Department of Intelligent Systems Engineering, Indiana University, Bloomington, Indiana 47405, United States.
Gill Center for Biomolecular Science, and Department of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana 47405, United States.
Anal Chem. 2022 Jan 18;94(2):1365-1372. doi: 10.1021/acs.analchem.1c04641. Epub 2021 Dec 20.
The discovery of new pain therapeutics targeting human nociceptive circuitry is an emerging, exciting, and rewarding field. However, current models for evaluating prospective new therapeutics [e.g., animals and two-dimensional (2D) cultures] fail to fully recapitulate the complexity of human nociceptive neuron and dorsal horn neuron biology, significantly limiting the development of novel pain therapeutics. Here, we report human spinal organoid-on-a-chip devices for modeling the biology and electrophysiology of human nociceptive neurons and dorsal horn interneurons in nociceptive circuitry. Our device can be simply made through the integration of a membrane with a three-dimensional (3D)-printed organoid holder. By combining air-liquid interface culture and spinal organoid protocols, our devices can differentiate human stem cells into human sensori-spinal-cord organoids with dorsal spinal cord interneurons and sensory neurons. By easily transferring from culture well plates to the multiple-electrode array (MEA) system, our device also allows the plug-and-play measurement of organoid activity for testing nociceptive modulators (e.g., mustard oil, capsaicin, velvet ant venom, etc.). Our organoid-on-a-chip devices are cost-efficient, scalable, easy to use, and compatible with conventional well plates, allowing the plug-and-play measurement of spinal organoid electrophysiology. By the integration of human sensory-spinal-cord organoids with our organoid-on-a-chip devices, our method may hold the promising potential to screen and validate novel therapeutics for human pain medicine discovery.
针对人类伤害感受回路的新型疼痛治疗药物的发现是一个新兴的、令人兴奋的和有益的领域。然而,目前用于评估潜在新型治疗药物的模型[例如,动物和二维(2D)培养物]未能充分再现人类伤害感受神经元和背角神经元生物学的复杂性,这极大地限制了新型疼痛治疗药物的开发。在这里,我们报告了用于模拟人类伤害感受神经元和背角中间神经元在伤害感受回路中的生物学和电生理学的人类脊髓类器官芯片设备。我们的设备可以通过将膜与三维(3D)打印的类器官支架集成来简单地制造。通过结合气液界面培养和脊髓类器官方案,我们的设备可以将人类干细胞分化为具有背角脊髓中间神经元和感觉神经元的人类感觉-脊髓-器官。通过从培养孔板轻松转移到多电极阵列(MEA)系统,我们的设备还允许即插即用测量类器官的活性,以测试伤害感受调节剂(例如,芥末油、辣椒素、毛毡蚁毒素等)。我们的类器官芯片设备具有成本效益、可扩展性、易于使用且与常规孔板兼容,允许即插即用测量脊髓类器官的电生理学。通过将人类感觉-脊髓器官与我们的类器官芯片设备集成,我们的方法可能具有很大的潜力,可用于筛选和验证新型人类疼痛医学治疗药物。