A static magnetic field reduces lipopolysaccharide-induced proinflammatory cytokine levels of fibroblasts by altering membrane fluidity

被引:0
作者
Lin, Che-Tong [1 ,2 ]
Chen, Chi-An [1 ]
Chen, Yu-Fu [3 ]
Chen, Chun-Yang [3 ]
Lee, Shengnang [3 ,4 ]
Huang, Haw-Ming [1 ]
机构
[1] Taipei Med Univ, Grad Inst Oral Sci, Taipei 11042, Taiwan
[2] Taipei Med Univ Hosp, Dept Dent, Taipei, Taiwan
[3] Taipei Med Univ, Sch Dent, Taipei, Taiwan
[4] Taipei Med Univ, Wan Fang Hosp, Dept Dent, Taipei, Taiwan
关键词
static magnetic field; fibroblast; lipopolysaccharide; proinflammatory cytokine; membrane fluidity;
D O I
暂无
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Lipopolysaccharide (LPS) is one of the major substances that initiate an immune host response in microbial infections which results in cytotoxicity. In terms of the treatment of the immune response, much research on endotoxin tolerance that can reduce LPS-induced damages has been conducted. In this experiment, cultured fibroblasts were challenged with LPS in order to initiate an inflammatory reaction. Cell numbers and various proinflammatory cytokine levels were compared between a static magnetic field (SMF)-exposed group and an unexposed group. Our results showed that with LPS challenge, fibroblasts exposed to a 4000-G SMF demonstrated a higher cell density (8.28 +/- 0.14 10(4) cells/ml) when compared to the unexposed (control) group (4.5 +/- 0.16 10(4) cells/ml, p < 0.05). Meanwhile, levels of LPS-induced interleukin-1 beta and tumor necrosis factor-alpha in the SMF-exposed groups were significantly lower at 32.9% and 61.4% than those of the unexposed counterparts, respectively (p < 0.05). The change in the fluorescence anisotropy of TMA-DPH increased when cells were exposed to SMF. These results indicate that a static magnetic field may decrease LPS-induced proinflammatory cytokine levels by altering the membrane fluidity.
引用
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页码:11 / 18
页数:8
相关论文
共 42 条
[21]   A POSSIBLE EXPLANATION FOR EFFECT OF MAGNETIC FIELDS ON BIOLOGICAL SYSTEMS [J].
LABES, MM .
NATURE, 1966, 211 (5052) :968-&
[22]   MEMBRANE FLUIDITY AS DETECTED BY DIPHENYLHEXATRIENE PROBES [J].
LENTZ, BR .
CHEMISTRY AND PHYSICS OF LIPIDS, 1989, 50 (3-4) :171-190
[23]  
Mathiak G, 2003, INT J MOL MED, V11, P41
[24]   Mechanotransduction of bone cells in vitro:: mechanobiology of bone tissue [J].
Mullender, M ;
El Haj, AJ ;
Yang, Y ;
van Duin, MA ;
Burger, EH ;
Klein-Nulend, J .
MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING, 2004, 42 (01) :14-21
[25]  
NAIRN R, 2002, IMMUNOLOGY MED STUDE, P71
[26]   The sirens' songs of confirmatory sepsis trials: Selection bias and sampling error [J].
Natanson, C ;
Esposito, CJ ;
Banks, SM .
CRITICAL CARE MEDICINE, 1998, 26 (12) :1927-1931
[27]   Effect of 0.2 T static magnetic field on human neurons: remodeling and inhibition of signal transduction without genome instability [J].
Pacini, S ;
Vannelli, GB ;
Barni, T ;
Ruggiero, M ;
Sardi, I ;
Pacini, P ;
Gulisano, M .
NEUROSCIENCE LETTERS, 1999, 267 (03) :185-188
[28]   THE ROLE OF INFLAMMATORY MEDIATORS IN THE PATHOGENESIS OF PERIODONTAL-DISEASE [J].
PAGE, RC .
JOURNAL OF PERIODONTAL RESEARCH, 1991, 26 (03) :230-242
[29]   Cytotoxicity of daunorubicin in trisomic (+21) human fibroblasts:: Relation to drug uptake and cell membrane fluidity [J].
Przybylska, M ;
Koceva-Chyla, A ;
Rózga, B ;
Józwiak, Z .
CELL BIOLOGY INTERNATIONAL, 2001, 25 (02) :157-170
[30]   Magnets in prosthetic dentistry [J].
Riley, MA ;
Walmsley, AD ;
Harris, IR .
JOURNAL OF PROSTHETIC DENTISTRY, 2001, 86 (02) :137-142