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DOI: 10.3791/52750-v
Boudewijn P.T. Kruithof1, Samuel C. Lieber2, Marianna Kruithof-de Julio3, Vincian Gaussin4, Marie José Goumans1
1Department of Molecular Cell Biology,Leiden University Medical Center, 2Department of Engineering Technology,New Jersey Institute of Technology, 3Department of Urology,Leiden University Medical Center, 4Cardiovascular Research Institute, Department of Cell Biology and Molecular Medicine,Rutgers New Jersey Medical School
This article presents a method for culturing murine cardiac valves using a miniature tissue culture system (MTCS). The procedure allows for the study of valve biology through histological analysis.
Here, we present an ex vivo flow model in which murine cardiac valves can be cultured allowing the study of the biology of the valve.
The overall goal of this procedure is to culture mouse cardiac valves using the miniature tissue culture system or MTCS. This is accomplished by first assembling the MTCS without the profusion chamber and circulating the medium to precondition the system. In the second step, the mouse heart is harvested and prepared for cannulation.
Next, the heart is placed in the profusion chamber where it is cannulated for a culture of the mitral or aortic valve. The perfusion chamber is then placed in the MTCS and the pump has started. Ultimately, histological analysis is used to assess the viability, morphology and extracellular matrix distribution of the valve.
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