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细胞监测平台中分泌信号分子感应的整合:一项关键综述。

Integration of secreted signaling molecule sensing on cell monitoring platforms: a critical review.

机构信息

Microfluidics Cluster UPV/EHU, BIOMICs Microfluidics Group, Lascaray Research Center, University of the Basque Country UPV/EHU, Vitoria-Gasteiz, Spain.

BIOMICs Research Group, Lascaray Research Center, University of the Basque Country UPV/EHU, Vitoria-Gasteiz, Spain.

出版信息

Anal Bioanal Chem. 2024 Dec;416(30):7249-7266. doi: 10.1007/s00216-024-05435-1. Epub 2024 Jul 24.

DOI:10.1007/s00216-024-05435-1
PMID:39048740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11584473/
Abstract

Monitoring cell secretion in complex microenvironments is crucial for understanding cellular behavior and advancing physiological and pathological research. While traditional cell culture methods, including organoids and spheroids, provide valuable models, real-time monitoring of cell secretion of signaling molecules remains challenging. Integrating advanced monitoring technologies into these systems often disrupts the delicate balance of the microenvironment, making it difficult to achieve sensitivity and specificity. This review explored recent strategies for integrating the monitoring of cell secretion of signaling molecules, crucial for understanding and replicating cell microenvironments, within cell culture platforms, addressing challenges such as non-adherent cell models and the focus on single-cell methodologies. We highlight advancements in biosensors, microfluidics, and three-dimensional culture methods, and discuss their potential to enhance real-time, multiplexed cell monitoring. By examining the advantages, limitations, and future prospects of these technologies, we aim to contribute to the development of integrated systems that facilitate comprehensive cell monitoring, ultimately advancing biological research and pharmaceutical development.

摘要

监测复杂微环境中的细胞分泌对于理解细胞行为和推进生理及病理研究至关重要。虽然传统的细胞培养方法,包括类器官和球体,提供了有价值的模型,但对细胞分泌的信号分子进行实时监测仍然具有挑战性。将先进的监测技术整合到这些系统中往往会破坏微环境的微妙平衡,难以实现灵敏度和特异性。本综述探讨了将信号分子细胞分泌监测整合到细胞培养平台中的最新策略,这些策略对于理解和复制细胞微环境至关重要,同时解决了非贴壁细胞模型的挑战以及对单细胞方法的关注。我们重点介绍了生物传感器、微流控和三维培养方法的进展,并讨论了它们在增强实时、多重细胞监测方面的潜力。通过检查这些技术的优势、限制和未来前景,我们旨在为开发促进全面细胞监测的综合系统做出贡献,从而最终推进生物研究和药物开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/fe5e59d2c24e/216_2024_5435_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/7fec9305477c/216_2024_5435_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/8cbad15997dc/216_2024_5435_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/71caeb92a73a/216_2024_5435_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/574a56909b41/216_2024_5435_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/fe5e59d2c24e/216_2024_5435_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/7fec9305477c/216_2024_5435_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/8cbad15997dc/216_2024_5435_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/71caeb92a73a/216_2024_5435_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/574a56909b41/216_2024_5435_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52c/11584473/fe5e59d2c24e/216_2024_5435_Fig5_HTML.jpg

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本文引用的文献

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Proteomic Profiling of Fallopian Tube-Derived Extracellular Vesicles Using a Microfluidic Tissue-on-Chip System.
使用微流控芯片组织系统对输卵管来源的细胞外囊泡进行蛋白质组学分析。
Bioengineering (Basel). 2023 Mar 27;10(4):423. doi: 10.3390/bioengineering10040423.
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Dual-ratiometric aptasensor for simultaneous detection of malathion and profenofos based on hairpin tetrahedral DNA nanostructures.基于发夹四面体DNA纳米结构的双比率适体传感器用于同时检测马拉硫磷和丙溴磷。
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A Microfluidic Cell Co-Culture Chip for the Monitoring of Interactions between Macrophages and Fibroblasts.一种用于监测巨噬细胞和成纤维细胞相互作用的微流控细胞共培养芯片。
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