Summary of Study ST002376

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001529. The data can be accessed directly via it's Project DOI: 10.21228/M8298N This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002376
Study TitleHepatic Phosphatidylcholine Catabolism Driven by PNPLA7 and PNPLA8 Supplies Endogenous Choline to Replenish the Methionine Cycle with Methyl Groups(Pnpla8-knockout)
Study SummaryCholine supplies methyl groups for regeneration of methionine and the methyl donor S-adenosylmethionine in the liver. Here we demonstrate that the catabolism of membrane phosphatidylcholine (PC) into water-soluble glycerophosphocholine (GPC) by the phospholipase/lysophospholipase PNPLA8-PNPLA7 axis enables endogenous choline stored in hepatic PC to be utilized in methyl metabolism. PNPLA7-deficient mice show marked decreases in hepatic GPC, choline, and several metabolites related to the methionine cycle, accompanied by various signs of methionine insufficiency including growth retardation, hypoglycemia, hypolipidemia, increased energy consumption, reduced adiposity, increased FGF21, and an altered histone/DNA methylation landscape. Moreover, PNPLA8-deficient mice recapitulate most of these phenotypes. In contrast to wild-type mice fed a methionine/choline-deficient diet, both knockout strains display a decreased hepatic triglyceride likely via reductions of lipogenesis and GPC-derived glycerol flux. Collectively, our findings highlight the biological importance of phospholipid catabolism driven by PNPLA8/PNPLA7 in methyl group flux and triglyceride synthesis in the liver.
Institute
Tokyo Metropolitan Institute of Medical Science
Last NameHirabayashi
First NameTetsuya
Address2-6-1 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan
Emailhirabayashi-tt@igakuken.or.jp
Phone+81-3-5316-3100
Submit Date2022-11-29
Analysis Type DetailLC-MS
Release Date2022-12-15
Release Version1
Tetsuya Hirabayashi Tetsuya Hirabayashi
https://dx.doi.org/10.21228/M8298N
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Genotype
SA237375KO3Pnpla8-knockout
SA237376KO4Pnpla8-knockout
SA237377KO6Pnpla8-knockout
SA237378KO2Pnpla8-knockout
SA237379KO5Pnpla8-knockout
SA237380KO1Pnpla8-knockout
SA237381WT3Wild-type
SA237382WT2Wild-type
SA237383WT4Wild-type
SA237384WT5Wild-type
SA237385WT6Wild-type
SA237386WT1Wild-type
Showing results 1 to 12 of 12
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