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金黄色葡萄球菌衍生的L型菌诱导巨噬细胞介导产生肿瘤坏死因子α

Induction of macrophage-mediated production of tumor necrosis factor alpha by an L-form derived from Staphylococcus aureus.

作者信息

Kuwano K, Akashi A, Matsu-ura I, Nishimoto M, Arai S

机构信息

Department of Microbiology, Kurume University School of Medicine, Japan.

出版信息

Infect Immun. 1993 May;61(5):1700-6. doi: 10.1128/iai.61.5.1700-1706.1993.

Abstract

We investigated the capability of an L-form derived from Staphylococcus aureus to induce tumor necrosis factor alpha (TNF-alpha) production in murine peritoneal macrophages. The activity for TNF-alpha induction was found in the membrane fraction of the L-form but not in the cytoplasmal fraction purified by the sucrose step gradient centrifugation. TNF-alpha mRNA was also detected in macrophages stimulated with L-form membranes. L-form induced TNF-alpha production in macrophages from both lipopolysaccharide-responsive and -unresponsive mouse strains. Regardless of the presence of polymyxin B, the activity of TNF-alpha induction of L-form was mostly found in the phenol layer, but not in the aqueous layer, both of which were prepared by phenol extraction method. Fractions of L-form membranes representing molecular masses of approximately between 29 and 36 kDa were primarily responsible for inducing the production of TNF-alpha consistently. Moreover, this stimulatory effect was abolished by digestion with Streptomyces griseus protease. In Western blot (immunoblot) analysis with anti-lipoteichoic acid antibody, two bands (65 and 45 kDa) were observed in the sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the phenol layer, whereas one band (14 kDa) was observed in either the aqueous layer or lipoteichoic acid of S. aureus. These results suggest that the component in the membrane of the L-form, distinct from cell wall components such as teichoic acid or lipopolysaccharide, possesses the capability to stimulate TNF-alpha production by macrophages.

摘要

我们研究了源自金黄色葡萄球菌的L型菌诱导小鼠腹腔巨噬细胞产生肿瘤坏死因子α(TNF-α)的能力。发现L型菌的膜组分具有诱导TNF-α的活性,而通过蔗糖阶梯梯度离心纯化的细胞质组分则没有该活性。在用L型菌膜刺激的巨噬细胞中也检测到了TNF-α mRNA。L型菌可诱导脂多糖反应性和非反应性小鼠品系的巨噬细胞产生TNF-α。无论是否存在多粘菌素B,L型菌诱导TNF-α的活性主要存在于通过苯酚提取法制备的苯酚层中,而不存在于水层中。L型菌膜中分子量约在29至36 kDa之间的组分主要负责持续诱导TNF-α的产生。此外,用灰色链霉菌蛋白酶消化可消除这种刺激作用。在用抗脂磷壁酸抗体进行的蛋白质印迹(免疫印迹)分析中,在苯酚层的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳中观察到两条带(65和45 kDa),而在水层或金黄色葡萄球菌的脂磷壁酸中观察到一条带(14 kDa)。这些结果表明,L型菌膜中的成分不同于细胞壁成分如磷壁酸或脂多糖,具有刺激巨噬细胞产生TNF-α的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27c/280754/a76becd7b8fd/iai00017-0118-a.jpg

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