Structure and biological activities of β-glucans from yeast and mycelial forms of Candida albicans

被引:32
|
作者
Miura, NN
Adachi, Y
Yadomae, T
Tamura, H
Tanaka, S
Ohno, N
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Pharm, Lab Immunopharmacol Microbial Prod, Hachioji, Tokyo 1920392, Japan
[2] Seikagaku Corp, Tokyo Res Inst, Tokyo 2070021, Japan
关键词
beta-glucan; Candida albicans; mycelial form; macrophage inflammatory protein-2;
D O I
10.1111/j.1348-0421.2003.tb03382.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have achieved the extraction of cell wall beta-glucan from the mycelial form of Candida albicans (C albicans) IFO 0579 (M-CSBG) by using acetic acid, sodium hypochlorite (NaCIO), and dimethylsulfoxide (DMSO) treatments. The yield of M-CSBG was significantly lower (7.5% from dried mycelial cells) than that of the yeast form from C. albicans IFO 1385 (Y-CSBG, 25.9% from dried yeast cells). The properties of M-CSBG were similar to those of Y-CSBG in terms of nuclear magnetic resonance (NMR) spectra and limulus reactivity. Molecular weight (Mw) of M-CSBG was slightly higher than that of Y-CSBG. Both Y-CSBG and M-CSBG induced the production of comparable amounts of macrophage inflammatory protein-2 (MIP-2), a chemotactic factor, from mouse peritoneal exudate cells (PEC) in vitro. These findings suggest that the structure and properties of CSBG from yeast and mycelial cells are similar to each other.
引用
收藏
页码:173 / 182
页数:10
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