Localised delivery of interleukin-13 from a PLGA microparticle embedded GelMA hydrogel improves functional and histopathological recovery in a mouse contusion spinal cord injury model

脊髓损伤 PLGA公司 大鼠模型 微粒 医学 脊髓 生物医学工程 病理 材料科学 生物 纳米技术 内科学 纳米颗粒 天体生物学 精神科
作者
Ciara Walsh,Ruth Colbert,James R. Reynolds,Emily Dunne,Emmanuelle Damilola Aiyegbusi,Ross O'Carroll,Jacek K. Wychowaniec,Takahiro Masuda,Klaus‐Peter Knobeloch,Marco Prinz,Dermot F. Brougham,Dearbhaile Dooley
出处
期刊:Bioactive Materials [Elsevier BV]
卷期号:53: 855-874 被引量:3
标识
DOI:10.1016/j.bioactmat.2025.07.018
摘要

Spinal cord injury (SCI) is a severe neurological condition with limited regenerative capacity and no effective curative treatments. Interleukin-13 (IL-13), an immunomodulatory cytokine, has shown therapeutic potential by promoting alternative immune activation and improving recovery after SCI in mice. However, cell-based IL-13 delivery is hindered by poor graft survival and limited localisation at the injury site. Here, we developed an injectable hydrogel-based delivery system (HGIL13) composed of IL-13-loaded poly(lactic-co-glycolic acid) (PLGA) microparticles embedded in a photocrosslinkable gelatin methacrylate (GelMA) matrix, enabling sustained and localised IL-13 release. HGIL13 achieved IL-13 release for up to six weeks and significantly reduced lipopolysaccharide (LPS)-induced inflammation in BV2 microglia in vitro . In a mouse contusion SCI model, HGIL13 enhanced functional recovery, reduced lesion volume, and decreased demyelinated area. Using the Hexb tdTomato mouse we show that HGIL13 modulated the neuroimmune response by decreasing resident microglia density, downregulating CD86 expression, and upregulating Arginase-1 in both microglia and infiltrating monocyte-derived macrophages. RT-qPCR and RNA-seq analyses confirmed sustained immunomodulation over 28 days and indicated early reduction of activated microglia at 7 days post-injury as a key therapeutic mechanism. This study presents a safe, effective, and translatable strategy for localised cytokine delivery, demonstrating strong potential for immunomodulation and improved functional recovery following SCI. • HGIL13 is an injectable delivery system consisting of IL-13/PLGA microparticles in a GelMA hydrogel. • HGIL13 releases IL-13 for up to 6 weeks and retains its bioactivity in vitro . • HGIL13 improves functional and histopathological recovery in a mouse contusion SCI model.
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