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环氧化酶和前列腺素E2在肥大细胞分泌颗粒中的定位。

Localization of cyclo-oxygenase and prostaglandin E2 in the secretory granule of the mast cell.

作者信息

Schmauder-Chock E A, Chock S P

机构信息

Department of Experimental Hematology, Armed Forces Radiobiology Research Institute, Bethesda, Maryland 20814-5145.

出版信息

J Histochem Cytochem. 1989 Sep;37(9):1319-28. doi: 10.1177/37.9.2504812.

Abstract

The application of anti-cyclo-oxygenase and anti-prostaglandin E2 immunoglobulins to A23187-stimulated rat connective tissue mast cells has permitted the localization of cyclooxygenase activity (prostaglandin H2 synthetase) and the site of prostaglandin E2 (PGE2) formation in the secretory granules. Because binding was carried out after stimulation but before dehydration and embedding, we have limited the loss of these antigens due to normal degradation and to aqueous and solvent washes. As this method permits labeling of exposed cell surfaces, only granules that have been exteriorized can be labeled. Contrary to what might have been expected, no labeling was associated with plasma membranes or with any portion of damaged cells. Antibodies to PGE2 were bound evenly over the surface of the granule matrix, whereas antibodies to cyclo-oxygenase appeared to be bound to strands of proteo-heparin projecting from the surface of the granule matrix. Where granule matrix had become unraveled and dispersed, label appeared to adhere throughout the ribbon-like proteo-heparin strands. These results support our previous conclusion that the secretory granule is the site of the arachidonic acid cascade during exocytosis.

摘要

将抗环氧化酶和抗前列腺素E2免疫球蛋白应用于A23187刺激的大鼠结缔组织肥大细胞,已使环氧化酶活性(前列腺素H2合成酶)和前列腺素E2(PGE2)在分泌颗粒中的形成位点得以定位。由于结合是在刺激后但在脱水和包埋前进行的,我们限制了这些抗原因正常降解以及水洗和溶剂洗而造成的损失。由于该方法允许对暴露的细胞表面进行标记,所以只有已外化的颗粒才能被标记。与预期相反,质膜或受损细胞的任何部分均未出现标记。抗PGE2抗体均匀地结合在颗粒基质表面,而抗环氧化酶抗体似乎结合在从颗粒基质表面伸出的蛋白聚糖链上。在颗粒基质已解开并分散的地方,标记似乎附着在整个带状蛋白聚糖链上。这些结果支持了我们之前的结论,即分泌颗粒是胞吐过程中花生四烯酸级联反应的位点。

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