Evidence map›Paper›PMID 42241389›Full record

ArticlePloS one2026

Reconstruction of a segmental bone defect using vascularized tissue-engineered bone substitutes: An animal study.

Yulei Wang, Qian Lv, Xu Zhang, Jinlong Liang, Fanzhe Feng, Jingyuan Li, Yi Cui

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Article in PloS one, 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

7 authors.

Yulei WangPain Department, Second People's Hospital of Qujing City, Qujing, China.
Qian LvDepartment of Orthopedics, 920th Hospital of Joint Logistics Support Force, People's Liberation Army, Kunming, China.
Xu ZhangDepartment of Hand Surgery, Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Jinlong LiangDepartment of Orthopedics, 920th Hospital of Joint Logistics Support Force, People's Liberation Army, Kunming, China.
Fanzhe FengDepartment of Orthopedics, 920th Hospital of Joint Logistics Support Force, People's Liberation Army, Kunming, China.
Jingyuan LiDepartment of Traumatology and Orthopedics, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Yi CuiDepartment of Orthopedics, 920th Hospital of Joint Logistics Support Force, People's Liberation Army, Kunming, China.ORCID https://orcid.org/0009-0003-6547-0476

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRepairing large segmental bone defects remains a major challenge in orthopedics, with conventional autografting and allografting limited by donor shortages and high complication rates. Tissue-engineered bone substitutes have emerged as a potential solution. This study aimed to assess the vascular regeneration of dual-vascularized tissue-engineered bone substitutes in the reconstruction of large segmental bone defects in rabbits.

methodDemineralized bone matrix (DBM) was used as a scaffold, with endothelial progenitor cells (EPCs) seeded onto it. A vascular channel was created within the DBM-EPCs composite scaffold, and the radial artery was implanted into this channel. New Zealand white rabbits were used to create a 15-mm critical-sized rabbit radial bone defect model, with animals divided into four groups: DBM, DBM+EPCs, DBM+Vascular Bundle,and DBM+EPCs+Vascular Bundle (n = 9 per group).X-ray examinations,gross morphological observations,and CD31 immunofluorescence staining were conducted at 4, 8,and 12 weeks post-surgery. Micro-CT was used to reconstruct the three-dimensional structures of the defects after 12 weeks.

resultsThe DBM+EPCs+Vascular Bundle group demonstrated the most significant bone regeneration and vascularization across all time points.X-ray,gross morphology, Micro-CT analysis,HE staining,and CD31 immunofluorescence staining all revealed superior bone regeneration and vascular density in this group compared to the others.

conclusionsIn conclusion, the dual vascularization strategy significantly enhanced bone regeneration and angiogenesis in the reconstruction of large bone defects. This approach has potential clinical applications for repairing critical-sized bone defects, particularly in anatomical regions with multiple arterial supplies such as the upper limbs and lower legs.

Indexed as

Bone and BonesBone SubstitutesTissue EngineeringAnimalsBone MatrixBone RegenerationEndothelial Progenitor CellsMaleNeovascularization, PhysiologicRabbitsRadiusTissue ScaffoldsX-Ray MicrotomographyBone Substitutes

Identifiers

PMID42241389
PMCPMC13235905

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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.