The protective effect of caffeic acid against inflammation injury of primary bovine mammary epithelial cells induced by lipopolysaccharide

Journal of Dairy Science

Volumn 97, Issue 5, 2014, Pages 2856-2865

  Liu, Mingjiang ^a   Song, Shixiu ^a   Li, Huanrong ^b   Jiang, Xiaoyu ^a   Yin, Peng ^a   Wan, Changrong ^a   Liu, Xiaoxi ^a   Liu, Fenghua ^b   Xu, Jianqin ^a  

^a CHINA AGRICULTURAL UNIVERSITY   (China)

^b BEIJING UNIVERSITY OF AGRICULTURE   (China)

Author keywords

Bovine mammary epithelial cell; Caffeic acid; Inflammation; Lipopolysaccharide

Indexed keywords

BOS; BOVINAE; ESCHERICHIA COLI;

ANTIINFLAMMATORY AGENT; CAFFEIC ACID; CAFFEIC ACID DERIVATIVE; CYTOKINE; LIPOPOLYSACCHARIDE;

ANIMAL; APOPTOSIS; BOVINE; CELL CULTURE; CYTOLOGY; DRUG EFFECTS; EPITHELIUM CELL; FEMALE; GENETICS; INFLAMMATION; METABOLISM; PHYSIOLOGY; UDDER;

ANIMALS; ANTI-INFLAMMATORY AGENTS; APOPTOSIS; CAFFEIC ACIDS; CATTLE; CELLS, CULTURED; CYTOKINES; EPITHELIAL CELLS; FEMALE; INFLAMMATION; LIPOPOLYSACCHARIDES; MAMMARY GLANDS, ANIMAL;

EID: 84899078284     PISSN: 00220302     EISSN: 15253198     Source Type: Journal    
DOI: 10.3168/jds.2013-7600     Document Type: Article

References (48)

