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钙离子载体A23187诱导大鼠嗜碱性白血病(2H3)细胞发生的形态学变化。

Morphological changes induced by the calcium ionophore A23187 in rat basophilic leukemia (2H3) cells.

作者信息

Sahara N, Siraganian R P, Oliver C

机构信息

Laboratory of Immunology, National Institute of Dental Research, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Histochem Cytochem. 1990 Jul;38(7):975-83. doi: 10.1177/38.7.1693935.

Abstract

RBL-2H3 cells have been widely used to study histamine release in vitro. It was previously shown that these cells undergo striking morphological changes after IgE-mediated secretion. The present study was undertaken to examine if the morphological changes were dependent on activation of the Fc epsilon receptor. Therefore, the cells were stimulated to release histamine by two different mechanisms: activation of the Fc epsilon receptor by antigen and treatment with the calcium ionophore A23187. Cell surface and cytoskeletal changes were examined by fluorescence microscopy and scanning electron microscopy after either IgE- or ionophore-mediated histamine release. After exposure of the cells to either secretagogue, the cells spread over the surface of the culture dish and underwent rearrangement of the cytoskeleton. In addition, scanning electron microscopy revealed that deep ruffles developed on the surface of the cells undergoing IgE-mediated release. The surface changes were not as pronounced with the ionophore. The distribution of the cytoskeletal elements was examined by immunofluorescence using FITC-phalloidin and antibodies against vimentin and tubulin. In unstimulated cells actin was localized at the cell periphery, just under the plasma membrane. In the stimulated cells it was associated with the cell periphery and concentrated in the surface ruffles. As the stimulated cells spread, intermediate filaments and microtubules became distributed throughout the cell body, but there was no obvious association with the membrane ruffles. These morphological changes were dependent on the presence of extracellular calcium and on the concentration of ionophore or antigen, and were also correlated with the amount of histamine released. Additionally, IgE-mediated stimulation led to increased uptake of the soluble-phase tracer Lucifer yellow, whereas stimulation with the ionophore A23187 showed no increase in Lucifer yellow internalization. Ionophore A23187 produced changes similar but not identical to those seen in the RBL-2H3 cells after IgE-mediated histamine release. The differences may be owing to the involvement of the Fc epsilon receptor in IgE-mediated secretion.

摘要

RBL - 2H3细胞已被广泛用于体外研究组胺释放。先前的研究表明,这些细胞在IgE介导的分泌后会发生显著的形态变化。本研究旨在检验这些形态变化是否依赖于Fcε受体的激活。因此,通过两种不同机制刺激细胞释放组胺:抗原激活Fcε受体和用钙离子载体A23187处理。在IgE或离子载体介导的组胺释放后,通过荧光显微镜和扫描电子显微镜检查细胞表面和细胞骨架的变化。将细胞暴露于任何一种促分泌剂后,细胞会在培养皿表面铺展并经历细胞骨架重排。此外,扫描电子显微镜显示,在经历IgE介导释放的细胞表面形成了深褶皱。离子载体处理时表面变化不那么明显。使用异硫氰酸荧光素 - 鬼笔环肽以及抗波形蛋白和微管蛋白的抗体通过免疫荧光检查细胞骨架成分的分布。在未受刺激的细胞中,肌动蛋白定位于细胞周边,就在质膜下方。在受刺激的细胞中,它与细胞周边相关并集中在表面褶皱中。随着受刺激细胞的铺展,中间丝和微管分布于整个细胞体,但与膜褶皱没有明显关联。这些形态变化依赖于细胞外钙的存在以及离子载体或抗原的浓度,并且也与释放的组胺量相关。此外,IgE介导的刺激导致可溶性示踪剂路西法黄摄取增加,而用离子载体A23187刺激则未显示路西法黄内化增加。离子载体A23187产生的变化与IgE介导组胺释放后RBL - 2H3细胞中观察到的变化相似但不完全相同。差异可能是由于Fcε受体参与了IgE介导的分泌。

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