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通过在缺氧条件下支架内的内源性氧气产生建立缺氧微环境以促进骨再生。

Hypoxic niches established via endogenous oxygen production in scaffold under anoxia for enhanced bone regeneration.

作者信息

Gan Kaifeng, Lian Leidong, Luo Zhe, Dong Yanxue, Xu Dingli, Li Xufeng, Li Jie, Zhang Xuyang, Chen Jian, Lu Liangjie, Zhao Fengdong

机构信息

Department of Orthopaedic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310016, China.

Zhejiang Key Laboratory of Mechanism Research and Precision Repair of Orthopaedic Trauma and Aging Diseases, Hangzhou, Zhejiang 310016, China.

出版信息

Regen Biomater. 2025 Jun 26;12:rbaf070. doi: 10.1093/rb/rbaf070. eCollection 2025.

Abstract

Anoxia remains a challenging problem to effective graft implantation in bone tissue engineering for managing large-size bone defects. One promising strategy is to provide immediate oxygen required for cell viability and graft maturation by introducing oxygen-generating biomaterials. In this study, we present a novel composite oxygen-generating scaffold by integrating oxygen-generating microspheres (OMs) comprised of emulsified calcium peroxides (CPOs) encapsulated in poly (lactic-co-glycolic acid; PLGA) into the gelatin methacryloyl (GelMA) hydrogel. The results reveal that the scaffold encapsulating 2% (w/v) OMs (OM@GelMA) mildly sustained oxygen production for approximately 16 days, and hence, established hypoxic niches with low oxygen tension (10-46 mmHg) under anoxic culture condition (0.2% oxygen) for the viability of bone marrow-derived mesenchymal stem cells (BMSCs) and their enhanced osteogenic differentiation, which may be induced by activation of HIF-1/β-catenin signaling pathway by the compatibly hypoxic level as one of the underlying molecular mechanisms verified via transcriptome sequencing, western blotting (WB) and quantitative real-time polymerase chain reaction (qRT-PCR) tests on samples. Moreover, the oxygen-generating hydrogel could enhance angiogenesis of human umbilical vein endothelial cells (HUVECs) under anoxia by preserving cell viability, accelerating cell migration, promoting tube formation and activating angiogenic genes and proteins expression. studies using rat cranial critical-size defect models demonstrated that OM@GelMA significantly enhanced bone regeneration, effectively promoting bone defect repair. In summary, the OM@GelMA, as a novel endogenously oxygen-generating scaffold, holds great potential to facilitate bone tissue regeneration subject to oxygen-deprived scenarios. This study provides a new insight for future research and clinical applications in bone tissue engineering, particularly for large bone defect repair.

摘要

在骨组织工程中,缺氧仍然是影响大型骨缺损有效移植植入的一个具有挑战性的问题。一种有前景的策略是通过引入产氧生物材料来提供细胞存活和移植物成熟所需的即时氧气。在本研究中,我们通过将由包裹在聚(乳酸-乙醇酸共聚物;PLGA)中的乳化过氧化钙(CPO)组成的产氧微球(OM)整合到甲基丙烯酰化明胶(GelMA)水凝胶中,提出了一种新型的复合产氧支架。结果表明,包裹2%(w/v)OM的支架(OM@GelMA)可温和持续产氧约16天,因此,在缺氧培养条件(0.2%氧气)下建立了低氧张力(10 - 46 mmHg)的低氧微环境,以维持骨髓间充质干细胞(BMSC)的活力并增强其成骨分化,这可能是通过转录组测序、蛋白质免疫印迹(WB)和定量实时聚合酶链反应(qRT-PCR)测试验证的潜在分子机制之一,即通过适度缺氧水平激活HIF-1/β-连环蛋白信号通路来诱导。此外,产氧水凝胶可通过维持细胞活力、加速细胞迁移、促进管腔形成以及激活血管生成基因和蛋白质表达,在缺氧条件下增强人脐静脉内皮细胞(HUVEC)的血管生成。使用大鼠颅骨临界尺寸缺损模型的研究表明,OM@GelMA显著增强了骨再生,有效促进了骨缺损修复。总之,OM@GelMA作为一种新型的内源性产氧支架,在缺氧情况下促进骨组织再生具有巨大潜力。本研究为骨组织工程的未来研究和临床应用提供了新的见解,特别是对于大型骨缺损修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5acc/12306443/f3e389d13162/rbaf070f8.jpg

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