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A role for the polysialic acid - neural cell adhesion molecule in PDGF-induced chemotaxis of oligodendrocyte precursor cells

机译:唾液酸-神经细胞粘附分子在PDGF诱导的少突胶质前体细胞趋化中的作用

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Directed migration of oligodendrocyte precursor cells (OPCs) is important for myelin formation and repair but the mechanisms of directional control are poorly understood. Here we have tested the role of polysialic acid-neural cell adhesion molecule (PSA-NCAM) in the directional migration of OPCs towards platelet-derived growth factor (PDGF). Using a Boyden microchemotaxis chamber and the Dunn direct viewing chamber, we show that in concentration gradients of PDGF, PSA-positive OPCs polarize and efficiently migrate towards the source of PDGF (chemotaxis). The loss or inactivation of the polysialic tail of NCAM leads to an altered pattern of OPC migration in response to PDGF gradients. Cells under these conditions, while being polarized and migrating, show no bias of displacement towards the source of PDGF and make random turns. By contrast, directed migration of OPCs towards basic fibroblast growth factor was not affected by the removal of PSA. Moreover, inactivation of PSA does not interfere with the random migration pattern of cells in uniform concentrations of PDGF (chemokinesis). These results suggest that PSA-NCAM is specifically involved in establishing the directionality of OPC migration in response to the concentration gradient of PDGF, but it is not essential for cell motility per se.
机译:少突胶质细胞前体细胞(OPCs)的定向迁移对于髓磷脂的形成和修复很重要,但对方向控制的机制了解甚少。在这里,我们测试了唾液酸神经细胞粘附分子(PSA-NCAM)在OPC向血小板衍生生长因子(PDGF)定向迁移中的作用。使用Boyden微趋化室和Dunn直视室,我们显示在PDGF的浓度梯度中,PSA阳性OPC极化并有效地向PDGF的来源迁移(趋化)。 NCAM的多唾液酸尾的丧失或失活导致响应于PDGF梯度的OPC迁移模式改变。在这些条件下的细胞在极化和迁移的同时,没有表现出向PDGF来源位移的偏向,并且随机转弯。相比之下,去除PSA不会影响OPC向碱性成纤维细胞生长因子的定向迁移。此外,PSA的失活不会干扰PDGF浓度均匀的细胞的随机迁移模式(趋化作用)。这些结果表明,PSA-NCAM专门参与建立响应于PDGF浓度梯度的OPC迁移的方向性,但对于细胞运动本身并不是必需的。

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