Skip to main content
Log in

Effect of acetate, β-hydroxybutyrate and their interaction on lipogenic gene expression, triglyceride contents and lipid droplet formation in dairy cow mammary epithelial cells

  • Published:
In Vitro Cellular & Developmental Biology - Animal Aims and scope Submit manuscript

Abstract

The purpose of this study was to assess the effects of acetate and β-hydroxybutyrate alone or in combination on lipogenic genes and their associated regulatory proteins in dairy cow mammary epithelial cells (DCMEC) using quantitative reverse transcription polymerase chain reaction (qRT-PCR), western blotting, lipid droplet staining and a triglyceride content detection kit, to determine whether SCFA are related to milk fat synthesis regulation in DCMEC. Our experiment shows that addition of different concentrations of acetate, β-hydroxybutyrate and their combinations to DCMEC increase in relative mRNA abundance of lipogenic genes and key transcription factors suggest an increase in lipogenic capacity, which is supported by an increased in cytosolic triglyceride content. Similarly, the protein expression level of acetyl-coenzyme A carboxylase (ACACA), fatty acid synthase (FASN) and sterol-coenzyme desaturase-1 (SCD1) genes and the transcription factor sterol regulatory element-binding protein-1 (SREBP1) were found to be increased by addition of acetate, β-hydroxybutyrate and their combinations. The expression pattern of fat-related genes and proteins showed similar trends in almost all treatments, suggesting that common transcription factor are regulating these genes. These results show that acetate and β-hydroxybutyrate regulate fat synthesis, further confirming that SCFAs work by targeting genes to activate the SREBP1 and insulin-induced gene 1 protein (INSIG1) signalling pathways in DCMEC.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1.
Figure 2.
Figure 3.
Figure 4.
Figure 5.

Similar content being viewed by others

References

  • Alex S, Lange K, Amolo T, Grinstead JS, Haakonsson AK, Szalowska E, Koppen A, Mudde K, Haenen D, Roelofsen H (2013) Short-chain fatty acids stimulate angiopoietin-like 4 synthesis in human colon adenocarcinoma cells by activating peroxisome proliferator-activated receptor γ. Mol Cell Biol 33:1303–1316

    Article  CAS  Google Scholar 

  • Bauman D, Griinari J (2001) Regulation and nutritional manipulation of milk fat: low-fat milk syndrome. Livest Prod Sci 70:15–29

    Article  Google Scholar 

  • Bauman DE, Griinari JM (2003) Nutritional regulation of milk fat synthesis. Annu Rev Nutr 23:203–227

    Article  CAS  Google Scholar 

  • Bernard L, Leroux C, Chilliard Y (2008) Expression and nutritional regulation of lipogenic genes in the ruminant lactating mammary gland. Adv Exp Med Biol 606:67–108. https://doi.org/10.1007/978-0-387-74087-4_2

  • Bionaz M, Loor JJ (2008) Gene networks driving bovine milk fat synthesis during the lactation cycle. BMC Genomics 9:366. https://doi.org/10.1186/1471-2164-9-366

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Boutinaud M, Guinard-Flament J (2004) The number and activity of mammary epithelial cells, determining factors for milk production. Reprod Nutr Dev 44:499–508

    Article  Google Scholar 

  • Brown MS, Goldstein JL (1997) The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor. Cell 89:331–340

    Article  CAS  Google Scholar 

  • Chilliard Y, Ferlay A, Mansbridge RM, Doreau M (2000) Ruminant milk fat plasticity: nutritional control of saturated, polyunsaturated, trans and conjugated fatty acids. Annales de zootechnie. EDP Sciences:181–205

  • Cui W, Li Q, Feng L, Ding W (2011) MiR-126-3p regulates progesterone receptors and involves development and lactation of mouse mammary gland. Mol Cell Biochem 355:17–25

    Article  CAS  Google Scholar 

  • Dong X-Y, Tang S-Q, Chen J-D (2012) Dual functions of Insig proteins in cholesterol homeostasis. Lipids Health Dis 11:173

    Article  CAS  Google Scholar 

  • Harvatine KJ, Bauman DE (2006) SREBP1 and thyroid hormone responsive spot 14 (S14) are involved in the regulation of bovine mammary lipid synthesis during diet-induced milk fat depression and treatment with CLA. J Nutr 136:2468–2474

    Article  CAS  Google Scholar 

  • Heid H, Keenan T (2005) Intracellular origin and secretion of milk fat globules. Eur J Cell Biol 84:245–258

