在体内沿着自我生成的硬度梯度进行集体硬度测试
Adam Shellard1, Roberto Mayor2
1Department of Cell and Developmental Biology, University College London, London, UK.
Nature
|December 9, 2021
概括
胚胎细胞在Xenopus laevis中自我生成并通过硬度梯度,这是以前未被证明的体内过程. 这种机械指导与化学信号一起工作,
科学领域:
- 发育生物学
- 细胞生物学
- 生物物理
背景情况:
- 集体细胞迁移对于发育,愈合和疾病至关重要.
- 化学反应 (遵循化学梯度) 是指向细胞运动的已知机制.
- 在实验室中观察到硬度 (随着硬度梯度),但其在体内的相关性是未知的.
研究的目的:
- 在体内调查durotaxis的存在和机制.
- 确定胚胎细胞是否能够产生和响应基质刚度梯度.
- 了解机械和化学线索如何协作指导细胞迁移.
主要方法:
- 使用Xenopus laevis胚胎研究神经细胞迁移.
- 研究了神经细胞在斑点组织中自我生成的刚度梯度.
- 分析了细胞矩阵粘附,N-cadherin相互作用和下游信号通路 (Rac活性,actomyosin收缩性).
主要成果:
- 证明了Xenopus神经细胞在相邻组织中自行产生动态刚度梯度.
- 表明神经细胞通过遵循这种自我生成的刚度梯度 (durotaxis) 来朝向迁移.
- 发现durotaxis与化疗作用协同作用,通过协调的actomyosin活动增强集体细胞迁移.
结论:
- 提供了第一个在体内证据的durotaxis和动态基板刚度梯度.
- 已确定N-cadherin相互作用和细胞矩阵粘附介导渐变传感和反应.
- 结论是化学和机械线索在体内协同驱动有效的定向集体细胞迁移.
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