Green C R, Noirot-Timothée C, Noirot C
J Cell Sci. 1983 Jul;62:351-70. doi: 10.1242/jcs.62.1.351.
Using modifications of techniques used for the isolation of macula type intercellular junctions (gap junctions and desmosomes) the arthropod smooth septate junction has been isolated from insect midgut tissue. Midguts from cockroaches or mealworms were used and membrane fractions were obtained by sucrose gradient and ultracentrifugation techniques. Preparations with reasonable concentrations of septate junction were obtained and have been studied by thin-section, negative-stain and freeze-fracture electron microscopy. The junctions appeared to be well preserved, although there was evidence that the junction strands were able to slide within the plane of the membrane. Septa were seen to have a cross-striated appearance when viewed after negative staining but their exact structure remained difficult to determine. Polyacrylamide gel electrophoretic studies demonstrated the reproducibility of the isolation procedure and showed that septa may have a 47 000 molecular weight glycoprotein component. Gel electrophoresis also gave some indication of the intramembrane biochemistry of the smooth septate junction, with proteins of 31 000 and 32 000 molecular weight always occurring in the junction fractions. The junctions were, however, very sensitive to both mechanical and chemical treatments, the septa were destroyed by rough homogenization or by treatment with urea at a concentration as low as 1 M. Freeze-fracture of untreated, isolated junctions demonstrated no differences from junctions in intact tissue, while replicas of urea-treated material were more difficult to interpret as the component parts of the junctions became separated once the septa had been destroyed. Gap junctions were also obtained and resisted both mechanical and chemical treatment, which destroyed the septate junctions. Their major protein component appeared to have a molecular weight of 36 000. Attempts to isolate pleated septate junctions (from insects, molluscs and annelids) by the same techniques failed, implying a significant difference in the structures of the two types of septate junction.
利用用于分离黄斑型细胞间连接(间隙连接和桥粒)的技术改进方法,从昆虫中肠组织中分离出节肢动物的光滑分隔连接。使用蟑螂或黄粉虫的中肠,通过蔗糖梯度和超速离心技术获得膜组分。获得了具有合理浓度分隔连接的制剂,并通过超薄切片、负染色和冷冻断裂电子显微镜进行了研究。这些连接似乎保存完好,尽管有证据表明连接链能够在膜平面内滑动。负染色后观察到隔膜具有横纹外观,但其确切结构仍难以确定。聚丙烯酰胺凝胶电泳研究证明了分离过程的可重复性,并表明隔膜可能有一个分子量为47000的糖蛋白成分。凝胶电泳还给出了一些关于光滑分隔连接膜内生物化学的指示,分子量为31000和32000的蛋白质总是出现在连接组分中。然而,这些连接对机械和化学处理都非常敏感,隔膜会被粗暴匀浆或用低至1M浓度的尿素处理破坏。未经处理的分离连接的冷冻断裂显示与完整组织中的连接没有差异,而尿素处理材料的复制品更难解释,因为一旦隔膜被破坏,连接的组成部分就会分离。间隙连接也被获得,并且抵抗破坏分隔连接的机械和化学处理。它们的主要蛋白质成分似乎分子量为36000。尝试用相同技术分离(来自昆虫、软体动物和环节动物的)褶皱分隔连接失败了,这意味着两种类型的分隔连接在结构上存在显著差异。