Collard J G, Temmink J H
J Cell Sci. 1975 Oct;19(1):21-32. doi: 10.1242/jcs.19.1.21.
Calculations of the density of Concanavalin A (Con A)-binding sites on normal and transformed fibroblasts have, as yet, been based on the unproven assumption that suspended cells are smooth spheres. We studied the surface morphology of suspended normal and transformed fibroblasts with scanning and transmission electron microscopes, and found a large difference in surface morphology between suspended normal and transformed 3T3 cells. When this difference in surface morphology was taken into account, the estimated cell surface area of normal 3T3 cells was approximately seven times larger than that of transformed 3T3 cells. Since equal numbers of 3H-Con A molecules are bound on normal and transformed cells, the density of Con A-binding sites is approximately seven times greater on transformed than on normal 3T3 cells. The difference in density of Con A-binding sites between normal and transformed fibroblasts might be sufficient to explain the difference in agglutination response, as originally suggested by Burger, and may also be the cause of the different degrees of clustering of Con A-binding sites on the plasma membrane of these cells.
迄今为止,对正常和成纤维细胞上伴刀豆球蛋白A(Con A)结合位点密度的计算是基于悬浮细胞为光滑球体这一未经证实的假设。我们用扫描电子显微镜和透射电子显微镜研究了悬浮的正常和成纤维细胞的表面形态,发现悬浮的正常3T3细胞和转化的3T3细胞在表面形态上有很大差异。当考虑到这种表面形态的差异时,正常3T3细胞的估计细胞表面积大约是转化3T3细胞的七倍。由于正常细胞和转化细胞上结合的3H-Con A分子数量相等,Con A结合位点的密度在转化的3T3细胞上大约比正常3T3细胞大七倍。正常和成纤维细胞之间Con A结合位点密度的差异可能足以解释最初由伯格提出的凝集反应差异,也可能是这些细胞质膜上Con A结合位点不同程度聚集的原因。