RAW 264.7 세포에 있어 t10c12-CLA의 ROS를 통한 TNF-${\alpha}$ 생산 및 NF-${\kappa}B$ 활성 조절

Trans-10, cis-12 Conjugated Linoleic Acid Modulates Tumor Necrosis Factor-${\alpha}$ Production and Nuclear Factor-${\kappa}B$ Activation in RAW 264.7 Macrophages Through Formation of Reactive Oxygen Species

  • Park, So-Young (Laboratory of Veterinary Internal Medicine, Department of Veterinary Medicine, College of Veterinary Medicine, Chungbuk National University) ;
  • Kang, Byeong-Teck (Laboratory of Veterinary Dermatology, Department of Veterinary Medicine, College of Veterinary Medicine, Chungbuk National University) ;
  • Kang, Ji-Houn (Laboratory of Veterinary Internal Medicine, Department of Veterinary Medicine, College of Veterinary Medicine, Chungbuk National University) ;
  • Yang, Mhan-Pyo (Laboratory of Veterinary Internal Medicine, Department of Veterinary Medicine, College of Veterinary Medicine, Chungbuk National University)
  • 심사 : 2014.10.13
  • 발행 : 2014.12.31

초록

본 연구는 염증상태에서의 CLA의 효과와 작용기전을 알아보기 위해 LPS-자극 RAW 264.7 macrophages에 있어 ROS 생성과 TNF-${\alpha}$ 생산, NF-${\kappa}B$$PPAR{\gamma}$ 활성을 검토하였다. t10c12-CLA는 LPS로 자극하지 않은 비염증시의 RAW 세포에서는 ROS 생성을 증가시켜 TNF-${\alpha}$ 생산을 유도하였으며, 이 효과는 $PPAR{\gamma}$ 활성화에 의존해서 NF-${\kappa}B$ 활성 증가에 의해 매개되었다. 반면, LPS로 자극한 염증조건의 RAW 세포에서는 t10c12-CLA가 $PPAR{\gamma}$ 활성화에 의존하지 않는 경로로 ROS 생성 및 과도한 TNF-${\alpha}$ 생산을 억제하였다. 본 결과로부터 CLA는 ROS 생성을 통해 TNF-${\alpha}$ 생산 및 NF-${\kappa}B$ 활성을 염증 유무에 따라 조절하는 것으로 사료되었다.

The aims of this study were to explore the effects of conjugated linoleic acid (CLA) on reactive oxygen species (ROS) production in lipopolysaccharide (LPS)-naïve and LPS-stimulated RAW 264.7 macrophages and to examine whether these effects affect the regulation of tumor necrosis factor-alpha (TNF-${\alpha}$) production, and nuclear factor-kappa B (NF-${\kappa}B$) and peroxisome proliferator-activated receptor gamma ($PPAR{\gamma}$) activation. Trans-10, cis-12(t10c12)-CLA increased the production of ROS, as well as TNF-${\alpha}$ in LPS-naïve RAW 264.7 cells. The CLA-induced TNF-${\alpha}$ production was suppressed by treatment of diphenyleneiodonium chloride (DPI), a NADPH oxidase inhibitor. In addition, CLA enhanced the activities of NF-${\kappa}B$ and $PPAR{\gamma}$ in LPS-naïve RAW 264.7 cells, and this effect was abolished with DPI treatment. LPS treatment increased ROS production, whereas CLA reduced LPS-induced ROS production. LPS increased both TNF-${\alpha}$ production and NF-${\kappa}B$ activity, whereas t10c12-CLA reduced TNF-${\alpha}$ production and NF-${\kappa}B$ activity in LPS-stimulated RAW 264.7 cells. DPI treatment suppressed LPS-induced ROS production and NF-${\kappa}B$ activity. Moreover, DPI enhanced the inhibitory effects of t10c12-CLA on TNF-${\alpha}$ production and NF-${\kappa}B$ activation in LPS-stimulated RAW 264.7 cells. However, neither t10c12-CLA nor DPI affected $PPAR{\gamma}$ activity in LPS-stimulated RAW 264.7 cells. Taken together, these data indicate that t10c12-CLA induces TNF-${\alpha}$ production by increasing ROS production in LPS-naïve RAW 264.7 cells, which is mediated by the enhancement of NF-${\kappa}B$ activity via $PPAR{\gamma}$ activation. By contrast, t10c12-CLA suppresses TNF-${\alpha}$ production by inhibiting ROS production and NF-${\kappa}B$ activation via a $PPAR{\gamma}$-independent pathway in LPS-stimulated RAW 264.7 cells. These results suggest that t10c12-CLA can modulate TNF-${\alpha}$ production and NF-${\kappa}B$ activation through formation of ROS in RAW 264.7 macrophages.

