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Ethanol Extract of Ulmus pumila Ameliorates Heat Stress through the Induction of Heat Shock Proteins Expression in RAW264.7 Macrophage Cells 원문보기

한국축산시설환경학회지 = Journal of animal environmental science, v.20 no.4, 2014년, pp.147 - 154  

dela Cruz, Joseph (Department of Animal Life and Environmental Science, Hankyong National University) ,  Byambaragchaa, Munkhzaya (Department of Animal Life and Environmental Science, Hankyong National University) ,  Choi, Seok-Geun (Department of Animal Life and Environmental Science, Hankyong National University) ,  Hwang, Seong-Gu (Department of Animal Life and Environmental Science, Hankyong National University)

Abstract AI-Helper 아이콘AI-Helper

Heat stress is a significant burden to animal production in most areas of the world. Improving our knowledge of physiological and metabolic mechanisms of acclimation may contribute to the development of procedures that may help to maintain health and production efficiency under hot temperature. The ...

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제안 방법

  • But the cytoprotective effect of Ulmus pumila against heat stress has not been reported so far. In this study our aim was to determine the cytoprotective ability of Ulmus pumila ethanol extract on the heat stressed Raw264.7 cells, as well as to reveal a potential gene transduction which are involved in cytoprotective function of this plant extract.
  • Thus, phagocytosis is an important indicator of macrophage effector activity. In this study, we evaluated the effect of heat stress on the phagocytic activity of RAW264.7 macrophage cells.
  • 7 cells. To further investigate the mechanism of action behind the cytoprotective activity of UP, we analyzed the expressions of heat stress related genes and proteins.

대상 데이터

  • RAW264.7 cells were obtained from the Korean Cell Line Bank (KCLB). The cells were maintained in Dulbecco’s Modified Eagle’s medium (DMEM), supplemented with 10% heat inactivated fetal bovine serum (FBS), penicillin (100 U/ml), streptomycin (100 mg/ml), and 3.

데이터처리

  • All quantitative data are representative of at least three independent experiments and the results were expressed as means + S.D. Differences between means were evaluated using ANOVA test (one-way) followed by Duncan’s Multiple Range Test.

이론/모형

  • Cell viability was quantified by CCK-8 assay. Briefly, the cells were plated in 96-well plates at a density of 1×105 cells/mL and allowed to adhere at 37℃ for 3h.
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참고문헌 (17)

  1. Cheng, A.W., Wan, F.C., Wang, J.Q., Jin, Z.Y., Xu, X.M., 2008. Macrophage immunomodulatory activity of polysaccharides isolated from Glycyrrhiza uralensis fish. International Immunopharmacology. 8:43-50. 

  2. Collier, R.J., Baumgard, L.H., Lock, A.L., Bauman, D.E., 2005. Physiological Limitations, Nutrient Partitioning. In Yield of Farmed Species. Constraints and Opportunities in the 21st Century. Nottingham University Press, Nottingham UK, pp.351-377. 

  3. Johnson, J.D., Fleshner, M., 2006. Releasing signals, secretory pathways, and immune function of endogenous extracellular heat shock protein 72. J. Leukoc. Biol. 79:425-434. 

  4. Kapila, N., Kishore, A., Sodhi, M., Sharma, A., Mohanty, A.K., Kumar, P., Mukesh, A., 2013. Temporal Changes In mRNA Expression Of Heat Shock Protein Genes In Mammary Epithelial Cells Of Riverine Buffalo In Response To Heat Stress In Vitro. I. J. Anim. Bio. 3:5-9. 

  5. Kregel, K.C., 2002. Molecular Biology of Thermoregulation Invited Review: Heat shock proteins: modifying factors in physiological stress responses and acquired thermotolerance. J. Appl. Physiol. 92:2177-2186. 

  6. Lee, W.C., Wen, H.C., Chang, C.P., Chen, M.Y., Lin, M.T., 2006. Heat Shock Protein 72 Overexpression Protects Against Hyperthermia, Circulatory Shock and Cerebral Ischemia During Heat Stroke. J. Appl. Pysiol. 100:2073-2082. 

  7. Mayor, A., Martinon, F., De Smedt, T., Petrilli, V., Tschopp, J., 2007. A crucial function of SGT1 and HSP90 in inflammasome activity links mammalian and plant innate immune responses. Nat. Immunol. 8:497-503. 

  8. Morange, F., 2006. HSFs in Development. Handbook of Experimental Pharmacology. 172:153-169. 

  9. Prohaszka, Z., Fust, G., 2004. Immunological Aspects of Heat-Shock Proteins - The Optimum Stress of Life. Molecular Immunology. 41:29-44. 

  10. Ross, O.A., Curran, M.D., Crum, K.A., Rea, I.M., Barnett, Y.A., Middleton D., 2003. Increased Frequency of the 2437 T Allele of the Heat Shock Protein 70-Hom Gene in an Aged Irish Population. Experimental Gerontology. 38:561-565. 

  11. Terao, J., 2009. Dietary flavonoids as antioxidants. Forum Nutr. 61:87-94. 

  12. Wang, R., Kovalchin, J.T., Muhlenkamp, P., Chandawarkar, R.Y., 2006. Exogenous heat shock protein 70 binds macrophage lipid raft micro domain and stimulates phagocytosis, processing and MHC-II presentation of antigens. Blood. 107:1636-1642. 

  13. Wang, D., Xia, M., Cui, Z., 2006. New triterpenoids isolated from the root bark of Ulmus pumila L. Chem. Pharm. Bull. 54:775-778. 

  14. Van Morelle, W., Wielockx, B., Mahieu, T., Takada, M., Taniguchi, T., Sekikawa, K., Libert, C., 2002. HSP70 protects against TNF-induced lethal inflammatory shock. Immunity 16:685-695. 

  15. Voellmy, R., 1994. Transduction of the stress signal and mechanisms of transcriptional regulation of heat shock/stress protein gene expression in higher eukaryotes. Crit. Rev. Eukaryot. Gene Expr. 4:357-401. 

  16. Zuo, J., Baler, R., Dahl, G., Voellmy, R., 1994. Activation of the DNA-binding ability of human heat shock transcription factor 1 may involve the transition from an intramolecular triple-stranded coiled-coil structure. Mol. Cell Biol. 14:7447-68. 

  17. Zou, J., Guo, Y., Guettouche, T., Smith, D.F., Voellmy, R., 1998. Repression of heat shock transcription factor HSF1 activation by HSP90 (HSP90 complex) that forms a stress-sensitive complex with HSF1. Cell. 94:471-480. 

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