口腔医学 ›› 2026, Vol. 46 ›› Issue (7): 514-520.doi: 10.13591/j.cnki.kqyx.2026.07.005

• 基础与临床研究 • 上一篇    下一篇

重组人源化Ⅲ型胶原涂层促进聚醚醚酮表面细胞黏附与成骨分化的研究

穆文清1,2,3, 吕子昂1,2,3, 孙佳骏1,2,3, 郑凯3(), 张玮1,2,3()   

  1. 1 南京医科大学附属口腔医院口腔特诊科, 江苏南京 (210029)
    2 口腔疾病研究与防治国家级重点实验室培育建设点(南京医科大学), 江苏南京 (210029)
    3 江苏省口腔转化医学工程研究中心(南京医科大学), 江苏南京 (210029)
  • 收稿日期:2026-02-07 出版日期:2026-07-28 发布日期:2026-07-23
  • 通讯作者: 张 玮 E-mail:zhangwei0508@njmu.edu.cn;
    郑 凯 E-mail:kaizheng@njmu.edu.cn
  • 基金资助:
    江苏省自然科学基金青年科技人才专项基金(BK20171057);江苏省科教能力提升工程——江苏省研究型医院(YJXYYJSDW4);江苏省医学创新中心(CXZX202227)

Recombinant humanized type Ⅲ collagen coating enhances cell adhesion and osteogenic differentiation on polyetheretherketone

MU Wenqing1,2,3, LYU Ziang1,2,3, SUN Jiajun1,2,3, ZHENG Kai3(), ZHANG Wei1,2,3()   

  1. 1 Department of Oral Special Consultation, The Affiliated Stomatological Hospital of Nanjing Medical University, Nanjing 210029, China
  • Received:2026-02-07 Online:2026-07-28 Published:2026-07-23

摘要:

目的 本研究旨在构建聚多巴胺(polydopamine,PDA)介导的重组人源化Ⅲ型胶原涂层,以改善聚醚醚酮(polyetheretherketone,PEEK)的表面生物活性。方法 采用两步浸渍法构建复合涂层。首先将PEEK浸泡于多巴胺(dopamine,DA)溶液中原位自聚,形成PDA-PEEK中间层,随后浸入重组人源化Ⅲ型胶原溶液制备Col-PEEK,利用扫描电子显微镜(scanning electron microscopy,SEM)、水接触角测量、傅里叶变换红外光谱(Fourier transform infrared spectrum,FTIR)和X射线光电子能谱(X-ray photoelectron spectroscopy,XPS)进行表面表征。以人颌骨骨髓间充质干细胞(human jaw bone marrow mesenchymal stem cells,hjBMMSCs)为模型,分别采用完全培养基(Control组)或不同材料的浸提液(PEEK、PDA-PEEK、Col-PEEK组)进行培养,通过CCK-8法检测细胞增殖,显微镜观察黏附形态,使用碱性磷酸酶(alkaline phosphatase,ALP)活性定量及茜素红S(alizarin red S,ARS)染色半定量评估成骨分化与矿化能力,RT-qPCR检测成骨相关基因表达水平。结果 SEM显示涂层均匀附着,表面改性未改变基材微观形貌;Col-PEEK水接触角显著降低(P<0.05),亲水性明显改善;FTIR与XPS证实Ⅲ型胶原成功固定于PDA层;CCK-8结果表明改性材料无细胞毒性;Col-PEEK组细胞呈现更多丝状伪足、铺展更充分;Col-PEEK组细胞ALP活性显著升高,钙结节沉积量明显增加(P<0.05),成骨分化关键基因表达水平显著上调(P<0.05)。结论 PDA介导的重组人源化Ⅲ型胶原涂层可显著提升PEEK表面的亲水性、细胞黏附能力和成骨诱导活性,为PEEK在口腔种植及颌骨修复领域的临床转化提供了新型表面改性策略和实验依据。

关键词: 聚醚醚酮, 表面改性, 生物活性, 细胞黏附, 成骨分化

Abstract:

Objective To improve the surface bioactivity of polyetheretherketone (PEEK) by constructing a polydopamine (PDA)-mediated recombinant humanized type Ⅲ collagen coating. Methods A composite coating was fabricated using a two-step immersion method. Briefly, PEEK substrates were first immersed in a dopamine (DA) solution to form an in situ self-polymerized PDA intermediate layer (PDA-PEEK), followed by immersion in a recombinant humanized type Ⅲ collagen solution to obtain Col-PEEK. Surface characteristics were analyzed using scanning electron microscopy (SEM), water contact angle measurement, Fourier transform infrared spectrum (FTIR), and X-ray photoelectron spectroscopy (XPS). Human jaw bone marrow mesenchymal stem cells (hjBMMSCs) were used as a model. Cells were cultured either with complete medium (Control group) or with material extracts (PEEK, PDA-PEEK, and Col-PEEK groups), and cell proliferation was then evaluated using the CCK-8 assay. Cell adhesion morphology was observed microscopically. Osteogenic differentiation and mineralization were assessed by quantitative alkaline phosphatase (ALP) activity analysis and semi-quantitative alizarin red S (ARS) staining. The expression levels of osteogenesis-related genes were determined by RT-qPCR. Results SEM observations revealed that the coating was uniformly distributed without altering the microstructure of the substrate. The water contact angle of Col-PEEK was significantly reduced (P<0.05), indicating markedly improved hydrophilicity. FTIR and XPS analyses confirmed the successful immobilization of type Ⅲ collagen onto the PDA layer. CCK-8 assays demonstrated that the modified materials exhibited no cytotoxicity. Cells cultured on Col-PEEK displayed enhanced spreading and more filopodia formation. ALP activity and calcium nodule deposition were significantly increased(P<0.05), accompanied by a marked upregulation of key osteogenic gene expression(P<0.05). Conclusion The PDA-mediated recombinant humanized type Ⅲ collagen composite coating significantly enhances the hydrophilicity, cell adhesion, and osteoinductive activity of PEEK surfaces. This modification strategy provides a novel surface modification approach and experimental evidence for the clinical translation of PEEK in oral implantation and maxillofacial bone regeneration.

Key words: polyetheretherketone, surface modification, bioactivity, cell adhesion, osteogenic differentiation

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