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Alteration of payload in extracellular vesicles by crosstalk with mesenchymal stem cells from different origin

  • Dong Jun Park*
  • , Jeong Eun Park
  • , Tae Hoon Kong
  • , Young Joon Seo*
  • *Corresponding author for this work
  • Yonsei University Wonju College of Medicine
  • Research Institute of Hearing Enhancement
  • University of California at San Diego
  • Curtin University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Background: The application of extracellular vesicles (EVs) derived from mesenchymal stem cells (MSCs) requires customized materials to target disease or cell damage. We hypothesized that EVs exert different inflammatory effects on one recipient cell, although stem cells of different origins in humans have similar payloads. Results: Here, the payload of EVs released by crosstalk between MSCs and human middle ear epithelial cells (HMEECs) extracted from adipose tissue, bone marrow and tonsils significantly increased the level of anti-inflammatory factors. EVs derived from the co-culture medium decreased TNF-α, COX-2, IL-1β, and IL-6 levels to approximately zero within 3 h in HMEECs. Expression of miR-638 and amyloid-β A4 precursor protein-binding family A member 2 was analyzed using microarrays and gene ontology analysis, respectively. Conclusions: In conclusion, stem cells of different origins have different payloads through crosstalk with recipient-specific cells. Inducing specific factors in EVs by co-culture with MSCs could be valuable in regenerative medicine. Graphical abstract: [Figure not available: see fulltext.].

Original languageEnglish
Article number148
JournalJournal of Nanobiotechnology
Volume19
Issue number1
DOIs
StatePublished - 2021.12

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Amyloid-β A4 precursor protein-binding family A member 2
  • Antiinflammation
  • Extracellular vesicles
  • Mesenchymal stem cell
  • miR-638

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