Suppr超能文献

肌球蛋白同工型在去神经支配、交叉神经支配和电刺激兔肌肉中的表达。

Expression of myosin isoforms in denervated, cross-reinnervated, and electrically stimulated rabbit muscles.

作者信息

Bacou F, Rouanet P, Barjot C, Janmot C, Vigneron P, d'Albis A

机构信息

Laboratoire de Différenciation cellulaire et Croissance, Institut National de la Recherche Agronomique, Montpellier, France.

出版信息

Eur J Biochem. 1996 Mar 1;236(2):539-47. doi: 10.1111/j.1432-1033.1996.00539.x.

Abstract

The expression of myosin heavy (MyHC) and light (MyLC) chain isoforms was analyzed after denervation and cross-reinnervation by a fast nerve of the slow-twitch Semimembranosus proprius (SMp) muscle, and after denervation and electrical stimulation at low frequency of the fast-twitch Semimembranous accessorius (SMa) muscle of the rabbit. The control SMp (100% type I fibers) expressed 100% type I MyHC and 100% slow-type (1S', 1S and 2S) MyLC isoforms. Five month denervation did not alter significantly the MyHC expression of the muscle, but induced the expression of a new type 1 MyLC corresponding most probably to an embryonic MyLC. Five-month cross-reinnervation of the SMp by the fast SMa nerve induced a large change of its fiber type properties. As shown by immunocytochemistry, almost all fibers were stained by fast myosin antibody, but a high proportion of them co-expressed slow myosin. This result was in agreement with biochemical data showing that fast MyHC and MyLC isoforms became predominant. The control SMa (nearly 100% type II fibers) expressed almost 100% type II MyHC (70% type IIb and 22% IIx/d) and 100% fast-type (1F, 2F and 3F) MyLC isoforms. Five month denervation of the SMa induced a shift in its MyHC, with 98% type IIx/d and 2% type IIb isoforms, and no change in the proportions of its MyLC. Three month electrical stimulation at 10 Hz of the SMa transformed its fiber type composition. All fibers reacted with the slow myosin antibody and a minor proportion of them were stained by the fast myosin antibody. These observations were in agreement with the biochemical analysis showing a large predominance of the slow-type MyHC and MyLC isoforms. Taken together, these results obtained from rabbit muscles which are normally homogeneous in either fast-twitch or slow-twitch fiber types, further support the idea that the different myosin isoforms, particularly the MyHC, are differentially regulated by motor innervation. Type I MyHC is maintained in denervated SMp muscle, but is not expressed in denervated SMa. Type IIb isoform is the most sensitive to neural influence, as it disappears rapidly in denervated and electrically stimulated fast-twitch SMa muscle, and is barely expressed in cross-reinnervated slow-twitch SMp muscle. In contrast, type IIa and type IIx/d are less dependent upon motor innervation. In addition to the previous studies of d'Albis et al. analysis of these results leads us to conclude that, in the rabbit, sensitivity to motor innervation increases from the glycolytic to the oxydative types of fibers, in the order IIB > IIX/IID > IIA > I.

摘要

在慢肌半膜肌固有部(SMp)由快神经进行去神经支配和交叉神经支配后,以及在兔的快肌半膜肌副部(SMa)进行去神经支配和低频电刺激后,对肌球蛋白重链(MyHC)和轻链(MyLC)同工型的表达进行了分析。对照SMp(100%为I型纤维)表达100%的I型MyHC和100%的慢型(1S'、1S和2S)MyLC同工型。去神经支配5个月并未显著改变该肌肉的MyHC表达,但诱导了一种新型I型MyLC的表达,其很可能对应于胚胎MyLC。由快SMa神经对SMp进行5个月的交叉神经支配诱导了其纤维类型特性的巨大变化。免疫细胞化学显示,几乎所有纤维都被快肌球蛋白抗体染色,但其中很大一部分同时表达慢肌球蛋白。这一结果与生化数据一致,表明快MyHC和MyLC同工型占主导地位。对照SMa(近100%为II型纤维)表达近100%的II型MyHC(70%为IIb型和22%为IIx/d型)和100%的快型(1F、2F和3F)MyLC同工型。对SMa进行5个月的去神经支配导致其MyHC发生转变,IIx/d型占98%,IIb型占2%,其MyLC比例无变化。对SMa进行3个月10Hz的电刺激改变了其纤维类型组成。所有纤维都与慢肌球蛋白抗体发生反应,其中一小部分被快肌球蛋白抗体染色。这些观察结果与生化分析一致,表明慢型MyHC和MyLC同工型占主导地位。综上所述,从正常情况下快肌或慢肌纤维类型单一的兔肌肉获得的这些结果,进一步支持了不同肌球蛋白同工型,特别是MyHC,受运动神经支配差异调节的观点。I型MyHC在去神经支配的SMp肌肉中得以维持,但在去神经支配的SMa中不表达。IIb型同工型对神经影响最为敏感,因为它在去神经支配和电刺激的快肌SMa肌肉中迅速消失,在交叉神经支配的慢肌SMp肌肉中几乎不表达。相比之下,IIa型和IIx/d型对运动神经支配的依赖性较小。除了d'Albis等人之前的研究外,对这些结果的分析使我们得出结论,在兔中,对运动神经支配的敏感性从糖酵解型纤维到氧化型纤维逐渐增加,顺序为IIB > IIX/IID > IIA > I。

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