Katow H
Exp Cell Res. 1986 Feb;162(2):401-10. doi: 10.1016/0014-4827(86)90345-9.
The primary mesenchyme cells (PMCs) were separated from the mesenchyme blastulae of Pseudocentrotus depressus using differential adhesiveness of these cells to plastic Petri dishes. These cells were incubated in various artificial extracellular matrices (ECMs) including horse serum plasma fibronectin, mouse EHS sarcoma laminin, mouse EHS sarcoma type IV collagen, and porcine skin dermatan sulfate. The cell behavior was monitored by a time-lapse videomicrograph and analysed with a microcomputer. The ultrastructure of the artificial ECM was examined by transmission electron microscopy (TEM), while the ultrastructure of the PMCs was examined by scanning electron microscopy (SEM). The PMCs did not migrate in type IV collagen gel, laminin or dermatan sulfate matrix either with or without collagen gel, whereas PMCs in the matrix which was composed of fibronectin and collagen gel migrated considerably. However, the most active and extensive PMC migration was seen in the matrix which contained dermatan sulfate in addition to fibronectin and collagen gel. This PMC migration involved an increase not only of migration speed but also of proportion of migration-promoted cells. These results support the hypothesis that the mechanism of PMC migration involves fibronectin, collagen and sulfated proteoglycans which contain dermatan sulfate.
利用原代间充质细胞(PMCs)对塑料培养皿的不同黏附性,从凹顶伪球海胆的间充质囊胚中分离出这些细胞。将这些细胞置于各种人工细胞外基质(ECM)中培养,包括马血清血浆纤连蛋白、小鼠EHS肉瘤层粘连蛋白、小鼠EHS肉瘤IV型胶原和猪皮硫酸皮肤素。通过延时视频显微镜监测细胞行为,并用微型计算机进行分析。通过透射电子显微镜(TEM)检查人工ECM的超微结构,而通过扫描电子显微镜(SEM)检查PMCs的超微结构。无论有无胶原凝胶,PMCs在IV型胶原凝胶、层粘连蛋白或硫酸皮肤素基质中均不迁移,而在由纤连蛋白和胶原凝胶组成的基质中的PMCs则有明显迁移。然而,在除纤连蛋白和胶原凝胶外还含有硫酸皮肤素的基质中,观察到PMCs最活跃且迁移范围最广。这种PMCs迁移不仅涉及迁移速度的增加,还涉及迁移促进细胞比例的增加。这些结果支持了以下假设:PMCs迁移的机制涉及纤连蛋白、胶原和含有硫酸皮肤素的硫酸化蛋白聚糖。