Jorgensen A O, Jones L R
J Biol Chem. 1986 Mar 15;261(8):3775-81.
Phospholamban, originally described as a cardiac sarcoplasmic reticulum protein, was localized in cryostat sections of three adult canine skeletal muscles (gracilis, extensor carpi radialis, and superficial digitalis flexor) by immunofluorescence labeling with highly specific phospholamban antibodies. Only some myofibers were strongly labeled with phospholamban antibodies. The labeling of myofibers with phospholamban antibodies was compared to the distribution of Type I (slow) and Type II (fast) myofibers as determined by staining adjacent sections cytochemically for the alkali-stable myosin ATPase, a specific marker for Type II myofibers. All the skeletal myofibers labeled for phospholamban above background levels corresponded to Type I (slow) myofibers. The presence of phospholamban in microsomal fractions isolated from canine superficial digitalis flexor (89 +/- 3% Type I) and extensor carpi radialis skeletal muscle (14 +/- 6% Type I) was confirmed by immunoblotting. Antiserum to cardiac phospholamban bound to proteins of apparent Mr values of 25,000 (oligomeric phospholamban) and 5,000-6,000 (monomeric phospholamban) in sarcoplasmic reticulum vesicles from both muscles. Quantification of phospholamban in sarcoplasmic reticulum vesicles from cardic, slow, and fast skeletal muscle tissues following phosphorylation with [gamma-32P] ATP suggested that superficial digitalis flexor and extensor carpi radialis skeletal muscle contained about 16 and 3%, respectively, as much phospholamban as cardiac muscle per unit of sarcoplasmic reticulum. The presence of phospholamban in both Type I (slow) and cardiac muscle fibers supports the possibility that the Ca2+ fluxes across the sarcoplasmic reticulum in both fiber types are similarly regulated, and is consistent with the idea that the relaxant effect of catecholamines on slow skeletal muscle is mediated in part by phosphorylation of phospholamban.
磷酸受磷蛋白最初被描述为一种心肌肌浆网蛋白,通过用高度特异性的磷酸受磷蛋白抗体进行免疫荧光标记,将其定位在三只成年犬的三种骨骼肌(股薄肌、桡侧腕伸肌和指浅屈肌)的低温切片中。只有一些肌纤维被磷酸受磷蛋白抗体强烈标记。将磷酸受磷蛋白抗体对肌纤维的标记与通过对相邻切片进行细胞化学染色以检测碱稳定肌球蛋白ATP酶(II型肌纤维的特异性标志物)所确定的I型(慢)和II型(快)肌纤维的分布进行比较。所有高于背景水平被标记为磷酸受磷蛋白的骨骼肌纤维均对应于I型(慢)肌纤维。通过免疫印迹证实了从犬指浅屈肌(89±3%为I型)和桡侧腕伸肌(14±6%为I型)分离的微粒体组分中存在磷酸受磷蛋白。抗心肌磷酸受磷蛋白抗血清与来自这两种肌肉的肌浆网小泡中表观分子量为25,000(寡聚磷酸受磷蛋白)和5,000 - 6,000(单体磷酸受磷蛋白)的蛋白质结合。用[γ-32P]ATP磷酸化后,对心脏、慢肌和快肌骨骼肌组织的肌浆网小泡中的磷酸受磷蛋白进行定量分析表明,指浅屈肌和桡侧腕伸肌每单位肌浆网中所含的磷酸受磷蛋白分别约为心肌的16%和3%。I型(慢)肌纤维和心肌纤维中均存在磷酸受磷蛋白,这支持了两种纤维类型中跨肌浆网的Ca2+通量受到类似调节的可能性,并且与儿茶酚胺对慢肌骨骼肌的舒张作用部分是由磷酸受磷蛋白的磷酸化介导的观点一致。