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在三维自组装肽支架中培养的胰腺癌细胞中,硬度增加下调粘着斑激酶表达。

Increased Stiffness Downregulates Focal Adhesion Kinase Expression in Pancreatic Cancer Cells Cultured in 3D Self-Assembling Peptide Scaffolds.

作者信息

Betriu Nausika, Andreeva Anna, Alonso Anna, Semino Carlos E

机构信息

Tissue Engineering Research Laboratory, Department of Bioengineering, IQS-School of Engineering, Ramon Llull University, 08017 Barcelona, Spain.

出版信息

Biomedicines. 2022 Jul 29;10(8):1835. doi: 10.3390/biomedicines10081835.

Abstract

The focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that participates in integrin-mediated signal transduction and contributes to different biological processes, such as cell migration, survival, proliferation and angiogenesis. Moreover, FAK can be activated by autophosphorylation at position Y397 and trigger different signaling pathways in response to increased extracellular matrix stiffness. In addition, FAK is overexpressed and/or hyperactivated in many epithelial cancers, and its expression correlates with tumor malignancy and invasion potential. One of the characteristics of solid tumors is an over deposition of ECM components, which generates a stiff microenvironment that promotes, among other features, sustained cell proliferation and survival. Researchers are, therefore, increasingly developing cell culture models to mimic the increased stiffness associated with these kinds of tumors. In the present work, we have developed a new 3D in vitro model to study the effect of matrix stiffness in pancreatic ductal adenocarcinoma (PDAC) cells as this kind of tumor is characterized by a desmoplastic stroma and an increased stiffness compared to its normal counterpart. For that, we have used a synthetic self-assembling peptide nanofiber matrix, RAD16-I, which does not suffer a significant degradation in vitro, thus allowing to maintain the same local stiffness along culture time. We show that increased matrix stiffness in synthetic 3D RAD16-I gels, but not in collagen type I scaffolds, promotes FAK downregulation at a protein level in all the cell lines analyzed. Moreover, even though it has classically been described that stiff 3D matrices promote an increase in pFAK/FAK proteins, we found that this ratio in soft and stiff RAD16-I gels is cell-type-dependent. This study highlights how cell response to increased matrix stiffness greatly depends on the nature of the matrix used for 3D culture.

摘要

粘着斑激酶(FAK)是一种非受体酪氨酸激酶,参与整合素介导的信号转导,并促成不同的生物学过程,如细胞迁移、存活、增殖和血管生成。此外,FAK可在Y397位点通过自身磷酸化被激活,并在细胞外基质硬度增加时触发不同的信号通路。另外,FAK在许多上皮癌中过表达和/或过度激活,其表达与肿瘤恶性程度和侵袭潜力相关。实体瘤的特征之一是细胞外基质(ECM)成分过度沉积,这会产生一个坚硬的微环境,除其他特征外,还能促进细胞持续增殖和存活。因此,研究人员越来越多地开发细胞培养模型来模拟与这类肿瘤相关的硬度增加。在本研究中,我们开发了一种新的三维体外模型,以研究基质硬度对胰腺导管腺癌(PDAC)细胞的影响,因为这类肿瘤的特征是促纤维增生性基质,且与其正常对应物相比硬度增加。为此,我们使用了一种合成的自组装肽纳米纤维基质RAD16-I,它在体外不会发生显著降解,从而能够在培养过程中保持相同的局部硬度。我们发现,合成的三维RAD16-I凝胶而非I型胶原支架中基质硬度的增加,会促使所有分析的细胞系中FAK在蛋白水平下调。此外,尽管传统上认为坚硬的三维基质会促使pFAK/FAK蛋白增加,但我们发现软质和硬质RAD16-I凝胶中的这一比例因细胞类型而异。这项研究突出了细胞对基质硬度增加的反应如何在很大程度上取决于用于三维培养的基质的性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93d4/9405295/e19fb1174cd4/biomedicines-10-01835-g001.jpg

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