Rosen D M, Stempien S A, Thompson A Y, Brennan J E, Ellingsworth L R, Seyedin S M
Exp Cell Res. 1986 Jul;165(1):127-38. doi: 10.1016/0014-4827(86)90538-0.
The role of cell shape in chondrogenesis was studied by using rat mesenchymal cells cultured with cartilage-inducing factor (CIF). Here we report that enhanced expression of chondroblastic markers by induced cells was attained by culturing cells in monolayer in the presence of dihydrocytochalasin B (DHCB). This effect was optimal at 3 microM DHCB and was apparent after 3 days in culture. Mesenchymal cells cultured with DHCB alone exhibited no detectable increase in cartilage proteoglycan synthesis, whereas cells cultured with 3 microM DHCB and 0.1 nM CIF showed a 4-5 fold increase in proteoglycan synthesis. When cells were cultured with CIF alone on plastic, only small increases in proteoglycan synthesis were observed. Cells cultured with CIF in monolayer and then transferred to a permissive environment (either agarose or cultured with DHCB) showed enhanced synthesis of chondroblastic proteins. These results suggest that expression, but not induction, of a chondroblastic phenotype by CIF is inhibited by growth in monolayer. The altering of cell shape with DHCB releases that inhibition.
通过使用与软骨诱导因子(CIF)一起培养的大鼠间充质细胞,研究了细胞形状在软骨形成中的作用。在此我们报告,通过在二氢细胞松弛素B(DHCB)存在下将细胞单层培养,诱导细胞的成软骨细胞标志物表达增强。这种效应在3 microM DHCB时最为显著,培养3天后即可显现。单独用DHCB培养的间充质细胞未显示出软骨蛋白聚糖合成有可检测到的增加,而用3 microM DHCB和0.1 nM CIF培养的细胞蛋白聚糖合成增加了4至5倍。当细胞单独在塑料上用CIF培养时,仅观察到蛋白聚糖合成有小幅增加。在单层中用CIF培养然后转移到允许环境(琼脂糖或用DHCB培养)中的细胞显示出成软骨细胞蛋白的合成增强。这些结果表明,单层生长抑制了CIF对成软骨细胞表型的表达而非诱导。用DHCB改变细胞形状可解除这种抑制。