthetic genes in an AGPAT3-dependent mannerCellular Physiology; Molecular Physiology; Molecular Biology
