Choi Jin-Ha, Choi Hye Kyu, Lee Ki-Bum
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey,123 Bevier Road, Piscataway, NJ 08854, USA.
School of Chemical Engineering, Jeonbuk National University, Jeonju, 54896, Korea.
Adv Funct Mater. 2023 Nov 9;33(46). doi: 10.1002/adfm.202304382. Epub 2023 Sep 1.
The human neurovascular system is a complex network of blood vessels and brain cells that is essential to the proper functioning of the brain. In recent years, researchers have become increasingly interested in the role of this system in developing drugs to treat neuroinflammation. This process is believed to contribute to the development of several neurodegenerative diseases, including Alzheimer's and Parkinson's diseases. While much remains to be learned about the precise mechanisms by which the neurovascular system interacts with the brain and how it can be targeted for therapeutic purposes, this area of research holds great promise for the future of neurology and medicine. Currently, creating neurovascular models begins with animal models, followed by testing on humans in clinical trials. However, the high number of medication failures that pass through animal testing indicates that animal models do not always reflect the outcome of human clinical trials. To overcome the challenges of neurovascular systems and the issues with animal models, we have developed a one-of-a-kind neurovascular unit-on-a-chip to accurately replicate the human neurovascular microenvironment. This neuroinflammation-on-a-chip platform has the potential to enhance the current methods of drug development and testing to treat neurodegenerative diseases. By replicating the human neurovascular unit in vitro, a more accurate representation of human physiology can be achieved compared to animal models. The ability to detect pro-inflammatory cytokines in situ and monitor physiological changes, such as barrier function, in real-time can provide an invaluable tool for evaluating the efficacy and safety of drugs. Moreover, using nano-sized graphene oxide for in situ detection of inflammatory responses is an innovative approach that can advance the field of neuroinflammation research. , our developed neuroinflammation-on-a-chip system has the potential to provide a more efficient and effective method for developing drugs for treating neurodegenerative diseases and other central nervous system (CNS) diseases.
人类神经血管系统是一个由血管和脑细胞组成的复杂网络,对大脑的正常运作至关重要。近年来,研究人员对该系统在开发治疗神经炎症药物中的作用越来越感兴趣。据信,这一过程会促使包括阿尔茨海默病和帕金森病在内的几种神经退行性疾病的发展。虽然关于神经血管系统与大脑相互作用的确切机制以及如何将其作为治疗靶点还有很多有待了解,但这一研究领域对神经病学和医学的未来具有巨大的潜力。目前,创建神经血管模型首先从动物模型开始,然后在临床试验中对人类进行测试。然而,大量通过动物测试的药物却失败了,这表明动物模型并不总是能反映人类临床试验的结果。为了克服神经血管系统的挑战以及动物模型存在的问题,我们开发了一种独一无二的芯片上神经血管单元,以精确复制人类神经血管微环境。这种芯片上神经炎症平台有潜力改进目前治疗神经退行性疾病的药物开发和测试方法。通过在体外复制人类神经血管单元,与动物模型相比,可以更准确地呈现人类生理学特征。原位检测促炎细胞因子以及实时监测诸如屏障功能等生理变化的能力,可为评估药物的疗效和安全性提供一个非常有价值的工具。此外,使用纳米尺寸的氧化石墨烯进行炎症反应的原位检测是一种创新方法,可推动神经炎症研究领域的发展。我们开发的芯片上神经炎症系统有潜力为开发治疗神经退行性疾病和其他中枢神经系统(CNS)疾病的药物提供一种更高效、更有效的方法。