Suppr超能文献

在有调理素和无调理素情况下人类多形核白细胞与金黄色葡萄球菌之间的相互作用。

Interaction between human polymorphonuclear leucocytes and Staphylococcus aureus in the presence and absence of opsonins.

作者信息

Vandenbroucke-Grauls C M, Thijssen H M, Verhoef J

出版信息

Immunology. 1984 Jul;52(3):427-35.

Abstract

Phagocytosis of Staphylococcus aureus by human polymorphonuclear leucocytes (PMN) in the presence and absence of opsonins was studied with an assay which allows interaction between PMN and bacteria on a surface. The kinetics of uptake, the activity of the metabolic burst, and the degranulation during phagocytosis of opsonized and unopsonized bacteria were compared. Uptake of unopsonized S. aureus proceeded at a slower rate, but unopsonized staphylococci induced metabolic activity and degranulation in the PMN to the same extent as opsonized bacteria. Treatment of PMN with a metabolic inhibitor (2-deoxy-D-glucose) or with an inhibitor of microfilament function (cytochalasin B) totally inhibited the capacity of PMN to ingest unopsonized S. aureus, whereas uptake of opsonized bacteria was much less affected. Treatment of the PMN with pronase prevented uptake of unopsonized bacteria, but had no effect on the uptake of opsonized bacteria. Uptake was not inhibited by mannose. Recognition of S. aureus by the PMN was not dependent on the presence of the cell wall components protein A or teichoic acid. The presence of a capsule inhibited uptake.

摘要

在有调理素和无调理素的情况下,使用一种能使多形核白细胞(PMN)与细菌在表面相互作用的检测方法,研究了人多形核白细胞对金黄色葡萄球菌的吞噬作用。比较了调理和未调理细菌吞噬过程中的摄取动力学、代谢爆发活性和脱颗粒情况。未调理的金黄色葡萄球菌摄取速度较慢,但未调理的葡萄球菌诱导PMN的代谢活性和脱颗粒程度与调理细菌相同。用代谢抑制剂(2-脱氧-D-葡萄糖)或微丝功能抑制剂(细胞松弛素B)处理PMN,完全抑制了PMN摄取未调理金黄色葡萄球菌的能力,但调理细菌的摄取受影响较小。用链霉蛋白酶处理PMN可阻止未调理细菌的摄取,但对调理细菌的摄取没有影响。甘露糖不抑制摄取。PMN对金黄色葡萄球菌的识别不依赖于细胞壁成分蛋白A或磷壁酸的存在。荚膜的存在会抑制摄取。

相似文献

引用本文的文献

5
Modulation of phagocytic cell function.吞噬细胞功能的调节。
Vet Res Commun. 1986 May;10(3):165-88. doi: 10.1007/BF02213979.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验