扫描声学显微镜在智能探针评估多种癌细胞中MMP激活的应用。

Hasan Ozan Otaş, Nasire Uluç, İrem Demirkan, Aylin Alkan, Açelya Yilmazer, Seda Yaşa, Davod Khalafkhany, Nesrin Özören, Mehmet Burçin Ünlü
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引用次数: 0

摘要

背景/目的:基质金属蛋白酶(Matrix metalloproteinases, MMPs)在多种癌症类型的评估中发挥着重要作用;然而,检测通常会带来挑战。为了更好地了解MMPs在病理生理中的基本作用,还需要进一步的分析。我们的目的是在扫描声学显微镜(SAM)中使用可激活探针来评估探针是否可以帮助可视化体外MMP活性的效果。材料和方法:我们应用扫描声阻抗显微镜获得HT1080、THP-1和SK-MEL-28细胞系模型在MMPSense 680探针孵育和不孵育时的声阻抗图。我们使用共聚焦激光扫描显微镜成像视觉验证了我们的结果。我们进一步分析了MMPSense 680探针对细胞活力的影响,以消除任何伪影。结果:这是第一个通过声阻抗测量来展示SAM在细胞介质中MMPSense 680探针劈裂声学评估中的适用性的研究。我们提出用可激活探针测量SAM可以作为研究细胞系中MMP活性的声学变化的有效工具。结果,我们在HT1080人纤维肉瘤细胞系中检测到MMPSense 680探针的分裂。结论:通过声阻抗测量,我们发现带有智能探针的SAM可以检测体外HT1080细胞株的MMPSense 680蛋白水解活性。SAM可以作为一种替代工具,在临床设置之前更好地了解MMPs在癌症进展中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Application of scanning acoustic microscopy for evaluation of MMP activation in multiple cancer cell lines with a smart probe.

Application of scanning acoustic microscopy for evaluation of MMP activation in multiple cancer cell lines with a smart probe.

Application of scanning acoustic microscopy for evaluation of MMP activation in multiple cancer cell lines with a smart probe.

Application of scanning acoustic microscopy for evaluation of MMP activation in multiple cancer cell lines with a smart probe.

Background/aim: Matrix metalloproteinases (MMPs) play an important role in the evaluation of many cancer types; however, the detection usually presents a challenge. Further assays for a better understanding of the fundamental roles of MMPs in pathophysiology are still needed. We aimed to use an activatable probe in scanning acoustic microscopy (SAM) to evaluate acoustically if the probe can aid the visualization of the effects of in vitro MMP activity.

Materials and methods: We applied scanning acoustic impedance microscopy to obtain acoustic impedance maps of the cell line models of HT1080, THP-1, and SK-MEL-28 with and without MMPSense 680 probe incubation. We visually validated our results using confocal laser scanning microscopy imaging. We further analyzed the effects of MMPSense 680 probe on cell viabilities to eliminate any artifacts.

Results: This is the first study presenting the applicability of SAM in the acoustical evaluation of MMPSense 680 probe cleavage in a cellular medium through acoustic impedance measurements. We proposed that SAM measurement with the activatable probe can be used as an effective tool for studying the acoustical variations of MMP activities in cell lines. As a result, we detected MMPSense 680 probe cleavage in HT1080 human fibrosarcoma cell line.

Conclusion: We showed that SAM with the smart probe can detect proteolytic activity using MMPSense 680 in in vitro HT1080 cell line by acoustic impedance measurements. SAM could be proposed as an alternative tool leading a novel way for a better understanding of the roles of MMPs in cancer progression before clinical settings.

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