# Modular parallel plate flow chamber with tunable substrate mechanics and defined shear stress

**Authors:** Bryan J. Ferrick, Jason P. Gleghorn

PMC · DOI: 10.1007/s10544-025-00787-6 · 2026-01-29

## TL;DR

This paper introduces a new lab tool that lets researchers study how cells respond to both surface stiffness and fluid flow at the same time.

## Contribution

A modular flow chamber that independently controls substrate stiffness and fluid shear stress using polyacrylamide gels.

## Key findings

- PAA substrates support cell growth across a range of stiffnesses.
- The chamber maintains consistent fluid channel height for controlled shear stress.
- Substrate stiffness and shear stress synergistically affect F-actin filament length.

## Abstract

Cells integrate multiple mechanical cues simultaneously, yet most in vitro models examine extracellular matrix (ECM) stiffness and fluid shear stress (FSS) in isolation, limiting our understanding of mechanotransduction. We developed a parallel plate flow chamber with a polyacrylamide (PAA) substratum enabling independent, tunable control of substrate stiffness and FSS using readily available materials. We confirm that the PAA substratum has controllable mechanical properties that support the growth of Madin-Darby canine kidney epithelial cells across a range of stiffnesses. Furthermore, the flow chamber design accommodates the volumetric equilibrium swelling of the gel, maintaining a predictable fluid channel height that allows for the application of controlled fluid shear stress to cells within the device, confirmed through particle image velocimetry of perfused microspheres. Single flow chambers support the growth of sufficient cellular numbers for endpoint analyses, such as Western blots. Finally, quantitative analysis of F-actin organization revealed that substrate stiffness and FSS synergistically increase filament length with independent effects on filament width, demonstrating the ability and usefulness of this model as a tool for studying the effect of multiple concurrent forces on cell behavior.

## Linked entities

- **Proteins:** Act5C (Actin 5C)

## Full-text entities

- **Genes:** RHO (rhodopsin) [NCBI Gene 493763] {aka RHO1}, AQP2 (aquaporin 2) [NCBI Gene 486552] {aka AQP-2, AQP-CD, WCH-CD}, PIEZO1 (piezo type mechanosensitive ion channel component 1) [NCBI Gene 489662] {aka FAM38A}, CDH1 (cadherin 1) [NCBI Gene 442858] {aka Cadherin-1, Uvomorulin}, TAZ [NCBI Gene 612975]
- **Diseases:** endothelial dysfunction (MESH:D014652), swelling (MESH:D004487), atherosclerosis (MESH:D050197), fibrosis (MESH:D005355), cancer (MESH:D009369)
- **Chemicals:** water (MESH:D014867), alginate (MESH:D000464), HEPES (MESH:D006531), oil (MESH:D009821), PAA (MESH:C016679), (3-aminopropyl) triethoxysilane (MESH:C477625), PBS (MESH:D007854), CO2 (MESH:D002245), DPBS (MESH:C012939), streptomycin (MESH:D013307), Hoechst 33342 (MESH:C017807), DMSO (MESH:D004121), Triton-X 100 (MESH:D017830), sulfo-SANPAH (MESH:C062325), paraformaldehyde (MESH:C003043), penicillin (MESH:D010406), Silicone (MESH:D012828), APTES (-), isopropanol (MESH:D019840), phalloidin (MESH:D010590), PAA hydrogel (MESH:C016680), glutaraldehyde (MESH:D005976), N2 (MESH:D009584), calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** JMP — Homo sapiens (Human), Mantle cell lymphoma, Cancer cell line (CVCL_UJ14), MDCK — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_0422)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12855244/full.md

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Source: https://tomesphere.com/paper/PMC12855244