키워드

참고문헌

  1. Bai XC, Lu D, Liu AL Zhang ZM, Li XM, Zou ZP, Zeng WS, Cheng BL, Luo SQ. Reactive oxygen species stimulates receptor activator of NF-kappaB ligand expression in osteoblast. J Biol Chem 2005; 280: 17497-17506. https://doi.org/10.1074/jbc.M409332200
  2. Belury MA. Dietary conjugated linoleic acid in health: physiological effects and mechanisms of action. Annu Rev Nutr 2002; 22: 505-531. https://doi.org/10.1146/annurev.nutr.22.021302.121842
  3. Belury MA. Inhibition of carcinogenesis by conjugated linoleic acid: potential mechanisms of action. J Nutr 2002; 132: 2995-2998. https://doi.org/10.1093/jn/131.10.2995
  4. Changhua L, Jindong Y, Defa L, Lidan Z, Shiyan Q, Jianjun X. Conjugated linoleic acid attenuates the production and gene expression of proinflammatory cytokines in weaned pigs challenged with lipopolysaccharide. J Nutr 2005; 135: 239-244. https://doi.org/10.1093/jn/135.2.239
  5. Chung S, Brown JM, Provo JN, Hopkins R, McIntosh MK. Conjugated linoleic acid promotes human adipocyte insulin resistance through NF$\kappa$B-dependent cytokine production. J Biol Chem 2005; 280: 38445-38456. https://doi.org/10.1074/jbc.M508159200
  6. Cook ME, Miller CC, Park Y, Pariza M. Immune modulation by altered nutrient metabolism: nutritional control of immuneinduced growth depression. Poult Sci 1993; 72: 1301-1305. https://doi.org/10.3382/ps.0721301
  7. Granlund L, Juvet LK, Pedersen JI, Nebb HI. Trans10, cis12- conjugated linoleic acid prevents triacylglycerol accumulation in adipocytes by acting as a PPARgamma modulator. J Lipid Res 2003; 44: 1441-1452. https://doi.org/10.1194/jlr.M300120-JLR200
  8. Halliwell B, Gutteridge JM. Role of free radicals and catalytic metal ions in human disease: an overview. Methods Enzymol 1990; 186: 1-85. https://doi.org/10.1016/0076-6879(90)86093-B
  9. Hassan Eftekhari M, Aliasghari F, Babaei-Beigi MA, Hasanzadeh J. Effect of conjugated linoleic acid and omega-3 fatty acid supplementation on inflammatory and oxidative stress markers in atherosclerotic patients. ARYA Atheroscler 2013; 9: 311-318.
  10. Houseknecht KL, Vanden Heuvel JP, Moya-Camarena SY, et al.: Dietary conjugated linoleic acid normalizes impaired glucose tolerance in the Zucker diabetic fatty fa/fa rat. Biochem Biophys Res Commun 1998; 244: 678-682. https://doi.org/10.1006/bbrc.1998.8303
  11. Hu X. Proteolytic signaling by TNFalpha: caspase activation and IkappaB degradation. Cytokine 2003; 21: 286-294. https://doi.org/10.1016/S1043-4666(03)00107-8
  12. Kim DI, Kim KH, Kang JH, Jung EM, Kim SS, Jeung EB, Yang MP. Trans-10, cis-12-conjugated linoleic acid modulates NF-$\kappa$B activation and TNF-$\alpha$ production in porcine peripheral blood mononuclear cells via a PPAR$\gamma$- dependent pathway. Br J Nutr 2011; 105: 1329-1336. https://doi.org/10.1017/S000711451000499X
  13. Kim KH, Kim DI, Kim SH, Jung EM, Kang JH, Jeung EB, Yang MP. Trans-10, cis-12-conjugated linoleic acid attenuates tumor necrosis factor-$\alpha$ production by lipopolysaccharide- stimulated porcine peripheral blood mononuclear cells through induction of interleukin-10. Cytokine 2011; 56: 224-230. https://doi.org/10.1016/j.cyto.2011.06.019
