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合成的胞壁酰二肽及其类似物对化学发光的刺激作用。

Stimulation of chemiluminescence by synthetic muramyl dipeptide and analogs.

作者信息

Masihi K N, Azuma I, Brehmer W, Lange W

出版信息

Infect Immun. 1983 Apr;40(1):16-21. doi: 10.1128/iai.40.1.16-21.1983.

Abstract

The effect on respiratory burst of murine splenic cells after in vitro exposure to synthetic muramyl dipeptide (MDP) and 6-O-acyl and quinonyl derivatives was studied at an early phase of interaction by luminol-dependent chemiluminescence (CL) in response to stimulation by zymosan. The MDP molecule enhanced CL, but the degree of CL response varied with the kinds of fatty acids introduced in the chemical structure of synthetic glycopeptide analogs. A 6-O-acyl derivative possessing an alpha-branched fatty acid chain, B30-MDP, stimulated maximum levels of CL activity. High CL responses were obtained with L8-MDP having a short chain of linear fatty acids and with QS-10-MDP-66 containing a ubiquinone compound. CL was also stimulated by MDP and its analogs in the spleen cells of nude mice lacking mature T lymphocytes, but the extent of stimulation was decreased compared with that of normal spleen cells.

摘要

在相互作用的早期阶段,通过鲁米诺依赖性化学发光(CL)研究了体外暴露于合成的胞壁酰二肽(MDP)以及6 - O - 酰基和醌基衍生物后对小鼠脾细胞呼吸爆发的影响,该呼吸爆发是对酵母聚糖刺激的响应。MDP分子增强了CL,但CL反应的程度随合成糖肽类似物化学结构中引入的脂肪酸种类而变化。具有α - 分支脂肪酸链的6 - O - 酰基衍生物B30 - MDP刺激了最大水平的CL活性。具有直链脂肪酸短链的L8 - MDP和含有泛醌化合物的QS - 10 - MDP - 66也获得了高CL反应。缺乏成熟T淋巴细胞的裸鼠脾细胞中的MDP及其类似物也刺激了CL,但与正常脾细胞相比,刺激程度有所降低。

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本文引用的文献

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Stimulation of nonspecific resistance to infection induced by 6-O-acyl muramyl dipeptide analogs in mice.
Infect Immun. 1981 May;32(2):748-58. doi: 10.1128/iai.32.2.748-758.1981.
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Adjuvant activities of quinonyl-N-acetyl muramyl dipeptides in mice and guinea pigs.
Infect Immun. 1981 Jan;31(1):114-21. doi: 10.1128/iai.31.1.114-121.1981.
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Components of mycobacteria and muramyl dipeptide with adjuvant activity induce lymphocyte activating factor.
Cell Immunol. 1980 Mar 1;50(1):71-81. doi: 10.1016/0008-8749(80)90007-6.
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Association of neutrophil chemiluminescence with microbicidal activity.
Clin Immunol Immunopathol. 1982 Feb;22(2):259-69. doi: 10.1016/0090-1229(82)90042-3.

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