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      Pneumatic microfluidic cell compression device for high-throughput study of chondrocyte mechanobiology

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          Abstract

          Hyaline cartilage is a specialized type of connective tissue that lines many moveable joints (articular cartilage) and contributes to bone growth (growth plate cartilage). Hyaline cartilage is composed of a single cell type, the chondrocyte, which produces a unique hydrated matrix to resist compressive stress. Although compressive stress has profound effects on transcriptional networks and matrix biosynthesis in chondrocytes, mechanistic relationships between strain, signal transduction, cell metabolism, and matrix production remain superficial. Here, we describe development and validation of a polydimethylsiloxane (PDMS)-based pneumatic microfluidic cell compression device which generates multiple compression conditions in a single platform. The device contained an array of PDMS balloons of different sizes which were actuated by pressurized air, and the balloons compressed chondrocytes cells in alginate hydrogel constructs. Our characterization and testing of the device showed that the developed platform could compress chondrocytes with various magnitudes simultaneously with negligible effect on cell viability. Also, the device is compatible with live cell imaging to probe early effects of compressive stress, and it can be rapidly dismantled to facilitate molecular studies of compressive stress on transcriptional networks. Therefore, the proposed device will enhance the productivity of chondrocyte mechanobiology studies, and it can be applied to study mechanobiology of other cell types.

          Table of contents entry:

          We demonstrate a pneumatically operated microfluidic device that can apply compressive stress of various magnitudes to multiple alginate-chondrocyte constructs simultaneously.

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          Author and article information

          Journal
          101128948
          31848
          Lab Chip
          Lab Chip
          Lab on a chip
          1473-0197
          1473-0189
          22 August 2018
          10 July 2018
          10 July 2019
          : 18
          : 14
          : 2077-2086
          Affiliations
          [a ]Department of Mechanical and Materials Engineering, University of Nebraska-Lincoln, Lincoln, NE 68588
          [b ]Department of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE 68198
          [c ]Houston District, Texas Department of Transportation, Houston, TX 77007
          [d ]Nebraska Center for Materials and Nanoscience, University of Nebraska-Lincoln, Lincoln, NE 68588
          []Current affiliation: Department of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE 68198
          Author notes
          [* ]Corresponding authors
          Article
          PMC6467204 PMC6467204 6467204 nihpa975183
          10.1039/c8lc00320c
          6467204
          29897088
          a9cab8ad-d6e2-4915-a333-88d067717941
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