首页|期刊导航|解放军医学院学报|甲基丙烯酰化明胶/β-磷酸三钙/黑色素纳米颗粒复合水凝胶对小鼠胚胎成骨细胞促成骨和抗活性氧作用的影响

甲基丙烯酰化明胶/β-磷酸三钙/黑色素纳米颗粒复合水凝胶对小鼠胚胎成骨细胞促成骨和抗活性氧作用的影响OA

Effects of GelMA/β-tricalcium-phosphate/melanin nanoparticle composite hydrogel on osteogenesis promotion and reactive oxygen species scavenging in mouse embryonic osteoblasts

中文摘要英文摘要

背景 通过组织工程技术将甲基丙烯酰化明胶(gelatin methacryloyl,GelMA)与具有良好骨传导性的β-磷酸三钙(β-tricalcium phosphate,β-TCP)复合,开发可植入骨缺损区域的材料,有望解决骨缺损的修复与功能重建难题.目的 合成GelMA/β-TCP/黑色素纳米颗粒(melanin nanoparticles,MNPs)复合水凝胶,并探究其对MC3T3-E1细胞的生物相容性、抗活性氧活性、生物学特性和促成骨分化作用.方法 采用5%GelMA、1%β-TCP和1 mg/mL MNPs,在0.25%苯基-2,4,6-三甲基苯甲酰基次膦酸锂(光引发剂)和 405 nm 光下合成单纯 GelMA、GelMA/β-TCP(GT)、GelMA/MNPs(GM)和GelMA/β-TCP/MNPs(GTM)4组材料,对其进行扫描电镜表征其微观结构.提取4组材料浸提液,并以普通培养基作为空白对照组,检测各组材料的生物相容性(CCK-8法、活死细胞染色、TUNEL染色)、抗活性氧活性(DCFH-DA荧光染色)、生物学特性(鬼笔环肽染色、Ki-67免疫荧光染色、划痕实验)及成骨作用(RUNX2和OCN免疫荧光染色、碱性磷酸酶染色、茜素红染色及实时荧光定量PCR检测成骨相关基因表达).结果 GTM水凝胶冻干后呈现出粗糙的三维孔隙结构,孔径大小为(103.61±16.90)μm,有利于细胞的黏附和增殖.GTM水凝胶有良好的生物相容性,CCK-8法、活死细胞染色、TUNEL染色检测结果显示各组水凝胶均未见明显细胞毒性.细胞内DCFH-DA染色结果表明,在GelMA中加入MNPs,可提高材料的抗细胞内活性氧能力(P<0.05).鬼笔环肽染色显示GTM水凝胶可提高细胞黏附性能;划痕实验表明其相较于对照组可以有效促进细胞迁移(P<0.001),Ki-67免疫荧光染色显示其相较于对照组和其他材料组可以促进细胞增殖(P<0.05).ALP染色结果显示,诱导7 d后GTM水凝胶组的ALP活性高于对照组及其他材料组;诱导14 d后,GTM水凝胶组诱导形成的钙结节数量多于其他组,覆盖面积也更大.RUNX2和OCN免疫荧光和qRT-PCR结果显示,相较于对照组和其他材料组,GTM水凝胶具有最强的成骨诱导能力(P<0.001).结论 GTM水凝胶具有良好的生物相容性和抗活性氧性能,可增强细胞增殖、迁移和黏附,促进MC3T3-E1细胞成骨分化,在骨组织工程领域具有应用前景.

Background By integrating gelatin methacryloyl(GelMA)with osteoconductive β-tricalcium phosphate(β-TCP)via tissue engineering strategies,we developed an implantable scaffold designed for bone defect regions.This composite material holds promise for addressing the challenges associated with bone repair and functional reconstruction.Objective To synthesize a GelMA/β-TCP/melanin nanoparticle(MNP)composite hydrogel and investigate its biocompatibility,reactive oxygen species(ROS)-scavenging capacity,biological properties,and osteogenic differentiation potential in MC3T3-E1 cells.Methods Four types of hydrogels were prepared under 0.25%LAP(photoinitiator)and 405 nm light:GelMA,GelMA/β-TCP,GelMA/MNPs,and GelMA/β-TCP/MNPs,using 5%GelMA,1%β-TCP,and 1 mg/mL MNPs.The microstructures of freeze-dried samples were characterized by scanning electron microscopy.Extracts from the four hydrogel groups were collected,with complete culture medium serving as a blank control.Biocompatibility was assessed using CCK-8 assay,live/dead staining,and TUNEL staining;anti-ROS activity was evaluated with DCFH-DA staining;biological property regulation was determined via phalloidin staining,Ki-67 immunofluorescence,and scratch wound assay;and osteogenic potential was assessed by RUNX2 and OCN immunofluorescence staining.Results Freeze-dried GelMA/β-TCP/MNP hydrogel exhibited a rough,three-dimensional porous structure with an average pore size of(103.61±16.90)μm,favorable for cell adhesion and proliferation.Biocompatibility assays indicated no obvious cytotoxicity in any group.Incorporation of MNPs into GelMA significantly enhanced intracellular ROS-scavenging activity.Biological property evaluations showed increased cell adhesion(phalloidin staining),promoted cell migration(scratch assay),and enhanced cell proliferation(Ki-67)in the GelMA/β-TCP/MNP group.Osteogenesis-related staining revealed that GelMA/β-TCP/MNP hydrogel exhibited the strongest osteoinductive ability compared with the control and other material groups.Conclusion GelMA/β-TCP/MNP hydrogel demonstrates excellent biocompatibility and effective ROS-scavenging activity,and enhances cell adhesion,migration,and proliferation,promote osteogenic differentiation of MC3T3-E1 cells,indicating promising potential for bone tissue engineering applications.

张鲁岳;黄萌;张敏;王朝祥;刘醒钊;刘天驰;王碧莹;曹均凯

解放军医学院,北京 100853||解放军总医院第一医学中心口腔科,北京 100853解放军总医院第六医学中心口腔科,北京 100048解放军总医院第八医学中心口腔科,北京 100091解放军医学院,北京 100853||解放军总医院第一医学中心口腔科,北京 100853解放军医学院,北京 100853||解放军总医院第一医学中心口腔科,北京 100853解放军医学院,北京 100853||解放军总医院第一医学中心口腔科,北京 100853解放军总医院第一医学中心口腔科,北京 100853解放军总医院第一医学中心口腔科,北京 100853

医药卫生

β-磷酸三钙黑色素水凝胶活性氧成骨

β-tricalcium phosphatemelanin nanoparticleshydrogelreactive oxygen speciesosteogenesis

《解放军医学院学报》 2026 (5)

473-483,11

10.12435/j.issn.2095-5227.25122301

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