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April 4, 2026Journal of Extracellular Vesicles0 citationsOpen Access

Development of Anti‐Inflammatory Extracellular Vesicles by Surface Expression of Syndecan‐4

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LYLi YuJiangnan UniversityMBMarkus BergqvistUniversity of GothenburgKPKyong‐Su ParkUniversity of Gothenburg

Key Points

  • This research aims to explore the anti-inflammatory properties of a specific subpopulation of extracellular vesicles (miniEVs) from HEK293F cells and the role of Syndecan-4.
  • Isolation of miniEVs from HEK293F cells and characterization via quantitative proteomics.
  • Engineering HEK293F cells to overexpress Syndecan-4 to investigate its effects on EV composition.
  • Testing anti-inflammatory effects of Syndecan-4 expressing miniEVs both in vitro and in vivo.
  • miniEVs demonstrated significant anti-inflammatory properties compared to larger EVs.
  • Syndecan-4 was identified on miniEVs, absent in larger EV populations.
  • Syndecan-4 expression increased heparan sulfate levels on EV surface.
  • Heparinase treatment reduced the anti-inflammatory effects of SDC4 EVs.
  • SDC4-expressing miniEVs showed efficacy in reducing inflammation in a peritonitis model.

Abstract

ABSTRACT The biological functions of extracellular vesicles (EVs) depend on their cellular source. Further, different subpopulations of EVs from the same cells carry different cargo, but differences in their biological functions are less understood. We here identify a very small EV subpopulation released by HEK293F cells (miniEVs). These EVs, in contrast to the larger EVs, were found to have anti‐inflammatory properties. Quantitative proteomics identified a potential anti‐inflammatory molecule, Syndecan‐4 (SDC4), on the surface of the miniEVs, but not on larger EVs. We engineered HEK293F cells to overexpress SDC4, which results in the molecule being highly expressed in all EV subpopulations. Expression of SDC4, a proteoglycan, also increased the presence of heparan sulfate on the EV surface. Furthermore, these EVs were found to have potent anti‐inflammatory effects in vitro, which heparinase treatment could slightly reduce. Furthermore, the SDC4 EVs showed anti‐inflammatory effects in vivo in a model of peritonitis. We conclude that HEK293F miniEVs convey anti‐inflammatory properties, and SDC4‐expressing HEK293F‐EV potentially could become an anti‐inflammatory therapeutic.

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Cite This Study

Yu et al. (2026) studied this question.

synapsesocial.com/papers/69d0af68659487ece0fa55d6https://doi.org/10.1002/jev2.70266
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