Details

Autor(en) / Beteiligte

• Fletcher, Nicola F
• Wilson, Garrick K
• Murray, Jacinta
• Hu, Ke
• Lewis, Andrew
• Reynolds, Gary M
• Stamataki, Zania
• Meredith, Luke W
• Rowe, Ian A
• Luo, Guangxiang
• Lopez–Ramirez, Miguel A
• Baumert, Thomas F
• Weksler, Babette
• Couraud, Pierre–Olivier
• Kim, Kwang Sik
• Romero, Ignacio A
• Jopling, Catherine
• Morgello, Susan
• Balfe, Peter
• McKeating, Jane A

Titel

Hepatitis C Virus Infects the Endothelial Cells of the Blood-Brain Barrier

Ist Teil von

• Gastroenterology (New York, N.Y. 1943), 2012-03, Vol.142 (3), p.634-643.e6

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2012

Link zum Volltext

Quelle

ScienceDirect

Beschreibungen/Notizen

• Background & Aims Hepatitis C virus (HCV) infection leads to progressive liver disease and is associated with a variety of extrahepatic syndromes, including central nervous system (CNS) abnormalities. However, it is unclear whether such cognitive abnormalities are a function of systemic disease, impaired hepatic function, or virus infection of the CNS. Methods We measured levels of HCV RNA and expression of the viral entry receptor in brain tissue samples from 10 infected individuals (and 3 uninfected individuals, as controls) and human brain microvascular endothelial cells by using quantitative polymerase chain reaction and immunochemical and confocal imaging analyses. HCV pseudoparticles and cell culture–derived HCV were used to study the ability of endothelial cells to support viral entry and replication. Results Using quantitative polymerase chain reaction, we detected HCV RNA in brain tissue of infected individuals at significantly lower levels than in liver samples. Brain microvascular endothelia and brain endothelial cells expressed all of the recognized HCV entry receptors. Two independently derived brain endothelial cell lines, hCMEC/D3 and HBMEC, supported HCV entry and replication. These processes were inhibited by antibodies against the entry factors CD81, scavenger receptor BI, and claudin-1; by interferon; and by reagents that inhibit NS3 protease and NS5B polymerase. HCV infection promotes endothelial permeability and cellular apoptosis. Conclusions Human brain endothelial cells express functional receptors that support HCV entry and replication. Virus infection of the CNS might lead to HCV-associated neuropathologies.