Walker J L, Menko A S
Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, 571 Jefferson Alumni Hall, Philadelphia, Pennsylvania, 19107, USA.
Dev Biol. 1999 Jun 15;210(2):497-511. doi: 10.1006/dbio.1999.9277.
The developing chicken embryo lens provides a unique model for examining the relationship between alpha6 integrin expression and cell differentiation, since multiple stages of differentiation are expressed concurrently at one stage of development. We demonstrate that alpha6 integrin is likely to mediate the inductive effects of laminin on lens differentiation as well as to function in a matrix-independent manner along the cell-cell interfaces of the differentiating cortical lens fiber cells. Both alpha6 isoform expression and its linkage to the cytoskeleton were regulated in a differentiation-specific manner. The association of alpha6 integrin with the Triton-insoluble cytoskeleton increased as the lens cells differentiated, reaching its highest levels in the cortical fiber region where the lens fiber cells are formed. In this region of the lens alpha6 integrin was uniquely localized along the cell-cell borders of the differentiating fiber cells, similar to beta1. alpha6beta4, the primary transmembrane protein of hemidesmosomes, is also expressed in the lens, but in the absence of hemidesmosomes. Differential expression of alpha6A and alpha6B isoforms with lens cell differentiation was seen at both the mRNA and the protein levels. RT-PCR studies demonstrated that alpha6B was the predominant isoform expressed both early in development, embryonic day 4, and in the epithelial regions of the day 10 embryonic lens. Isoform switching, with alpha6A now the predominant isoform, occurred in the fiber cell zones. Immunoprecipitation studies showed that alpha6B, which is characteristic of undifferentiated cells, was expressed by the lens epithelial cells but was dramatically reduced in the lens fiber zones. Expression of alpha6B began to drop as the cells initiated their differentiation and then dropped precipitously in the cortical fiber zone. In contrast, expression of the alpha6A isoform remained high until the cells became terminally differentiated. alpha6A was the predominant isoform expressed in the cortical fiber region. The down-regulation of alpha6B relative to alpha6A provides a developmental switch in the process of lens fiber cell differentiation.
发育中的鸡胚晶状体为研究α6整合素表达与细胞分化之间的关系提供了一个独特的模型,因为在发育的一个阶段会同时表达多个分化阶段。我们证明,α6整合素可能介导层粘连蛋白对晶状体分化的诱导作用,并在分化的皮质晶状体纤维细胞的细胞-细胞界面以不依赖基质的方式发挥作用。α6亚型的表达及其与细胞骨架的连接均以分化特异性方式受到调节。随着晶状体细胞的分化,α6整合素与不溶于曲拉通的细胞骨架的结合增加,在形成晶状体纤维细胞的皮质纤维区域达到最高水平。在晶状体的这个区域,α6整合素与β1相似,独特地定位于分化纤维细胞的细胞-细胞边界。半桥粒的主要跨膜蛋白α6β4也在晶状体中表达,但不存在半桥粒。在mRNA和蛋白质水平均观察到α6A和α6B亚型随晶状体细胞分化的差异表达。RT-PCR研究表明,α6B是在发育早期(胚胎第4天)和第10天胚胎晶状体的上皮区域均表达的主要亚型。在纤维细胞区发生了亚型转换,此时α6A成为主要亚型。免疫沉淀研究表明,未分化细胞特有的α6B由晶状体上皮细胞表达,但在晶状体纤维区显著减少。随着细胞开始分化,α6B的表达开始下降,然后在皮质纤维区急剧下降。相反,α6A亚型的表达一直保持较高水平,直到细胞终末分化。α6A是在皮质纤维区域表达的主要亚型。相对于α6A,α6B的下调为晶状体纤维细胞分化过程提供了一个发育开关。