首页> 外文期刊>Journal of cell biology >Targeted deletion of beta 1 integrins in F9 embryonal carcinoma cells affects morphological differentiation but not tissue-specific gene expression.
【24h】

Targeted deletion of beta 1 integrins in F9 embryonal carcinoma cells affects morphological differentiation but not tissue-specific gene expression.

机译:有针对性地删除F9胚胎癌细胞中的β1整合素会影响形态分化,但不会影响组织特异性基因表达。

获取原文
           

摘要

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.
机译:异二聚跨膜粘附受体的整联蛋白超家族介导许多细胞-细胞和细胞-基质相互作用,其功能被认为对正常形态发生和分化至关重要。通过消除同源重组的β1整合素基因,我们已经评估了β1整合素家族在F9胚胎癌模型内胚层分化中的作用。出乎意料地发现F9细胞可以维持三个拷贝的beta 1基因,并且要完全消除,需要连续进行三轮靶向,才能产生三级敲除系(beta 1 TKO)。从F9细胞中消除β1整合素家族的粘附受体,导致与纤连蛋白,层粘连蛋白和胶原蛋白的粘附力降低,但与玻连蛋白的粘附力大大增强。缺少β1整合素并不会促进β3或β5亚基的明显补偿性上调,当它们与αv结合时,它们都可作为玻连蛋白受体。β1整合素的丧失严重影响了β的形态分化。 1-缺陷细胞被诱导分化为顶内膜或内脏内胚层。来自β1缺陷细胞的顶叶内胚层保留了圆形的形态,并且在纤连蛋白和玻连蛋白上的迁移能力很差。来自β1缺陷细胞的内脏内胚层也不能形成正常的,融合的上皮单层。取而代之的是,观察到了一个非连续的层,其中包含成簇的杂乱无章的细胞。但是,β1整联蛋白的丢失不会干扰分化为内脏或壁皮内胚层组织特异性基因产物的诱导剂。这些结果表明,β1整合素介导诱导的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,并且这两个过程在该系统中不一定连接。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号