Fathi Parinaz, Holland Glenn, Pan Dipanjan, Esch Mandy B
Biomedical Technologies Group, Microsystems and Nanotechnology Division, Physical Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, United States.
Departments of Bioengineering, Materials Science and Engineering, and Beckman Institute, University of Illinois at Urbana-Champaign, Champaign, Illinois 61801, United States.
ACS Appl Bio Mater. 2020 Oct 19;3(10):6697-6707. doi: 10.1021/acsabm.0c00609. Epub 2020 Sep 21.
The lymphatic system is a complex organ system that is essential in regulating the development of host immune responses. Because of the complexity of the lymphatic system and the existence of few models that replicate human lymphatic vessels, there is a need for a primary cell-based lymphatic model that can provide a better understanding of the effects of flow parameters, therapeutics, and other stimuli on lymphatic vessel behavior. In this report, a fluidic device models the cyclical lymphatic flow under normal and disease conditions. The device utilizes a pumpless design, operating with gravitational forces to simulate normal conditions with a shear of 0.092 Pa (0.92 dyn/cm) as well as disease conditions with an increased shear of (0.67 Pa, 6.7 dyn/cm). The cyclical pumping present in lymphatic vessels is replicated by applying shear stress for a period of 10 s multiple times per minute. Primary human lymphatic endothelial cells (HLECs) cultured in the device for 10 days produce less interleukin 8 (IL-8), and tumor necrosis factor alpha (TNF-α) per cell than cells cultured under static conditions. The results are consistent with previously published measurements, indicating that the fluidic device mimics conditions for IL-8 and TNF-α expression well. Data obtained with the devices also indicate that primary HLECs proliferate faster under high-shear than under low-shear conditions.
淋巴系统是一个复杂的器官系统,在调节宿主免疫反应的发展中至关重要。由于淋巴系统的复杂性以及很少有能复制人类淋巴管的模型,因此需要一种基于原代细胞的淋巴模型,以便更好地理解流动参数、治疗方法和其他刺激对淋巴管行为的影响。在本报告中,一种流体装置模拟了正常和疾病条件下的周期性淋巴流动。该装置采用无泵设计,利用重力运行,以模拟正常条件下0.092帕(0.92达因/平方厘米)的剪切力以及疾病条件下增加到(0.67帕,6.7达因/平方厘米)的剪切力。通过每分钟多次施加10秒的剪切应力来复制淋巴管中存在的周期性泵送。在该装置中培养10天的原代人淋巴管内皮细胞(HLEC),与在静态条件下培养的细胞相比,每个细胞产生的白细胞介素8(IL-8)和肿瘤坏死因子α(TNF-α)更少。结果与先前发表的测量结果一致,表明该流体装置能很好地模拟IL-8和TNF-α的表达条件。该装置获得的数据还表明,原代HLEC在高剪切条件下比在低剪切条件下增殖更快。