Author:
Yu Zhihang,Chen Yiqun,Li Jingjing,Chen Chang,Lu Huaxiu,Chen Siyuan,Zhang Tingting,Guo Tianruo,Zhu Yonggang,Jin Jing,Yan Sheng,Chen Huaying
Abstract
AbstractPathological conditions linked to shear stress have been identified in hematological diseases, cardiovascular diseases, and cancer. These conditions often exhibit significantly elevated shear stress levels, surpassing 1000 dyn/cm2 in severely stenotic arteries. Heightened shear stress can induce mechanical harm to endothelial cells, potentially leading to bleeding and fatal consequences. However, current technology still grapples with limitations, including inadequate flexibility in simulating bodily shear stress environments, limited range of shear stress generation, and spatial and temporal adaptability. Consequently, a comprehensive understanding of the mechanisms underlying the impact of shear stress on physiological and pathological conditions, like thrombosis, remains inadequate. To address these limitations, this study presents a microfluidic-based shear stress generation chip as a proposed solution. The chip achieves a substantial 929-fold variation in shear stress solely by adjusting the degree of constriction in branch channels after PDMS fabrication. Experiments demonstrated that a rapid increase in shear stress up to 1000 dyn/cm2 significantly detached 88.2% cells from the substrate. Long-term exposure (24 h) to shear stress levels below 8.3 dyn/cm2 did not significantly impact cell growth. Furthermore, cells exposed to shear stress levels equal to or greater than 8.3 dyn/cm2 exhibited significant alterations in aspect ratio and orientation, following a normal distribution. This microfluidic chip provides a reliable tool for investigating cellular responses to the wide-ranging shear stress existing in both physiological and pathological flow conditions.
Graphical Abstract
Funder
National Natural Science Foundation of China
Natural Science Foundation of Guangdong Province
Science, Technology and Innovation Commission of Shenzhen Municipality
Shenzhen University 2035 Program for Excellent Research
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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