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巨噬细胞对固定免疫复合物进行受挫吞噬作用期间高尔基体膜的快速碎片化和重组。

Rapid fragmentation and reorganization of Golgi membranes during frustrated phagocytosis of immobile immune complexes by macrophages.

作者信息

Bainton D F, Takemura R, Stenberg P E, Werb Z

机构信息

Department of Pathology, University of California, San Francisco 94143-0506.

出版信息

Am J Pathol. 1989 Jan;134(1):15-26.

Abstract

The authors have observed the rapid reorganization of the cellular membranes of macrophages during Fc receptor-mediated frustrated phagocytosis of immune complex-coated surfaces. As the macrophages spread, large, clear basal vacuoles and anastamosing tubules were formed, occasionally contiguous with the adherent surface. Coated vesicles also were observed. This process was accompanied by a rapid reorganization of the Golgi complex region of the macrophages, which was observed using trimetaphosphatase histochemistry and an antibody to a Golgi membrane antigen as markers. On contact of the macrophages with the immune complexes, the Golgi complexes, which were tightly clustered around the centrioles, dispersed into vesicles and reorganized near the basal surface. The Golgi cisternae swelled, fragmented, and decreased in number. Golgi membrane antigen was found in the large basal vacuoles and also associated with the adherent basal surface of the macrophages. This indicates that the Golgi complexes were reorganized, in part, by a direct recruitment of their membranes to the increasing basal surface area of the spreading macrophages. The changes in the structure of the Golgi complexes were reversible; by 2 hours, the complexes had recovered their normal organization, with an accompanying decrease in the number of large basal vacuoles. These data suggest that the dynamic interrelationship among the Golgi membranes, intracellular vacuoles, and the plasma membrane can be perturbed by membrane spreading on a nonphagocytosable surface.

摘要

作者观察到,在Fc受体介导的对免疫复合物包被表面的吞噬受阻过程中,巨噬细胞的细胞膜会迅速重组。随着巨噬细胞铺展,会形成大的、清晰的基底空泡和相互吻合的小管,偶尔与黏附表面相连。还观察到了有被小泡。这一过程伴随着巨噬细胞高尔基体复合体区域的迅速重组,利用焦磷酸酶组织化学和针对高尔基体膜抗原的抗体作为标志物对其进行了观察。巨噬细胞与免疫复合物接触时,紧密聚集在中心粒周围的高尔基体复合体会分散成小泡,并在基底表面附近重新组织。高尔基体潴泡肿胀、破碎且数量减少。在大的基底空泡中发现了高尔基体膜抗原,其也与巨噬细胞的黏附基底表面相关。这表明高尔基体复合体的重组部分是通过将其膜直接募集到铺展的巨噬细胞不断增加的基底表面积上实现的。高尔基体复合体结构的变化是可逆的;到2小时时,复合体已恢复其正常组织,同时大的基底空泡数量减少。这些数据表明,高尔基体膜、细胞内空泡和质膜之间的动态相互关系会因膜在不可吞噬表面上的铺展而受到干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b8c/1879551/54b15af1b364/amjpathol00121-0024-a.jpg

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