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      Dielectrophoretic characterization of dendritic cell deformability upon maturation

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          Abstract

          We have developed a rapid technique for characterizing the biomechanical properties of dendritic cells using dielectrophoretic forces. It is widely recognized that maturing of dendritic cells modulates their stiffness and migration capabilities, which results in T-cell activation triggering the adaptive immune response. Therefore it is important to develop techniques for mechanophenotyping of immature and mature dendritic cells. The technique reported here utilizes nonuniform electric fields to exert a substantial force on the cells to induce cellular elongation for optical measurements. In addition, a large array of interdigitated electrodes allows multiple cells to be stretched simultaneously. Our results indicate a direct correlation between F-actin activity and deformability observed in dendritic cells, determined through mean fluorescence signal intensity of phalloidin.

          Method summary

          A device with an array of interdigitated microelectrodes was developed using standard photolithography approaches. The dendritic cells used were differentiated human leukemic cells. Differentiated dendritic cells were treated with cytochalasin B to decrease F-actin expression. Subsequently, cells were detached and used for dielectrophoresis experimentation and F-actin quantification. Suspended cells were loaded to the device, then immobilized and stretched using a multistep dielectrophoresis approach. Cell deformation was measured from microscopic images.

          Most cited references39

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          Remodeling and homeostasis of the extracellular matrix: implications for fibrotic diseases and cancer

          Dynamic remodeling of the extracellular matrix (ECM) is essential for development, wound healing and normal organ homeostasis. Life-threatening pathological conditions arise when ECM remodeling becomes excessive or uncontrolled. In this Perspective, we focus on how ECM remodeling contributes to fibrotic diseases and cancer, which both present challenging obstacles with respect to clinical treatment, to illustrate the importance and complexity of cell-ECM interactions in the pathogenesis of these conditions. Fibrotic diseases, which include pulmonary fibrosis, systemic sclerosis, liver cirrhosis and cardiovascular disease, account for over 45% of deaths in the developed world. ECM remodeling is also crucial for tumor malignancy and metastatic progression, which ultimately cause over 90% of deaths from cancer. Here, we discuss current methodologies and models for understanding and quantifying the impact of environmental cues provided by the ECM on disease progression, and how improving our understanding of ECM remodeling in these pathological conditions is crucial for uncovering novel therapeutic targets and treatment strategies. This can only be achieved through the use of appropriate in vitro and in vivo models to mimic disease, and with technologies that enable accurate monitoring, imaging and quantification of the ECM.
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            Dendritic cell migration in health and disease

            Dendritic cells (DCs) are potent and versatile antigen-presenting cells, and their ability to migrate is key for the initiation of protective pro-inflammatory as well as tolerogenic immune responses. Recent comprehensive studies have highlighted the importance of DC migration in the maintenance of immune surveillance and
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              Ac electrokinetics: a review of forces in microelectrode structures

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                Author and article information

                Journal
                BTN
                BioTechniques
                Future Science Ltd (London, UK )
                0736-6205
                1940-9818
                03 November 2020
                October 2020
                : 70
                : 1
                : 29-36
                Affiliations
                1Institute of Engineering & Transport, Electrical & Electronics, Malta College for Arts, Science & Technology, Malta
                2Laboratory for Immuno Bioengineering Research & Applications, Division of Engineering, New York University Abu Dhabi, Abu Dhabi, UAE
                3Advanced Microfluidics & Microdevices Laboratory, Division of Engineering, New York University Abu Dhabi, Abu Dhabi, UAE
                4Department of Mechanical Engineering, Tandon School of Engineering, New York University, NY, USA
                Author notes
                [* ]Author for correspondence: anoop.menachery@ 123456mcast.edu.mt
                [** ]Author for correspondence: jeremy.teo@ 123456nyu.edu
                ***Author for correspondence: mohammad.qasaimeh@ 123456nyu.edu
                [‡]

                Authors contributed equally

                Author information
                https://orcid.org/0000-0002-0201-6052
                https://orcid.org/0000-0001-6627-7713
                https://orcid.org/0000-0001-6869-3833
                https://orcid.org/0000-0003-1122-9698
                Article
                10.2144/btn-2020-0126
                b83ff338-e477-4cb9-b8cd-4dfa7959ba86
                © 2020 Anoop Menachery

                This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License

                History
                : 19 August 2020
                : 15 October 2020
                : 03 November 2020
                Page count
                Pages: 8
                Funding
                Funded by: Al Jalila Foundation
                Award ID: AJF2018085
                Categories
                Reports

                General life sciences,Cell biology,Molecular biology,Biotechnology,Genetics,Life sciences
                actin,cytoskeleton,dielectrophoresis,deformability,dendritic cells,stretching,biochip

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