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小鼠巨噬细胞对支原体的黏附和摄取。II. 扫描电子显微镜观察结果

Attachment and ingestion of mycoplasmas by mouse macrophages. II. Scanning electron microscopic observations.

作者信息

Jones T C, Minick R, Yang L

出版信息

Am J Pathol. 1977 May;87(2):347-58.

Abstract

Mycoplasmas adhere closely to the central region of the surface of mouse peritoneal macrophages in vitro. They do not appear connected to each other or the macrophage membrane, and they induce no change in the surface of the cell. After addition of antimycoplasma antibody, mycoplasmas show interconnections and the cell shows an increase occurrence of ruffled membrane and folding over the mycoplasmas. Large and small lacunae appear in the membrane at sites other than those taking in organisms, and the cell develops a diffusely granular appearance. These changes are associated with an increase in pinocytosis of horseradish peroxidase that is 85% above controls. Five minutes after addition of antibody, the macrophage appears contracted and engorged and has persistent membrane changes consisting of pits, openings, and membrane folds. Trypsin causes slow ingestion of surface mycoplasmas without the obvious membrane folding over organisms but with evidence of a predominantly invaginating process of phagocytosis. The macrophage surface has numerous microprojections, but is does not have the granular appearance seen after addition of antibody. Trypsin and Mycoplasma pulmonis antigen do not enhance macrophage pinocytic rates. (Am J Pathol 87:347-358, 1977).

摘要

在体外,支原体紧密附着于小鼠腹腔巨噬细胞表面的中央区域。它们彼此之间或与巨噬细胞膜似乎没有连接,并且不会引起细胞表面的变化。加入抗支原体抗体后,支原体出现相互连接,细胞出现皱膜增加以及在支原体上方折叠的现象。在摄取微生物以外的部位,细胞膜出现大小不等的腔隙,细胞呈现弥漫性颗粒状外观。这些变化与辣根过氧化物酶的胞饮作用增加有关,其增加幅度比对照组高85%。加入抗体五分钟后,巨噬细胞出现收缩和肿胀,并持续存在由凹陷、开口和膜褶皱组成的膜变化。胰蛋白酶导致表面支原体被缓慢摄取,微生物上方没有明显的膜折叠,但有主要为内吞过程的吞噬作用证据。巨噬细胞表面有许多微突起,但没有加入抗体后所见的颗粒状外观。胰蛋白酶和肺支原体抗原不会提高巨噬细胞的胞饮速率。(《美国病理学杂志》87:347 - 358, 1977)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61bf/2032027/29075aa1f440/amjpathol00399-0096-a.jpg

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