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03452nam a2200685Ia 4500 |
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10.1002-cpz1.144 |
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220427s2021 CNT 000 0 und d |
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|a 26911299 (ISSN)
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|a Characterization and Functional Analysis of Tumor-Derived Microparticles
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|b Blackwell Publishing Inc.
|c 2021
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|z View Fulltext in Publisher
|u https://doi.org/10.1002/cpz1.144
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|a Microparticles (MPs) are heterogeneous populations of cell-derived vesicles that play an important role in intercellular communications. The release of MPs by tumor cells is a very common event in tumor microenvironments (TMEs). Tumor cell−derived MPs (T-MPs) contain a variety of bioactive molecules, thus modulating various biological processes, including the regulation of immune cell phenotype and function, as well as immune responses. Moreover, T-MPs can be used as natural carriers to deliver therapeutic drugs into tumor cells and immune cells, thus remodeling TMEs and modifying anti-tumor immune responses. These features allow T-MPs to function as potential biomaterials to be applied in tumor immunotherapies and vaccines. This article describes protocols for the isolation of T-MPs from supernatants of cultured tumor cells by multi-step centrifugations. Tools and protocols are also provided in order to characterize and validate the isolated MPs and to analyze the interaction between T-MPs and different target cells. © 2021 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Isolation of tumor cell-derived microparticles by multi-step centrifugations. Basic Protocol 2: Characterization and validation of tumor cell−derived microparticles. Basic Protocol 3: Functional analysis of the uptake of tumor cell−derived microparticles by different cell types. © 2021 The Authors. Current Protocols published by Wiley Periodicals LLC.
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|a analysis
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|a apoptosis assay
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|a Article
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|a biomaterial
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|a bone marrow derived dendritic cell
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|a bone marrow derived macrophage
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|a cell communication
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|a Cell Communication
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|a cell surface marker
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|a Cell-Derived Microparticles
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|a centrifugation
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|a centrifugation
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|a dendritic cell vaccine
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|a doxorubicin
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|a electron microscopy
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|a encapsulation
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|a exosome
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|a extracellular vesicles
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|a flow cytometry
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|a functional analysis
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|a H22 cell line
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|a high performance liquid chromatography
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|a human
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|a Humans
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|a immunotherapy
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|a Immunotherapy
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|a isolation
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|a isolation procedure
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|a M2 macrophage
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|a membrane microparticle
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|a methotrexate
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|a microparticles
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|a nanoparticle tracking analysis
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|a neoplasm
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|a Neoplasms
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|a nonhuman
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|a tumor cell
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|a tumor cells
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|a tumor derived microparticle
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|a tumor microenvironment
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|a Tumor Microenvironment
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|a Western blotting
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|a Huang, B.
|e author
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|a Ma, J.
|e author
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|a Tang, K.
|e author
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|a Wei, K.
|e author
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|a Zhang, H.
|e author
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|t Current Protocols
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