Czech J. Anim. Sci., 2015, 60(12):531-541 | DOI: 10.17221/8595-CJAS

Effect of the ratios of acetate and β-hydroxybutyrate on the expression of milk fat- and protein-related genes in bovine mammary epithelial cellsOriginal Paper

R. Sheng, S.M. Yan, L.Z. Qi, Y.L. Zhao, L. Jin, X.Y. Guo
College of Animal Science, Inner Mongolia Agricultural University, Huhhot, P.R. China

The objective of this study was to evaluate the effects of the different ratios of acetate and β-hydroxybutyrate (BHBA) on cell viability, triacylglycerol (TAG) content, and mRNA expression of the genes related to lipid and protein synthesis in bovine mammary epithelial cells (BMECs). Primary cells were isolated from the mammary glands of Holstein dairy cows and were passaged twice. Then, the cells were cultured with different ratios of acetate and BHBA (1 : 3, 1 : 2, 1 : 1, 2 : 1, 3 : 1, 4 : 1, and 1 : 1, Group 1 to Group 7, respectively) for 48 h, and the fetal bovine serum in the culture media was replaced with fatty acid-free bovine serum albumin (BSA) (1 g/l). The control culture media contained only fatty acid-free BSA without unsaturated fatty acids (0mM). Cell viability was not affected by adding different ratios of acetate and BHBA, but TAG accumulation was significantly influenced by supplementing the culture media with different ratios of acetate and BHBA. The expression levels of genes related to milk fat (FASN, ACACA, CD36, SCD, FABP3, LPL, PPARG, and SPEBF1) and milk protein-related genes (CSN1S1, CSN3, mTOR, 4E-BP1, S6KB1, STAT5, JAK2, and LEPTIN) were significantly affected by the addition of different ratios of acetate and BHBA to the BMECs. Our results suggested that Groups 3 and 4 (1 : 1 and 2 : 1) had a stronger acceleration of milk fat synthesis, and Group 4 (2 : 1) had the strongest effect. The expression of the CSN1S1 and LEPTIN mRNAs was more effectively promoted in Groups 3 and 4 (1 : 1 and 2 : 1), and Group 3 (1 : 1) had the strongest acceleration. Expressions of genes related to milk protein synthesis (mTOR, 4E-BP1, S6KB1, JAK2, and STAT5) were up-regulated using a ratio of acetate and BHBA of 2 : 1. Taken together, the 2 : 1 ratio of acetate and BHBA had the best effect for both the milk fat synthesis and milk protein synthesis genes. However, further studies are necessary to elucidate the mechanism for regulating milk fat and protein synthesis by different ratios of acetate and BHBA.

Keywords: ratio of short chain fatty acids; milk fat precursor; dairy cow; milk fat; milk protein; gene expression

Published: December 31, 2015  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Sheng R, Yan SM, Qi LZ, Zhao YL, Jin L, Guo XY. 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 J. Anim. Sci. 2015;60(12):531-541. doi: 10.17221/8595-CJAS.
Download citation

