首页> 外文期刊>Development Growth and Differentiation >Rapid patterning in 2-D cultures of Dictyostelium cells and its relationship to zonal differentiation
【24h】

Rapid patterning in 2-D cultures of Dictyostelium cells and its relationship to zonal differentiation

机译:Dictyostelium细胞的二维培养中的快速模式及其与区域分化的关系

获取原文
获取原文并翻译 | 示例
           

摘要

Rapid patterning has been observed in confined 2-D cultures of Dictyostelium discoideum Ax-2 cells as an outer dark zone and a inner light zone. The width of outer zone was usually ~100 #mu#m, irrespective of the size of cell masses under atmospheric conditions. The width of the outer zone, however, changed depending on external 0_2 concentrations and reached up to 250 #mu#m at 100% 0_2. A clear regional difference in tetramethyl rhodamine methyl ester (TMRM) staining was noticed between the outer zone and the inner zone: the inner zone was more strongly stained with TMRM than the outer zone, which faced the air. Using inhibitors of oxidative phosphorylation (dinitrophenol (DNP) or NaN_3) and a specific inhibitor of CN-resistant respiration (benzohydroxamic acid (BHAM)), it has been demonstrated that the outer zone is basically formed by the 0_2 threshold for oxidative phosphorylation, while the inner cells mainly perform cyanide-resistant respiration. When cells around the early mound stage (just before prestalk and prespore differentiation) were cultured as 2-D cell masses, ecmA-expressing cells (pstA cells), ecmB-expressing cells (pstB cells) and D19-expressing cells (prespore; psp cells), arose in a position-dependent manner in the outer zone. In the inner zone, cell motility seemed to be markedly impaired and neither prestalk nor prespore differentiation occurred. In addition, oncedifferentiated prespore cells were found to dedifferentiate rapidly in the inner zone. The reason for dedifferentiation as well as for failure of cells to differentiate in the inner zone is discussed with reference to 0_2 radicals.
机译:已在Disctyostelium discoideum Ax-2细胞的受限2-D培养物中观察到快速图案化,即外部暗区和内部亮区。不论大气条件下细胞团的大小如何,外部区域的宽度通常约为100#mu#m。但是,外部区域的宽度根据外部0_2浓度而变化,在100%0_2时达到250#mu#m。在外部区域和内部区域之间发现四甲基若丹明甲酯(TMRM)染色存在明显的区域差异:内部区域比面对空气的外部区域更易被TMRM染色。使用氧化磷酸化抑制剂(二硝基苯酚(DNP)或NaN_3)和抗CN呼吸的特异性抑制剂(苯并异羟肟酸(BHAM)),已证明外部区域基本上由氧化磷酸化的0_2阈值形成,而内部细胞主要进行抗氰化物呼吸。当将堆丘早期(前茎和芽孢分化之前)的细胞培养成二维细胞团时,表达ecmA的细胞(pstA细胞),表达ecmB的细胞(pstB细胞)和表达D19的细胞(prespore; psp)细胞)在外部区域中以位置相关的方式出现。在内部区域,细胞运动似乎受到明显损害,并且未发生前茎或孢子分化。此外,发现曾经分化的孢子细胞在内部区域迅速去分化。参照0_2基团讨论了去分化的原因以及细胞在内部区域的分化失败的原因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号