Singer I I
Cell. 1979 Mar;16(3):675-85. doi: 10.1016/0092-8674(79)90040-0.
A possible connection between external fibronectin-containing fibers and cytoplasmic 5 nm actin microfilaments within dense submembranous plaques has been observed by transmission electron microscopy. We refer to this transmembranous association as the fibronexus. Hamster embryo fibroblasts, transformed by wild-type or temperature-sensitive mutant (A28) SV40 virus, and human lung fibroblasts (WI-38, MRC-5) were studied using the tannic acid method of Simionescu and Simionescu (1976), which preferentially stained external carbohydrates. Fibronectin antigens were also localized on the extracellular fibers of the fibronexus with fibronectin antibody and immunoferritin staining. Goniometric studies of sections cut parallel to the plasmalemma demonstrated that the actin- and fibronectin-containing fibers of the fibronexus remained colinear when the specimen was tilted through a 40 degree angle about the fibrillar long axis. Sections cut perpendicular to the cell surface also showed that these fibers were apparently colinear. Our results suggest that the fibronectin and actin fibers of the fibronexus are closely associated (maximum separation distances of 8--22 nm), if not co-axial. Fibronexuses remained after expression of SV40-induced transformation, despite alteration of microfilament bundles and reduction in the amount of fibronectin (observed by immunofluorescence microscopy). The possible roles of fibronectin and the fibronexus in regulating actin polymerization are discussed.
通过透射电子显微镜观察到,在致密的膜下斑块中,含纤连蛋白的外部纤维与细胞质中5纳米的肌动蛋白微丝之间可能存在联系。我们将这种跨膜联系称为纤维连接。利用西米奥内斯库和西米奥内斯库(1976年)的单宁酸法对经野生型或温度敏感突变型(A28)SV40病毒转化的仓鼠胚胎成纤维细胞以及人肺成纤维细胞(WI-38、MRC-5)进行了研究,该方法能优先对外部碳水化合物进行染色。纤连蛋白抗原也通过纤连蛋白抗体和免疫铁蛋白染色定位在纤维连接的细胞外纤维上。对平行于质膜切割的切片进行测角研究表明,当标本围绕纤维长轴倾斜40度角时,纤维连接中含肌动蛋白和纤连蛋白的纤维仍保持共线。垂直于细胞表面切割的切片也显示这些纤维明显共线。我们的结果表明,纤维连接中的纤连蛋白纤维和肌动蛋白纤维即使不是同轴的,也是紧密相连的(最大间距为8 - 22纳米)。尽管微丝束发生了改变且纤连蛋白的量有所减少(通过免疫荧光显微镜观察到),但在SV40诱导的转化表达后纤维连接仍然存在。本文讨论了纤连蛋白和纤维连接在调节肌动蛋白聚合中的可能作用。