Wilkens Christina M, Beam Kurt G
Department of Anatomy and Neurobiology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
J Muscle Res Cell Motil. 2003;24(1):99-109. doi: 10.1023/a:1024830132118.
The L-type Ca2+ channel in skeletal muscle (alpha1S) is essential for excitation-contraction (EC) coupling. Previous studies using chimeras composed of alpha1S together with alpha1C or alpha1M demonstrated the importance of the alpha1S II-III loop and of a smaller subdomain (residues 720-764; 'ECC') in skeletal EC coupling. However, these chimeras failed to test the significance of regions outside the II-III loop, which are highly conserved between alpha1S and alpha1C. Therefore, we have injected dysgenic (alpha1S-lacking) myotubes with cDNAs encoding chimeras between alpha1S and the highly divergent T-type Ca2+ channel, alpha1H. The chimeras consisted of GFP-tagged alpha1H with one or more of the following substitutions: alpha1S II-III loop residues 720-764 ('ECC'), a putative targeting domain of the alpha1S C terminus ('target'; residues 1543-1662) or the entire alpha1S C terminus ('Cterm'; residues 1382-1873). The presence of either target or Cterm affected the expression and/or kinetics of whole-cell currents recorded from both dysgenic muscle cells and tsa-201 cells. Importantly, substitution of ECC alone into GFP-alpha1H (GFP-alpha1H + ECC), or together with either target (GFP-alpha1H + ECC + target) or Cterm (GFP-alpha1H + ECC + Cterm), was insufficient to restore electrically evoked contractions. Depolarization-induced fluorescence transients for GFP-alpha1H + ECC, GFP-alpha1H + ECC + target or GFP-alpha1H + ECC + Cterm had a bell shaped dependence upon membrane voltage (inconsistent with skeletal EC coupling) and were also exceedingly small (unlike cardiac EC coupling). The absence of EC coupling for these chimeras raises the possibility that regions of alpha1S outside of ECC and target are necessary for providing the context that allows these two domains to function in EC coupling and targeting, respectively. Additionally, an inadequate membrane density of the chimeras may have contributed to the lack of coupling.
骨骼肌中的L型Ca2+通道(α1S)对于兴奋-收缩(EC)偶联至关重要。先前使用由α1S与α1C或α1M组成的嵌合体进行的研究表明,α1S II-III环以及一个较小的亚结构域(残基720-764;“ECC”)在骨骼肌EC偶联中具有重要性。然而,这些嵌合体未能测试II-III环之外区域的重要性,这些区域在α1S和α1C之间高度保守。因此,我们向发育不全的(缺乏α1S的)肌管中注射了编码α1S与高度不同的T型Ca2+通道α1H之间嵌合体的cDNA。这些嵌合体由带有绿色荧光蛋白(GFP)标签的α1H组成,并具有以下一个或多个替换:α1S II-III环残基720-764(“ECC”)、α1S C末端的一个假定靶向结构域(“靶向”;残基1543-1662)或整个α1S C末端(“C末端”;残基1382-1873)。靶向或C末端的存在影响了从发育不全的肌肉细胞和tsa-201细胞记录的全细胞电流的表达和/或动力学。重要的是,仅将ECC替换到GFP-α1H中(GFP-α1H + ECC),或与靶向(GFP-α1H + ECC +靶向)或C末端(GFP-α1H + ECC + C末端)一起替换,不足以恢复电诱发的收缩。GFP-α1H + ECC、GFP-α1H + ECC +靶向或GFP-α1H + ECC + C末端的去极化诱导荧光瞬变对膜电压呈钟形依赖性(与骨骼肌EC偶联不一致),并且也非常小(与心脏EC偶联不同)。这些嵌合体缺乏EC偶联增加了一种可能性,即ECC和靶向之外的α1S区域对于提供允许这两个结构域分别在EC偶联和靶向中发挥作用的背景是必要的。此外,嵌合体的膜密度不足可能导致了偶联的缺乏。