Proteomic analysis of endogenous conjugated linoleic acid biosynthesis in lactating rats and mouse mammary gland epithelia cells (HC11)

Biochimica et Biophysica Acta - Proteins and Proteomics

Volumn 1804, Issue 4, 2010, Pages 745-751

  Jin, Yong Cheng ^a   Lee, Hong Gu ^b   Xu, Cheng Xiong ^c   Han, Jeng A ^a   Choi, Seong Ho ^d   Song, Man Kang ^d   Kim, Young Jun ^e   Lee, Ki Beom ^f   Kim, Seon Ku ^b   Kang, Han Seok ^b   Cho, Byung Wook ^b   Shin, Teak Soon ^b   Choi, Yun Jaie ^a  

^a Seoul National University   (South Korea)

^b Pusan National University   (South Korea)

^c EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d Chungbuk National University   (South Korea)

^e Korea University   (South Korea)

^f Department of Biotechnology ^*  (South Korea)

Author keywords

Conjugated linoleic acid; Real time PCR; Stearoyl CoA desaturase; Trans vaccenic acid; Two dimensional electrophoresis

Indexed keywords

FATTY ACID; LAMININ RECEPTOR; LAMININ RECEPTOR 1; LINOLEIC ACID; MESSENGER RNA; PEROXIREDOXIN 2; UNCLASSIFIED DRUG; VACCENIC ACID;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIOSYNTHESIS; BREAST EPITHELIUM; CELL MOTILITY; CELL STRUCTURE; CONJUGATION; CONTROLLED STUDY; FEMALE; GENETIC CODE; IMMUNOLOGY; LACTATION; MOLECULAR MECHANICS; MOUSE; NONHUMAN; PRECURSOR; PRIORITY JOURNAL; PRODUCTIVITY; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN METABOLISM; PROTEOMICS; RAT; REAL TIME POLYMERASE CHAIN REACTION; SAMPLE; UPREGULATION;

AMINO ACID SEQUENCE; ANIMALS; CELL LINE; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; EPITHELIAL CELLS; FEMALE; LACTATION; LINOLEIC ACIDS, CONJUGATED; MAMMARY GLANDS, ANIMAL; METABOLIC NETWORKS AND PATHWAYS; MICE; MODELS, BIOLOGICAL; MOLECULAR SEQUENCE DATA; OLEIC ACIDS; PEROXIREDOXINS; POLYMERASE CHAIN REACTION; PROTEIN DISULFIDE-ISOMERASES; PROTEOMICS; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, LAMININ; RIBOSOMAL PROTEINS; RNA, MESSENGER; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; TANDEM MASS SPECTROMETRY;

RATTUS;

EID: 76849109300     PISSN: 15709639     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbapap.2009.11.016     Document Type: Article

References (58)

