...
首页> 外文期刊>Kurume Medical Journal >Surface Charge of Fractionated Guinea Pig Keratinocytes Measured by Free-flow Cell Electrophoresis
【24h】

Surface Charge of Fractionated Guinea Pig Keratinocytes Measured by Free-flow Cell Electrophoresis

机译:自由流动细胞电泳测量豚鼠角质形成细胞的表面电荷

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Keratinocytes differentiate from basal cells to spinous, granular, and horny layer cells. It is known that alterations in the surface charge of cell membranes in most cases reflect the processes of differentiation. By using a continuous colloidal silica (Percoll) density gradient, keratinocytes may be separated into three fractions which correspond to their arrangement in vivo. Using a free-flow cell electrophoretic technique, we measured the electrophoretic mobility of guinea pig keratinocytes. Electrophoretic mobility histograms of basal and granular cells showed slow and fast monophasic patterns, respectively. In spinous cells, a biphasic pattern of slow and fast electrophoretc mobility was present. The electrophoretic mobility level of guinea pig keratinocytes was slightly reduced with neuraminidase digestion. Those of human red blood cells and lymphocytes, however, were markedly decreased. These results indicate that membrane charge density is lower in basal cells and higher in granular cells and that the membrane charge density of guinea pig keratinocytes involves not only neuraminic acid residues but also other substance (s). Our results illustrate the alterations of cell membrane charge properties during epidermal cell differentiation.
机译:角质形成细胞从基底细胞分化为棘突,颗粒和角质层细胞。众所周知,大多数情况下细胞膜表面电荷的变化反映了分化过程。通过使用连续的胶体二氧化硅(Percoll)密度梯度,可以将角质形成细胞分为三个部分,这三个部分与它们在体内的排列相对应。使用自由流动的细胞电泳技术,我们测量了豚鼠角质形成细胞的电泳迁移率。基底细胞和颗粒细胞的电泳迁移率直方图分别显示缓慢和快速的单相模式。在棘细胞中,存在缓慢和快速电泳等迁移率的两相模式。神经氨酸酶消化后,豚鼠角质形成细胞的电泳迁移率水平略有降低。然而,人红细胞和淋巴细胞的那些明显减少。这些结果表明,基底细胞中的膜电荷密度较低,而粒状细胞中的膜电荷密度较高,并且豚鼠角质形成细胞的膜电荷密度不仅涉及神经氨酸残基,还涉及其他物质。我们的结果说明了表皮细胞分化过程中细胞膜电荷性质的变化。

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