The additive effects of photobiomodulation and bioactive glasses on enhancing early angiogenesis

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Lidong Huang, W. Gong, Gui-qin Huang, Jingyi Li, Jilin Wu, Yuguang Wang, Yanmei Dong
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引用次数: 1

Abstract

Bioactive glasses (BG) have been widely utilized as a biomaterial for bone repair. However, the early angiogenesis of BG may be inadequate, which weakens its osteogenic effects in large-sized bone defects and often leads to the failure of bone regeneration. In this study, we explored the effects of photobiomodulation (PBM) combined with BG on early angiogenesis to solve this bottleneck problem of insufficient early angiogenesis. In vitro, human umbilical vein endothelial cells (HUVECs) were cultured with BG extracts and treated with PBM using 1 J cm−2. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, real-time reverse transcription-polymerase chain reaction (real-time RT-PCR) and tubule formation assay were utilized to detect HUVECs’ proliferation, vascular growth factor genes expression and tubules formation. In vivo, bone defects at the femoral metaphysis in Sprague-Dawley rats were treated with BG particulates and PBM at 120 J cm−2. Hematoxylin–eosin staining was used to observe the inflammatory response, tissue formation and biomaterial absorption of bone defects. Immunohistochemical staining was applied to observe the vascular-like structure formation. The in vitro results showed that PBM combined with BG significantly promoted HUVECs’ proliferation, genes expression and mature tubules formation. On days 2, 4 and 7, the mRNA expression of VEGF in BG + PBM group was 2.70-, 2.59- and 3.05-fold higher than control (P< 0.05), and significantly higher than PBM and BG groups (P< 0.05). On days 4 and 7, the bFGF gene expression in BG + PBM group was 2.42- and 1.82-fold higher than control (P< 0.05), and also higher than PBM and BG groups (P< 0.05). Tube formation assay showed that mature tubules were formed in BG + PBM and PBM groups after 4 h, and the number in BG + PBM group was significantly higher than other groups (P< 0.05). In vivo results further confirmed PBM induced early angiogenesis, with more vascular-like structures observed in BG + PBM and PBM groups 2 week post-surgery. With the optimum PBM fluence and BG concentration, PBM combined with BG exerted additive effects on enhancing early angiogenesis.
光生物调节剂和生物活性玻璃对促进早期血管生成的叠加效应
生物活性玻璃(BG)作为一种用于骨修复的生物材料已被广泛应用。然而,BG的早期血管生成可能不足,这削弱了其在大型骨缺损中的成骨作用,并经常导致骨再生失败。在本研究中,我们探讨了光生物调节(PBM)与BG联合对早期血管生成的影响,以解决早期血管生成不足的瓶颈问题。在体外,用BG提取物培养人脐静脉内皮细胞(HUVECs),并用1 J cm−2的PBM处理。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)法、实时逆转录聚合酶链式反应(RT-PCR)法和小管形成法检测HUVECs增殖、血管生长因子基因表达和小管形成。在体内,用BG颗粒和PBM在120 J cm−2下处理Sprague-Dawley大鼠股干骺端的骨缺损。苏木精-伊红染色观察骨缺损的炎症反应、组织形成和生物材料吸收。免疫组化染色观察血管样结构的形成。体外实验结果表明,PBM与BG联合应用可显著促进HUVECs的增殖、基因表达和成熟小管的形成。在第2、4和7天,BG+PBM组VEGF的mRNA表达分别是对照组的2.70、2.59和3.05倍(P<0.05),显著高于PBM和BG组(P<0.05),造管实验显示,BG+PBM和PBM组在4h后形成成熟小管,且BG+PBM组的数量明显高于其他组(P<0.05)。体内结果进一步证实了PBM诱导的早期血管生成,术后2周,BG+PDM和PBM两组观察到更多的血管样结构。在最佳PBM注量和BG浓度下,PBM与BG联合对促进早期血管生成具有加性作用。
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来源期刊
Biomedical materials
Biomedical materials 工程技术-材料科学:生物材料
CiteScore
6.70
自引率
7.50%
发文量
294
审稿时长
3 months
期刊介绍: The goal of the journal is to publish original research findings and critical reviews that contribute to our knowledge about the composition, properties, and performance of materials for all applications relevant to human healthcare. Typical areas of interest include (but are not limited to): -Synthesis/characterization of biomedical materials- Nature-inspired synthesis/biomineralization of biomedical materials- In vitro/in vivo performance of biomedical materials- Biofabrication technologies/applications: 3D bioprinting, bioink development, bioassembly & biopatterning- Microfluidic systems (including disease models): fabrication, testing & translational applications- Tissue engineering/regenerative medicine- Interaction of molecules/cells with materials- Effects of biomaterials on stem cell behaviour- Growth factors/genes/cells incorporated into biomedical materials- Biophysical cues/biocompatibility pathways in biomedical materials performance- Clinical applications of biomedical materials for cell therapies in disease (cancer etc)- Nanomedicine, nanotoxicology and nanopathology- Pharmacokinetic considerations in drug delivery systems- Risks of contrast media in imaging systems- Biosafety aspects of gene delivery agents- Preclinical and clinical performance of implantable biomedical materials- Translational and regulatory matters
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