Sieber-Blum M, Cohen A M
J Cell Biol. 1978 Mar;76(3):628-38. doi: 10.1083/jcb.76.3.628.
To examine possible changes in cell surface carbohydrates, fluorescent lectins were applied at various times during differentiation of neural crest cells in vitro. The pattern and intensity of binding of several lectins changed as the crest cells developed into melanocytes and adrenergic cells. Considerable amounts of concanavalin A (Con A) and wheat germ agglutinin (WGA) bound to all unpigmented cells throughout the culture period. Melanocytes, however, bound much less of these lectins. Soy bean agglutinin (SBA), unlike Con A and WGA, only bound later in development to unpigmented cells at about the time when catecholamines were detected histochemically. Binding of SBA could be induced in younger cultures by pretreating the cells with neuraminidase. Melanocytes, however, did not bind detectable amounts of SBA even if treated with neuraminidase. The SBA-binding sites were often concentrated on cytoplasmic extensions and on contact points between neighboring cells, even when receptor mobility was restricted by prefixation of the cells or adsorption of lectin at 0 degrees C. All three lectins bound to cell processes resembling nerve fibers in particularly high amounts.
为了检测细胞表面碳水化合物可能发生的变化,在体外神经嵴细胞分化的不同时间应用了荧光凝集素。随着嵴细胞发育成黑素细胞和肾上腺素能细胞,几种凝集素的结合模式和强度发生了变化。在整个培养期间,大量的伴刀豆球蛋白A(Con A)和麦胚凝集素(WGA)与所有未着色的细胞结合。然而,黑素细胞与这些凝集素的结合要少得多。与Con A和WGA不同,大豆凝集素(SBA)仅在发育后期大约在组织化学检测到儿茶酚胺时才与未着色的细胞结合。通过用神经氨酸酶预处理细胞,可以在较年轻的培养物中诱导SBA的结合。然而,即使经过神经氨酸酶处理,黑素细胞也不会结合可检测量的SBA。即使细胞的受体流动性因细胞预固定或在0℃下吸附凝集素而受到限制,SBA结合位点也常常集中在细胞质延伸部分和相邻细胞之间的接触点上。所有三种凝集素都特别大量地与类似神经纤维的细胞突起结合。