4.6 Article

Real-time monitoring of liver fibrosis through embedded sensors in a microphysiological system

Journal

NANO CONVERGENCE
Volume 8, Issue 1, Pages -

Publisher

SPRINGER
DOI: 10.1186/s40580-021-00253-y

Keywords

Liver fibrosis-on-chip; TEER sensor; ROS sensor; Embedded sensors; TGF-β 1

Funding

  1. Program of National Research Foundation of Korea through the Ministry of Education
  2. Ministry of Health & Welfare (MOHW), Republic of Korea [P0006848] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Hepatic fibrosis is a warning sign for future adverse events like liver cirrhosis, liver failure, and cancer, mainly caused by hepatic stellate cell activation leading to excessive extracellular matrix deposition and hepatic parenchyma disintegration. In a dynamic cell culture microphysiological system, measuring trans-epithelial electrical resistance (TEER) can be used to monitor fibrosis development effectively, serving as a potential substitute for conventional assays.
Hepatic fibrosis is a foreshadowing of future adverse events like liver cirrhosis, liver failure, and cancer. Hepatic stellate cell activation is the main event of liver fibrosis, which results in excessive extracellular matrix deposition and hepatic parenchyma's disintegration. Several biochemical and molecular assays have been introduced for in vitro study of the hepatic fibrosis progression. However, they do not forecast real-time events happening to the in vitro models. Trans-epithelial electrical resistance (TEER) is used in cell culture science to measure cell monolayer barrier integrity. Herein, we explored TEER measurement's utility for monitoring fibrosis development in a dynamic cell culture microphysiological system. Immortal HepG2 cells and fibroblasts were co-cultured, and transforming growth factor beta 1 (TGF-beta 1) was used as a fibrosis stimulus to create a liver fibrosis-on-chip model. A glass chip-based embedded TEER and reactive oxygen species (ROS) sensors were employed to gauge the effect of TGF-beta 1 within the microphysiological system, which promotes a positive feedback response in fibrosis development. Furthermore, albumin, Urea, CYP450 measurements, and immunofluorescent microscopy were performed to correlate the following data with embedded sensors responses. We found that chip embedded electrochemical sensors could be used as a potential substitute for conventional end-point assays for studying fibrosis in microphysiological systems.

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