    Article  CAS  Google Scholar 

  • Jacobs A, Dijkstra J, Liesman J, Vandehaar M, Lock A, Van Vuuren A, Hendriks W, Van Baal J (2013) Effects of short-and long-chain fatty acids on the expression of stearoyl-CoA desaturase and other lipogenic genes in bovine mammary epithelial cells. Animal 7:1508–1516

    Article  CAS  Google Scholar 

  • Jensen RG (2002) The composition of bovine milk lipids: January 1995 to December 2000. J Dairy Sci 85:295–350

    Article  CAS  Google Scholar 

  • Kadegowda A, Bionaz M, Piperova L, Erdman R, Loor JJ (2009) Peroxisome proliferator-activated receptor-γ activation and long-chain fatty acids alter lipogenic gene networks in bovine mammary epithelial cells to various extents. J Dairy Sci 92:4276–4289

    Article  CAS  Google Scholar 

  • Kast-Woelbern HR, Dana SL, Cesario RM, Sun L, de Grandpre LY, Brooks ME, Osburn DL, Reifel-Miller A, Klausing K, Leibowitz MD (2004) Rosiglitazone induction of Insig-1 in white adipose tissue reveals a novel interplay of peroxisome proliferator-activated receptor γ and sterol regulatory element-binding protein in the regulation of adipogenesis. J Biol Chem 279:23908–23915

    Article  CAS  Google Scholar 

  • Kim Y-M, Shin H-T, Seo Y-H, Byun H-O, Yoon S-H, Lee I-K, Hyun D-H, Chung H-Y, Yoon G (2010) Sterol regulatory element-binding protein (SREBP)-1-mediated lipogenesis is involved in cell senescence. J Biol Chem 285:29069–29077

    Article  CAS  Google Scholar 

  • Li C, Li L, Chen K, Wang Y, Yang F, Wang G (2019, 2019) UFL1 alleviates lipopolysaccharide-induced cell damage and inflammation via regulation of the TLR4/NF-κB pathway in bovine mammary epithelial cells. Oxidative Med Cell Longev

  • Li N, Zhao F, Wei C, Liang M, Zhang N, Wang C, Li Q-Z, Gao X-J (2014) Function of SREBP1 in the milk fat synthesis of dairy cow mammary epithelial cells. Int J Mol Sci 15:16998–17013

    Article  CAS  Google Scholar 

  • Lindmark Månsson H (2008) Fatty acids in bovine milk fat. Food Nutr Res 52:1821

    Article  Google Scholar 

  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods 25:402-408

  • Lv Y, Guan W, Qiao H, Wang C, Chen F, Zhang Y, Liao Z (2015) Veterinary medicine and omics (veterinomics): metabolic transition of milk triacylglycerol synthesis in sows from late pregnancy to lactation. Omics: a journal of integrative biology 19:602–616

    Article  CAS  Google Scholar 

  • Ma L, Corl B (2012) Transcriptional regulation of lipid synthesis in bovine mammary epithelial cells by sterol regulatory element binding protein-1. J Dairy Sci 95:3743–3755

    Article  CAS  Google Scholar 

  • Man WC, Miyazaki M, Chu K, Ntambi J (2006) Colocalization of SCD1 and DGAT2: implying preference for endogenous monounsaturated fatty acids in triglyceride synthesis. J Lipid Res 47:1928–1939

    Article  CAS  Google Scholar 

  • McCarthy S, Smith G (1972) Synthesis of milk fat from β-hydroxybutyrate and acetate by ruminant mammary tissue in vitro. Biochimica et Biophysica Acta (BBA)-Lipids and Lipid Metabolism 260:185–196

  • McPherson R, Gauthier A (2004) Molecular regulation of SREBP function: the Insig-SCAP connection and isoform-specific modulation of lipid synthesis. Biochem Cell Biol 82:201–211

    Article  CAS  Google Scholar 

  • Palmquist D, Beaulieu AD, Barbano D (1993) Feed and animal factors influencing milk fat composition. J Dairy Sci 76:1753–1771

    Article  CAS  Google Scholar 

  • Paton CM, Ntambi JM (2009) Biochemical and physiological function of stearoyl-CoA desaturase. American Journal of Physiology-Endocrinology and Metabolism 297:E28–E37

