Kil S H, Krull C E, Cann G, Clegg D, Bronner-Fraser M
Division of Biology 139-74, California Institute of Technology, Pasadena, California, 91125, USA.
Dev Biol. 1998 Oct 1;202(1):29-42. doi: 10.1006/dbio.1998.8985.
We identify the alpha4 subunit of integrin as a predominant integrin expressed by neural crest cells in both avian and murine embryos. Using degenerate primers, we obtained a PCR fragment of the chick integrin alpha4 subunit that was subsequently used to clone the full-length subunit with a predicted amino acid sequence 60% identical to human and mouse alpha4 subunits. In situ hybridization demonstrates that chick integrin alpha4 mRNA is expressed at high levels by migrating neural crest cells and neural crest-derived ganglia at both cranial and trunk levels. An antibody against the murine alpha4 subunit revealed similar distribution patterns in mouse to chick. In addition to neural crest cells, the integrin alpha4 subunit was later observed on the muscle masses of the limb, the apical ectodermal ridge, and the developing liver. To examine the functional role of the integrin alpha4 subunit in neural crest cell migration, we used an explant preparation that allows visualization of neural crest cells in their normal environment with or without perturbing reagents. In the presence of a blocking antibody against the mouse integrin alpha4 subunit, there was a profound abrogation of neural crest cell migration at trunk and hindbrain levels. Both the numbers of migrating neural crest cells and the total distance traversed were markedly reduced. Similarly, avian embryos injected with synthetic peptides that contain the integrin alpha4 binding site in fibronectin displayed abnormal neural crest cell migration. Our results suggest that the integrin alpha4 subunit is important for normal neural crest cell migration and may be one of the primary alpha subunits used for neural crest cell migration in vivo. Furthermore, the integrin alpha4 subunit represents a useful neural crest marker in the mouse.
我们确定整联蛋白的α4亚基是鸟类和鼠类胚胎中神经嵴细胞表达的主要整联蛋白。利用简并引物,我们获得了鸡整联蛋白α4亚基的PCR片段,随后用该片段克隆了全长亚基,其预测的氨基酸序列与人和小鼠的α4亚基有60%的同源性。原位杂交显示,鸡整联蛋白α4 mRNA在颅部和躯干部位迁移的神经嵴细胞以及神经嵴衍生的神经节中高水平表达。一种针对鼠α4亚基的抗体在小鼠中显示出与鸡相似的分布模式。除神经嵴细胞外,后来在肢体的肌肉块、顶端外胚层嵴和发育中的肝脏上也观察到了整联蛋白α4亚基。为了研究整联蛋白α4亚基在神经嵴细胞迁移中的功能作用,我们使用了一种外植体制备方法,该方法可以在有或没有干扰试剂的情况下,在正常环境中观察神经嵴细胞。在存在针对小鼠整联蛋白α4亚基的阻断抗体时,躯干部位和后脑部位的神经嵴细胞迁移受到了显著抑制。迁移的神经嵴细胞数量和总迁移距离都明显减少。同样,注射了含有纤连蛋白中整联蛋白α4结合位点的合成肽的鸟类胚胎,其神经嵴细胞迁移也出现异常。我们的结果表明,整联蛋白α4亚基对正常神经嵴细胞迁移很重要,可能是体内神经嵴细胞迁移所使用的主要α亚基之一。此外,整联蛋白α4亚基是小鼠中一种有用的神经嵴标记物。