Geiger B, Tokuyasu K T, Singer S J
Proc Natl Acad Sci U S A. 1979 Jun;76(6):2833-7. doi: 10.1073/pnas.76.6.2833.
alpha-Actinin was localized in chicken intestinal epithelial cells by immunofluorescence and immunoferritin labeling of thin frozen sections. Most of the label of the brush border was confined to the terminal web area. The label there was concentrated mainly along the "roots" of the microvilli core microfilaments and in the vicinity of the zonula adherens. In the latter structure, the narrow electron-dense zones adjacent to the cell membranes, however, were not significantly labeled. This suggests that alpha-actinin does not mediate directly the association of the transverse terminal web microfilaments to the membrane at the zonula adherens. Sparse ferritin labeling was found near the tight junction, whereas the staining associated with the spot desmosome was negligible. The microvilli were not significantly labeled by either immunofluorescence or immunoferritin staining unless the sections were previously treated with detergent. Moreover, alpha-actinin (or a structurally related protein) was not detected in preparations of purified microvillar vesicles, suggesting the possibility that the alpha-actinin staining in the microvilli may be an artificial due to its translocation by the detergent from the terminal web onto the microvilli. The possible roles of alpha-actinin in the organization and function of the brush border are discussed.
通过对薄冰冻切片进行免疫荧光和免疫铁蛋白标记,α-辅肌动蛋白定位于鸡肠道上皮细胞中。刷状缘的大部分标记局限于终末网区域。那里的标记主要集中在微绒毛核心微丝的“根部”以及黏着小带附近。然而,在后者结构中,紧邻细胞膜的狭窄电子致密区没有明显的标记。这表明α-辅肌动蛋白并不直接介导终末网横向微丝与黏着小带处细胞膜的结合。在紧密连接附近发现了稀疏的铁蛋白标记,而与点状桥粒相关的染色可忽略不计。除非切片事先用去污剂处理,否则微绒毛在免疫荧光或免疫铁蛋白染色中均无明显标记。此外,在纯化的微绒毛小泡制剂中未检测到α-辅肌动蛋白(或结构相关蛋白),这表明微绒毛中α-辅肌动蛋白染色可能是由于去污剂将其从终末网转移到微绒毛上而产生的人为现象。本文讨论了α-辅肌动蛋白在刷状缘的组织和功能中的可能作用。