Microphysiological Systems

Microphysiological systems are engineered in vitro models that recreate key structural, mechanical, and biochemical features of human tissues or organs, providing a more physiologically relevant platform for biological research. They typically combine living human cells with microfluidic devices, biomaterials, and controlled fluid flow to reproduce tissue interfaces, nutrient delivery, and organ-specific physical cues. In biology, these systems support studies of development, disease mechanisms, cell interactions, and responses to drugs or environmental exposures. By enabling precise, repeatable experiments under defined conditions, they can complement conventional cell cultures and improve preclinical testing while contributing to efforts to reduce reliance on animal models.

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Research

JoVE Journal - Bioengineering

Transforming Static Barrier Tissue Models into Dynamic Microphysiological Systems

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Cited by 3 •

2024

This protocol describes a reconfigurable membrane-based cell culture platform that integrates the open-well format with fluid flow capabilities. This platform is compatible with standard protocols and allows for reversible transitions between open-well and microfluidic culture modes, accommodating the needs of both engineering and bioscience laboratories.

Isolation of Primary Human Proximal Tubule Epithelial Cells and Their Use in Creating a Microphysiological Model of the Renal Proximal Tubule

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Cited by 3 •

2025

We present an optimized protocol for processing whole human kidneys to isolate and culture primary renal proximal tubule epithelial cells and the application of these cells in a three-dimensional, microfluidic, microphysiological platform to recapitulate the renal proximal tubule.

The Use of Chemostats in Microbial Systems Biology

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Cited by 67 •

2013

Cell growth rate is a regulated process and a primary determinant of cell physiology. Continuous culturing using chemostats enables extrinsic control of cell growth rate by nutrient limitation facilitating the study of molecular networks that control cell growth and how those networks evolve to optimize cell growth.

An Intestine/Liver Microphysiological System for Drug Pharmacokinetic and Toxicological Assessment

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Cited by 3 •

2020

We exposed a microphysiological system (MPS) with intestine and liver organoids to acetaminophen (APAP). This article describes the methods for organoid production and APAP pharmacokinetic and toxicological property assessments in the MPS. It also describes the tissue functionality analyses necessary to validate the results.

A Microphysiological System to Study Leukocyte-Endothelial Cell Interaction during Inflammation

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Cited by 6 •

2021

In this protocol, a biomimetic microfluid assay, which can reproduce a physiologically relevant microvascular environment and reproduce the entire leukocyte adhesion/migration cascade, is employed to study leukocyte-endothelial cell interactions in inflammatory disease.

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