A facile fluid pressure system reveals differential cellular response to interstitial pressure gradients and flow

Author:

Wang Hao1ORCID,Lu Jingming1ORCID,Rathod Mitesh1ORCID,Aw Wen Yih1ORCID,Huang Stephanie A.1ORCID,Polacheck William J.123ORCID

Affiliation:

1. Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University 1 , Chapel Hill, North Carolina 27514, USA

2. Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill School of Medicine 2 , Chapel Hill, North Carolina 27514, USA

3. McAllister Heart Institute, University of North Carolina at Chapel Hill 3 , Chapel Hill, North Carolina 27514, USA

Abstract

Interstitial fluid pressure gradients and interstitial flow have been shown to drive morphogenic processes that shape tissues and influence progression of diseases including cancer. The advent of porous media microfluidic approaches has enabled investigation of the cellular response to interstitial flow, but questions remain as to the critical biophysical and biochemical signals imparted by interstitial fluid pressure gradients and resulting flow on resident cells and extracellular matrix (ECM). Here, we introduce a low-cost method to maintain physiological interstitial fluid pressures that is built from commonly accessible laboratory equipment, including a laser pointer, camera, Arduino board, and a commercially available linear actuator. We demonstrate that when the system is connected to a microfluidic device containing a 3D porous hydrogel, physiologic pressure is maintained with sub-Pascal resolution and when basic feedback control is directed using an Arduino, constant pressure and pressure gradient can be maintained even as cells remodel and degrade the ECM hydrogel over time. Using this model, we characterized breast cancer cell growth and ECM changes to ECM fibril structure and porosity in response to constant interstitial fluid pressure or constant interstitial flow. We observe increased collagen fibril bundling and the formation of porous structures in the vicinity of cancer cells in response to constant interstitial fluid pressure as compared to constant interstitial flow. Collectively, these results further define interstitial fluid pressure as a driver of key pathogenic responses in cells, and the systems and methods developed here will allow for future mechanistic work investigating mechanotransduction of interstitial fluid pressures and flows.

Funder

National Institute of General Medical Sciences

American Heart Association

National Science Foundation

Lymphatic Malformation Institute the CLOVES Foundation

Publisher

AIP Publishing

Subject

Condensed Matter Physics,General Materials Science,Fluid Flow and Transfer Processes,Colloid and Surface Chemistry,Biomedical Engineering

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