# Choline attenuates NEFA-induced hepatic steatosis via GNMT regulation in hepatocytes

**Authors:** Xueer Du, Lamei Wang, Yanfei Dai, Jing Lu, Hongrui Li, Dangdang Wang, Jun Zhang, Chuanjiang Cai, Shimin Liu, Junhu Yao, Jianguo Wang, Yangchun Cao

PMC · DOI: 10.1007/s44154-025-00264-3 · 2025-11-14

## TL;DR

Choline reduces liver fat buildup in calf and human liver cells by regulating GNMT and related metabolic pathways.

## Contribution

Identifies GNMT as a key target of choline in mitigating hepatic steatosis and reveals the AMPK/Myc/GNMT signaling axis as a novel regulatory mechanism.

## Key findings

- Choline reduces NEFA-induced triglyceride accumulation and cytotoxicity in hepatocytes.
- GNMT expression is upregulated by choline, and its knockdown reverses choline's protective effects on lipid and bile acid metabolism.
- AMPK inhibition reduces GNMT expression and increases Myc, suggesting AMPK/Myc axis mediates choline's effects.

## Abstract

To elucidate the molecular mechanisms by which choline regulates hepatic lipid metabolism under negative energy balance conditions, we established non-esterified fatty acid (NEFA)-induced hepatic steatosis models in both calf primary hepatocytes and human LO2 hepatocytes. Choline supplementation significantly reduced intracellular triglyceride accumulation and cytotoxicity induced by NEFA exposure. Transcriptomic profiling identified glycine N-methyltransferase (GNMT) as a key differentially expressed gene. Subsequent experiments confirmed that choline upregulated GNMT expression at both the mRNA and protein levels in a concentration-dependent manner. Knockdown of GNMT reversed the beneficial effects of choline on genes related to lipid synthesis (FAS, ACC), fatty acid oxidation (CPT1), lipoprotein assembly (ApoB100, MTTP), and bile acid metabolism (CYP7A1, CYP27A1, BSEP). Furthermore, inhibition of AMP-activated protein kinase (AMPK) reduced GNMT protein expression and elevated Myc, a negative transcriptional regulator of GNMT, suggesting that choline may regulate GNMT through the AMPK/Myc axis. Collectively, our findings demonstrate that choline alleviates NEFA-induced lipid accumulation and hepatocellular damage by modulating lipid and bile acid metabolism through GNMT, with the AMPK/Myc/GNMT signaling axis playing a pivotal regulatory role. These results provide mechanistic insights into the hepatic protective effects of choline and suggest GNMT as a potential therapeutic target for metabolic disorders in dairy cows and beyond.

The online version contains supplementary material available at 10.1007/s44154-025-00264-3.

## Linked entities

- **Genes:** GNMT (glycine N-methyltransferase) [NCBI Gene 27232], FAS (Fas cell surface death receptor) [NCBI Gene 355], ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 31], CPT1A (carnitine palmitoyltransferase 1A) [NCBI Gene 1374], APOB (apolipoprotein B) [NCBI Gene 338], MTTP (microsomal triglyceride transfer protein) [NCBI Gene 4547], CYP7A1 (cytochrome P450 family 7 subfamily A member 1) [NCBI Gene 1581], CYP27A1 (cytochrome P450 family 27 subfamily A member 1) [NCBI Gene 1593], ABCB11 (ATP binding cassette subfamily B member 11) [NCBI Gene 8647], MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609]
- **Proteins:** PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1), GNMT (glycine N-methyltransferase)
- **Chemicals:** choline (PubChem CID 305), NEFA (PubChem CID 57426056)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** MTTP (microsomal triglyceride transfer protein) [NCBI Gene 280868] {aka MTP}, CYP27A1 (cytochrome P450 family 27 subfamily A member 1) [NCBI Gene 511960], CYP7A1 (cytochrome P450 family 7 subfamily A member 1) [NCBI Gene 510507], APOB (apolipoprotein B) [NCBI Gene 494004] {aka APOB-100, ApoB(100)}, GNMT (glycine N-methyltransferase) [NCBI Gene 538212], MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 511077] {aka CMYC}
- **Diseases:** metabolic disorders (MESH:D008659), cytotoxicity (MESH:D064420), hepatic steatosis (MESH:D005234)
- **Chemicals:** NEFA (MESH:D005230), Choline (MESH:D002794), triglyceride (MESH:D014280), fatty acid (MESH:D005227), lipid (MESH:D008055), bile acid (MESH:D001647)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]
- **Cell lines:** LO2 — Homo sapiens (Human), Amelanotic melanoma, Cancer cell line (CVCL_C7SD)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12615869/full.md

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Source: https://tomesphere.com/paper/PMC12615869