4.7 Article

A microfluidic platform for the high-throughput study of pathological cardiac hypertrophy

Journal

LAB ON A CHIP
Volume 17, Issue 19, Pages 3264-3271

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7lc00415j

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Funding

  1. NIH [HL076485, EB002520, GM007367]
  2. NYSTEM [C028119]

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Current in vitro models fall short in deciphering the mechanisms of cardiac hypertrophy induced by volume overload. We developed a pneumatic microfluidic platform for high-throughput studies of cardiac hypertrophy that enables repetitive (hundreds of thousands of times) and robust (over several weeks) manipulation of cardiac mu tissues. The platform is reusable for stable and reproducible mechanical stimulation of cardiac mu tissues (each containing only 5000 cells). Heterotypic and homotypic mu tissues produced in the device were pneumatically loaded in a range of regimes, with real-time on-chip analysis of tissue phenotypes. Concentrated loading of the three-dimensional cardiac tissue faithfully recapitulated the pathology of volume overload seen in native heart tissue. Sustained volume overload of mu tissues was sufficient to induce pathological cardiac remodeling associated with upregulation of the fetal gene program, in a dosedependent manner.

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