Suppr超能文献

猿猴肉瘤病毒转化细胞的细胞质和细胞核中血小板衍生生长因子/v-sis相关蛋白的超微结构定位

Ultrastructural localization of a platelet-derived growth factor/v-sis-related protein(s) in cytoplasm and nucleus of simian sarcoma virus-transformed cells.

作者信息

Yeh H J, Pierce G F, Deuel T F

出版信息

Proc Natl Acad Sci U S A. 1987 Apr;84(8):2317-21. doi: 10.1073/pnas.84.8.2317.

Abstract

The subcellular distribution of v-sis-related protein(s) was analyzed in three simian sarcoma virus (SSV)-transformed cell lines with immunofluorescence and protein A-gold labeling techniques using rabbit polyclonal anti-platelet-derived-growth factor (PDGF) antisera. Antigenically reactive proteins were recognized in subcellular organelles related to protein synthesis and processing, including polyribosomes, endoplasmic reticulum, and the Golgi apparatus, as well as on the cytoplasmic surface of plasma membranes. Prominent immunoreactive proteins were also shown in association with nuclear chromatin in intact cells and in isolated nuclei using Lowicryl K4M resin embedding techniques. Protein A-gold labeling was markedly reduced in sections of non-SSV-transformed fibroblasts incubated with anti-PDGF and absent from SSV-transformed cells if Epon resin was substituted for Lowicryl in the embedding process or if sections were with irrelevant antisera. Nuclear localization of v-sis-related antigens was confirmed in a nitrocellulose-based immunoassay using nuclei isolated from SSV-transformed fibroblasts. Thus, polypeptides recognized antigenically as related to the v-sis gene product not only may be found in subcellular organelles associated with protein synthesis and packaging but also may be found in the nucleus of SSV-transformed cells. These results raise the possibility that v-sis- or PDGF-like proteins may function within the nucleus of SSV-transformed cells.

摘要

利用兔抗血小板衍生生长因子(PDGF)多克隆抗血清,通过免疫荧光和蛋白A-金标记技术,分析了三种猿猴肉瘤病毒(SSV)转化细胞系中v-sis相关蛋白的亚细胞分布。在与蛋白质合成和加工相关的亚细胞器中识别出了抗原反应性蛋白,包括多核糖体、内质网和高尔基体,以及质膜的细胞质表面。使用Lowicryl K4M树脂包埋技术,在完整细胞和分离的细胞核中,也显示出显著的免疫反应性蛋白与核染色质相关。在用抗PDGF孵育的非SSV转化成纤维细胞切片中,蛋白A-金标记明显减少;如果在包埋过程中用Epon树脂代替Lowicryl,或者切片用无关抗血清处理,则在SSV转化细胞中没有蛋白A-金标记。在基于硝酸纤维素的免疫测定中,使用从SSV转化成纤维细胞分离的细胞核,证实了v-sis相关抗原的核定位。因此,抗原性上被识别为与v-sis基因产物相关的多肽,不仅可能存在于与蛋白质合成和包装相关的亚细胞器中,还可能存在于SSV转化细胞的细胞核中。这些结果增加了v-sis或PDGF样蛋白可能在SSV转化细胞的细胞核内发挥作用的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bee5/304641/ddbf4fc9fb24/pnas00273-0216-a.jpg

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