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大鼠神经丝蛋白NF-L和NF-M在转染的非神经元细胞中的表达。

Expression of rat neurofilament proteins NF-L and NF-M in transfected non-neuronal cells.

作者信息

Chin S S, Liem R K

机构信息

Department of Pharmacology, New York University Medical Center, NY.

出版信息

Eur J Cell Biol. 1989 Dec;50(2):475-90.

PMID:2516804
Abstract

Two cDNA clones fully encoding the rat neurofilament proteins NF-L and NF-M were subcloned into eukaryotic expression vectors behind the strong constitutive viral promoters from SV40 and Rous sarcoma viruses. Transient transfection of L tk- and Cos cell lines with these expression constructs resulted in cells expressing the neurofilament proteins in an intermediate filament-type pattern. Additionally, a putative juxtanuclear organizing center or region was observed in the transfected cells, most noticeable shortly after the transfection procedure. Stable transfections were performed on mouse L tk- and Swiss 3T6 cells using NF-L and NF-M constructs bearing an SV40 early promoter driven neomycin selectable marker. Although G418-resistant clones were recovered with both the NF-L and the NF-M constructs, only clones expressing immunofluorescently stainable amounts of NF-M were detected and established. Immunoelectron microscopic analysis revealed NF-M and vimentin proteins to be colocalized on the same intermediate filaments.

摘要

两个完全编码大鼠神经丝蛋白NF-L和NF-M的cDNA克隆被亚克隆到真核表达载体中,置于来自SV40和劳氏肉瘤病毒的强组成型病毒启动子之后。用这些表达构建体对L tk-和Cos细胞系进行瞬时转染,导致细胞以中间丝类型模式表达神经丝蛋白。此外,在转染细胞中观察到一个假定的近核组织中心或区域,在转染过程后不久最为明显。使用带有SV40早期启动子驱动的新霉素选择标记的NF-L和NF-M构建体对小鼠L tk-和瑞士3T6细胞进行稳定转染。尽管用NF-L和NF-M构建体都回收了G418抗性克隆,但仅检测到并建立了表达免疫荧光可染色量的NF-M的克隆。免疫电子显微镜分析显示NF-M和波形蛋白在同一中间丝上共定位。

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