Human hepatocytes secrete soluble CD14, a process not directly influenced by HBV and HCV infection
Meuleman, P.; Steyaert, S.; Libbrecht, L.; Couvent, S.; Van Houtte, F.; Clinckspoor, F.; de Hemptinne, B.; Roskams, T.; Vanlandschoot, P.; Leroux-Roels, G.
Clinica Chimica Acta; International Journal of Clinical Chemistry 366(1-2): 156-162
2006
ISSN/ISBN: 0009-8981 PMID: 16253217 DOI: 10.1016/j.cca.2005.09.022
Accession: 012159713
Chronic hepatitis B (HBV) and hepatitis C (HCV) patients have elevated plasma levels of soluble CD14 (sCD14). We examined whether human hepatocytes produce sCD14 in vivo, and whether HBV or HCV infections influence this chimeric production. uPA-SCID mice were transplanted with primary human hepatocytes and some animals were subsequently infected with HBV or HCV. Plasma from these mice was analyzed for the presence of human sCD14. The liver was examined via immunohistochemistry. A soluble form of human CD14 could be detected in the plasma from successfully transplanted mice, while it was completely absent in non-transplanted control animals. The isoform of this human sCD14 corresponded with the most abundant isoform found in human plasma. CD14 levels in circulation were not significantly different between non-infected, HBV infected and HCV infected animals. Our data indicate that human hepatocytes produce sCD14 in vivo, and that liver cells might be the major source of sCD14 in normal human plasma. In addition we demonstrate that HBV and HCV infections have no direct influence on the production of sCD14 by human hepatocytes in this chimeric model.