Comparison of nitric oxide, hydrogen peroxide, and cytokine production in RAW 264.7 cells by Bifidobacterium and other intestinal bacteria

被引:0
作者
Om, AS
Park, SY
Hwang, IK
Ji, GE [1 ]
机构
[1] Seoul Natl Univ, Dept Food Sci & Nutr, Seoul 151742, South Korea
[2] Michigan State Univ, Dept Food Sci & Human Nutr, E Lansing, MI 48824 USA
[3] Seoul Natl Univ, Coll Med, Canc Res Ctr, Seoul 110744, South Korea
关键词
Bifidobacterium; intestinal bacteria; macrophage; H2O2; nitric oxide; cytokine;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Intestinal bacteria comprise one-third of the contents of the large intestine in humans. Their interactions with the gastrointestinal immune system induce characteristic immunological responses which stimulate or suppress the host's defense system. RAW 264.7 murine cell line was used as a macrophage model to assess the effects of the exposure to the isolated human intestinal bacteria, Bacteroides, Bifidobacterium, Eubacterium, Streptococcus, and E. coli, on NO (nitric oxide), H2O2 (hydrogen peroxide), and cytokines IL (interleukin)-6 and TNF (tumor necrosis factor)-alpha production. RAW 264.7 cells were cultured in the presence of heat-killed bacteria for 24 h at concentrations of 0 similar to 50 mu g/ml. Our results showed that Bacteroides and E. coli stimulated IL-6. TNF-alpha, NO, and H2O2 production at high levels even at 1 mu g/ml, whereas Bifidobacterium, Eubacterium, and Streptococcus showed a low level of stimulation at 1 mu g/ml and a gradual increase as the cell concentration increased up to 50 mu g/ml. This result suggests that gram-negative Bacteroides and E, coli are better able to stimulate macrophage than gram-positive Bifidobacterium, Streptococcus, and Eubacterium. The in vitro approaches employed here should be useful in further characterization of the effects of intestinal bacteria on gastrointestinal and systemic immunity.
引用
收藏
页码:98 / 105
页数:8
相关论文
共 53 条
[1]   INTERLEUKIN-6 IN BIOLOGY AND MEDICINE [J].
AKIRA, S ;
TAGA, T ;
KISHIMOTO, T .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :1-78
[2]  
[Anonymous], 1994, CYTOKINES CELLULAR M
[3]  
[Anonymous], 1994, Bifidobacteria Microflora, DOI DOI 10.12938/BIFIDUS1982.13.2_79
[4]   The indigenous gastrointestinal microflora [J].
Berg, RD .
TRENDS IN MICROBIOLOGY, 1996, 4 (11) :430-435
[5]  
BEZKOROVAINY A, 1989, BIOCH PHYSL BIFIDOBA, P30
[6]   CYTOKINES AND MACROPHAGES [J].
CAVAILLON, JM .
BIOMEDICINE & PHARMACOTHERAPY, 1994, 48 (10) :445-453
[7]  
Choi YJ, 1996, J MICROBIOL BIOTECHN, V6, P255
[8]   TUMOR-NECROSIS-FACTOR INDUCTION BY AN AQUEOUS PHENOL-EXTRACTED LIPOPOLYSACCHARIDE COMPLEX FROM BACTEROIDES SPECIES [J].
DELAHOOKE, DM ;
BARCLAY, GR ;
POXTON, IR .
INFECTION AND IMMUNITY, 1995, 63 (03) :840-846
[9]  
DESIMONE C, 1992, IMMUNOPHARM IMMUNOT, V14, P331, DOI 10.3109/08923979209009228
[10]   ELEVATED GENE-EXPRESSION AND PRODUCTION OF INTERLEUKIN-2, INTERLEUKIN-4, INTERLEUKIN-5, AND INTERLEUKIN-6 DURING EXPOSURE TO VOMITOXIN (DEOXYNIVALENOL) AND CYCLOHEXIMIDE IN THE EL-4 THYMOMA [J].
DONG, WM ;
AZCONAOLIVERA, JI ;
BROOKS, KH ;
LINZ, JE ;
PESTKA, JJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1994, 127 (02) :282-290