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由24.1D5单克隆抗体所界定的成肌细胞表面抗原的克隆与特性分析

Cloning and characterization of a myoblast cell surface antigen defined by 24.1D5 monoclonal antibody.

作者信息

Gower H J, Moore S E, Dickson G, Elsom V L, Nayak R, Walsh F S

机构信息

Institute of Neurology, Queen Square, London, UK.

出版信息

Development. 1989 Apr;105(4):723-31. doi: 10.1242/dev.105.4.723.

Abstract

Monoclonal antibody 24.1D5 reacts specifically with an epitope expressed on the cell surface of mononucleate myoblasts in primary cultures of human skeletal muscle cells, but not with either multinucleate myotubes or fibroblasts. Polypeptides of 60 and 100 X 10(3) Mr were identified by immunoblotting with the McAb. Human muscle cDNAs encoding the 24.1D5 epitope were used to study further the structure and expression of 24.1D5 during skeletal muscle development. Two mRNA species of 3.0 and 2.5 kb were identified in primary cultures of human skeletal muscle and in mouse muscle cell lines. The levels of both transcripts decreased during myotube formation in vitro and were similarly decreased during myogenesis in the mouse embryo. 24.1D5 mRNAs were expressed by multipotential cells and myoblast derivatives of the mouse embryonic cell line C3H10T1/2, suggesting that 24.1D5 is expressed at an early stage during skeletal muscle development.

摘要

单克隆抗体24.1D5能特异性地与人类骨骼肌细胞原代培养物中单核成肌细胞表面表达的一个表位发生反应,但与多核肌管或成纤维细胞均无反应。通过用该单克隆抗体进行免疫印迹鉴定出了分子量为60和100×10³的多肽。编码24.1D5表位的人类肌肉cDNA被用于进一步研究24.1D5在骨骼肌发育过程中的结构和表达。在人类骨骼肌原代培养物和小鼠肌肉细胞系中鉴定出了3.0和2.5 kb的两种mRNA。在体外肌管形成过程中,这两种转录本的水平均下降,并且在小鼠胚胎的肌生成过程中也同样下降。24.1D5 mRNA由小鼠胚胎细胞系C3H10T1/2的多能细胞和成肌细胞衍生物表达,这表明24.1D5在骨骼肌发育的早期阶段表达。

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