References

  1. Aoki N., Matsuda T. (2000): A cytosolic protein-tyrosine phosphatase PTP1B specifically dephosphorylates and deactivates prolactin-activated STAT5a and STAT5b. Journal of Biological Chemistry, 275, 39718-39726. Go to original source... Go to PubMed...
  2. Bernard L., Leroux C., Chilliard Y. (2008): Expression and nutritional regulation of lipogenic genes in the ruminant lactating mammary gland. Advances in Experimental Medicine and Biology, 606, 67-108. Go to original source... Go to PubMed...
  3. Bionaz M., Loor J. (2008): Gene networks driving bovine milk fat synthesis during the lactation cycle. BMC Genomics, 9, 366. Go to original source... Go to PubMed...
  4. Burgos S.A., Dai M., Cant J.P. (2010): Nutrient availability and lactogenic hormones regulate mammary protein synthesis through the mammalian target of rapamycin signaling pathway. Journal of Dairy Science, 93, 153-161. Go to original source... Go to PubMed...
  5. Chilliard Y., Ferlay A., Mansbridge R.M. (2000): Ruminant milk fat plasticity: nutritional control of saturated, polyunsaturated, trans and conjugated fatty acids. Annales de Zootechnie, 49, 181-205. Go to original source...
  6. Feuermann Y., Mabjeesh S.J., Shamay A. (2004): Leptin affects prolactin action on milk protein and fat synthesis in the bovine mammary gland. Journal of Dairy Science, 87, 2941-2946. Go to original source... Go to PubMed...
  7. Gebauer S.K., Psota T.L., Kris-Etherton P.M. (2007): The diversity of health effects of individual trans fatty acid isomers. Lipids, 42, 787-799. Go to original source... Go to PubMed...
  8. Harvatine K.J., Boisclair Y.R., Bauman D.E. (2009): Recent advances in the regulation of milk fat synthesis. Animal, 3, 40-54. Go to original source... Go to PubMed...
  9. Jacobs A.A.A., Dijkstra J., Liesman J.S., VandeHaar M.J., Lock A.L., van Vuuren A.M., Hendriks W.H., 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. Go to original source... Go to PubMed...
  10. Kadegowda A.K., Piperova L.S., Delmonte P. (2008): Abomasal infusion of butterfat increases milk fat in lactating dairy cows. Journal of Dairy Science, 91, 2370-2379. Go to original source... Go to PubMed...
  11. Keenan T.W., Mather I.H. (2006): Intracellular origin of milk fat globules and the nature of the milk fat globule membrane. In: Fox P.F and McSweeney P.L.H. (eds): Advanced Dairy Chemistry, Volume 2: Lipids. Springer Science + Business Media, Inc., New York, USA, 137-171. Go to original source...
  12. Kim J.E., Chen J. (2004): Regulation of peroxisome proliferator-activated receptor-gamma activity by mammalian target of rapamycin and amino acids in adipogenesis. Diabetes, 53, 2748-2756. Go to original source... Go to PubMed...
  13. Kong Q.Y. (2012): Effect of sodium acetate and sodium butyrate on expression of genes related to milk fat synthesis of dairy cow mammary epithelial cells and acinus. Master's Thesis. Harbin, China: Northeast Agricultural Univ. Available from: www.cnki.net.
  14. Laplante M., Sabatini D.M. (2009): mTOR signaling at a glance. Journal of Cell Science, 122, 3589-3594. Go to original source... Go to PubMed...
  15. Lehner R., Kuksis A. (1996): Biosynthesis of triacylglycerols. Lipid Research, 35, 169-201. Go to original source... Go to PubMed...
  16. Liu Y., Peterson D.A., Kimura H., David S. (1997): Mechanism of cellular 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction. Journal of Neurochemistry, 69, 581-593. Go to original source... Go to PubMed...
  17. Livak K.J., Schmittgen T.D. (2001): Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods, 25, 402-408. Go to original source... Go to PubMed...
  18. Ma L., Corl B.A. (2012): Transcriptional regulation of lipid synthesis in bovine mammary epithelial cells by sterol regulatory element binding protein-1. Journal of Dairy Science, 95, 3743-3755. Go to original source... Go to PubMed...
  19. Maxin G., Glasser F., Hurtaud C. (2011): Combined effects of trans-10, cis-12 conjugated linoleic acid, propionate, and acetate on milk fat yield and composition in dairy cows. Journal of Dairy Science, 94, 2051-2059. Go to original source... Go to PubMed...
  20. Mensink R.P., Zock P.L., Kester A.D., Katan M.B. (2003): Effects of dietary fatty acids and carbohydrates on the ratio of serum total to HDL cholesterol and on serum lipids and apolipoproteins: a meta-analysis of 60 controlled trials. American Journal of Clinical Nutrition, 77, 1146-1155. Go to original source... Go to PubMed...
  21. Palmquist D.L. (2006): Milk fat: origin of fatty acids and influence of nutritional factors thereon. In: Fox P.F., McSweeney P.L.H. (eds): Advanced Dairy Chemistry, Volume 2: Lipids. Springer Science + Business Media, Inc., New York, USA, 43-92. Go to original source...
  22. Purdie N.G., Trout D.R., Poppi D.P. (2008): Milk synthetic response of the bovine mammary gland to an increase in the local concentration of amino acids and acetate. Journal of Dairy Science, 91, 218-228. Go to original source... Go to PubMed...
  23. Ramirez-Zacarias J. L., Castro-Munozledo F., Kuri-Harcuch W. (1992): Quantitation of adipose conversion and triglycerides by staining intracytoplasmic lipids with Oil red O. Histochemistry, 97, 493-497. Go to original source... Go to PubMed...
  24. Salter A.M., Tarling E.J. (2007): Regulation of gene transcription by fatty acids. Animal, 1, 1314-1320. Go to original source... Go to PubMed...
  25. Sheng R., Yan S.M., Qi L.Z., Zhao Y.L. (2015): Effect of the ratios of unsaturated fatty acids on the expressions of genes related to fat and protein in the bovine mammary epithelial cells. In Vitro Cellular & Developmental Biology - Animal, 51, 381-389. Go to original source... Go to PubMed...
  26. Soliman M.M., Ahmed M.M., Salah-eldin A. (2011): Butyrate regulates leptin expression through different signaling pathways in adipocytes. Journal of Veterinary Science, 12, 319-323. Go to original source... Go to PubMed...
  27. Spitsberg V.L., Matitashvili E. (1995): Association and coexpression of fatty-acid-binding protein and glycoprotein CD36 in the bovine mammary gland. European Journal of Biochemistry, 230, 872-878. Go to original source... Go to PubMed...
  28. Yonezawa T., Yonekura S., Sanosaka M., Hagino A. (2004): Octanoate stimulates cytosolic triacylglycerol accumulation and CD36 mRNA expression but inhibits acetyl coenzyme A carboxylase activity in primary cultured bovine mammary epithelial cells. Journal of Dairy Research, 71, 398-404. Go to original source... Go to PubMed...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.