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Enhanced Auricular Cartilage Regeneration via 3D-Printed Hydrogel With miR-92a-3p-Enriched Platelet-Rich
Shan Hua1,2, Hongyi Zhang1,2, Jiawei Gu1,2
1Department of Plastic Surgery School of Medicine, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China.
Advanced Healthcare Materials
|May 10, 2026
Summary
Engineered platelet-derived extracellular vesicles (PEVs) carrying miRNA-92a-3p in a 3D-printed scaffold significantly enhance ear cartilage regeneration, overcoming key challenges in microtia reconstruction.
Area of Science:
- Regenerative Medicine
- Biomaterials Science
- Tissue Engineering
Background:
- Auricular cartilage reconstruction for microtia is challenging due to chondrocyte quiescence.
- Current cartilage tissue engineering methods struggle with efficient chondrogenesis.
Purpose of the Study:
- To develop an effective strategy for auricular cartilage regeneration using engineered extracellular vesicles and 3D bioprinting.
- To investigate the role of platelet-derived extracellular vesicles (PEVs) and miRNA-92a-3p in enhancing chondrogenesis.
Main Methods:
- Engineered PEVs carrying miRNA-92a-3p (miR@PEVs) were developed.
- A double-network hydrogel scaffold (ElaMA/GelMA) was fabricated using 3D bioprinting.
- In vitro and in vivo studies assessed chondrogenesis, biocompatibility, and mechanical properties.
Main Results:
- miR@PEV-laden scaffolds demonstrated superior chondrogenesis compared to controls in vivo.
- Scaffold's Young's modulus approached native cartilage after one month.
- In vitro, miR@PEVs promoted chondrocyte proliferation, migration, and M2 macrophage polarization via miR-92a-3p.
- miR-92a-3p suppressed SMAD7, activating TGFβ/Smad signaling.
Conclusions:
- Engineered miR@PEVs integrated into 3D-printed scaffolds offer a promising solution for auricular reconstruction.
- This approach overcomes limitations in chondrogenesis and ear regeneration.
- The strategy holds potential for total ear reconstruction in microtia patients.
