Suppr超能文献

大鼠基底动脉的血管周围神经纤维和内皮细胞:I型和III型一氧化氮合酶抗原位点的免疫金标记

Perivascular nerve fibres and endothelial cells of the rat basilar artery: immuno-gold labelling of antigenic sites for type I and type III nitric oxide synthase.

作者信息

Loesch A, Burnstock G

机构信息

Department of Anatomy and Developmental Biology, University College London, UK.

出版信息

J Neurocytol. 1998 Mar;27(3):197-204. doi: 10.1023/a:1026493425977.

Abstract

Ultrastructural localisation of type I (neuronal) and type III (endothelial) isoforms of nitric oxide synthase in perivascular nerve fibres (axons) and endothelial cells was studied in the Wistar rat cerebral basilar artery, using monoclonal antibodies either to type I or type III nitric oxide synthase and post-embedding colloidal-gold immunocytochemistry. Labelling signal (gold particles) for type I and type III nitric oxide synthase was localised both in axons and endothelial cells. In the axon profiles, labelling for either type I or type III nitric oxide synthase was localised in the axoplasm and the lumen and/or membrane of small agranular synaptic vesicles. In the endothelial cells, labelling for either type-I or type-III nitric oxide synthase was predominantly in the cytoplasm. The present qualitative data extends our previous study of cerebrovascular nerve fibres and endothelial cells employing monoclonal antibodies; the localisation of nitric oxide synthase in a subpopulation of synaptic vesicles in nitric oxide synthase-positive cerebrovascular nerves suggests that vesicular mechanisms may be involved in the production/release of nitric oxide.

摘要

利用抗I型或III型一氧化氮合酶的单克隆抗体及包埋后胶体金免疫细胞化学技术,在Wistar大鼠脑基底动脉中研究了血管周围神经纤维(轴突)和内皮细胞中I型(神经元型)和III型(内皮型)一氧化氮合酶的超微结构定位。I型和III型一氧化氮合酶的标记信号(金颗粒)定位于轴突和内皮细胞中。在轴突断面中,I型或III型一氧化氮合酶的标记定位于轴浆以及小的无颗粒突触小泡的管腔和/或膜上。在内皮细胞中,I型或III型一氧化氮合酶的标记主要位于细胞质中。目前的定性数据扩展了我们先前使用单克隆抗体对脑血管神经纤维和内皮细胞的研究;一氧化氮合酶阳性脑血管神经中一氧化氮合酶在一部分突触小泡中的定位表明,囊泡机制可能参与一氧化氮的产生/释放。

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