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肌动蛋白结合蛋白在营养不良的鸡和小鼠骨骼肌中的表达增加。

Increased expression of cofilin in dystrophic chicken and mouse skeletal muscles.

作者信息

Hayakawa K, Minami N, Ono S, Ogasawara Y, Totsuka T, Abe H, Tanaka T, Obinata T

机构信息

Department of Biology, Chiba University.

出版信息

J Biochem. 1993 Oct;114(4):582-7. doi: 10.1093/oxfordjournals.jbchem.a124220.

Abstract

A monoclonal antibody (McAb) specific for actin depolymerizing factor (ADF) was prepared. With this and previously prepared anti-cofilin McAb (MAB-22) and other antibodies, the expression of cofilin and ADF in the muscles of dystrophic (NH-413) chicken and dystrophic (C57BL/6J dy/dy) mice was compared with that in normal control animals by immunoblotting and immunocytochemical methods. Since cofilin expression is down-regulated during normal postnatal development of skeletal muscles [Abe et al. (1989) J. Biochem. 106, 696-702], cofilin was detected in the breast (pectoralis) muscle of normal adult chicken and the leg (femoris and tibialis anterior) muscles of normal mice only at a low level. ADF was not detectable in adult skeletal muscles. However, a significant increase of cofilin amount, but not of ADF amount, was observed in these muscles of the dystrophic animals, when the symptom of muscular dystrophy became evident. In order to localize cofilin in individual muscle fibers, serial cryosections of the dystrophic chicken muscle were examined with anti-cofilin antibody (MAB-22). The antibody stained cells of different size in the dystrophic muscle, indicating that cofilin expression was induced in the regenerating muscle cells as well as in the pre-existing myofibers. We suggest that cofilin is involved in disassembly or reorganization of actin in the dystrophic muscle.

摘要

制备了一种针对肌动蛋白解聚因子(ADF)的单克隆抗体(McAb)。利用该抗体以及先前制备的抗丝切蛋白单克隆抗体(MAB - 22)和其他抗体,通过免疫印迹和免疫细胞化学方法,比较了营养不良型(NH - 413)鸡和营养不良型(C57BL / 6J dy/dy)小鼠肌肉中丝切蛋白和ADF的表达与正常对照动物的差异。由于在骨骼肌正常出生后的发育过程中丝切蛋白表达下调[Abe等人(1989年)《生物化学杂志》106卷,696 - 702页],正常成年鸡的胸肌(胸大肌)和正常小鼠的腿部肌肉(股四头肌和胫骨前肌)中仅能检测到低水平的丝切蛋白。在成年骨骼肌中未检测到ADF。然而,当肌肉营养不良症状明显时,在这些营养不良动物的肌肉中观察到丝切蛋白量显著增加,但ADF量未增加。为了在单个肌纤维中定位丝切蛋白,用抗丝切蛋白抗体(MAB - 22)检查了营养不良鸡肌肉的连续冰冻切片。该抗体对营养不良肌肉中不同大小的细胞进行了染色,表明丝切蛋白表达在再生肌细胞以及已存在的肌纤维中均被诱导。我们认为丝切蛋白参与了营养不良肌肉中肌动蛋白的拆卸或重组。

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