Bornslaeger E A, Corcoran C M, Stappenbeck T S, Green K J
Department of Pathology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Cell Biol. 1996 Aug;134(4):985-1001. doi: 10.1083/jcb.134.4.985.
The desmosomal plaque protein desmoplakin (DP), located at the juncture between the intermediate filament (IF) network and the cytoplasmic tails of the transmembrane desmosomal cadherins, has been proposed to link IF to the desmosomal plaque. Consistent with this hypothesis, previous studies of individual DP domains indicated that the DP COOH terminus associates with IF networks whereas NH2-terminal sequences govern the association of DP with the desmosomal plaque. Nevertheless, it had not yet been demonstrated that DP is required for attaching IF to the desmosome. To test this proposal directly, we generated A431 cell lines stably expressing DP NH2-terminal polypeptides, which were expected to compete with endogenous DP during desmosome assembly. As these polypeptides lacked the COOH-terminal IF-binding domain, this competition should result in the loss of IF anchorage if DP is required for linking IF to the desmosomal plaque. In such cells, a 70-kD DP NH2-terminal polypeptide (DP-NTP) colocalized at cell-cell interfaces with desmosomal proteins. As predicted, the distribution of endogenous DP was severely perturbed. At cell-cell borders where endogenous DP was undetectable by immunofluorescence, there was a striking absence of attached tonofibrils (IF bundles). Furthermore, DP-NTP assembled into ultrastructurally identifiable junctional structures lacking associated IF bundles. Surprisingly, immunofluorescence and immunogold electron microscopy indicated that adherens junction components were coassembled into these structures along with desmosomal components and DP-NTP. These results indicate that DP is required for anchoring IF networks to desmosomes and furthermore suggest that the DP-IF complex is important for governing the normal spatial segregation of adhesive junction components during their assembly into distinct structures.
桥粒斑蛋白桥粒芯蛋白(DP)位于中间丝(IF)网络与跨膜桥粒钙黏蛋白的细胞质尾部之间的交界处,有人提出它将中间丝连接到桥粒斑。与这一假设一致的是,先前对单个DP结构域的研究表明,DP的COOH末端与中间丝网络相关联,而NH2末端序列则控制DP与桥粒斑的关联。然而,尚未证明DP是将中间丝连接到桥粒所必需的。为了直接测试这一假设,我们构建了稳定表达DP NH2末端多肽的A431细胞系,预计这些多肽在桥粒组装过程中会与内源性DP竞争。由于这些多肽缺乏COOH末端的中间丝结合结构域,如果DP是将中间丝连接到桥粒斑所必需的,那么这种竞争应该会导致中间丝锚定的丧失。在这类细胞中,一种70-kD的DP NH2末端多肽(DP-NTP)在细胞-细胞界面处与桥粒蛋白共定位。正如所预测的,内源性DP的分布受到严重干扰。在免疫荧光检测不到内源性DP的细胞-细胞边界处,明显没有附着的张力原纤维(中间丝束)。此外,DP-NTP组装成超微结构上可识别的连接结构,但缺乏相关的中间丝束。令人惊讶的是,免疫荧光和免疫金电子显微镜显示,黏着连接成分与桥粒成分和DP-NTP一起共组装到这些结构中。这些结果表明,DP是将中间丝网络锚定到桥粒所必需的,此外还表明DP-中间丝复合物对于在黏附连接成分组装成不同结构的过程中控制其正常的空间分离很重要。