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建立背根神经节培养的体外模型:研究癌症与神经串扰的互补方法。

Establishing In Vitro Models of Dorsal Root Ganglia Culture: Complementary Approaches for Investigating Cancer-Nerve Crosstalk.

作者信息

Oliveira Larissa C B, Pereira Erica R, Hyndman Brandy D, Thomson Bryanna, Serpeloni Juliana M, Mulligan Lois M

机构信息

Division of Cancer Biology and Genetics, Sinclair Cancer Research Institute, and Department of Pathology and Molecular Medicine, Queen's University.

Division of Cancer Biology and Genetics, Sinclair Cancer Research Institute, and Department of Pathology and Molecular Medicine, Queen's University; Laboratory of Mutagenesis and Oncogenetics, Department of General Biology - Center for Biological Science, State University of Londrina.

出版信息

J Vis Exp. 2025 Jul 11(221). doi: 10.3791/68552.

Abstract

The contribution of the nervous system to the tumor microenvironment and the importance of neural invasion as a route for cancer dissemination are being increasingly recognized. Interactions of cancer cells with neurons can promote their invasion around and into nerves, a feature of many cancers with poor clinical outcomes. In vitro models to study reciprocal interactions between neurons and cancer cells provide valuable tools for understanding cancer spread and identifying approaches to mitigate it. Here, we describe a protocol for murine dorsal root ganglia (DRG) isolation and the establishment of both whole mount and dissociated monolayer cultures that can be used to visualize neuron morphology and neurite outgrowth over time. Whole DRGs mounted in Matrigel preserve nerve architecture and responses to stimuli in a heterogeneous environment more similar to the in vivo nerve, while dissociated nerve cultures allow assessment of direct cell-cell interactions more closely. Once DRG cultures are established, cancer cells can be added to generate co-cultures that can be used to visualize changes in neurite outgrowth and nerve morphology in response to cancer cells. Growth or motility of cancer cells in response to nerve-derived signals over time or under conditions of growth stimulation or inhibition can be assessed, as well as visualizing the effects of direct contact between cancer cells and nerve extensions. As both co-culture models can be generated simultaneously, this protocol provides a more comprehensive view of the impact of cancer-neuron interactions and facilitates comparisons of treatment conditions and integration of information from the cellular level and whole ganglia. This protocol will facilitate the study of nerve-tumor interactions and can be used for a wide range of applications, including studies of cell signaling, drug screening, or study of the heterogeneity of the tumor-nerve environment and the mechanisms of tumor dissemination along nerves.

摘要

神经系统对肿瘤微环境的贡献以及神经侵袭作为癌症传播途径的重要性正日益得到认可。癌细胞与神经元的相互作用可促进其在神经周围及进入神经的侵袭,这是许多临床预后不良的癌症的一个特征。用于研究神经元与癌细胞之间相互作用的体外模型为理解癌症扩散及确定减轻扩散的方法提供了有价值的工具。在此,我们描述了一种小鼠背根神经节(DRG)分离及建立整装和分离单层培养物的方案,可用于随时间观察神经元形态和神经突生长。安装在基质胶中的完整DRG在更类似于体内神经的异质环境中保留神经结构和对刺激的反应,而分离的神经培养物则更便于评估直接的细胞 - 细胞相互作用。一旦建立了DRG培养物,就可以添加癌细胞以生成共培养物,用于观察神经突生长和神经形态因癌细胞而发生的变化。可以评估癌细胞随时间或在生长刺激或抑制条件下对神经源性信号的生长或运动反应,以及观察癌细胞与神经延伸之间直接接触的影响。由于两种共培养模型可以同时生成,该方案提供了对癌症 - 神经元相互作用影响的更全面视图,并有助于比较治疗条件以及整合细胞水平和整个神经节的信息。该方案将促进神经 - 肿瘤相互作用的研究,并可用于广泛的应用,包括细胞信号传导研究、药物筛选或肿瘤 - 神经环境异质性及肿瘤沿神经扩散机制的研究。

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