2021
DOI: 10.3390/polym13173016
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Extracellular Matrix Optimization for Enhanced Physiological Relevance in Hepatic Tissue-Chips

Abstract: The cellular microenvironment is influenced explicitly by the extracellular matrix (ECM), the main tissue support biomaterial, as a decisive factor for tissue growth patterns. The recent emergence of hepatic microphysiological systems (MPS) provide the basic physiological emulation of the human liver for drug screening. However, engineering microfluidic devices with standardized surface coatings of ECM may improve MPS-based organ-specific emulation for improved drug screening. The influence of surface coatings… Show more

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Cited by 27 publications
(15 citation statements)
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“…The integrin binding sites in fibronectin and collagen have been confirmed to promote cell adhesion. Therefore, dual ECM (collagen and fibronectin) coating is an optimal method to mimic the liver microenvironment to facilitate cell development and stabilize the cell functions in engineered albumin-based cryogel liver tissues [ 53 , 54 ].…”
Section: Resultsmentioning
confidence: 99%
“…The integrin binding sites in fibronectin and collagen have been confirmed to promote cell adhesion. Therefore, dual ECM (collagen and fibronectin) coating is an optimal method to mimic the liver microenvironment to facilitate cell development and stabilize the cell functions in engineered albumin-based cryogel liver tissues [ 53 , 54 ].…”
Section: Resultsmentioning
confidence: 99%
“…The level of relevance of a microphysiological system (MPS) with human physiology makes them ideal for identifying the novel therapeutics. The organ-on-a-chip and spheroid culture systems are evolving to better mimic human pathophysiology, which is being enhanced by the integration of sensors and robotics [1][2][3][4][5][6][7][8]. Among MPS, spheroids are emerging with the potential to mimic human tissues in a 3D shape and function [9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…After 80 to 90% confluency, the cells were expanded up to 3 passages before seeding and washed with Dulbecco’s phosphate buffer saline (DPBS) (Cat# 14190144, ThermoFisher, Waltham, MA, USA) to remove cell debris and metabolites before adding fresh media. Cells at 90% confluency were trypsinized with 0.05% Trypsin-EDTA solution (Cat# 25300054, Thermo Fisher, USA), then suspended in freshly prepared RPMI-1640 media containing a specified concentration of FBS [ 22 , 33 , 34 , 35 ]. Human primary pulmonary alveolar epithelial cells (HPAEpiC) (Science Cell Research laboratories, Carlsbad, CA, USA) were revived according to the manufacturer’s instructions.…”
Section: Methodsmentioning
confidence: 99%