Toh B H, Yildiz A, Sotelo J, Osung O, Holborow E J, Fairfax A
Cell Tissue Res. 1979 Jun 8;199(1):117-26. doi: 10.1007/BF00237731.
Specific anti-actin and anti-myosin antibodies were shown to react in single and double immunofluorescence sandwich tests with identical sites in non-muscle cells in frozen sections of tissues and in cultured cells. In tissues, both antibodies reacted with liver cell membranes, parts of renal glomeruli, brush borders and peritubular fibrils of renal tubules, brain synaptic junctions, and membranes of lymphoid cells in thymic medulla, lymph nodes and spleen. Both antibodies reacted strongly with long parallel cytoplasmic fibrils in cultured fibroblasts, and with disrupted fibrils in cytochalasin-B treated cells. In neuroblastoma cells both antibodies gave prominent staining of growth cones and microspikes. The observation that the distribution of myosin parallels that of actin in non-muscle cells argues strongly in favour of a functional interaction between the two molecules in the generation of contractile activity in non-muscle cells.
特异性抗肌动蛋白和抗肌球蛋白抗体在组织冰冻切片的非肌肉细胞以及培养细胞中进行的单重和双重免疫荧光夹心试验中,被证明可与相同位点发生反应。在组织中,两种抗体均与肝细胞膜、部分肾小球、肾小管刷状缘和肾小管周围纤维、脑突触连接以及胸腺髓质、淋巴结和脾脏中淋巴细胞的膜发生反应。两种抗体均与培养的成纤维细胞中长的平行细胞质纤维以及用细胞松弛素B处理的细胞中破坏的纤维强烈反应。在神经母细胞瘤细胞中,两种抗体均使生长锥和微刺呈现显著染色。在非肌肉细胞中肌球蛋白的分布与肌动蛋白的分布平行这一观察结果有力地支持了这两种分子在非肌肉细胞收缩活性产生过程中存在功能相互作用的观点。