Author/Authors :
Simon N. Waddington، نويسنده , , John H. McVey
، نويسنده , , David Bhella، نويسنده , , Alan L. Parker، نويسنده , , Kristeen Barker، نويسنده , , Hideko Atoda، نويسنده , , Rebecca Pink، نويسنده , , Suzanne M.K. Buckley، نويسنده , , Jenny A. Greig، نويسنده , , Laura Denby، نويسنده , , Jerome Custers، نويسنده , , Takashi Morita، نويسنده , , Ivo M.B. Francischetti، نويسنده , , Robson Q. Monteiro، نويسنده , , Dan H. Barouch، نويسنده , , Nico van Rooijen، نويسنده , , Claudio Napoli، نويسنده , , Menzo J.E. Havenga، نويسنده , , Stuart A. Nicklin، نويسنده , , Andrew H. Baker، نويسنده , , et al.، نويسنده ,
Abstract :
Adenoviruses are used extensively as gene transfer agents, both experimentally and clinically. However, targeting of liver cells by adenoviruses compromises their potential efficacy. In cell culture, the adenovirus serotype 5 fiber protein engages the coxsackievirus and adenovirus receptor (CAR) to bind cells. Paradoxically, following intravascular delivery, CAR is not used for liver transduction, implicating alternate pathways. Recently, we demonstrated that coagulation factor (F)X directly binds adenovirus leading to liver infection. Here, we show that FX binds to the Ad5 hexon, not fiber, via an interaction between the FX Gla domain and hypervariable regions of the hexon surface. Binding occurs in multiple human adenovirus serotypes. Liver infection by the FX-Ad5 complex is mediated through a heparin-binding exosite in the FX serine protease domain. This study reveals an unanticipated function for hexon in mediating liver gene transfer in vivo.
