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成纤维细胞 EXT1 水平影响复合球体中的肿瘤细胞增殖和迁移。

Fibroblast EXT1-levels influence tumor cell proliferation and migration in composite spheroids.

机构信息

Department of Biomedicine, University of Bergen, Bergen, Norway.

出版信息

PLoS One. 2012;7(7):e41334. doi: 10.1371/journal.pone.0041334. Epub 2012 Jul 25.

Abstract

BACKGROUND

Stromal fibroblasts are important determinants of tumor cell behavior. They act to condition the tumor microenvironment, influence tumor growth, support tumor angiogenesis and affect tumor metastasis. Heparan sulfate proteoglycans, present both on tumor and stromal cells, interact with a large number of ligands including growth factors, their receptors, and structural components of the extracellular matrix. Being ubiquitously expressed in the tumor microenvironment heparan sulfate proteoglycans are candidates for playing central roles in tumor-stroma interactions. The objective of this work was to investigate the role of heparan sulfate expressed by stromal fibroblasts in modulating the growth of tumor cells and in controlling the interstitial fluid pressure in a 3-D model.

METHODOLOGY/PRINCIPAL FINDINGS: We generated spheroids composed of fibroblasts alone, or composite spheroids, composed of fibroblasts and tumor cells. Here we show that stromal fibroblasts with a mutation in the heparan sulfate elongating enzyme Ext1 and thus a low heparan sulfate content, formed composite fibroblast/tumor cell spheroids with a significant lower interstitial fluid pressure than corresponding wild-type fibroblast/tumor cell composite spheroids. Furthermore, immunohistochemistry of composite spheroids revealed that the cells segregated, so that after 6 days in culture, the wild-type fibroblasts formed an inner core and the tumor cells an outer layer of cells. For composite spheroids containing Ext1-mutated fibroblasts this segregation was less obvious, indicating impaired cell migration. Analysis of tumor cells expressing the firefly luciferase gene revealed that the changes in tumor cell migration in mutant fibroblast/tumor cell composite spheroids coincided with a lower proliferation rate.

CONCLUSIONS/SIGNIFICANCE: This is the first demonstration that stromal Ext1-levels modulate tumor cell proliferation and affect the interstitial fluid pressure in a 3-D spheroid model. Learning how structural changes in stromal heparan sulfate influence tumor cells is essential for our understanding how non-malignant cells of the tumor microenvironment influence tumor cell progression.

摘要

背景

基质成纤维细胞是肿瘤细胞行为的重要决定因素。它们作用于调节肿瘤微环境,影响肿瘤生长,支持肿瘤血管生成并影响肿瘤转移。硫酸乙酰肝素蛋白聚糖,存在于肿瘤细胞和基质细胞上,与包括生长因子、其受体和细胞外基质结构成分在内的大量配体相互作用。硫酸乙酰肝素蛋白聚糖在肿瘤微环境中广泛表达,是在肿瘤-基质相互作用中发挥核心作用的候选物。本工作的目的是研究基质成纤维细胞表达的硫酸乙酰肝素在调节肿瘤细胞生长和控制 3-D 模型中细胞间质压力中的作用。

方法/主要发现:我们生成了仅由成纤维细胞组成的球体,或由成纤维细胞和肿瘤细胞组成的复合球体。在这里,我们表明,具有硫酸乙酰肝素延长酶 Ext1 突变且因此硫酸乙酰肝素含量低的基质成纤维细胞,形成的复合成纤维细胞/肿瘤细胞球体的细胞间质压力明显低于相应的野生型成纤维细胞/肿瘤细胞复合球体。此外,复合球体的免疫组织化学显示细胞发生了分离,因此在培养 6 天后,野生型成纤维细胞形成了球体的内部核心,而肿瘤细胞形成了球体的外层细胞。对于包含 Ext1 突变成纤维细胞的复合球体,这种分离现象不太明显,表明细胞迁移受损。对表达萤火虫荧光素酶基因的肿瘤细胞的分析表明,在突变的成纤维细胞/肿瘤细胞复合球体中,肿瘤细胞迁移的变化与增殖率降低相一致。

结论/意义:这是首次证明基质 Ext1 水平调节肿瘤细胞增殖并影响 3-D 球体模型中的细胞间质压力。了解基质硫酸乙酰肝素结构变化如何影响肿瘤细胞对于我们理解肿瘤微环境中非恶性细胞如何影响肿瘤细胞进展至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbb/3405129/c563c11ac86f/pone.0041334.g001.jpg

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