A Structured Framework of Cytoskeletal Proteins and Non-centrosomal Microtubules Promote the Initiation and Elongation of Invadopodia.

IF 2.7 3区 生物学 Q3 CELL BIOLOGY
Mark Garewal, Pedro Ramos, Kenneth A Myers
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引用次数: 0

Abstract

Cancer deaths are largely attributed to the dissemination of cancer cells from a primary tumor to a secondary metastatic site. The metastatic cascade is initiated by cancer cell invasion that is facilitated by cytoskeletal remodeling to produce ventral cell protrusions, termed invadopodia, that degrade the extracellular matrix to promote motility. Conventional invadopodia studies rely on techniques with embedded cells in 3D matrices to observe and determine protein behavior, which often utilize immunolabeling strategies and struggle to visualize individual invadopodia, thereby limiting investigations of protein and invadopodia dynamics. Here, the design and utilization of an Axial Invasion Chamber is described for live-cell imaging of elongating invadopodia in 3D. Results identify that cytoskeletal and microtubule associated proteins within invadopodia exist in an organized framework, and determine the functional contribution by which non-centrosomal microtubules promote cancer cell invasion and migration. [Media: see text].

细胞骨架蛋白和非中心体微管的结构框架促进Invadopodia的起始和延伸。
癌症死亡主要归因于癌细胞从原发肿瘤扩散到继发转移部位。转移级联是由癌细胞侵袭引发的,细胞骨架重塑促进了癌细胞侵袭,产生腹侧细胞突起,称为浸润性突起,降解细胞外基质,促进运动。传统的侵过体研究依赖于将细胞嵌入3D基质中的技术来观察和确定蛋白质行为,这些技术通常使用免疫标记策略,难以可视化单个侵过体,从而限制了对蛋白质和侵过体动力学的研究。在这里,设计和利用轴向侵入室描述了活细胞成像的延长侵入足在三维。结果表明,细胞骨架蛋白和微管相关蛋白存在于一个有组织的框架中,并确定了非中心体微管促进癌细胞侵袭和迁移的功能贡献。[媒体:见文本]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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