Methodology for the formation of functional, cell-based cardiac pressure generation constructs in vitro.

In Vitro Cell Dev Biol Anim

Section of Cardiac Surgery, University of Michigan, Biomedical Science Research Building, Ann Arbor, MI 48109-2200, USA.

Published: January 2009

AI Article Synopsis

  • Researchers developed a new method to create a functional cardiac pressure generating construct (CPGC) using primary cardiac cells and chitosan scaffolds.
  • The CPGCs were formed by plating cardiac cells on fibrin gels surrounding tubular constructs, leading to a complete monolayer of cells by 14 days.
  • The CPGCs exhibited visible contractility and generated measurable intraluminal pressures, demonstrating their potential for cardiac tissue engineering.

Article Abstract

We have previously described a model to engineer three-dimensional (3-D) heart muscle in vitro. In the current study, we extend our model of 3-D heart muscle to engineer a functional cell-based cardiac pressure generating construct (CPGC). Tubular constructs were fabricated utilizing a phase separation method with chitosan as the scaffolding material. Primary cardiac cells isolated from rat hearts were plated on the surface of fibrin gels cast in 35 mm tissue culture dishes. CPGCs (N = 8) were formed by anchoring the tubular constructs to the center of the plate with primary cardiac cells seeded in fibrin gels wrapped around the tubular constructs. Intraluminal pressure measurements were evaluated with and without external electrical stimulation and histological evaluation performed. The fibrin gel spontaneously compacted due to the traction force of the cardiac cells. By 14 d after original cell plating, the cardiac cells had completely formed a monolayer around the tubular construct resulting in the formation of a cell-based CPGC. The spontaneous contractility of the CPGC was macroscopically visible and resulted in intraluminal pressure spikes of 0.08 mmHg. Upon electrical stimulation, the CPGCs generated twitch pressures of up to 0.05 mmHg. In addition, the CPGC constructs were electrically paced at frequencies of up to 3 Hz. Histological evaluation showed the presence of a continuous cell monolayer around the surface of the tubular construct. In this study, we describe a novel in vitro method to engineer functional cell-based CPGCs and demonstrate several physiological metrics of functional performance.

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Source
http://dx.doi.org/10.1007/s11626-008-9098-9DOI Listing

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