Evidence map›Paper›PMID 42469849›Full record

ArticleJournal of orthopaedic surgery and research2026

3D bioprinted bilayer GelMA/HAp hydrogel scaffold functionalized with miR-140-5p-modified MSCs for enhanced osteochondral regeneration.

Yingjie Xu, Junhui Xing, Ziyu Zhang, Minghui Li, Jing Qu, Hongtao Zhang

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Article in Journal of orthopaedic surgery and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yingjie Xu *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China.
Junhui Xing *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China.
Ziyu ZhangDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China.
Minghui LiDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China.
Jing QuSchool of Biology and Basic of Medical Science, Medical College of Soochow University, Suzhou, China. qujing@suda.edu.cn.
Hongtao ZhangDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China. htzhangsz@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteochondral defects remain a major clinical challenge due to the limited intrinsic healing capacity of articular cartilage and the complex structural integration required between cartilage and subchondral bone. Tissue-engineered scaffolds offer a promising strategy for improving repair outcomes.

methodsWe developed a 3D bioprinted bilayer GelMA/hydroxyapatite (HAp) hydrogel scaffold incorporating miR-140-5p-modified mesenchymal stem cells (MSCs). The upper chondral-oriented layer consisted of 5% GelMA60, while the lower relatively stiffer HAp-containing layer comprised 5% GelMA90 with 1% HAp. Mechanical properties, cell viability, migration, and differentiation were evaluated in vitro. Osteochondral repair efficacy was further assessed in a rabbit femoral condyle defect model using macroscopic scoring, Micro-CT, and histological analysis.

resultsThe bilayer scaffold demonstrated enhanced compressive strength and maintained favorable swelling characteristics. MSC viability remained high in both scaffold groups and exceeded 90% by day 5 after bioprinting. miR-140-5p modification significantly promoted MSC migration and upregulated chondrogenic markers. In vivo, the functionalized scaffold markedly improved cartilage surface integrity, subchondral bone reconstruction, and ICRS scores compared with controls.

conclusionThe 3D bioprinted bilayer GelMA/HAp scaffold combined with miR-140-5p-modified MSCs significantly enhances osteochondral repair in a rabbit model and represents a promising strategy for clinical translation.

Indexed as

BioprintingBone RegenerationCartilage, ArticularDurapatiteHydrogelsMesenchymal Stem CellsMicroRNAsPrinting, Three-DimensionalTissue EngineeringTissue ScaffoldsAnimalsHumansRabbitsDurapatiteHydrogelsMicroRNAsMIR140, human3D bio-printingHybrid scaffoldMesenchymal stem cellsmicroRNA-140-5pOsteochondral defectRabbit femoral condyle osteochondral defects

Identifiers

PMID42469849
PMCPMC13660108

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.