Dissection of the molecular determinants and pathways involved in Hepatitis B virus (HBV) entry into hepatocytes

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Title: Dissection of the molecular determinants and pathways involved in Hepatitis B virus (HBV) entry into hepatocytes
Authors: Evripioti, Antonia Alexandra
Item Type: Thesis or dissertation
Abstract: HBV entry into cells is mediated through a precisely orchestrated interaction of the pre-S1 glycoprotein domain of the virus principally with the sodium taurocholate cotransporting polypeptide (NTCP) receptor on the surface of hepatocytes. However, in vitro this typically relies on high multiplicities of infections, and even in this case a very small majority of the hepatocytes become infected with the virus. Here we describe a mechanism by which DMSO facilitates overexpression of human NTCP, resulting in the bulk trafficking of the receptor to the cell surface and hence enhancing susceptibility of these cells to HBV infection. This mechanism is an intricate network of intracellular interactions, with the main one being the inhibition of particular phosphodiesterases (PDEs), including PDE4, by DMSO. This outcome can hopefully now open the door for the study of new small molecule inhibitors to prevent HBV entry into hepatocytes by specifically targeting the levels of NTCP on the cells’ surface. It is highly likely, however, that HBV entry into hepatocytes additionally relies on other, yet not fully characterised, cell surface receptors or host factors. Such an example may be the asialoglycoprotein receptor (ASGPR), which our data suggests may possibly be important and play a role during HBV entry. In particular, we found that the simultaneous presence of NTCP and ASGPR enhanced entry of HBV-mimicking particles into hepatocytes, more so than when only the NTCP receptor was overexpressed on those cells. This is the first study to have established positive HBV infection of a mouse hepatic cell line overexpressing a chimeric form of the NTCP receptor. This outcome should hopefully now open the road towards further research and understanding of the HBV interspecies transmission barrier, as well as identification of those host factors vital for productive HBV infection in vitro and in vivo.
Content Version: Open Access
Issue Date: Jul-2017
Date Awarded: Oct-2017
URI: http://hdl.handle.net/10044/1/65070
Supervisor: Dorner, Marcus
O'Hare, Peter
Thursz, Mark
Sponsor/Funder: Imperial College London
Department: Department of Medicine
Publisher: Imperial College London
Qualification Level: Doctoral
Qualification Name: Doctor of Philosophy (PhD)
Appears in Collections:Medicine PhD theses



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