  14. Kim YS, Morgan MJ, Choksi S, Liu ZG. TNF-induced activation of the Nox1 NADPH oxidase and its role in the induction of necrotic cell death. Mol Cell 2007; 26: 675-687. https://doi.org/10.1016/j.molcel.2007.04.021
  15. Kritchevsky D, Tepper SA, Wright S, Czarnecki SK, Wilson TA, Nicolosi RJ. Conjugated linoleic acid isomer effects in atherosclerosis: growth and regression of lesions. Lipids 2004; 39: 611-616. https://doi.org/10.1007/s11745-004-1273-8
  16. Lee MJ, Kang BT, Kang JH, Yang MP. Effect of Conjugated Linoleic Acid on Nuclear Factor-$\kappa$B Activation and Tumor Necrosis Factor-$\alpha$ Production in RAW 264.7 Cells Exposed to High Concentration of Glucose. J Vet Clin 2012; 10: 361-367.
  17. Li G, Barnes D, Butz D, Bjorling D, Cook ME. 10t,12cconjugated linoleic acid inhibits lipopolysaccharide-induced cyclooxygenase expression in vitro and in vivo. J Lipid Res 2005; 46: 2134-2142. https://doi.org/10.1194/jlr.M500064-JLR200
  18. Loscher CE, Draper E, Leavy O, Kelleher D, Mills KH, Roche HM. Conjugated linoleic acid suppresses NF-kappa B activation and IL-12 production in dendritic cells through ERK-mediated IL-10 induction. J Immunol 2005; 175: 4990-4998. https://doi.org/10.4049/jimmunol.175.8.4990
  19. Morgan MJ, Liu ZG. Crosstalk of reactive oxygen species and NF-$\kappa$B signaling. Cell Res 2011; 21: 103-115. https://doi.org/10.1038/cr.2010.178
  20. Nakamura YK, Omaye ST. Conjugated linoleic acid isomers' roles in the regulation of PPAR-gamma and NF-kappaB DNA binding and subsequent expression of antioxidant enzymes in human umbilical vein endothelial cells. Nutrition 2009; 25: 800-811. https://doi.org/10.1016/j.nut.2009.01.003
  21. Park NY, Valacchi G, Lim Y. Effect of dietary conjugated linoleic acid supplementation on early inflammatory responses during cutaneous wound healing. Mediators Inflamm 2010; 2010: 342328.
  22. Petrova TV, Akama KT, Van Eldik LJ. Cyclopentenone prostaglandins suppress activation of microglia: down-regulation of inducible nitric-oxide synthase by 15-deoxy- Delta12,14-prostaglandin J2. Proc Natl Acad Sci U S A 1999; 96: 4668-4673. https://doi.org/10.1073/pnas.96.8.4668
  23. Ricote M, Li AC, Willson TM, Kelly CJ, Glass CK. The peroxisome proliferator-activated receptor-gamma is a negative regulator of macrophage activation. Nature 1998; 391: 79-82. https://doi.org/10.1038/34178
  24. Ringseis R, Müller A, Herter C, Gahler S, Steinhart H, Eder K. CLA isomers inhibit TNFalpha-induced eicosanoid release from human vascular smooth muscle cells via a PPARgamma ligand-like action. Biochim Biophys Acta 2006; 1760: 290-300. https://doi.org/10.1016/j.bbagen.2005.12.002
  25. Schoonbroodt S, Legrand-Poels S, Best-Belpomme M, Piette J. Activation of the NF-kappaB transcription factor in a Tlymphocytic cell line by hypochlorous acid. Biochem J 1997; 321: 777-785. https://doi.org/10.1042/bj3210777