1. Aro A., Männistö S., Salminen I., Ovaskainen M.L., Kataja V., and Uusitupa M. Inverse association between dietary and serum conjugated linoleic acid and risk of breast cancer in postmenopausal women. Nutr. Cancer 38 2 (2000) 151-157
2. Houseknecht K.L., Vanden Heuvel J.P., Moya-Camarena S.Y., Portocarrero C.P., Peck L.W., Nickel K.P., and Belury M.A. Dietary conjugated linoleic acid normalizes impaired glucose tolerance in the Zucker diabetic fatty fa/fa rat. Biochem. Biophys. Res. Commun. 244 3 (1998) 678-682
3. Hayek M.G., Han S.N., Wu D., Watkins B.A., Meydani M., Dorsey J.L., Smith D.E., and Meydani S.N. Dietary conjugated linoleic acid influences the immune response of young and old C57BL/6NCrlBR mice. J. Nutr. 129 1 (1999) 32-38
4. Lee K.N., Kritchevsky D., and Pariza M.W. Conjugated linoleic acid and atherosclerosis in rabbits. Atherosclerosis 108 1 (1994) 19-25
5. Blankson H., Stakkestad J.A., Fagertun H., Thom E., Wadstein J., and Gudmundsen O. Conjugated linoleic acid reduces body fat mass in overweight and obese humans. J. Nutr. 130 12 (2000) 2943-2948
6. Griinari J.M., Corl B.A., Lacy S.H., Chouinard P.Y., Nurmela K.V., and Bauman D.E. Conjugated linoleic acid is synthesized endogenously in lactating dairy cows by Delta(9)-desaturase. J. Nutr. 130 9 (2000) 2285-2291
7. Bauman D.E., Corl B.A., Baumgard L.H., and Griinari J.M. Conjugated linoleic acid (CLA) and the dairy cow. In: Garnsworthy P.C., and Cole D.J. (Eds). Recent Advances in Animal Nutrition (2001), Nottingham University Press, Nottingham, UK 237-266
8. Corl B.A., Baumgard L.H., Dwyer D.A., Griinari J.M., Phillips B.S., and Bauman D.E. The role of Delta(9)-desaturase in the production of cis-9, trans-11 CLA. J. Nutr. Biochem. 12 11 (2001) 622-630
9. Banni S., Angioni E., Murru E., Carta G., Melis M.P., Bauman D., Dong Y., and Ip C. Vaccenic acid feeding increases tissue levels of conjugated linoleic acid and suppresses development of premalignant lesions in rat mammary gland. Nutr. Cancer 41 1-2 (2001) 91-97
10. Corl B.A., Barbano D.M., Bauman D.E., and Ip C. Cis-9, trans-11 CLA derived endogenously from trans-11 18:1 reduces cancer risk in rats. J. Nutr. 133 9 (2003) 2893-2900
11. Santora J.E., Palmquist D.L., and Roehrig K.L. Trans-vaccenic acid is desaturated to conjugated linoleic acid in mice. J. Nutr. 130 2 (2000) 208-215
12. Loor J.J., Lin X., and Herbein J.H. Dietary trans-vaccenic acid (trans11-18:1) increases concentration of cis9, trans11-conjugated linoleic acid (rumenic acid) in tissues of lactating mice and suckling pups. Reprod. Nutr. Dev. 42 2 (2002) 85-99
13. Salminen I., Mutanen M., Jauhiainen M., and Aro A. Dietary trans fatty acids increase conjugated linoleic acid levels in human serum. J. Nutr. Biochem. 9 2 (1998) 93-98
14. Adlof R.O., Duval S., and Emken E.A. Biosynthesis of conjugated linoleic acid in humans. Lipids 35 2 (2000) 131-135
15. Pollard M.R., Gunstone F.D., James A.T., and Morris L.J. Desaturation of positional and geometric isomers of monoenoic fatty acids by microsomal preparations from rat liver. Lipids 15 5 (1980) 306-314
16. Ntambi J.M. The regulation of setaroyl-CoA desaturase(SCD). Prog. Lipid Res. 34 2 (1995) 139-150
17. de Roos B., Rucklidge G., Reid M., Ross K., Duncan G., Navarro M.A., Arbones-Mainar J.M., Guzman-Garcia M.A., Osada J., Browne J., Loscher C.E., and Roche H.M. Divergent mechanisms of cis9, trans11-and trans10, cis12-conjugated linoleic acid affecting insulin resistance and inflammation in apolipoprotein E knockout mice: a proteomics approach. FASEB J. 19 12 (2005) 1746-1748
18. Viswanadha S., Giesy J.G., Hanson T.W., and McGuire M.A. Dose response of milk fat to intravenous administration of the trans-10, cis-12 isomer of conjugated linoleic acid. J. Dairy Sci. 86 10 (2003) 3229-3236
19. Ball R.K., Friis R.R., Schoenenberger C.A., Doppler W., and Groner B. Prolactin regulation of beta-casein gene expression and of a cytosolic 120-kd protein in a cloned mouse mammary epithelial cell line. EMBO J. 7 7 (1998) 2089-2095