    Article  CAS  Google Scholar 

  • Santos SJ, Aupperlee MD, Xie J, Durairaj S, Miksicek R, Conrad SE, Leipprandt JR, Tan YS, Schwartz RC, Haslam SZ (2009) Progesterone receptor A-regulated gene expression in mammary organoid cultures. J Steroid Biochem Mol Biol 115:161–172

    Article  CAS  Google Scholar 

  • Schoeler M, Caesar R (2019) Dietary lipids, gut microbiota and lipid metabolism. Reviews in Endocrine and Metabolic Disorders 20:461–472

    Article  CAS  Google Scholar 

  • Sheng R, Yan S, Qi L, Zhao Y, Jin L, Guo X (2015) Effect of the ratios of acetate and β-hydroxybutyrate on the expression of milk fat-and protein-related genes in bovine mammary epithelial cells. Czech Journal of Animal Science 60:531–541

    Article  CAS  Google Scholar 

  • Sun Y, Luo J, Zhu J, Shi H, Li J, Qiu S, Wang P, Loor JJ (2016) Effect of short-chain fatty acids on triacylglycerol accumulation, lipid droplet formation and lipogenic gene expression in goat mammary epithelial cells. Anim Sci J 87:242–249

    Article  CAS  Google Scholar 

  • Takeuchi Y, Yahagi N, Izumida Y, Nishi M, Kubota M, Teraoka Y, Yamamoto T, Matsuzaka T, Nakagawa Y, Sekiya M (2010) Polyunsaturated fatty acids selectively suppress sterol regulatory element-binding protein-1 through proteolytic processing and autoloop regulatory circuit. J Biol Chem 285:11681–11691

    Article  CAS  Google Scholar 

  • Tracey TJ, Steyn FJ, Wolvetang EJ, Ngo ST (2018) Neuronal lipid metabolism: multiple pathways driving functional outcomes in health and disease. Front Mol Neurosci 11:10

    Article  Google Scholar 

  • Wei Z, Xiao C, Guo C, Zhang X, Wang Y, Wang J, Yang Z, Fu Y (2017) Sodium acetate inhibits Staphylococcus aureus internalization into bovine mammary epithelial cells by inhibiting NF-κB activation. Microb Pathog 107:116–121

    Article  CAS  Google Scholar 

  • Xu J, Teran-Garcia M, Park JH, Nakamura MT, Clarke SD (2001) Polyunsaturated fatty acids suppress hepatic sterol regulatory element-binding protein-1 expression by accelerating transcript decay. J Biol Chem 276:9800–9807

    Article  CAS  Google Scholar 

  • Yonezawa T, Sanosaka M, Haga S, Katoh K, Obara Y (2008) Regulation of uncoupling protein 2 expression by long-chain fatty acids and hormones in bovine mammary epithelial cells. Biochem Biophys Res Commun 375:280–285

    Article  CAS  Google Scholar 

  • Yonezawa T, Yonekura S, Sanosaka M, Hagino A, Katoh K, Obara Y (2004) Octanoate stimulates cytosolic triacylglycerol accumulation and CD36 mRNA expression but inhibits acetyl coenzyme A carboxylase activity in primary cultured bovine mammary epithelial cells. J Dairy Res 71:398–404

    Article  CAS  Google Scholar 

  • Yu Y, Zhen Z, Qi H, Yuan X, Gao X, Zhang M (2019) U2AF65 enhances milk synthesis and growth of bovine mammary epithelial cells by positively regulating the mTOR-SREBP-1c signalling pathway. Cell Biochem Funct 37:93–101

    Article  CAS  Google Scholar 

  • Zambell KL, Fitch MD, Fleming SE (2003) Acetate and butyrate are the major substrates for de novo lipogenesis in rat colonic epithelial cells. J Nutr 133:3509–3515

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors are grateful to C.L, L.L, K.M, M.S., W.Y, Y.M and G. W for their assistance during the experiment.

Funding

The authors gratefully acknowledge the financial support by the National Key Research and Development Program of China (2018YFD0501600).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Lian Li.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Editor: Tetsuji Okamoto

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ali, I., Li, C., Li, L. et al. Effect of acetate, β-hydroxybutyrate and their interaction on lipogenic gene expression, triglyceride contents and lipid droplet formation in dairy cow mammary epithelial cells. In Vitro Cell.Dev.Biol.-Animal 57, 66–75 (2021). https://doi.org/10.1007/s11626-020-00538-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11626-020-00538-2

Keywords

Navigation