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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.5301/ijao.5000096</dc:identifier><dc:language>eng</dc:language><dc:creator>Chouhan, M.</dc:creator><dc:creator>Puppi, J.</dc:creator><dc:creator>Solanas, E.</dc:creator><dc:creator>Mitry, R.</dc:creator><dc:creator>Dhawan, A.</dc:creator><dc:creator>Hughes, R.D.</dc:creator><dc:title>Hepatocyte labeling with Tc-99m-gsa: a potential non-invasive technique for tracking cell transplantation</dc:title><dc:identifier>ART-2012-136571</dc:identifier><dc:description>Background: Hepatocyte transplantation is a promising alternative to orthotopic liver transplantation, however, the fate of transplanted hepatocytes is not well defined. 99mTc-galactosyl-serum albumin (99mTc-GSA) is a clinical scintigraphic agent which is specifically taken up by the hepatocyte asialoglycoprotein receptor (ASGPR). Aims: To investigate labeling of fresh and cryopreserved human hepatocytes and fresh rat hepatocytes in vitro using 99mTc-GSA Methods: Human and rat hepatocytes were isolated from liver tissue by collagenase perfusion. The ASGPR were characterized using immunohistochemistry and RT-PCR. Hepatocytes were incubated with 99mTc-GSA in suspension at 4°C and 37°C. Cell viability and function was determined using cell mitochondrial dehydrogenase (MTS) and sulphorhodamine B (SRB) assays. Results: Fresh and cryopreserved human hepatocytes expressed the ASGPR. Incubation of hepatocytes in suspension with 99mTc-GSA reduced the viability of hepatocytes, but this was similar to unlabeled control cells. Greater loss of viability was seen on incubation at 37°C compared to 4°C, but there was a significantly greater uptake of 99mTc-GSA at the physiological temperature (6.6 ± SE 0.6-fold increase, p&amp;lt;0.05) consistent with ASGPR-mediated endocytosis. MTS and SRB assays were not significantly affected by labeling with 99mTc-GSA in all three cell types. A mean of 18.5% of the radioactivity was released over 120 min when 99mTc-GSA - labeled hepatocytes were shaken in vitro at 37°C. Conclusions: Human and rat hepatocytes can be labeled with 99mTc-GSA, which may have potential application for in vivo imaging after hepatocyte transplantation.</dc:description><dc:date>2012</dc:date><dc:source>http://zaguan.unizar.es/record/130544</dc:source><dc:doi>10.5301/ijao.5000096</dc:doi><dc:identifier>http://zaguan.unizar.es/record/130544</dc:identifier><dc:identifier>oai:zaguan.unizar.es:130544</dc:identifier><dc:identifier.citation>INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS 35, 6 (2012), 450-457</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/closedAccess</dc:rights></dc:dc>

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