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微病理芯片模拟神经血管单元对炎症性骨病的反应。

Micropathological Chip Modeling the Neurovascular Unit Response to Inflammatory Bone Condition.

机构信息

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, Porto, 4200-135, Portugal.

INEB - Instituto Nacional de Engenharia Biomédica, Universidade do Porto, Rua Alfredo Allen, 208, Porto, 4200-135, Portugal.

出版信息

Adv Healthc Mater. 2022 Jun;11(11):e2102305. doi: 10.1002/adhm.202102305. Epub 2022 Feb 25.

DOI:10.1002/adhm.202102305
PMID:35158409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11468530/
Abstract

Organ-on-a-chip in vitro platforms accurately mimic complex microenvironments offering the ability to recapitulate and dissect mechanisms of physiological and pathological settings, revealing their major importance to develop new therapeutic targets. Bone diseases, such as osteoarthritis, are extremely complex, comprising of the action of inflammatory mediators leading to unbalanced bone homeostasis and de-regulation of sensory innervation and angiogenesis. Although there are models to mimic bone vascularization or innervation, in vitro platforms merging the complexity of bone, vasculature, innervation, and inflammation are missing. Therefore, in this study a microfluidic-based neuro-vascularized bone chip (NVB chip) is proposed to 1) model the mechanistic interactions between innervation and angiogenesis in the inflammatory bone niche, and 2) explore, as a screening tool, novel strategies targeting inflammatory diseases, using a nano-based drug delivery system. It is possible to set the design of the platform and achieve the optimized conditions to address the neurovascular network under inflammation. Moreover, this system is validated by delivering anti-inflammatory drug-loaded nanoparticles to counteract the neuronal growth associated with pain perception. This reliable in vitro tool will allow understanding the bone neurovascular system, enlightening novel mechanisms behind the inflammatory bone diseases, bone destruction, and pain opening new avenues for new therapies discovery.

摘要

器官芯片体外平台能够准确模拟复杂的微环境,具有重现和剖析生理和病理状态下机制的能力,这揭示了它们对于开发新的治疗靶点的重要性。骨疾病,如骨关节炎,极其复杂,包含炎症介质的作用,导致骨稳态失衡和感觉神经支配和血管生成的失调。虽然有模拟骨血管生成或神经支配的模型,但缺乏将骨、血管、神经支配和炎症的复杂性融合在一起的体外平台。因此,在这项研究中,提出了一种基于微流控的神经血管化骨芯片(NVB 芯片),以 1)模拟炎症性骨龛中神经支配和血管生成之间的机械相互作用,2)探索针对炎症性疾病的新型策略,使用纳米药物递送系统作为筛选工具。可以设定平台的设计并实现优化条件,以解决炎症下的神经血管网络问题。此外,该系统通过递送载有抗炎药物的纳米颗粒来对抗与疼痛感知相关的神经元生长,从而得到验证。这种可靠的体外工具将有助于理解骨神经血管系统,阐明炎症性骨疾病、骨破坏和疼痛背后的新机制,为新疗法的发现开辟新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/7073ca9e4e7e/ADHM-11-2102305-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/81a6089c5d95/ADHM-11-2102305-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/b97bd8831ef1/ADHM-11-2102305-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/12157b1878ae/ADHM-11-2102305-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/7073ca9e4e7e/ADHM-11-2102305-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/81a6089c5d95/ADHM-11-2102305-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/a68fd2751c57/ADHM-11-2102305-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/dcf231e5274e/ADHM-11-2102305-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/b97bd8831ef1/ADHM-11-2102305-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e875/11468530/7073ca9e4e7e/ADHM-11-2102305-g005.jpg

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