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      Conscription of Immune Cells by Light‐Activatable Silencing NK‐Derived Exosome (LASNEO) for Synergetic Tumor Eradication

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          Abstract

          Exosomes derived from natural killer (NK) cells (NEO) constitute promising antineoplastic nano‐biologics because of their versatile functions in immune regulation. However, a significant augment of their immunomodulatory capability is an essential need to achieve clinically meaningful treatment outcomes. Light‐activatable silencing NK‐derived exosomes (LASNEO) are orchestrated by engineering the NEO with hydrophilic small interfering RNA (siRNA) and hydrophobic photosensitizer Ce6. Profiling of genes involved in apoptosis pathway with Western blot and RNA‐seq in cells receiving NEO treatment reveals that NEO elicits effective NK cell‐like cytotoxicity toward tumor cells. Meanwhile, reactive oxygen species (ROS) generation upon laser irradiation not only triggers substantial photodynamic therapy effect but also boosts M1 tumor‐associated macrophages polarization and DC maturation in the tumor microenvironment (TME). In addition, ROS also accelerates the cellular entry and endosomal escape of siRNA in TME. Finally, siRNAs targeting PLK1 or PD‐L1 induce robust gene silencing in cancer cells, and downregulation of PD‐L1 restores the immunological surveillance of T cells in TME. Therefore, the proposed LASNEO exhibit excellent antitumor effects by conscripting multiple types of immune cells. Considering that its manufacture is quite simple and controllable, LASNEO show compelling potential for clinical translational application.

          Abstract

          Light‐activatable silencing natural killer (NK)‐derived exosome (LASNEO) enables robust immuno‐oncotherapy by conscripting multiple types of immune cells. It elicits inherited NK cell‐like cytotoxicity. Reactive oxygen species photogeneration triggers effective photodynamic therapy, boosts M1 macrophage polarization and DC maturation, and facilitates endosomal escape of small interfering RNA. PD‐L1 silencing and soluble factors further restore T cell immune surveillance.

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          Author and article information

          Contributors
          yyhuang@bit.edu.cn
          Journal
          Adv Sci (Weinh)
          Adv Sci (Weinh)
          10.1002/(ISSN)2198-3844
          ADVS
          Advanced Science
          John Wiley and Sons Inc. (Hoboken )
          2198-3844
          04 June 2022
          August 2022
          : 9
          : 22 ( doiID: 10.1002/advs.v9.22 )
          : 2201135
          Affiliations
          [ 1 ] School of Life Science Advanced Research Institute of Multidisciplinary Science School of Medical Technology (Institute of Engineering Medicine) Key Laboratory of Molecular Medicine and Biotherapy Key Laboratory of Medical Molecule Science and Pharmaceutics Engineering Beijing Institute of Technology Beijing 100081 China
          [ 2 ] Department of Radiation Oncology the First Affiliated Hospital of Zhengzhou University Erqi Zhengzhou 450000 China
          [ 3 ] Chinese Academy of Sciences (CAS) Center for Excellence in Nanoscience CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety National Center for Nanoscience and Technology Beijing 100190 China
          Author notes
          [*] [* ]E‐mail: yyhuang@ 123456bit.edu.cn

          Author information
          https://orcid.org/0000-0003-3935-7245
          Article
          ADVS4162
          10.1002/advs.202201135
          9353410
          35665496
          5a5911c7-d9d0-4da7-a8bc-5e845a836576
          © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH

          This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

          History
          : 11 April 2022
          : 26 February 2022
          Page count
          Figures: 7, Tables: 0, Pages: 15, Words: 10686
          Funding
          Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
          Award ID: 31871003
          Award ID: 31901053
          Award ID: 32001008
          Funded by: Beijing Nova Program from the Beijing Municipal Science & Technology Commission
          Award ID: Z201100006820005
          Funded by: Beijing‐Tianjin‐Hebei Basic Research Cooperation Project
          Award ID: 19JCZDJC64100
          Funded by: National Key R&D Program of China
          Award ID: 2021YFE0106900
          Award ID: 2021YFA1201000
          Funded by: Beijing Natural Science Foundation , doi 10.13039/501100004826;
          Award ID: 7214283
          Award ID: 7214302
          Funded by: Natural Science Foundation of Guangdong Province , doi 10.13039/501100003453;
          Award ID: 2019A1515010776
          Categories
          Research Article
          Research Articles
          Custom metadata
          2.0
          August 5, 2022
          Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.7 mode:remove_FC converted:05.08.2022

          exosome,immunotherapy,natural killer cells,reactive oxygen species,small interfering rna

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