1. Boehmer J.L. Proteomic analyses of host and pathogen responses during bovine mastitis. J. Mammary Gland Biol. Neoplasia 2011, 16:323-338.
2. Botrel M.-A., Haenni M., Morignat E., Sulpice P., Madec J.-Y., Calavas D. Distribution and antimicrobial resistance of clinical and subclinical mastitis pathogens in dairy cows in RhÔne-Alpes, France. Foodborne Pathog. Dis 2010, 7:479-487.
3. Bougarn S., Cunha P., Harmache A., Fromageau A., Gilbert F.B., Rainard P. Muramyl dipeptide synergizes with Staphylococcus aureus lipoteichoic acid to recruit neutrophils in the mammary gland and to stimulate mammary epithelial cells. Clin. Vaccine Immunol 2010, 17:1797-1809.
4. Bradley A.J., Leach K.A., Breen J.E., Green L.E., Green M.J. Survey of the incidence and aetiology of mastitis on dairy farms in England and Wales. Vet. Rec 2007, 160:253-257.
5. Búfalo M.C., Ferreira I., Costa G., Francisco V., Liberal J., Cruz M.T., Lopes M.C., Batista M.T., Sforcin J.M. Propolis and its constituent caffeic acid suppress LPS-stimulated pro-inflammatory response by blocking NF-κB and MAPK activation in macrophages. J. Ethnopharmacol 2013, 149:84-92.
6. Burvenich C., Van Merris V., Mehrzad J., Diez-Fraile A., Duchateau L. Severity of E. coli mastitis is mainly determined by cow factors. Vet. Res 2003, 34:521-564.
7. Calvinho L.F., Almeida R.A., Oliver S.P. Influence of bacterial factors on proliferation of bovine mammary epithelial cells. Rev. Argent. Microbiol 2001, 33:28-35.
8. Calzado M.A., Bacher S., Schmitz M.L. NF-kappaB inhibitors for the treatment of inflammatory diseases and cancer. Curr. Med. Chem 2007, 14:367-376.
9. Cario E., Rosenberg I.M., Brandwein S.L., Beck P.L., Reinecker H.-C., Podolsky D.K. Lipopolysaccharide activates distinct signaling pathways in intestinal epithelial cell lines expressing toll-like receptors. J. Immunol 2000, 164:966-972.
10. Ghosh S., Hayden M.S. New regulators of NF-κB in inflammation. Nat. Rev. Immunol 2008, 8:837-848.
11. Günther J., Petzl W., Zerbe H., Schuberth H.-J., Koczan D., Goetze L., Seyfert H.-M. Lipopolysaccharide priming enhances expression of effectors of immune defence while decreasing expression of pro-inflammatory cytokines in mammary epithelia cells from cows. BMC Genomics 2012, 13:17.
12. Hines D.J., Choi H.B., Hines R.M., Phillips A.G., MacVicar B.A. Prevention of LPS-induced microglia activation, cytokine production and sickness behavior with TLR4 receptor interfering peptides. PLoS ONE 2013, 8:e60388.
13. Hoeben D., Burvenich C., Trevisi E., Bertoni G., Hamann J., Bruckmaier R.M., Blum J.W. Role of endotoxin and TNF-alpha in the pathogenesis of experimentally induced coliform mastitis in periparturient cows. J. Dairy Res 2000, 67:503-514.
14. Hoffmann A., Baltimore D. Circuitry of nuclear factor κB signaling. Immunol. Rev 2006, 210:171-186.
15. Hoffmann A., Levchenko A., Scott M.L., Baltimore D. The IκB-NF-κB signaling module: Temporal control and selective gene activation. Science 2002, 298:1241-1245.
16. Ibeagha-Awemu E.M., Lee J.-W., Ibeagha A.E., Bannerman D.D., Paape M.J., Zhao X. Bacterial lipopolysaccharide induces increased expression of toll-like receptor (TLR) 4 and downstream TLR signaling molecules in bovine mammary epithelial cells. Vet. Res 2008, 39:11.
17. Jung J.E., Kim H.S., Lee C.S., Park D.-H., Kim Y.-N., Lee M.-J., Lee J.W., Park J.-W., Kim M.-S., Ye S.K., Chung M.-H. Caffeic acid and its synthetic derivative CADPE suppress tumor angiogenesis by blocking STAT3-mediated VEGF expression in human renal carcinoma cells. Carcinogenesis 2007, 28:1780-1787.
18. Jung W.-K., Choi I., Lee D.-Y., Yea S.S., Choi Y.H., Kim M.-M., Park S.-G., Seo S.-K., Lee S.-W., Lee C.-M., Park Y.-M., Choi I.-W. Caffeic acid phenethyl ester protects mice from lethal endotoxin shock and inhibits lipopolysaccharide-induced cyclooxygenase-2 and inducible nitric oxide synthase expression in RAW 264.7 macrophages via the p38/ERK and NF-κB pathways. Int. J. Biochem. Cell Biol 2008, 40:2572-2582.
19. Karin M., Ben-Neriah Y. Phosphorylation meets ubiquitination: The control of NF-κB activity. Annu. Rev. Immunol 2000, 18:621-663.
20. Kerro Dego O., Oliver S.P., Almeida R.A. Host-pathogen gene expression profiles during infection of primary bovine mammary epithelial cells with Escherichia coli strains associated with acute or persistent bovine mastitis. Vet. Microbiol 2012, 155:291-297.
21. Klement J.F., Rice N.R., Car B.D., Abbondanzo S.J., Powers G.D., Bhatt P.H., Chen C.-H., Rosen C.A., Stewart C.L. IκBα deficiency results in a sustained NF-κB response and severe widespread dermatitis in mice. Mol. Cell. Biol 1996, 16:2341-2349.
22. Lahouassa H., Moussay E., Rainard P., Riollet C. Differential cytokine and chemokine responses of bovine mammary epithelial cells to Staphylococcus aureus and Escherichia coli. Cytokine 2007, 38:12-21.
23. Lee Y., Shin D., Kim J.-H., Hong S., Choi D., Kim Y.-J., Kwak M.-K., Jung Y. Caffeic acid phenethyl ester-mediated Nrf2 activation and IκB kinase inhibition are involved in NFκB inhibitory effect: Structural analysis for NFκB inhibition. Eur. J. Pharmacol 2010, 643:21-28.
24. Li Q., Verma I.M. NF-κB regulation in the immune system. Nat. Rev. Immunol 2002, 2:725-734.
