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[抗菌肽生物功能化二氧化钛纳米管对人角质形成细胞生物学行为的影响及其抗菌作用]

[Influence of antimicrobial peptide biofunctionalized TiO nanotubes on the biological behavior of human keratinocytes and its antibacterial effect].

作者信息

Li Y, Wang J J, He Y D, Xu M, Li X Y, Xu B Y, Zhang Y M

机构信息

Department of Prosthodontics, School of Stomatology, The Fourth Military Medical University & State Key Laboratory of Military Stomatology & National Clinical Research Center for Oral Diseases & Shaanxi Key Laboratory of Stomatology, Xi'an 710032, China.

Department of Periodontology, School of Stomatology, The Fourth Military Medical University & State Key Laboratory of Military Stomatology & National Clinical Research Center for Oral Diseases & Shaanxi Engineering Research Center for Dental Materials and Advanced Manufacture, Xi'an 710032, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2023 Feb 9;58(2):165-173. doi: 10.3760/cma.j.cn112144-20221023-00550.

Abstract

To fabricate TiO nanotube material functionalized by antimicrobial peptide LL-37, and to explore its effects on biological behaviors such as adhesion and migration of human keratinocytes (HaCaT) and its antibacterial properties. The TiO nanotube array (NT) was constructed on the surface of polished titanium (PT) by anodization, and the antimicrobial peptide LL-37 was loaded on the surface of TiO nanotube (LL-37/NT) by physical adsorption. Three samples were selected by simple random sampling in each group. Surface morphology, roughness, hydrophilicity and release characteristics of LL-37 of the samples were analyzed with a field emission scanning electron microscope, an atomic force microscope, a contact angle measuring device and a microplate absorbance reader. HaCaT cells were respectively cultured on the surface of three groups of titanium samples. Each group had 3 replicates. The morphology of cell was observed by field emission scanning electron microscope. The number of cell adhesion was observed by cellular immunofluorescence staining. Cell counting kit-8 (CCK-8) assay was used to detect cell proliferation. Wound scratch assay was used to observe the migration of HaCaT. The above experiments were used to evaluate the effect of each group on the biological behavior of HaCaT cells. To evaluate their antibacterial effects, (Pg) was respectively inoculated on the surface of three groups of titanium samples. Each group had 3 replicates. The morphology of bacteria was observed by field emission scanning electron microscope. Bacterial viability was determined by live/dead bacterial staining. A uniform array of nanotubes could be seen on the surface of titanium samples in LL-37/NT group, and the top of the tube was covered with granular LL-37. Compared with PT group [the roughness was (2.30±0.18) nm, the contact angle was 71.8°±1.7°], the roughness [(20.40±3.10) and (19.10±4.11) nm] and hydrophilicity (the contact angles were 22.4°±3.1° and 25.3°±2.2°, respectively) of titanium samples increased in NT and LL-37/NT group (<0.001). The results of release test showed that the release of antimicrobial peptide LL-37 was characterized by early sudden release (1-4 h) and long-term (1-7 d) slow release. With the immunofluorescence, more cell attachment was found on NT and LL-37/NT than that on PT at the first 0.5 and 2.0 h of culture (<0.05). The results of CCK-8 showed that there was no significant difference in the proliferation of cells among groups at 1, 3 and 5 days after culture. Wound scratch assay showed that compared with PT and NT group, the cell moved fastest on the surface of titanium samples in LL-37/NT group at 24 h of culture [(96.4±4.9)%] (=35.55, <0.001). A monolayer cells could be formed and filled with the scratch in 24 h at LL-37/NT group. The results of bacterial test showed that compared with the PT group, the bacterial morphology in the NT and LL-37/NT groups was significantly wrinkled, and obvious bacterial rupture could be seen on the surface of titanium samples in LL-37/NT group. The results of bacteria staining showed that the green fluorescence intensity of titanium samples in LL-37/NT group was the lowest in all groups (=66.54,<0.001). LL-37/NT is beneficial to the adhesion and migration of HaCaT cells and has excellent antibacterial properties, this provides a new strategy for the optimal design of implant neck materials.

摘要

制备抗菌肽LL-37功能化的TiO纳米管材料,并探讨其对人角质形成细胞(HaCaT)黏附、迁移等生物学行为的影响及其抗菌性能。通过阳极氧化在抛光钛(PT)表面构建TiO纳米管阵列(NT),采用物理吸附法将抗菌肽LL-37负载于TiO纳米管表面(LL-37/NT)。每组通过简单随机抽样选取3个样本。用场发射扫描电子显微镜、原子力显微镜、接触角测量仪和酶标仪分析样本的表面形貌、粗糙度、亲水性及LL-37的释放特性。将HaCaT细胞分别培养于三组钛样本表面,每组设3个重复。用场发射扫描电子显微镜观察细胞形态,用细胞免疫荧光染色观察细胞黏附数量,采用细胞计数试剂盒-8(CCK-8)法检测细胞增殖,用划痕实验观察HaCaT细胞的迁移情况。上述实验用于评估每组对HaCaT细胞生物学行为的影响。为评估其抗菌效果,将牙龈卟啉单胞菌(Pg)分别接种于三组钛样本表面,每组设3个重复。用场发射扫描电子显微镜观察细菌形态,用死活细菌染色法测定细菌活力。LL-37/NT组钛样本表面可见均匀的纳米管阵列,管顶部覆盖有颗粒状LL-37。与PT组[粗糙度为(2.30±0.18)nm,接触角为71.8°±1.7°]相比,NT组和LL-37/NT组钛样本的粗糙度[分别为(20.40±3.10)和(19.10±4.11)nm]和亲水性(接触角分别为22.4°±3.1°和25.3°±2.2°)增加(P<0.001)。释放试验结果显示,抗菌肽LL-37的释放表现为初期突发释放(14 h)和长期(17 d)缓慢释放。免疫荧光结果显示,培养0.5 h和2.0 h时,NT组和LL-37/NT组黏附的细胞多于PT组(P<0.05)。CCK-8结果显示,培养1、3和5 d时,各组细胞增殖无显著差异。划痕实验显示,培养24 h时,与PT组和NT组相比,LL-37/NT组钛样本表面细胞迁移最快[(96.4±4.9)%](F=35.55,P<0.001)。LL-37/NT组在24 h时可形成单层细胞并填充划痕。细菌检测结果显示,与PT组相比,NT组和LL-37/NT组细菌形态明显皱缩,LL-37/NT组钛样本表面可见明显的细菌破裂。细菌染色结果显示,LL-37/NT组钛样本的绿色荧光强度在所有组中最低(F=66.54,P<0.001)。LL-37/NT有利于HaCaT细胞的黏附与迁移,具有优异的抗菌性能,为种植体颈部材料的优化设计提供了新策略。

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