3D mapping of native extracellular matrix reveals cellular responses to the microenvironment

IF 3.5 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Structural Biology: X Pub Date : 2019-01-01 DOI:10.1016/j.yjsbx.2018.100002
Zipora Lansky , Yael Mutsafi , Lothar Houben , Tal Ilani , Gad Armony , Sharon G. Wolf , Deborah Fass
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引用次数: 18

Abstract

Cells and extracellular matrix (ECM) are mutually interdependent: cells guide self-assembly of ECM precursors, and the resulting ECM architecture supports and instructs cells. Though bidirectional signaling between ECM and cells is fundamental to cell biology, it is challenging to gain high-resolution structural information on cellular responses to the matrix microenvironment. Here we used cryo-scanning transmission electron tomography (CSTET) to reveal the nanometer- to micron-scale organization of major fibroblast ECM components in a native-like context, while simultaneously visualizing internal cell ultrastructure including organelles and cytoskeleton. In addition to extending current models for collagen VI fibril organization, three-dimensional views of thick cell regions and surrounding matrix showed how ECM networks impact the structures and dynamics of intracellular organelles and how cells remodel ECM. Collagen VI and fibronectin were seen to distribute in fundamentally different ways in the cell microenvironment and perform distinct roles in supporting and interacting with cells. This work demonstrates that CSTET provides a new perspective for the study of ECM in cell biology, highlighting labeled extracellular elements against a backdrop of unlabeled but morphologically identifiable cellular features with nanometer resolution detail.

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原生细胞外基质的三维映射揭示了细胞对微环境的反应
细胞和细胞外基质(ECM)是相互依赖的:细胞引导ECM前体的自组装,由此产生的ECM结构支持和指导细胞。虽然ECM和细胞之间的双向信号传导是细胞生物学的基础,但获得细胞对基质微环境反应的高分辨率结构信息是具有挑战性的。在这里,我们使用低温扫描透射电子断层扫描(CSTET)在原生环境中揭示了主要成纤维细胞ECM成分的纳米到微米级组织,同时可视化了细胞内部的超微结构,包括细胞器和细胞骨架。除了扩展胶原VI原纤维组织的现有模型外,厚细胞区域和周围基质的三维视图显示了ECM网络如何影响胞内细胞器的结构和动力学以及细胞如何重塑ECM。胶原VI和纤维连接蛋白在细胞微环境中的分布方式完全不同,在支持细胞和与细胞相互作用方面发挥着不同的作用。这项工作表明,CSTET为细胞生物学中ECM的研究提供了一个新的视角,突出标记的细胞外元件,而不是未标记但形态可识别的细胞特征,具有纳米分辨率细节。
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
Journal of Structural Biology: X
Journal of Structural Biology: X Biochemistry, Genetics and Molecular Biology-Structural Biology
CiteScore
6.50
自引率
0.00%
发文量
20
审稿时长
62 days
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