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聚多巴胺界面涂层用于稳定的类器官芯片模型:在胰腺导管腺癌中的应用。

Polydopamine Interfacial Coating for Stable Tumor-on-a-Chip Models: Application for Pancreatic Ductal Adenocarcinoma.

机构信息

Multiscale in Mechanical & Biological Engineering Research Group, Aragon Institute of Engineering Research (I3A), School of Engineering and Architecture, University of Zaragoza, 50018 Zaragoza, Aragon, Spain.

Department of Biochemistry and Molecular and Cellular Biology, Faculty of Sciences, University of Zaragoza, 50009 Zaragoza, Aragon, Spain.

出版信息

Biomacromolecules. 2024 Aug 12;25(8):5169-5180. doi: 10.1021/acs.biomac.4c00551. Epub 2024 Jul 31.

Abstract

Addressing current challenges in solid tumor research requires advanced in vitro three-dimensional (3D) cellular models that replicate the inherently 3D architecture and microenvironment of tumor tissue, including the extracellular matrix (ECM). However, tumor cells exert mechanical forces that can disrupt the physical integrity of the matrix in long-term 3D culture. Therefore, it is necessary to find the optimal balance between cellular forces and the preservation of matrix integrity. This work proposes using polydopamine (PDA) coating for 3D microfluidic cultures of pancreatic cancer cells to overcome matrix adhesion challenges to sustain representative tumor 3D cultures. Using PDA's distinctive adhesion and biocompatibility, our model uses type I collagen hydrogels seeded with different pancreatic cancer cell lines, prompting distinct levels of matrix deformation and contraction. Optimizing the PDA coating enhances the adhesion and stability of collagen hydrogels within microfluidic devices, achieving a balance between the disruptive forces of tumor cells on matrix integrity and the maintenance of long-term 3D cultures. The findings reveal how this tension appears to be a critical determinant in spheroid morphology and growth dynamics. Stable and prolonged 3D culture platforms are crucial for understanding solid tumor cell behavior, dynamics, and responses within a controlled microenvironment. This advancement ultimately offers a powerful tool for drug screening, personalized medicine, and wider cancer therapeutics strategies.

摘要

解决当前实体瘤研究中的挑战需要先进的体外三维(3D)细胞模型,这些模型能够复制肿瘤组织固有的 3D 结构和微环境,包括细胞外基质(ECM)。然而,肿瘤细胞会产生机械力,从而在长期的 3D 培养中破坏基质的物理完整性。因此,有必要在细胞力和基质完整性的保护之间找到最佳平衡。本工作提出使用聚多巴胺(PDA)涂层来克服胰腺癌细胞 3D 微流控培养中的基质黏附挑战,以维持具有代表性的肿瘤 3D 培养。利用 PDA 的独特黏附性和生物相容性,我们的模型使用 I 型胶原水凝胶接种不同的胰腺癌细胞系,引发不同程度的基质变形和收缩。优化 PDA 涂层可增强胶原水凝胶在微流控装置中的黏附性和稳定性,在肿瘤细胞对基质完整性的破坏力和长期 3D 培养的维持之间取得平衡。研究结果揭示了这种张力如何成为球体形态和生长动力学的关键决定因素。稳定和长期的 3D 培养平台对于理解实体瘤细胞在受控微环境中的行为、动力学和反应至关重要。这一进展最终为药物筛选、个性化医疗和更广泛的癌症治疗策略提供了有力工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/790b/11323005/9c7746cb9358/bm4c00551_0001.jpg

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