Engineered Probiotics with Low Oxygen Targeting Porphyromonas gingivalis and Gingival Fibroblasts for the Treatment of Periodontitis.

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Shenghong Li, Zhibo Fan, Kaijun Zheng, Yujie Wu, Guannan Zhong, Xiaomei Xu
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引用次数: 0

Abstract

The overuse of antibiotics has increased the prevalence of drug-resistant bacteria in periodontitis. "Sentinel" gingival fibroblasts, stimulated by pathogenic bacteria, continue to release signaling factors that affect stem cell repair and recruit immune cells, resulting in persistent inflammation in periodontal tissues, eventually leading to the loosening and loss of teeth. Periodontal pathogenic bacteria cause surface hypoxia, and gingival fibroblasts in the inflammatory microenvironment express HIF-1α, promoting hypoxic areas in periodontal pockets. No drug delivery system is available for the hypoxic region of periodontal pockets. We synthesized BI NPs via berberine (BBR) and indocyanine green (ICG) and formed BIP NPs by wrapping BI NPs with polydopamine (PDA), and the BIP NPs were delivered to the hypoxic region of the periodontal pocket by hitchhiking with the anaerobic probiotic Bifidobacterium bifidum (Bif). The BIP NPs released berberin (BBR) under near-infrared (NIR) irradiation, which inhibited the sulfur metabolism of Porphyromonas gingivalis via mild photothermal action and BBR-targeted serine acetyltransferase, resulting in a decrease in resistance to oxidative stress, thus exerting a nonantibiotic bacteriostatic effect. This mild photothermal effect facilitated the uptake of BIP NPs bygingival fibroblasts. Moreover, BBR targeted nuclear factor-erythroid 2-related factor 2 (NRF2) to reduce ferroptosis, and the gingival fibroblast supernatant modulated macrophage polarization through the NF-κB pathway. In the periodontitis rat model, Bif@BIP+NIR treatment carried the drug to deep periodontal pockets, decreasing local gingival ferroptosis and alleviating periodontitis symptoms. To summarize, engineered probiotics target low-oxygen periodontal pockets for drug delivery, P. gingivalis for nonantibiotic bacterial inhibition, and gingival fibroblasts to mitigate ferroptosis, thus alleviating periodontitis to reduce periodontitis.

低氧靶向牙龈卟啉单胞菌和牙龈成纤维细胞的工程益生菌治疗牙周炎。
抗生素的过度使用增加了牙周炎中耐药细菌的患病率。“哨兵”牙龈成纤维细胞在病原菌的刺激下,不断释放影响干细胞修复的信号因子,招募免疫细胞,导致牙周组织持续炎症,最终导致牙齿松动和脱落。牙周致病菌引起表面缺氧,炎症微环境中的牙龈成纤维细胞表达HIF-1α,促进牙周袋缺氧区。目前尚无针对牙周袋缺氧区域的药物输送系统。我们通过小檗碱(BBR)和吲哚菁绿(ICG)合成BIP NPs,用聚多巴胺(PDA)包裹BIP NPs形成BIP NPs,并与厌氧益生菌两歧双歧杆菌(biidobacterium bifidium bifidum, biif)搭便车将BIP NPs传递到牙周袋缺氧区。BIP NPs在近红外(NIR)照射下释放小檗碱(berberin, BBR),通过轻度光热作用和BBR靶向丝氨酸乙酰转移酶抑制牙龈卟啉单胞菌的硫代谢,使其抗氧化应激能力下降,从而发挥非抗生素抑菌作用。这种轻微的光热效应促进了牙龈成纤维细胞对BIP NPs的摄取。此外,BBR靶向核因子-红细胞2相关因子2 (NRF2)减少铁凋亡,牙龈成纤维细胞上清通过NF-κB途径调节巨噬细胞极化。在牙周炎大鼠模型中,Bif@BIP+NIR治疗将药物输送到牙周深袋,减轻局部牙龈铁下垂,缓解牙周炎症状。综上所述,工程益生菌针对低氧牙周袋进行药物递送,针对牙龈卟啉卟啉进行非抗生素细菌抑制,针对牙龈成纤维细胞减轻铁下垂,从而减轻牙周炎,减少牙周炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
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