Isolation of human umbilical arterial smooth muscle cells (HUASMC).
J Vis Exp (2010) PMID 20644508 PMCID PMC3156078
<object style="float: right;" type="application/x-shockwave-flash" data="http://www.jove.com/Resources/ThumbPlayer/ThumbPlayer_gray.swf?f=http://source.jove.com/1940_MINI.flv" width="204" height="156" wmode="opaque" onclick="window.open('http://www.jove.com/Details.php?ID=1940')" <param name="movie" value="http://www.jove.com/Resources/ThumbPlayer/ThumbPlayer_gray.swf?f=http://source.jove.com/XXXX_MINI.flv" /> <param name="wmode" value="opaque"> <!-- <p>Sorry, to view this content, you need the latest version of the Adobe Flash Player. Please download the<a href="http://get.adobe.com/flashplayer/"> Flash Player here</a>. Thank you.</p> --> </object>The human umbilical cord (UC) is a biological sample that can be easily obtained just after birth. This biological sample is, most of the time, discarded and their collection does not imply any added risk to the newborn or mother s health. Moreover no ethical concerns are raised. The UC is composed by one vein and two arteries from which both endothelial cells (ECs) and smooth muscle cells (SMCs), two of the main cellular components of blood vessels, can be isolated. In this project the SMCs were obtained after enzymatic treatment of the UC arteries accordingly the experimental procedure previously described by Jaffe et al. After cell isolation they were kept in t-flash with DMEM-F12 supplemented with 5% of fetal bovine serum and were cultured for several passages. Cells maintained their morphological and other phenotypic characteristics in the different generations. The aim of this study was to isolate smooth muscle cells in order to use them as models for future assays with constrictor drugs, isolate and structurally characterize L-type calcium channels, to study cellular and molecular aspects of the vascular function and to use them in tissue engineering.
DOI: 10.3791/1940
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