Greenberg J H, Pratt R M
Cell Differ. 1977 Aug;6(2):119-32. doi: 10.1016/0045-6039(77)90034-3.
In the developing chick embryo, cranial neural crest cells, that will subsequently give rise to facial mesenchyme tissues, migrate beneath the surface ectoderm in a cell-free and hyaluronate-rich matrix. To determine how the crest cells could contribute to this matrix, we cultured crest cells from stage 9 embryos for 2 days and then labeled them for 18--20 h with various precursors of glycosaminoglycans (GAG) and glycoproteins. [3H]fucose and [3H]glucosamine were incorporated into Pronase-sensitive macromolecules associated with the cell layer, but little labeled glycoprotein was released into the medium. Hyaluronate was the major GAG synthesized and was distributed between the cells and medium. Less chondroitin-sulfate was synthesized. In comparison, older cultures as well as fibroblasts produced different proportions of GAG. Our results confirm the autoradiographic findings of Pratt et al. (1975) and suggest that crest cells may contribute GAG to the matrix during migration.
在发育中的鸡胚中,随后将形成面部间充质组织的颅神经嵴细胞在无细胞且富含透明质酸的基质中于表面外胚层下方迁移。为了确定嵴细胞如何对这种基质产生影响,我们将第9阶段胚胎的嵴细胞培养2天,然后用各种糖胺聚糖(GAG)和糖蛋白的前体对其进行18 - 20小时的标记。[3H]岩藻糖和[3H]葡萄糖胺被掺入与细胞层相关的对链霉蛋白酶敏感的大分子中,但很少有标记的糖蛋白释放到培养基中。透明质酸是合成的主要GAG,并分布于细胞和培养基之间。硫酸软骨素的合成较少。相比之下,较老的培养物以及成纤维细胞产生不同比例的GAG。我们的结果证实了普拉特等人(1975年)的放射自显影结果,并表明嵴细胞在迁移过程中可能为基质贡献GAG。