Klein I, Daood M, Whiteside T
J Cell Physiol. 1985 Jul;124(1):49-53. doi: 10.1002/jcp.1041240109.
Cultured neonatal rat heart cells can be used to study the factors that regulate cardiac contractility and myocyte development in vitro. An antibody to the 26,000 dalton light chain of myosin (MLC1), has been produced and purified on a Sepharose 4B affinity column prepared with rat heart myosin. When primary cultures of myocytes are studied by indirect immunofluorescence using this antibody a predictable pattern of myofibrillar structure is observed to develop over 72 h. This myosin cytoskeleton is highly organized and the myosin fibrils exhibit cross striations. The antibody does not stain non-muscle heart cells and there is no evidence for myocyte division in culture. The qualitative immunofluorescent pattern of myosin organization is the same in both spontaneously beating and in non-contracting cells.
培养的新生大鼠心脏细胞可用于在体外研究调节心脏收缩性和心肌细胞发育的因素。已制备出针对肌球蛋白26,000道尔顿轻链(MLC1)的抗体,并在以大鼠心脏肌球蛋白制备的琼脂糖4B亲和柱上进行了纯化。当使用该抗体通过间接免疫荧光研究心肌细胞的原代培养物时,可观察到在72小时内肌原纤维结构呈现出可预测的发育模式。这种肌球蛋白细胞骨架高度有序,肌球蛋白纤维呈现出横纹。该抗体不会对非肌肉心脏细胞进行染色,并且培养中没有心肌细胞分裂的证据。在自发跳动的细胞和非收缩细胞中,肌球蛋白组织的定性免疫荧光模式是相同的。