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Migration of nerve growth cones requires detergent-resistant membranes in a spatially defined and substrate-dependent manner

机译:神经生长锥的迁移需要在空间上限定且依赖于底物的方式使用耐洗涤剂的膜

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摘要

Motility of nerve growth cones (GCs) is regulated by region-specific activities of cell adhesion molecules (CAMs). CAM activities could be modified by their localization to detergent-resistant membranes (DRMs), specialized microdomains enriched in signaling molecules. This paper deals with a question of whether DRMs are involved in GC migration stimulated by three CAMs; L1, N-cadherin (Ncad), and β1 integrin. We demonstrate that L1 and Ncad are present in DRMs, whereas β1 integrin is exclusively detected in non-DRMs of neurons and that localization of L1 and Ncad to DRMs is developmentally regulated. GC migration mediated by L1 and Ncad but not by β1 integrin is inhibited after DRM disruption by micro-scale chromophore-assisted laser inactivation (micro-CALI) of GM1 gangliosides or by pharmacological treatments that deplete cellular cholesterol or sphingolipids, essential components for DRMs. Characteristic morphology of GCs induced by L1 and Ncad is also affected by micro-CALI–mediated DRM disruption. Micro-CALI within the peripheral domain of GCs, or even within smaller areas such as the filopodia and the lamellipodia, is sufficient to impair their migration. However, micro-CALI within the central domain does not affect GC migration. These results demonstrate the region-specific involvement of DRMs in CAM-dependent GC behavior.
机译:神经生长锥(GCs)的运动受细胞粘附分子(CAMs)的区域特定活动调节。可以通过将CAM活性定位于去污剂抗性膜(DRM)(富含信号分子的专门微域)来进行修饰。本文讨论了一个问题,即DRM是否参与了由三个CAM刺激的GC迁移? L1,N-钙粘蛋白(Ncad)和β1整联蛋白。我们证明L1和Ncad存在于DRM中,而β1整联蛋白仅在神经元的非DRM中检测到,并且L1和Ncad到DRM的定位受到发育调节。在DRM破坏后,通过GM1神经节苷脂的微型生色团辅助激光灭活(micro-CALI)或通过消耗细胞胆固醇或鞘脂的药物治疗,抑制了L1和Ncad介导但不受β1整联蛋白介导的GC迁移。由L1和Ncad诱导的GC的特征形态也受到微CALI介导的DRM破坏的影响。 GC外围区域内的Micro-CALI,或什至在丝状伪足和片状脂质体之类的较小区域内,都足以削弱它们的迁移。但是,中央域内的micro-CALI不会影响GC迁移。这些结果表明DRMs在CAM依赖GC行为中的区域特定参与。

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