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首页> 外文期刊>Seminars in cell and developmental biology >Cadherin-11 promotes neural crest cell spreading by reducing intracellular tension-Mapping adhesion and mechanics in neuralcrest explants by atomic force microscopy
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Cadherin-11 promotes neural crest cell spreading by reducing intracellular tension-Mapping adhesion and mechanics in neuralcrest explants by atomic force microscopy

机译:通过原子力显微镜通过减少神经系统外植体的细胞内张力测绘粘附和力学来促进神经嵴细胞扩散

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During development cranial neural crest cells (NCCs) display a striking transition from collective to single cell migration, but the mechanisms enabling individual NCCs to separate from the neural crest tissue are still incompletely understood. In this study we have employed atomic force microscopy (AFM) to investigate potential adhesive and mechanical changes associated with the dissociation of individual cells from cohesive Xenopus NCC explants at early stages of migration. AFM-based single-cell force spectroscopy (SCFS) revealed a uniform distribution of cell-cell adhesion forces within NCC explants, including semi-detached leader cells in the process of delaminating from the explant edge. This suggested that dissociation from the cell sheet may not require prior weakening of cell-cell contacts. However, mapping NCC sheet elasticity by AFM microbead indentation demonstrated strongly reduced cell stiffness in semi-detached leader cells compared to neighbouring cells in the NCC sheet periphery. Reduced leader cell stiffness coincided with enhanced cell spreading and high substrate traction, indicating a possible mechano-regulation of leader cell delamination. In support, AFM elasticity measurements of individual NCCs in optical side view mode demonstrated that reducing cell tension by inhibiting actomyosin contractility induces rapid spreading, possibly maximizing cell-substrate interactions as a result. Depletion of cadherin-11, a classical cadherin with an essential role in NCC migration and substrate adhesion, prevented the tension reduction necessary for NCC spreading, both in individual cells and at the edge of explanted sheets. In contrast, overexpression of cadherin-11 accelerated spreading of both individual cells and delaminating leader cells. As cadherin-11 expression increases strongly during NCC migration, this suggests an important role of cadherin-11 in regulating NCC elasticity and spreading at later stages of NCC migration. We therefore propose a mo
机译:在开发期间,颅神经顶部细胞(NCC)显示从集体到单细胞迁移的醒目过渡,但是使单独的NCC与神经顶部组织分离的机制仍然不完全理解。在这项研究中,我们使用了原子力显微镜(AFM)来研究与在迁移的早期阶段的粘性外爪蟾植体的单个细胞的解离潜在的粘合剂和机械变化。基于AFM的单细胞力光谱(SCFS)揭示了NCC外植体内细胞 - 细胞粘附力的均匀分布,包括在从外植入边缘分层的分层过程中的半脱离的前导细胞。这表明来自细胞片的解离可能在细胞 - 细胞触点的先前弱化。然而,与AFM微臂压痕的映射NCC片弹性在与NCC片外围中的相邻单元相比,半分离的领导单元中的细胞刚度明显降低。减少的引导池刚度与增强的电池扩散和高衬底牵引力一致,表明领导细胞分层的可能机械调节。在载体中,光学侧视图模式中的单个NCCs的AFM弹性测量表明,通过抑制肌动酶收缩性降低细胞张力,诱导迅速扩散,可能最大化细胞基底相互作用。钙粘蛋白-11的耗尽,一种具有基本作用的古典钙粘蛋白,具有在NCC迁移和基材粘附中的基本作用,防止了NCC散布所需的张力减少,无论是个单个细胞和涂抹片的边缘。相反,钙粘蛋白-11的过度表达肠蛋白-11加速展开单个细胞和分层前导细胞的扩散。随着在NCC迁移期间钙粘蛋白-11表达强烈增加,这表明Cadherin-11在调节NCC弹性和在NCC迁移的后期扩散的重要作用。因此,我们提出了一个莫

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