Stimulation of various functions in murine peritoneal macrophages by glucans produced by glucosyltransferases from Streptococcus mutans

被引:13
作者
Choi, I
Jo, G
Kim, S
Jung, CW
Kim, Y
Shin, K
机构
[1] Korea Food Res Inst, Seongnam 463420, Kyunggi Do, South Korea
[2] Kyonggi Univ, Dept Food Sci & Biotechnol, Suwon 442760, Kyunggi Do, South Korea
关键词
glucan; glucosyltransferases (GTFs); Streptococcus mutans; peritoneal macrophage; immunostimulating;
D O I
10.1271/bbb.69.1693
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The glucan that was produced by glucosyltransferases (GTFs) from Streptococcus mutans was examined for its stimulating functions toward murine peritoneal macrophages. Soluble glucan was obtained by the reaction with cell-free crude GTFs and sucrose, followed by ethanol precipitation, dispersion in water and reprecipitation by ethanol. Soluble glucan, those average molecular weight was about 3 x 101, was composed of mixture of alpha-1,6 and alpha-1,3 linkages in a 3:1 ratio. When 30 and 60 mu g/ml of the glucan was incubated with peritoneal macrophages, the lysosomal phosphatase activity was increased in a dose-dependant manner, indicating that soluble glucan may activate macrophages. To examine its effects on the various functions of macrophages, soluble glucan was orally administered daily at a level of 100 mg/kg of body weight to C57BL/6 mice. Significant stimulation of the production of H2O2 by the macrophages was observed without any increase in NO production. The production of tumor necrosis factor-alpha (TNF-alpha) by the macrophages was also stimulated from 538.73-555.06 pg/ml to 585.73-596.40 pg/ml during 15 days of oral administration of soluble glucan. The cytotoxicity of peritoneal macrophages against B16 tumor cells was significantly enhanced by 25-38% during 15 days of oral administration. These results may indicate that soluble glucan stimulates the immune functions of macrophages.
引用
收藏
页码:1693 / 1699
页数:7
相关论文
共 32 条
[1]  
ADACHI Y, 1993, BIOL PHARM BULL, V16, P462
[2]   Production of glucosyltransferases by clinical mutans streptococcal isolates as determined by semiquantitative cross-dot assay [J].
Alaluusua, S ;
Gronroos, L ;
Zhu, X ;
Saarela, M ;
Matto, J ;
Asikainen, S ;
Fukushima, K .
ARCHIVES OF ORAL BIOLOGY, 1997, 42 (06) :417-422
[3]  
BOGWALD J, 1984, J LEUKOCYTE BIOL, V35, P357
[4]   (1->3)-beta-D-glucans as biological response modifiers: A review of structure-functional activity relationships [J].
Bohn, JA ;
BeMiller, JN .
CARBOHYDRATE POLYMERS, 1995, 28 (01) :3-14
[5]   Echinacea-induced cytokine production by human macrophages [J].
Burger, RA ;
Torres, AR ;
Warren, RP ;
Caldwell, VD ;
Hughes, BG .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1997, 19 (07) :371-379
[6]  
CERENIUS L, 1994, J BIOL CHEM, V269, P29462
[7]  
CHOI EM, 2002, KOREAN J FOOD SCI TE, V34, P510
[8]   Sugar metabolism by mutans streptococci [J].
Colby, SM ;
Russell, RRB .
JOURNAL OF APPLIED MICROBIOLOGY, 1997, 83 :S80-S88
[9]   FUNCTIONS OF LYSOSOMES [J].
DEDUVE, C ;
WATTIAUX, R .
ANNUAL REVIEW OF PHYSIOLOGY, 1966, 28 :435-+
[10]  
DOITA M, 1991, J LEUKOCYTE BIOL, V49, P342, DOI 10.1002/jlb.49.4.342