Microsystems Research Section, Department of Mechanical Engineering, Eindhoven University of Technology, Eindhoven, 5600 MB, The Netherlands.
Institute for Complex Molecular Systems (ICMS), Eindhoven University of Technology, Eindhoven, 5600 MB, The Netherlands.
Adv Sci (Weinh). 2024 Aug;11(30):e2400970. doi: 10.1002/advs.202400970. Epub 2024 Jun 13.
Organ-on-a-chip (OOC) models based on microfluidic technology are increasingly used to obtain mechanistic insight into (patho)physiological processes in humans, and they hold great promise for application in drug development and regenerative medicine. Despite significant progress in OOC development, several limitations of conventional microfluidic devices pose challenges. First, most microfluidic systems have rectangular cross sections and flat walls, and therefore tubular/ curved structures, like blood vessels and nephrons, are not well represented. Second, polymers used as base materials for microfluidic devices are much stiffer than in vivo extracellular matrix (ECM). Finally, in current cell seeding methods, challenges exist regarding precise control over cell seeding location, unreachable spaces due to flow resistances, and restricted dimensions/geometries. To address these limitations, an alternative cell seeding technique and a corresponding workflow is introduced to create circular cross-sectioned tubular OOC models by pre-wrapping cells around sacrificial fiber templates. As a proof of concept, a perfusable renal proximal tubule-on-a-chip is demonstrated with a diameter as small as 50 µm, cellular tubular structures with branches and curvature, and a preliminary vascular-renal tubule interaction model. The cell pre-wrapping seeding technique promises to enable the construction of diverse physiological/pathological models, providing tubular OOC systems for mechanistic investigations and drug development.
基于微流控技术的器官芯片(OOC)模型越来越多地被用于获得人类(病理)生理学过程的机制见解,并且它们在药物开发和再生医学中的应用具有很大的前景。尽管 OOC 的发展取得了重大进展,但传统微流控设备的几个局限性带来了挑战。首先,大多数微流控系统具有矩形横截面和平壁,因此管状/弯曲结构,如血管和肾单位,不能很好地代表。其次,用作微流控设备基础材料的聚合物比体内细胞外基质(ECM)硬得多。最后,在当前的细胞播种方法中,存在关于细胞播种位置的精确控制、由于流动阻力而无法到达的空间以及受限的尺寸/几何形状的挑战。为了解决这些限制,引入了一种替代的细胞播种技术和相应的工作流程,通过将细胞预包裹在牺牲纤维模板周围来创建圆形横截面的管状 OOC 模型。作为概念验证,展示了一种可灌注的肾近端小管芯片,其直径小至 50 µm,具有分支和弯曲的细胞管状结构,以及初步的血管-肾小管相互作用模型。细胞预包裹播种技术有望能够构建多样化的生理/病理模型,为机制研究和药物开发提供管状 OOC 系统。