Niessen C M, Hulsman E H, Oomen L C, Kuikman I, Sonnenberg A
Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam.
J Cell Sci. 1997 Aug;110 ( Pt 15):1705-16. doi: 10.1242/jcs.110.15.1705.
The integrin alpha6 beta4 is a major component of hemidesmosomes, in which it mediates firm adhesion to laminin 5. Previous studies have shown that the incorporation of alpha6 beta4 into hemidesmosomes requires a 303 amino acid stretch of the cytoplasmic domain of beta4, comprising part of the first fibronectin type III (FNIII) repeat, the second FNIII repeat and the segment that connects the second to the third FNIII repeat (connecting segment). Now, we have further defined sequences within beta4 that are critical for its localization in hemidesmosomes and we demonstrate that these sequences also induce the redistribution of HD1/plectin into junctional complexes containing the integrin alpha6 beta4 in COS-7 cells, transfected with cDNAs encoding alpha6A and beta4. Truncation of the cytoplasmic domain of beta4 after amino acids 1,382 or 1,355 in the connecting segment, by which a potential tyrosine activation motif (TAM) is removed, does not prevent the localization of alpha6 beta4 in hemidesmosomes in the rat bladder carcinoma cell line 804G and neither did it eliminate the ability of alpha6 beta4 to change the subcellular distribution of HD1/plectin in COS-7 cells. In contrast, beta4 subunits in which the entire connecting segment had been deleted or which were truncated after amino acid 1,328, which removes almost the complete segment, had lost both of these functions. Furthermore, when beta4 subunits with either a deletion of the second FNIII repeat or a small deletion in this repeat were co-expressed with alpha6, the integrins were not localized in hemidesmosomes and did not induce the redistribution of HD1/plectin in COS-7 cells. Finally, the fourth FNIII repeat of beta4 could not replace the second in either of these activities. These findings establish that a region in beta4, which encompasses the second FNIII repeat and a stretch of 27 amino acids (1,329-1,355) of the connecting segment, is critical for the localization of alpha6beta4 in hemidesmosomes and that it regulates the distribution of HD1/plectin.
整合素α6β4是半桥粒的主要成分,在半桥粒中它介导与层粘连蛋白5的牢固黏附。先前的研究表明,α6β4整合到半桥粒中需要β4胞质结构域的一段303个氨基酸的序列,该序列包括第一个III型纤连蛋白(FNIII)重复序列的一部分、第二个FNIII重复序列以及连接第二个和第三个FNIII重复序列的片段(连接片段)。现在,我们进一步确定了β4中对于其在半桥粒中定位至关重要的序列,并且我们证明这些序列还能在转染了编码α6A和β4的cDNA的COS-7细胞中,诱导HD1/网蛋白重分布到含有整合素α6β4的连接复合体中。在连接片段中第1382或1355位氨基酸之后截断β4的胞质结构域,从而去除一个潜在的酪氨酸激活基序(TAM),这并不妨碍α6β4在大鼠膀胱癌细胞系804G的半桥粒中的定位,也没有消除α6β4改变COS-7细胞中HD1/网蛋白亚细胞分布的能力。相比之下,整个连接片段被删除或在第1328位氨基酸之后截断(几乎去除了整个片段)的β4亚基失去了这两种功能。此外,当缺失第二个FNIII重复序列或在该重复序列中有小缺失的β4亚基与α6共表达时,整合素不在半桥粒中定位,也不会在COS-7细胞中诱导HD1/网蛋白的重分布。最后,β4的第四个FNIII重复序列在这两种活性中都不能替代第二个。这些发现表明,β4中的一个区域,包括第二个FNIII重复序列和连接片段的一段27个氨基酸(1329 - 1355),对于α6β4在半桥粒中的定位至关重要,并且它调节HD1/网蛋白的分布。