Mechanical Stimulation: A Crucial Element of Organ-on-Chip Models

被引:87
作者
Thompson, Clare L. [1 ]
Fu, Su [1 ]
Knight, Martin M. [1 ]
Thorpe, Stephen D. [2 ]
机构
[1] Queen Mary Univ London, Sch Engn & Mat Sci, Ctr Predict In Vitro Models, London, England
[2] Univ Coll Dublin, UCD Conway Inst Biomol & Biomed Res, UCD Sch Med, Dublin, Ireland
基金
英国医学研究理事会;
关键词
microphysiological systems; organ-on-chip; mechanobiology; biomechanics; biomechanical stimulation; pre-clinical model; tensile strain; fluid shear; IN-VITRO MODEL; A-CHIP; HUMAN LIVER; STEM-CELLS; PERSONALIZED MEDICINE; FLUID SHEAR; 1ST STEP; LUNG; KIDNEY; COCULTURE;
D O I
10.3389/fbioe.2020.602646
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Organ-on-chip (OOC) systems recapitulate key biological processes and responses in vitro exhibited by cells, tissues, and organs in vivo. Accordingly, these models of both health and disease hold great promise for improving fundamental research, drug development, personalized medicine, and testing of pharmaceuticals, food substances, pollutants etc. Cells within the body are exposed to biomechanical stimuli, the nature of which is tissue specific and may change with disease or injury. These biomechanical stimuli regulate cell behavior and can amplify, annul, or even reverse the response to a given biochemical cue or drug candidate. As such, the application of an appropriate physiological or pathological biomechanical environment is essential for the successful recapitulation of in vivo behavior in OOC models. Here we review the current range of commercially available OOC platforms which incorporate active biomechanical stimulation. We highlight recent findings demonstrating the importance of including mechanical stimuli in models used for drug development and outline emerging factors which regulate the cellular response to the biomechanical environment. We explore the incorporation of mechanical stimuli in different organ models and identify areas where further research and development is required. Challenges associated with the integration of mechanics alongside other OOC requirements including scaling to increase throughput and diagnostic imaging are discussed. In summary, compelling evidence demonstrates that the incorporation of biomechanical stimuli in these OOC or microphysiological systems is key to fully replicating in vivo physiology in health and disease.
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页数:18
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