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双向单细胞迁移和检索芯片用于定量研究树突状细胞迁移。

A Bidirectional Single-Cell Migration and Retrieval Chip for Quantitative Study of Dendritic Cell Migration.

机构信息

Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.

The Third Xiangya Hospital, Central South University, Changsha, 410008, P. R. China.

出版信息

Adv Sci (Weinh). 2023 Mar;10(8):e2204544. doi: 10.1002/advs.202204544. Epub 2023 Jan 19.

DOI:10.1002/advs.202204544
PMID:36658690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10015900/
Abstract

Dendritic cell (DC) migration is a fundamental step during execution of its adaptive immunity functions. Studying DC migration characteristics is critical for development of DC-dependent allergy treatments, vaccines, and cancer immunotherapies. Here, a microfluidics-based single-cell migration platform is described that enables high-throughput and precise bidirectional cell migration assays. It also allows selective retrieval of cell subpopulations that have different migratory potentials. Using this microfluidic platform, DC migration is investigated in response to different chemoattractants and inhibitors, quantitatively describe DC migration patterns and retrieve DC subpopulations of different migratory potentials for differential gene expression analysis. This platform opens an avenue for precise characterization of cell migration and potential discovery of therapeutic modulators.

摘要

树突状细胞 (DC) 迁移是其执行适应性免疫功能的一个基本步骤。研究 DC 迁移特性对于开发依赖 DC 的过敏治疗、疫苗和癌症免疫疗法至关重要。在这里,描述了一种基于微流控的单细胞迁移平台,该平台可实现高通量和精确的双向细胞迁移分析。它还允许选择性回收具有不同迁移潜力的细胞亚群。使用这个微流控平台,研究了 DC 对不同趋化因子和抑制剂的迁移反应,定量描述了 DC 的迁移模式,并回收了具有不同迁移潜力的 DC 亚群,用于差异基因表达分析。该平台为精确表征细胞迁移和潜在治疗调节剂的发现开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/06ef10e9936a/ADVS-10-2204544-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/c51c47c46119/ADVS-10-2204544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/9ff0418c287c/ADVS-10-2204544-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/33826d04fea3/ADVS-10-2204544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/06ef10e9936a/ADVS-10-2204544-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/c51c47c46119/ADVS-10-2204544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/9ff0418c287c/ADVS-10-2204544-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/33826d04fea3/ADVS-10-2204544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f0/10015900/06ef10e9936a/ADVS-10-2204544-g004.jpg

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2
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Front Pharmacol. 2022 Feb 25;13:841687. doi: 10.3389/fphar.2022.841687. eCollection 2022.
3
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Cell Mol Immunol. 2021 Nov;18(11):2461-2471. doi: 10.1038/s41423-021-00726-4. Epub 2021 Jul 23.
4
The nucleus acts as a ruler tailoring cell responses to spatial constraints.细胞核作为一个标尺,对细胞响应的空间约束进行调整。
Science. 2020 Oct 16;370(6514). doi: 10.1126/science.aba2894.
5
Nuclear Membrane Rupture and Its Consequences.核膜破裂及其后果。
Annu Rev Cell Dev Biol. 2020 Oct 6;36:85-114. doi: 10.1146/annurev-cellbio-020520-120627. Epub 2020 Jul 21.
6
The Chemokine Receptor CCR7 Uses Distinct Signaling Modules With Biased Functionality to Regulate Dendritic Cells.趋化因子受体 CCR7 使用具有偏向功能的不同信号模块来调节树突状细胞。
Front Immunol. 2020 Apr 15;11:528. doi: 10.3389/fimmu.2020.00528. eCollection 2020.
7
CHMPions of repair: Emerging perspectives on sensing and repairing the nuclear envelope barrier.CHMP:修复的推动者:对核膜屏障的感应和修复的新观点。
Curr Opin Cell Biol. 2020 Jun;64:25-33. doi: 10.1016/j.ceb.2020.01.011. Epub 2020 Feb 24.
8
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Micromachines (Basel). 2019 Dec 5;10(12):851. doi: 10.3390/mi10120851.
9
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Anal Chem. 2020 Jan 7;92(1):892-898. doi: 10.1021/acs.analchem.9b03681. Epub 2019 Dec 16.
10
Dendritic cells in cancer immunology and immunotherapy.树突状细胞在癌症免疫和免疫治疗中的作用。
Nat Rev Immunol. 2020 Jan;20(1):7-24. doi: 10.1038/s41577-019-0210-z. Epub 2019 Aug 29.