基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
英文原题:Analysis of EMT induction in a non-invasive breast cancer cell line by mesenchymal stem cell supernatant: Study of 2D and 3D microfluidic based aggregate formation and migration ability, and cytoskeleton remodeling.
Analysis of EMT induction in a non-invasive breast cancer cell line by mesenchymal stem cell supernatant: Study of 2D and 3D microfluidic based aggregate formation and migration ability, and cytoskeleton remodeling.
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上皮-间质转化(EMT)是细胞获得侵袭性表型的转变过程,其机制和影响因素正受到广泛研究。将人脂肪来源间充质干细胞(hADMSC)上清液用于非侵袭性癌细胞,是一种常用的体外诱导EMT样过程的方法。既往研究主要关注hADMSC上清液通过不同蛋白质和基因表达影响细胞生化信号通路的作用;本研究则考察其潜在促癌性物理力学变化,包括三维微环境中的细胞运动性和聚集体形成变化,以及细胞骨架肌动蛋白-肌球蛋白含量和纤维排列。主要方法:采用饥饿培养48小时的hADMSC上清液处理MCF-7癌细胞,并评估波形蛋白/E-钙黏蛋白表达。通过聚集体形成和迁移能力,测定并比较处理与未处理细胞的侵袭潜能。此外,还研究细胞及细胞核形态变化,并检测F-肌动蛋白和肌球蛋白II的含量和排列改变。主要发现:结果表明,hADMSC上清液增强了EMT生物标志物波形蛋白表达,并通过提高细胞运动性和降低聚集体形成,增强非侵袭性癌细胞的侵袭潜能,从而产生促癌效应;同时还伴随肌动蛋白结构重排、应力纤维增多及肌球蛋白II增加,进而提高细胞运动性和牵引力。
间充质干细胞上清液在体外诱导EMT时,可通过细胞骨架重塑影响癌细胞的生物物理特征,凸显癌症进展和侵袭过程中化学与物理信号通路的联系。这些结果加深了对EMT过程以及促成该过程的生化与生物物理参数协同作用的理解,并最终有助于改进癌症治疗策略。
AIMS: The process of Epithelial-to-mesenchymal transition (EMT) as a phenotypic invasive shift and the factors affecting it, are under extensive research. Application of supernatants of human adipose-derived mesenchymal stem cells (hADMSCs) on non-invasive cancer cells is a well known method of in vitro induction of EMT like process.
While previous researches have focused on the effects of hADMSCs supernatant on the biochemical signaling pathways of the cells through expression of different proteins and genes, we investigated pro-carcinogic alterations of physico-mechanical cues in terms of changes in cell motility and aggregated formation in 3D microenvironments, and cytoskeletal actin-myosin content and fiber arrangement.
MAIN METHODS: MCF-7 cancer cells were treated by the supernatant from 48 hour-starved hADMSCs, and their vimentin/E-cadherin expressions were evaluated. The invasive potential of treated and non-treated cells was measured and compared through aggregate formation and migration capability.
Furthermore, alterations in cell and nucleus morphologies were studied, and F-actin and myosin-II alterations in terms of content and arrangement were investigated. KEY FINDINGS: Results indicated that application of hADMSCs supernatant enhanced vimentin expression as the biomarker of EMT, and induced pro-carcinogenic effects on non-invasive cancer cells through increased invasive potential by higher cell motility and reduced aggregate formation, rearrangement of actin structure and generation of more stress fibers, together with increased myosin II that lead to enhanced cell motility and traction force.
SIGNIFICANCE: Our results indicated that in vitro induction of EMT through mesenchymal supernatant influenced biophysical features of cancer cells through cytoskeletal remodeling that emphasizes the interconnection of chemical and physical signaling pathways during cancer progress and invasion. Results give a better insight to EMT as a biological process and the synergy between biochemical and biophysical parameters that contribute to this process, and eventually assist in improving cancer treatment strategies.
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