Li Chunyan, Chaung Wayne, Mozayan Cameron, Chabra Ranjeev, Wang Ping, Narayan Raj K
Cushing Neuromonitoring Laboratory, The Feinstein Institute for Medical Research, Manhasset, New York, United States of America.
Department of Neurosurgery, Hofstra Northwell School of Medicine, Manhasset, New York, United States of America.
PLoS One. 2016 May 24;11(5):e0155921. doi: 10.1371/journal.pone.0155921. eCollection 2016.
The development of in vitro disease models closely mimicking the functions of human disease has captured increasing attention in recent years. Oxygen tensions and gradients play essential roles in modulating biological systems in both physiologic and pathologic events. Thus, controlling oxygen tension is critical for mimicking physiologically relevant in vivo environments for cell, tissue and organ research. We present a new approach for on-demand generation of various oxygen tensions for in vitro hypoxia models. Proof-of-concept prototypes have been developed for conventional cell culture microplate by immobilizing a novel oxygen-consuming biomaterial on the 3D-printed insert. For the first time, rapid (~3.8 minutes to reach 0.5% O2 from 20.9% O2) and precisely controlled oxygen tensions/gradients (2.68 mmHg per 50 μm distance) were generated by exposing the biocompatible biomaterial to the different depth of cell culture media. In addition, changing the position of 3D-printed inserts with immobilized biomaterials relative to the cultured cells resulted in controllable and rapid changes in oxygen tensions (<130 seconds). Compared to the current technologies, our approach allows enhanced spatiotemporal resolution and accuracy of the oxygen tensions. Additionally, it does not interfere with the testing environment while maintaining ease of use. The elegance of oxygen tension manipulation introduced by our new approach will drastically improve control and lower the technological barrier of entry for hypoxia studies. Since the biomaterials can be immobilized in any devices, including microfluidic devices and 3D-printed tissues or organs, it will serve as the basis for a new generation of experimental models previously impossible or very difficult to implement.
近年来,能够紧密模拟人类疾病功能的体外疾病模型的开发受到了越来越多的关注。氧张力和梯度在生理和病理过程中调节生物系统方面发挥着重要作用。因此,控制氧张力对于模拟细胞、组织和器官研究中与生理相关的体内环境至关重要。我们提出了一种新方法,用于按需生成用于体外缺氧模型的各种氧张力。通过将一种新型耗氧生物材料固定在3D打印的插入物上,已为传统细胞培养微孔板开发了概念验证原型。首次通过将生物相容性生物材料暴露于细胞培养基的不同深度,快速(从20.9% O₂ 达到0.5% O₂ 约需3.8分钟)且精确地控制了氧张力/梯度(每50μm距离2.68 mmHg)。此外,改变固定有生物材料的3D打印插入物相对于培养细胞的位置会导致氧张力可控且快速变化(<130秒)。与当前技术相比,我们的方法提高了氧张力的时空分辨率和准确性。此外,它在保持易用性的同时不干扰测试环境。我们新方法引入的氧张力操纵的精妙之处将极大地改善控制并降低缺氧研究的技术准入门槛。由于生物材料可以固定在任何设备中,包括微流控设备和3D打印的组织或器官,它将成为新一代以前无法实现或很难实施的实验模型的基础。