25. Menzies F.D., Bryson D.G., McCallion T., Matthews D.I. A study of mortality among suckler and dairy cows in Northern Ireland in 1992. Vet. Rec 1995, 137:531-536.
26. Miyake K. Endotoxin recognition molecules, toll-like receptor 4-MD-2. Semin. Immunol 2004, 16:11-16.
27. Morimoto K., Kanda N., Shinde S., Isobe N. Effect of enterotoxigenic Escherichia coli vaccine on innate immune function of bovine mammary gland infused with lipopolysaccharide. J. Dairy Sci 2012, 95:5067-5074.
28. Petzl W., Zerbe H., Günther J., Yang W., Seyfert H.M., Nürnberg G., Schuberth H.J. Escherichia coli, but not Staphylococcus aureus triggers an early increased expression of factors contributing to the innate immune defense in the udder of the cow. Vet. Res 2008, 39:18.
29. Porcherie A., Cunha P., Trotereau A., Roussel P., Gilbert F.B., Rainard P., Germon P. Repertoire of Escherichia coli agonists sensed by innate immunity receptors of the bovine udder and mammary epithelial cells. Vet. Res 2012, 43:14.
30. Puangpraphant S., Berhow M.A., Vermillion K., Potts G., Gonzalez D.M.E. Dicaffeoylquinic acids in Yerba mate (Ilex paraguariensis St. Hilaire) inhibit NF-kappaB nucleus translocation in macrophages and induce apoptosis by activating caspases-8 and -3 in human colon cancer cells. Mol. Nutr. Food Res 2011, 55:1509-1522.
31. Quesnell R.R., Klaessig S., Watts J.L., Schukken Y.H. Bovine intramammary Escherichia coli challenge infections in late gestation demonstrate a dominant antiinflammatory immunological response. J. Dairy Sci 2012, 95:117-126.
32. Risco A., del Fresno C., Mambol A., Alsina-Beauchamp D., MacKenzie K.F., Yang H.-T., Barber D.F., Morcelle C., Arthur J.S.C., Ley S.C., Ardavin C., Cuenda A. p38γ and p38δ kinases regulate the toll-like receptor 4 (TLR4)-induced cytokine production by controlling ERK1/2 protein kinase pathway activation. Proc. Natl. Acad. Sci. USA 2012, 109:11200-11205.
33. Scheibel M., Klein B., Merkle H., Schulz M., Fritsch R., Greten F.R., Arkan M.C., Schneider G., Schmid R.M. IκBβ is an essential co-activator for LPS-induced IL-1β transcription in vivo. J. Exp. Med 2010, 207:2621-2630.
34. Schmitz S., Pfaffl M.W., Meyer H.H.D., Bruckmaier R.M. Short-term changes of mRNA expression of various inflammatory factors and milk proteins in mammary tissue during LPS-induced mastitis. Domest. Anim. Endocrinol 2004, 26:111-126.
35. Seegers H., Fourichon C., Beaudeau F. Production effects related to mastitis and mastitis economics in dairy cattle herds. Vet. Res 2003, 34:475-491.
36. Shimazu R., Akashi S., Ogata H., Nagai Y., Fukudome K., Miyake K., Kimoto M. MD-2, a molecule that confers lipopolysaccharide responsiveness on toll-like receptor 4. J. Exp. Med 1999, 189:1777-1782.
37. Shin K.-M., Kim I.-T., Park Y.-M., Ha J., Choi J.-W., Park H.-J., Lee Y.S., Lee K.-T. Anti-inflammatory effect of caffeic acid methyl ester and its mode of action through the inhibition of prostaglandin E2, nitric oxide and tumor necrosis factor-α production. Biochem. Pharmacol 2004, 68:2327-2336.
38. Shuster D.E., Kehrli M.J., Rainard P., Paape M. Complement fragment C5a and inflammatory cytokines in neutrophil recruitment during intramammary infection with Escherichia coli. Infect. Immun 1997, 65:3286-3292.
39. Strandberg Y., Gray C., Vuocolo T., Donaldson L., Broadway M., Tellam R. Lipopolysaccharide and lipoteichoic acid induce different innate immune responses in bovine mammary epithelial cells. Cytokine 2005, 31:72-86.
40. Sun S.C., Ganchi P.A., Ballard D.W., Greene W.C. NF-κB controls expression of inhibitor IκBα: Evidence for an inducible autoregulatory pathway. Science 1993, 259:1912-1915.
41. Tran K., Merika M., Thanos D. Distinct functional properties of IκBα and IκBβ. Mol. Cell. Biol 1997, 17:5386-5399.
42. + T cells. Clin. Exp. Immunol 2010, 160:223-232.
43. Wellnitz O., Baumert A., Saudenowa M., Bruckmaier R.M. Immune response of bovine milk somatic cells to endotoxin in healthy quarters with normal and very low cell counts. J. Dairy Res 2010, 77:452-459.
44. Wellnitz O., Bruckmaier R.M. The innate immune response of the bovine mammary gland to bacterial infection. Vet. J 2012, 192:148-152.
45. Wellnitz O., Kerr D.E. Cryopreserved bovine mammary cells to model epithelial response to infection. Vet. Immunol. Immunopathol 2004, 101:191-202.
46. Yamamoto M., Yamazaki S., Uematsu S., Sato S., Hemmi H., Hoshino K., Kaisho T., Kuwata H., Takeuchi O., Takeshige K., Saitoh T., Yamaoka S., Yamamoto N., Yamamoto S., Muta T., Takeda K., Akira S. Regulation of toll/IL-1-receptor-mediated gene expression by the inducible nuclear protein IκBζ. Nature 2004, 430:218-222.
47. Yu J., Yin P., Liu F., Cheng G., Guo K., Lu A., Zhu X., Luan W., Xu J. Effect of heat stress on the porcine small intestine: A morphological and gene expression study. Comp. Biochem. Physiol. A Mol. Integr. Physiol 2010, 156:119-128.
48. Yu J., Yin P., Yin J., Liu F., Zhu X., Cheng G., Guo K., Yin Y., Xu J. Involvement of ERK1/2 signalling and growth-related molecules' expression in response to heat stress-induced damage in rat jejunum and IEC-6 cells. Int. J. Hyperthermia 2010, 26:538-555.