20. Kim E.J., Kim W.Y., Kang Y.H., Ha Y.L., Bach L.A., and PARK J.H.Y. Inhibition of Caco-2 cell proliferation by (n-3) fatty acids: possible mediation by increased secretion of insulin-like growth factor binding protein-6. Nutr. Res. 20 10 (2000) 1409-1421
21. Aksu S., Scheler C., Focks N., Leenders F., Theuring F., Salnikow J., and Jungblut P.R. An iterative calibration method with prediction of post-translational modifications for the construction of a two-dimensional electrophoresis database of mouse mammary gland proteins. Proteomics 2 10 (2002) 1452-1463
22. Desrivières S., Prinz T., Castro-Palomino L.N., Meyer M., Boehm G., Bauer U., Schäfer J., Neumann T., Shemanko C., and Groner B. Comparative proteomic analysis of proliferating and functionally differentiated mammary epithelial cells. Mol. Cell Proteomics 2 10 (2003) 1039-1054
23. Shevchenko A., Jensen O.N., Podtelejnikov A.V., Sagliocco F., Wilm M., Vorm O., Mortensen P., Shevchenko A., Boucherie H., and Mann M. Linking genome and proteome by mass spectrometry: large-scale identification of yeast proteins from two dimensional gels. Proc. Natl. Acad. Sci. U. S. A. 93 25 (1996) 14440-14445
24. Folch J., Lees M., and Sloane Stanley G.H. A simple method for the isolation and purification of total lipids from animal tissues. J. Biol. Chem. 226 1 (1957) 497-509
25. Morrison W.R., and Smith L.M. Preparation of fatty acid methyl esters and dimethylacetals from lipids with boron fluoride-methanol. J. Lipid Res. 5 (1964) 600-608
26. Livak K.J., and Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25 4 (2001) 402-408
27. Mosley E.E., McGuire M.K., Williams J.E., and McGuire M.A. Cis-9, trans-11 conjugated linoleic acid is synthesized from vaccenic acid in lactating women. J. Nutr. 136 9 (2006) 2297-2301
28. Mosley E.E., Shafii Dagger B., Moate P.J., and McGuire M.A. Cis-9, trans-11 conjugated linoleic acid is synthesized directly from vaccenic acid in lactating dairy cattle. J. Nutr. 136 3 (2006) 570-575
29. Shingfield K.J., Reynolds C.K., Lupoli B., Toivonen V., Yurawecz M.P., Delmonte P., Griinari J.M., Grandison A.S., and Beever D.E. Effect of forage type and proportion of concentrate in diet on milk fatty acid composition in cows fed sunflower oil and fish oil. Anim. Sci. 80 (2005) 225-238
30. Bickerstaffe R., and Annison E.F. Lipid metabolism in the perfused chicken liver. The uptake and metabolism of oleic acid, elaidic acid, cis-vaccenic acid, trans-vaccenic acid and stearic acid. Biochem. J. 118 3 (1970) 433-442
31. Kinsella J.E. Stearic acid metabolism by mammary cells. J. Dairy Sci. 53 12 (1970) 1757-1765
32. McDonald T.M., and Kinsella J.E. Stearyl-CoA desaturase of bovine mammary microsomes. Arch. Biochem. Biophys. 156 1 (1973) 223-231
33. Ward R.J., Travers M.T., Richards S.E., Vernon R.G., Salter A.M., Buttery P.J., and Barber M.C. Stearoyl-CoA desaturase mRNA is transcribed from a single gene in the ovine genome. Biochim. Biophys. Acta 1391 2 (1998) 145-156
34. Corl B.A., Baumgard L.H., Dwyer D.A., Griinari J.M., Phillips B.S., and Bauman D.E. The role of Delta(9)-desaturase in the production of cis-9, trans-11 CLA. J. Nutr. Biochem. 12 11 (2001) 622-630
35. Griinari J.M., Corl B.A., Lacy S.H., Chouinard P.Y., Nurmela K.V., and Bauman D.E. Conjugated linoleic acid is synthesized endogenously in lactating dairy cows by Delta(9)-desaturase. J. Nutr. 130 9 (2000) 2285-2291
36. Loor J.J., Ferlay A., Ollier A., Ueda K., Doreau M., and Chilliard Y. High-concentrate diets and polyunsaturated oils alter trans and conjugated isomers in bovine rumen, blood, and milk. J. Dairy Sci. 88 11 (2005) 3986-3999
37. Banni S., Angioni E., Murru E., Carta G., Melis M.P., Bauman D., Dong Y., and Ip C. Vaccenic acid feeding increases tissue levels of conjugated linoleic acid and suppresses development of premalignant lesions in rat mammary gland. Nutr. Cancer 41 1-2 (2001) 91-97
38. Kraft J., Hanske L., Mockel P., Zimmermann S., Hartl A., Kramer J.K.G., and Jahreis G. The conversion efficiency of trans-11 and trans-12 18:1 by {Delta}9-Desaturation differs in rats. J. Nutr. 136 5 (2006) 1209-1214
