MDRCBB-Minnesota Dental Research Center for Biomaterials and Biomechanics, University of Minnesota, 16-212 Moos Tower, 515 Delaware St. SE, Minneapolis, Minnesota 55455, United States.
Institute of Stomatology, School and Hospital of Stomatology, Department of Prosthodontics, Wenzhou Medical University, 373 Xueyuan Xi Road, Wenzhou, Zhejiang 325027, China.
Acta Biomater. 2022 Mar 15;141:70-88. doi: 10.1016/j.actbio.2021.12.030. Epub 2021 Dec 29.
Teeth, long-lasting percutaneous organs, feature soft tissue attachment through adhesive structures, hemidesmosomes, in the junctional epithelium basement membrane adjacent to teeth. This soft tissue attachment prevents bacterial infection of the tooth despite the rich - and harsh - microbial composition of the oral cavity. Conversely, millions of percutaneous devices (catheters, dental, and orthopedic implants) fail from infection yearly. Standard of care antibiotic usage fuels antimicrobial resistance and is frequently ineffective. Infection prevention strategies, like for dental implants, have failed in generating durable soft tissue adhesion - like that seen with the tooth - to prevent bacterial colonization at the tissue-device interface. Here, inspired by the impervious natural attachment of the junctional epithelium to teeth, we synthesized four cell adhesion peptide (CAPs) nanocoatings, derived from basement membranes, to promote percutaneous device soft tissue attachment. The two leading nanocoatings upregulated integrin-mediated hemidesmosomes, selectively increased keratinocyte proliferation compared to fibroblasts, which cannot form hemidesmosomes, and expression of junctional epithelium adhesive markers. CAP nanocoatings displayed marked durability under simulated clinical conditions and the top performer CAP nanocoating was validated in a percutaneous implant murine model. Basement membrane CAP nanocoatings, inspired by the tooth and junctional epithelium, may provide an alternative anti-infective strategy for percutaneous devices to mitigate the worldwide threat of antimicrobial resistance. STATEMENT OF SIGNIFICANCE: Prevention and management of medical device infection is a significant healthcare challenge. Overzealous antibiotic use has motivated alternative material innovations to prevent infection. Here, we report implant cell adhesion peptide nanocoatings that mimic a long-lasting, natural "medical device," the tooth, through formation of cell adhesive structures called hemidesmosomes. Such nanocoatings sidestep the use of antimicrobial or antibiotic elements to form a soft-tissue seal around implants. The top performing nanocoatings prompted expression of hemidesmosomes and defensive factors to mimic the tooth and was validated in an animal model. Application of cell adhesion peptide nanocoatings may provide an alternative to preventing, rather that necessarily treating, medical device infection across a range of device indications, like dental implants.
牙齿是持久的经皮器官,通过附着在牙齿相邻的连接上皮基底膜中的黏附结构(半桥粒)与软组织相连。尽管口腔中微生物组成丰富且恶劣,但这种软组织附着可防止细菌感染牙齿。相反,每年有数百万人因感染而导致经皮器械(导管、牙科和骨科植入物)失效。标准的抗生素使用会助长抗菌药物耐药性,并且通常无效。感染预防策略,如牙科植入物,未能产生类似于牙齿的持久软组织附着,以防止细菌在组织-器械界面处定植。在这里,受连接上皮与牙齿之间不可渗透的天然附着的启发,我们合成了四种来源于基底膜的细胞黏附肽(CAP)纳米涂层,以促进经皮器械的软组织附着。两种领先的纳米涂层上调了整合素介导的半桥粒,与不能形成半桥粒的成纤维细胞相比,选择性地增加了角质形成细胞的增殖,并表达了连接上皮黏附标志物。CAP 纳米涂层在模拟临床条件下具有显著的耐久性,表现最佳的 CAP 纳米涂层在经皮植入物的小鼠模型中得到了验证。受牙齿和连接上皮启发的基底膜 CAP 纳米涂层可能为经皮器械提供一种抗感染策略,以减轻全球范围内抗菌药物耐药性的威胁。
预防和管理医疗器械感染是一个重大的医疗保健挑战。过度使用抗生素已促使人们采用替代材料创新来预防感染。在这里,我们报告了模仿长期存在的天然“医疗器械”——牙齿的植入细胞黏附肽纳米涂层,通过形成称为半桥粒的细胞黏附结构。这种纳米涂层避免了使用抗菌或抗生素元素在植入物周围形成软组织密封。表现最佳的纳米涂层促使半桥粒和防御因子的表达,以模仿牙齿,并在动物模型中得到了验证。细胞黏附肽纳米涂层的应用可能为预防医疗器械感染提供一种替代方案,而不是治疗感染,适用于各种器械适应症,如牙科植入物。