Ishibashi Ken-ichi, Miura Noriko N, Adachi Yoshiyuki, Tamura Hiroshi, Tanaka Shigenori, Ohno Naohito
Laboratory for Immunopharmacology of Microbial Products, School of Pharmacy, Tokyo University of Pharmacy and Life Science, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
FEMS Immunol Med Microbiol. 2004 Oct 1;42(2):155-66. doi: 10.1016/j.femsim.2004.04.004.
We have recently demonstrated that the cell wall beta-glucan of Candida albicans could be solubilized by sodium hypochlorite, followed by dimethylsulfoxide-extraction (NaClO-DMSO method). In this study, applying this method to Aspergillus spp., we prepared mycelial cell wall beta-glucan and examined its physical properties and immunotoxicological activity. The acetone-dried mycelia of Aspergillus spp. were oxidized by the NaClO-DMSO method. An analysis of (13)C NMR spectra revealed the preparations to be composed of alpha-(1 --> 3) and beta-(1 --> 3)-D-glucan. Also, the proportion of alpha-(1 --> 3) and beta-(1 --> 3)-D-glucan varied. Furthermore, a solubilized Aspergillus beta-glucan (ASBG) was prepared from OX-Asp by urea-autoclave treatment. ASBG showed limulus activity similar to Candida solubilized beta-glucan (CSBG), and there was little difference in the activity of ASBG between various Aspergillus spp. ASBG affected the production of IL-8 by human peripheral blood mononuclear cells (PBMC). ASBG should be useful for analyzing the clinical role of beta-glucan.
我们最近证明,白色念珠菌的细胞壁β-葡聚糖可通过次氯酸钠溶解,随后用二甲基亚砜萃取(次氯酸钠-二甲基亚砜法)。在本研究中,将该方法应用于曲霉属真菌,我们制备了菌丝细胞壁β-葡聚糖,并检测了其物理性质和免疫毒理学活性。曲霉属真菌的丙酮干燥菌丝体通过次氯酸钠-二甲基亚砜法进行氧化。对(13)C NMR光谱的分析表明,制备物由α-(1→3)和β-(1→3)-D-葡聚糖组成。此外,α-(1→3)和β-(1→3)-D-葡聚糖的比例各不相同。此外,通过尿素高压釜处理从OX-Asp制备了可溶解的曲霉β-葡聚糖(ASBG)。ASBG显示出与念珠菌溶解β-葡聚糖(CSBG)相似的鲎试剂活性,并且不同曲霉属真菌之间ASBG的活性差异不大。ASBG影响人外周血单核细胞(PBMC)产生IL-8。ASBG应该有助于分析β-葡聚糖的临床作用。