Stephens L E, Sonne J E, Fitzgerald M L, Damsky C H
Department of Stomatology, University of California San Francisco 94143-0512.
J Cell Biol. 1993 Dec;123(6 Pt 1):1607-20. doi: 10.1083/jcb.123.6.1607.
The integrin superfamily of heterodimeric transmembrane adhesion receptors mediates many cell-cell and cell-matrix interactions whose functions are believed to be critical for normal morphogenesis and differentiation. By eliminating the beta 1 integrin gene through homologous recombination, we have assessed the role of the beta 1 integrin family in the F9 embryonal carcinoma model for endodermal differentiation. F9 cells were unexpectedly found to maintain three copies of the beta 1 gene and complete elimination required three sequential rounds of targeting to generate triple knockout lines (beta 1 TKO). Elimination of the beta 1 integrin family of adhesion receptors from F9 cells resulted in reduced adhesion to fibronectin, laminin and collagen, but strongly enhanced adhesion to vitronectin. The absence of beta 1 integrins did not promote significant compensatory upregulation of either beta 3 or beta 5 subunits, both of which are known to act as vitronectin receptors when associated with alpha v. The loss of beta 1 integrins severely affected morphological differentiation when the beta 1-deficient cells were induced to differentiate to either parietal or visceral endoderm. Parietal endoderm derived from beta 1-deficient cells retained a rounded morphology and migrated poorly on both fibronectin and vitronectin. Visceral endoderm derived from beta 1-deficient cells were also unable to form a normal, confluent epithelial monolayer; instead, a non-contiguous layer containing clumps of disorganized cells was observed. However, loss of beta 1 integrins did not interfere with induction by differentiating agents of tissue-specific gene products for either visceral or parietal endoderm. These results suggest that beta 1 integrins mediate morphological differentiation (migration and epithelial formation) but not tissue-specific gene expression in induced F9 cells, and that these two processes are not necessarily linked in this system.
异二聚体跨膜黏附受体的整合素超家族介导了许多细胞间和细胞与基质间的相互作用,其功能被认为对正常的形态发生和分化至关重要。通过同源重组消除β1整合素基因,我们评估了β1整合素家族在用于内胚层分化的F9胚胎癌细胞模型中的作用。意外地发现F9细胞维持着β1基因的三个拷贝,完全消除需要三轮连续的靶向操作以产生三敲除细胞系(β1 TKO)。从F9细胞中消除黏附受体的β1整合素家族导致对纤连蛋白、层粘连蛋白和胶原蛋白的黏附减少,但对玻连蛋白的黏附显著增强。β1整合素的缺失并未促进β3或β5亚基的显著代偿性上调,已知这两个亚基与αv结合时均作为玻连蛋白受体发挥作用。当β1缺陷细胞被诱导分化为壁内胚层或脏内胚层时,β1整合素的缺失严重影响了形态分化。源自β1缺陷细胞的壁内胚层保持圆形形态,在纤连蛋白和玻连蛋白上的迁移能力都很差。源自β1缺陷细胞的脏内胚层也无法形成正常的汇合上皮单层;相反,观察到一个包含杂乱细胞团块的不连续层。然而,β1整合素的缺失并不干扰分化剂对脏内胚层或壁内胚层组织特异性基因产物的诱导。这些结果表明,β1整合素介导了诱导的F9细胞中的形态分化(迁移和上皮形成),但不介导组织特异性基因表达,并且在这个系统中这两个过程不一定相关联。