Comparisons of extracellular vesicles from human epidural fat-derived mesenchymal stem cells and fibroblast cells

Soo Eun Sung, Kyung Ku Kang, Joo Hee Choi, Si Joon Lee, Kilsoo Kim, Ju Hyeon Lim, Seung Yun Yang, Seul Ki Kim, Min Soo Seo, Gun Woo Lee

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Extracellular vesicles (EVs) are generated and secreted by cells into the circulatory system. Stem cell-derived EVs have a therapeutic effect similar to that of stem cells and are considered an alternative method for cell therapy. Accordingly, research on the characteristics of EVs is emerging. EVs were isolated from human epidural fat-derived mesenchymal stem cells (MSCs) and human fibroblast culture media by ultracentrifugation. The characterization of EVs involved the typical evaluation of cluster of differentiation (CD antigens) marker expression by fluorescence-activated cell sorting, size analysis with dynamic laser scattering, and morphology analysis with transmission electron microscopy. Lastly, the secreted levels of cytokines and chemokines in EVs were determined by a cytokine assay. The isolated EVs had a typical size of approximately 30–200 nm, and the surface proteins CD9 and CD81 were expressed on human epidural fat MSCs and human fibroblast cells. The secreted levels of cytokines and chemokines were compared between human epidural fat MSCderived EVs and human fibroblast-derived EVs. Human epidural fat MSC-derived EVs showed anti-inflammatory effects and promoted macrophage polarization. In this study, we demonstrated for the first time that human epidural fat MSC-derived EVs exhibit inflammatory suppressive potency relative to human fibroblast-derived EVs, which may be useful for the treatment of inflammationrelated diseases.

Original languageEnglish
Article number2889
Pages (from-to)1-12
Number of pages12
JournalInternational Journal of Molecular Sciences
Volume22
Issue number6
DOIs
StatePublished - 2 Mar 2021

Keywords

  • Chemokine
  • Cytokine
  • Epidural fat
  • Extracellular vesicle
  • Fibroblast
  • Inflammation
  • Mesenchymal stem cell

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