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Molecular Weight-Driven Tunable Hyaluronic Acid–Based Hydrogels Modulate Immune Polarization in Three-Dimensional Microenvironments

  • Jaechang Kim
  • , Inwoo Son
  • , Vesper Evereux
  • , Vivekanandan Subramanian
  • , Daniel Kolpek
  • , James Ogidi
  • , Seungman Park
  • , Yongdoo Park
  • , Jonghyuck Park

Producción científica: Articlerevisión exhaustiva

2 Citas (Scopus)

Resumen

Macrophages exhibit phenotypic plasticity that is strongly influenced by their surrounding microenvironment, including extracellular matrix (ECM) components. Hyaluronic acid (HA), a major glycosaminoglycan in ECM, has immunomodulatory effects that are highly dependent on its molecular weight (MW). However, most previous studies have been limited to two-dimensional (2D) culture systems, which were unable to accurately replicate the in vivo environment. In this study, we utilized a three-dimensional (3D) culture system based on HA-based hydrogels to better understand the MW-dependent immunomodulatory effects of HA on macrophages under more physiologically relevant conditions. Three different MWs of HA were chemically modified and cross-linked with PEG-SH4 to form hydrogels with distinct biophysical properties. Immortalized macrophages were encapsulated within these hydrogels and assessed for the expression of both pro-inflammatory and anti-inflammatory markers. Notably, hydrogels with high-MW HA significantly upregulated the expression of anti-inflammatory markers, indicating that the immunomodulatory effects of HA in 3D culture are affected by its biophysical characteristics. Our findings demonstrate the potential of HA-based hydrogels as customizable ECM-mimetic scaffolds for modulating immune responses in regenerative medicine applications.

Idioma originalEnglish
Páginas (desde-hasta)2173-2188
Número de páginas16
PublicaciónACS Biomaterials Science and Engineering
Volumen12
N.º4
DOI
EstadoPublished - abr 13 2026

Nota bibliográfica

Publisher Copyright:
© 2026 The Authors. Published by American Chemical Society

Financiación

This work was supported by the National Institutes of Health through R01NS136272 and K25AG070286, the National Center for Advancing Translational Sciences UL1 TR001998, the UKY Bioelectronics and Nanomedicine Research Center, and the Center for Pharmaceutical Research and Innovation (CPRI, NIH P20 GM130456).

FinanciadoresNúmero del financiador
Center for Pharmaceutical Research and Innovation, University of Kentucky
National Institutes of Health (NIH)R01NS136272, P20 GM130456, K25AG070286
National Center for Advancing Translational Sciences (NCATS)UL1 TR001998

    ASJC Scopus subject areas

    • Biomaterials
    • Biomedical Engineering

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