39. Lock A.L., Corl B.A., Barbano D.M., Bauman D.E., and Clement I.p. The anticarcinogenic effect of trans-11 18:1 is dependent on its conversion to cis-9, trans-11 CLA by {Delta}9-desaturase in rats. J. Nutr. 134 10 (2004) 2698-2704
40. Turpeinen A.M., Mutanen M., Aro A., Salminen I., Basu S., Palmquist D.L., and Griinari J.M. Bioconversion of vaccenic acid to conjugated linoleic acid in humans. Am. J. Clin. Nutr. 76 3 (2002) 504-510
41. Matitashvili E., and Bauman D.E. Effect of different isomers of C18:1 and C18:2 fatty acids on lipogenesis in bovine mammary epithelial cells. J. Anim. Sci. 83 suppl. 1 (2000) 165 (abs.)
42. Jayan G.C., and Herbein J.H. "Healthier" dairy fat using trans-vaccenic acid. Nutr. Food Sci. 30 6 (2000) 304-309
43. Bernard L., Leroux C., and Chilliard Y. Expression and nutritional regulation of lipogenic genes in the ruminant lactating mammary gland. Adv. Exp. Med. Biol. 606 (2008) 67-108
44. Edman J.C., Ellis L., Blacher R.W., Roth R.A., and Rutter W.J. Sequence of protein disulphide isomerase and implications of its relationship to thioredoxin. Nature 317 6034 (1985) 267-270
45. Freedman R.B., Hirst T.R., and Tuite M.F. Protein disulphide isomerase: building bridges in protein folding. Trends Biochem. Sci. 19 8 (1994) 331-336
46. Turano C., Coppari S., Altieri F., and Ferraro A. Proteins of the PDI family: unpredicted non-ER locations and functions. J. Cell. Physiol. 193 2 (2002) 154-163
47. Wilkinson B., and Gilbert H.F. Protein disulfide isomerase. Biochim. Biophys. Acta 1699 1-2 (2004) 35-44
48. Janiszewski M., Lopes L.R., Carmo A.O., Pedro M.A., Brandes R.P., Santos C.X., and Laurindo F.R. Regulation of NAD(P)H oxidase by associated protein disulfide isomerase in vascular smooth muscle cells. J. Biol. Chem. 280 49 (2005) 40813-40819
49. Laurindo F.R., Fernandes D.C., Amanso A.M., Lopes L.R., and Santos C.X. Novel role of protein disulfide isomerase in the regulation of NADPH oxidase activity: pathophysiological implications in vascular diseases. Antioxid. Redox Signal. 10 6 (2008) 1101-1113
50. Fernandes D.C., Manoel A.H., Wosniak Jr. J., and Laurindo F.R. Protein disulfide isomerase overexpression in vascular smooth muscle cells induces spontaneous preemptive NADPH oxidase activation and Nox1 mRNA expression: effects of nitrosothiol exposure. Arch. Biochem. Biophys. 484 2 (2009) 197-204
51. Yim M.B., Chae H.Z., Rhee S.G., Chock P.B., and Stadtman E.R. On the protective mechanism of the thiol-specific antioxidant enzyme against the oxidative damage of biomacromolecules. J. Biol. Chem. 269 3 (1994) 1621-1626
52. Netto L.E.S., Chae H.Z., Kang S.W., Rhee S.G., and Stadtman E.R. Removal of hydrogen peroxide by thiol-specific antioxidant enzyme (TSA) is involved with its antioxidant properties. J. Biol. Chem. 271 26 (1996) 15315-15321
53. Sarafian T.A., Rajper N., Grigorian B., Kim A., and Shau H. Cellular antioxidant properties of human natural killer enhancing factor B. Free Radic. Res. 26 3 (1997) 281-289
54. Lim M.J., Chae H.Z., Rhee S.G., Yu D.Y., Lee K.K., and Yeom Y.I. The type II peroxiredoxin gene family of the mouse: molecular structure, expression and evolution. Gene 216 1 (1998) 197-205
55. Kang S.W., Chae H.Z., Seo M.S., Kim K., Bains I.C., and Rhee S.G. Mammalian peroxiredoxin isoforms can reduce hydrogen peroxide generated in response to growth factors and tumor necrosis factor-a. J. Biol. Chem. 273 11 (1998) 6297-6302
56. Kim H., Lee T.H., Park E.S., Suh J.M., Park S.J., Chung H.K., Kwon O.Y., Kim Y.K., Ro H.K., and Shong M. Role of peroxideroxins in regulating intracellular hydrogen peroxide and hydrogen peroxide-induced apoptosis in thyroid cells. J. Biol. Chem. 275 24 (2000) 18266-18270
57. Cordray P., Doyle K., Edes K., Moos P.J., and Fitzpatrick F.A. Oxidation of 2-Cys-peroxiredoxins by arachidonic acid peroxide metabolites of lipoxygenases and cyclooxygenase-2. J. Biol. Chem. 282 45 (2007) 32623-32629
58. Yamada K.M. Fibronectin and other cell interactive glycoproteins. In: Hay E.D. (Ed). Cell Biology of Extracellular Matrix (1991), Plenum, New York