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广泛可用的3D皮肤模型作为抗菌治疗筛选的综合平台

Broadly Accessible 3D Skin Model as a Comprehensive Platform for Antibacterial Therapy Screening.

作者信息

Villata Simona, Baruffaldi Désirée, Cue Lopez Raquel, Paoletti Camilla, Bosch Paula, Napione Lucia, Giovannozzi Andrea M, Pirri Candido Fabrizio, Martinez-Campos Enrique, Frascella Francesca

机构信息

Dipartimento di Scienza Applicata e Tecnologia, PolitoBIOMed Lab, Politecnico di Torino, Turin 10129, Italy.

Dipartimento di Ingegneria Meccanica e Aerospaziale, Politecnico di Torino, Turin 10129, Italy.

出版信息

ACS Appl Mater Interfaces. 2024 Dec 25;16(51):70284-70296. doi: 10.1021/acsami.4c16397. Epub 2024 Dec 12.

DOI:10.1021/acsami.4c16397
PMID:39667725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11672480/
Abstract

Skin infections are currently a worldwide emergency as antibiotic-resistant bacteria are spreading, leading to the ineffectiveness of most antibiotics and antibacterial strategies. Consequently, there is an urgency of developing and testing innovative antibacterial therapies. As traditional 2D cell culture and planktonic bacteria culture can be obsolete due to their incapability of resembling the complex infection environment, 3D skin models can be a powerful tool to test and validate therapies. In this article, a 3D epidermis-dermis skin model has been developed and biofabricated to be broadly available, reaching a balance between the simplicity and reproducibility of the model and its complexity in terms of wound, infection, and treatment response. The results are really promising, as the skin model developed a comprehensive physical barrier. To further investigate the skin model, controlled wounding, infection, and antibiotic treatments were performed. The results were remarkable: Not only was the unwounded epidermal barrier able to partially stop the bacterial proliferation, but the entire system reacted to both wound and infection in a complex and complete way. Extracellular matrix deposition and remodeling, inflammatory response, antimicrobial peptide production, and change in cellular behaviors, from epithelial to mesenchymal and from fibroblasts to myofibroblasts, were witnessed, with different extents depending on the bacterial strain. In addition, the inflammatory response to the antibiotic administration was opposite for the two bacterial infections, probably revealing the release of inflammatory endotoxins during death. In conclusion, the presented 3D skin model has all the characteristics to be a future landmark as a platform for antibacterial strategy therapy testing.

摘要

由于抗生素耐药性细菌正在传播,导致大多数抗生素和抗菌策略失效,皮肤感染目前已成为一个全球性的紧急情况。因此,开发和测试创新的抗菌疗法迫在眉睫。由于传统的二维细胞培养和浮游细菌培养无法模拟复杂的感染环境,可能已过时,三维皮肤模型可以成为测试和验证疗法的有力工具。在本文中,已经开发并生物制造了一种三维表皮-真皮皮肤模型,使其广泛可用,在模型的简单性、可重复性与其在伤口、感染和治疗反应方面的复杂性之间取得了平衡。结果非常有前景,因为该皮肤模型形成了一个全面的物理屏障。为了进一步研究该皮肤模型,进行了可控的伤口、感染和抗生素治疗。结果令人瞩目:不仅未受伤的表皮屏障能够部分阻止细菌增殖,而且整个系统对伤口和感染都做出了复杂而完整的反应。观察到细胞外基质沉积和重塑、炎症反应、抗菌肽产生以及细胞行为的变化,从上皮细胞到间充质细胞,从成纤维细胞到肌成纤维细胞,其程度因细菌菌株而异。此外,两种细菌感染对抗生素给药的炎症反应相反,这可能揭示了死亡期间炎症内毒素的释放。总之,所展示的三维皮肤模型具有成为未来作为抗菌策略治疗测试平台的标志性模型的所有特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/33fa28518d26/am4c16397_0008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/f342822550b9/am4c16397_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/cc619e026406/am4c16397_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/0af5b7f88c01/am4c16397_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/98bfbd0a206c/am4c16397_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/a8524d27f249/am4c16397_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/c291cd53f4c6/am4c16397_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26a/11672480/33fa28518d26/am4c16397_0008.jpg

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