# Vitamin A-activated PPARγ signaling enhances intramuscular fat accumulation by overriding AMPK-mediated inhibition in late-fattening beef cattle

**Authors:** Xinyue Yang, Chengxing Zhang, Jizhe Tan, Jinge Zhang, Junhao Cui, Yating Fan, Nan Wang, Yongcheng Jin, Dongqiao Peng

PMC · DOI: 10.1186/s40104-025-01343-1 · 2026-02-12

## TL;DR

Adding vitamin A late in fattening beef cattle improves marbling quality by activating PPARγ and managing AMPK signaling, leading to better fat accumulation and healthier fatty acids.

## Contribution

This study reveals that late vitamin A supplementation enhances marbling by overriding AMPK inhibition through PPARγ activation in beef cattle.

## Key findings

- Late vitamin A supplementation increased marbling grades and beneficial fatty acids like EPA and DHA in Woking black cattle.
- AMPK activation was found to act as a negative feedback regulator rather than an inhibitor during vitamin A-induced adipogenesis.
- PPARγ and lipogenic proteins were upregulated in cattle with high-grade marbling following vitamin A supplementation.

## Abstract

Intramuscular fat (IMF) deposition determines beef marbling quality, with current industry practices relying on vitamin A (VA) restriction throughout fattening to enhance marbling development. This study challenges the conventional approach by investigating late-fattening vitamin A supplementation effects on marbling formation in Woking black cattle.

Initial in vitro experiments using bovine skeletal muscle cells (BSMCs) demonstrated that all-trans-retinoic acid (ATRA) treatment during late differentiation (0.1–1 μmol/L) enhanced lipid accumulation with upregulated PPARγ and FABP4 expression. In vivo trials with late-fattening VA supplementation (3,000 IU/kg DM) significantly improved marbling grades, achieving 75% high-grade marbling (A3 or above) with enhanced nutritionally beneficial fatty acids including EPA and DHA levels. Large-scale analysis using 336 genetically homogeneous cattle revealed that superior marbling development correlated with serum VA depletion after VA supplementation, indicating active utilization rather than restriction. A4-grade cattle showed significantly lower serum VA levels than A1-grade cattle, with coordinated upregulation of lipogenic proteins (FASN, SCD, ACACA, PPARγ, FABP4). Transcriptomic analysis unexpectedly revealed significant AMPK pathway activation alongside enhanced marbling development, contradicting conventional understanding of AMPK as an adipogenesis inhibitor. Functional validation using AMPK modulators in BSMCs confirmed that while AMPK inhibition (Compound C) dramatically enhanced VA-induced adipogenesis, AMPK activation (AICAR) suppressed lipogenesis, demonstrating AMPK functions as a negative feedback regulator during VA-mediated adipogenesis rather than preventing intramuscular fat accumulation.

Strategic late-fattening VA supplementation enhances marbling development through PPARγ-mediated transcriptional networks, with AMPK serving as a metabolic sensor and negative feedback regulator rather than an absolute inhibitor. This stage-specific intervention achieved superior marbling quality and improved fatty acid composition in Woking black cattle, suggesting potential for optimization of premium beef production. Validation across diverse genetic backgrounds and production systems will be essential for broader industry implementation.

The online version contains supplementary material available at 10.1186/s40104-025-01343-1.

## Linked entities

- **Genes:** PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], FABP4 (fatty acid binding protein 4) [NCBI Gene 2167], FASN (fatty acid synthase) [NCBI Gene 2194], SCD (stearoyl-CoA desaturase) [NCBI Gene 6319], ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 31]
- **Chemicals:** vitamin A (PubChem CID 445354), all-trans-retinoic acid (PubChem CID 444795), Compound C (PubChem CID 11524144), AICAR (PubChem CID 65110)
- **Species:** Bos taurus (taxon 9913)

## Full-text entities

- **Genes:** PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 281993], FASN (fatty acid synthase) [NCBI Gene 281152], ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 281590] {aka ACC1, ACCA}, SCD (stearoyl-CoA desaturase) [NCBI Gene 280924] {aka SCD1}, FABP4 (fatty acid binding protein 4, adipocyte) [NCBI Gene 281759]
- **Chemicals:** DHA (MESH:C027493), ATRA (MESH:D014212), VA (MESH:D014801), AICAR (MESH:C031143), Compound C (-), lipid (MESH:D008055), fatty acid (MESH:D005227)
- **Species:** Bos taurus (bovine, species) [taxon 9913]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896250/full.md

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Source: https://tomesphere.com/paper/PMC12896250