Fatty acid remodeling by LPCAT3 enriches arachidonate in phospholipid membranes and regulates triglyceride transport

Author:

Hashidate-Yoshida Tomomi1,Harayama Takeshi1,Hishikawa Daisuke1,Morimoto Ryo12,Hamano Fumie23,Tokuoka Suzumi M2,Eto Miki12,Tamura-Nakano Miwa4,Yanobu-Takanashi Rieko5,Mukumoto Yoshiko6,Kiyonari Hiroshi6,Okamura Tadashi57,Kita Yoshihiro23,Shindou Hideo18,Shimizu Takao12

Affiliation:

1. Department of Lipid Signaling, National Center for Global Health and Medicine, Tokyo, Japan

2. Department of Lipidomics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

3. Life Sciences Core Facility, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

4. Communal Laboratory, National Center for Global Health and Medicine, Tokyo, Japan

5. Department of Laboratory Animal Medicine, National Center for Global Health and Medicine, Tokyo, Japan

6. Laboratory for Animal Resources and Genetic Engineering, RIKEN Center for Developmental Biology, Kobe, Japan

7. Section of Animal Models, Department of Infectious Diseases, National Center for Global Health and Medicine, Tokyo, Japan

8. Core Research for Evolutionary Science and Technology, Japan Science and Technology Agency, Kawaguchi, Japan

Abstract

Polyunsaturated fatty acids (PUFAs) in phospholipids affect the physical properties of membranes, but it is unclear which biological processes are influenced by their regulation. For example, the functions of membrane arachidonate that are independent of a precursor role for eicosanoid synthesis remain largely unknown. Here, we show that the lack of lysophosphatidylcholine acyltransferase 3 (LPCAT3) leads to drastic reductions in membrane arachidonate levels, and that LPCAT3-deficient mice are neonatally lethal due to an extensive triacylglycerol (TG) accumulation and dysfunction in enterocytes. We found that high levels of PUFAs in membranes enable TGs to locally cluster in high density, and that this clustering promotes efficient TG transfer. We propose a model of local arachidonate enrichment by LPCAT3 to generate a distinct pool of TG in membranes, which is required for normal directionality of TG transfer and lipoprotein assembly in the liver and enterocytes.

Funder

Japan Society for the Promotion of Science (JSPS)

Takeda Science Foundation

National Center for Global Health and Medicine

Japan Science and Technology Agency (JST)

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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