  26. Shang FJ, Wang JP, Zheng QS, Liu XT, Xue YS, Li J, Zhao LY. The relationship between reactive oxygen speciesdependent activation of p38 MAPK and the expression of tumor necrosis factor-$\alpha$ in cultured cardiomyocytes. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi 2011; 27: 7-10.
  27. Song DH, Kang JH, Lee GS, Jeung EB, Yang MP. Upregulation of tumor necrosis factor-alpha expression by trans10-cis12 conjugated linoleic acid enhances phagocytosis of RAW macrophages via a peroxisome proliferator-activated receptor gamma-dependent pathway. Cytokine 2007; 37: 227-235. https://doi.org/10.1016/j.cyto.2007.04.003
  28. Staal FJ, Roederer M, Herzenberg LA, Herzenberg LA. Intracellular thiols regulate activation of nuclear factor kappa B and transcription of human immunodeficiency virus. Proc Natl Acad Sci U S A 1990; 87: 9943-9947. https://doi.org/10.1073/pnas.87.24.9943
  29. Stachowska E, Ba kiewicz-Masiuk M, Dziedziejko V, Gutowska I, Baranowska-Bosiacka I, Marchlewicz M, Do egowska B, Wiszniewska B, Machali ski B, Chlubek D. Conjugated linoleic acid increases intracellular ROS synthesis and oxygenation of arachidonic acid in macrophages. Nutrition 2008; 24: 187-199. https://doi.org/10.1016/j.nut.2007.10.018
  30. Taylor JS, Williams SR, Rhys R, James P, Frenneaux MP. Conjugated linoleic acid impairs endothelial function. Arterioscler Thromb Vasc Biol 2006; 26: 307-312.
  31. Verstrepen L, Bekaert T, Chau TL, Tavernier J, Chariot A, Beyaert R. TLR-4, IL-1R and TNF-R signaling to NFkappaB: variations on a common theme. Cell Mol Life Sci 2008; 65: 2964-2978. https://doi.org/10.1007/s00018-008-8064-8
  32. Wright G, Singh IS, Hasday JD, Farrance IK, Hall G, Cross AS, Rogers TB. Endotoxin stress-response in cardiomyocytes: NF-kappaB activation and tumor necrosis factor-alpha expression. Am J Physiol Heart Circ Physiol 2002; 282: H872-879. https://doi.org/10.1152/ajpheart.00256.2001
  33. Yang M, Cook ME. Dietary conjugated linoleic acid decreased cachexia, macrophage tumor necrosis factor-alpha production, and modifies splenocyte cytokines production. Exp Biol Med (Maywood) 2003; 228: 51-58. https://doi.org/10.1177/153537020322800107
  34. Yu Y, Correll PH, Vanden Heuvel JP. Conjugated linoleic acid decreases production of pro-inflammatory products in macrophages: evidence for a PPAR gamma-dependent mechanism. Biochim Biophys Acta 2002; 1581: 89-99. https://doi.org/10.1016/S1388-1981(02)00126-9
  35. Zhao L, Yin J, Li D, Lai C, Chen X, Ma D. Conjugated linoleic acid can prevent tumor necrosis factor gene expression by inhibiting nuclear factor binding activity in peripheral blood mononuclear cells from weaned pigs challenged with lipopolysaccharide. Arch Anim Nutr 2005; 59: 429-438. https://doi.org/10.1080/17450390500353333
  36. Zhu W, Downey JS, Gu J, Di Padova F, Gram H, Han J. Regulation of TNF expression by multiple mitogen-activated protein kinase pathways. J Immunol 2000; 164: 6349-6358. https://doi.org/10.4049/jimmunol.164.12.6349