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芯片上的附着点炎——一种研究附着点急慢性炎症及其药物治疗的模型

Enthesitis on Chip - A Model for Studying Acute and Chronic Inflammation of the Enthesis and its Pharmacological Treatment.

作者信息

Giacomini Francesca, Rho Hoon Suk, Eischen-Loges Maria, Tahmasebi Birgani Zeinab, van Blitterswijk Clemens, van Griensven Martijn, Giselbrecht Stefan, Habibović Pamela, Truckenmüller Roman

机构信息

Department of Instructive Biomaterials Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Universiteitssingel 40, Maastricht, 6229 ER, The Netherlands.

Department of Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Universiteitssingel 40, Maastricht, 6229 ER, The Netherlands.

出版信息

Adv Healthc Mater. 2024 Dec;13(31):e2401815. doi: 10.1002/adhm.202401815. Epub 2024 Aug 27.

DOI:10.1002/adhm.202401815
PMID:39188199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11650547/
Abstract

Enthesitis, the inflammation of the enthesis, which is the point of attachment of tendons and ligaments to bones, is a common musculoskeletal disease. The inflammation often originates from the fibrocartilage region of the enthesis as a consequence of mechanical overuse or -load and consequently tissue damage. During enthesitis, waves of inflammatory cytokines propagate in(to) the fibrocartilage, resulting in detrimental, heterotopic bone formation. Understanding of human enthesitis and its treatment options is limited, also because of lacking in vitro model systems that can closely mimic the pathophysiology of the enthesis and can be used to develop therapies. In this study, an enthes(it)is-on-chip model is developed. On opposite sides of a porous culture membrane separating the chip's two microfluidic compartments, human mesenchymal stromal cells are selectively differentiated into tenocytes and fibrochondrocytes. By introducing an inflammatory cytokine cocktail into the fibrochondrocyte compartment, key aspects of acute and chronic enthesitis, measured as increased expression of inflammatory markers, can be recapitulated. Upon inducing chronic inflammatory conditions, hydroxyapatite deposition, enhanced osteogenic marker expression and reduced secretion of tissue-related extracellular matrix components are observed. Adding the anti-inflammatory drug celecoxib to the fibrochondrocyte compartment mitigates the inflammatory state, demonstrating the potential of the enthesitis-on-chip model for drug testing.

摘要

附着点炎是肌腱和韧带附着于骨骼处的附着点发生的炎症,是一种常见的肌肉骨骼疾病。这种炎症通常源于附着点的纤维软骨区域,是机械性过度使用或负荷以及由此导致的组织损伤的结果。在附着点炎期间,炎症细胞因子波在纤维软骨中传播,导致有害的异位骨形成。对人类附着点炎及其治疗选择的了解有限,这也是因为缺乏能够紧密模拟附着点病理生理学并可用于开发治疗方法的体外模型系统。在本研究中,开发了一种芯片上的附着点炎模型。在分隔芯片两个微流体隔室的多孔培养膜的相对两侧,人间充质基质细胞被选择性地分化为成纤维细胞和纤维软骨细胞。通过将炎症细胞因子混合物引入纤维软骨细胞隔室,可以重现急性和慢性附着点炎的关键方面,以炎症标志物表达增加来衡量。在诱导慢性炎症条件时,观察到羟基磷灰石沉积、成骨标志物表达增强以及组织相关细胞外基质成分的分泌减少。向纤维软骨细胞隔室添加抗炎药物塞来昔布可减轻炎症状态,证明了芯片上的附着点炎模型在药物测试中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21ec/11650547/d177c06649e3/ADHM-13-0-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21ec/11650547/7f0e4c7a5d9b/ADHM-13-0-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21ec/11650547/c6bb13064dc4/ADHM-13-0-g005.jpg
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