McLeod A G, Shen A C, Campbell K P, Michalak M, Jorgensen A O
Department of Anatomy, University of Toronto, Canada.
Circ Res. 1991 Aug;69(2):344-59. doi: 10.1161/01.res.69.2.344.
Calsequestrin is a calcium-binding protein known to sequester calcium accumulated in the sarcoplasmic reticulum (SR) of muscle cells during relaxation. In the present study, we used affinity-purified antibodies to chicken cardiac calsequestrin to identify a 60,000-Da calsequestrin in frog myocardium. Like previously identified cardiac calsequestrins, it is enriched in cardiac microsomes, it is enriched by biochemical procedures previously used to purify cardiac and skeletal calsequestrins, and it exhibits a pH-dependent shift in its apparent Mr on a two-dimensional gel system. Finally, the NH2-terminal amino acid sequence of this 60,000-Da immunoreactive protein purified by fast protein liquid chromatography was identical to that of rabbit skeletal and canine cardiac calsequestrin. Thus, we conclude that this protein corresponds to the calsequestrin isoform in frog ventricular muscle. Frog calsequestrin was localized in discrete foci present at the periphery but absent from the central regions of frog ventricular myocytes as determined by immunofluorescence labeling. Immunoelectron microscopic labeling demonstrated that calsequestrin was confined to the lumen of two structurally distinct regions of the SR, where it was localized in the subsarcolemmal region of the myofibers. One of these appeared to correspond to the terminal SR previously reported to be closely apposed to the sarcolemma of frog myofibers. The other region, although close to the sarcolemma, was not physically joined to it and appeared to correspond to corbular SR. It generally is believed that frog cardiac SR does not provide activator Ca2+ required for excitation-contraction coupling. However, the identification of a calsequestrin isoform very similar to mammalian cardiac calsequestrin that is confined to specialized regions of frog cardiac SR lends support to the idea that frog cardiac SR has the ability to store Ca2+ and thus function in some capacity in frog cardiac muscle contraction.
肌集钙蛋白是一种钙结合蛋白,已知在肌肉细胞舒张时能螯合积累于肌浆网(SR)中的钙。在本研究中,我们使用针对鸡心脏肌集钙蛋白的亲和纯化抗体,在蛙心肌中鉴定出一种60,000道尔顿的肌集钙蛋白。与先前鉴定的心脏肌集钙蛋白一样,它在心脏微粒体中富集,通过先前用于纯化心脏和骨骼肌肌集钙蛋白的生化方法可使其富集,并且在二维凝胶系统中其表观分子量呈现pH依赖性变化。最后,通过快速蛋白质液相色谱纯化的这种60,000道尔顿免疫反应性蛋白的氨基末端氨基酸序列与兔骨骼肌和犬心脏肌集钙蛋白的序列相同。因此,我们得出结论,该蛋白对应于蛙心室肌中的肌集钙蛋白同工型。通过免疫荧光标记确定,蛙肌集钙蛋白定位于蛙心室肌细胞周边的离散灶中,而中央区域没有。免疫电子显微镜标记表明,肌集钙蛋白局限于SR两个结构不同区域的腔内,位于肌纤维的肌膜下区域。其中一个区域似乎对应于先前报道的与蛙肌纤维肌膜紧密相邻的终末SR。另一个区域虽然靠近肌膜,但并未与之物理连接,似乎对应于球状SR。一般认为蛙心脏SR不提供兴奋 - 收缩偶联所需的激活钙。然而,在蛙心脏SR的特定区域鉴定出与哺乳动物心脏肌集钙蛋白非常相似的肌集钙蛋白同工型,这支持了蛙心脏SR具有储存钙的能力并因此在蛙心肌收缩中发挥某种作用的观点。