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Alteration of blood-brain barrier integrity by retroviral infection.
Afonso P. V., Ozden S., Cumont M.-C., Seilhean D., Cartier L., Rezaie P., Mason S., Lambert S., Huerre M., Gessain A. et al
PLoS Pathogens 4, 11 (2008) e1000205 - http://hal-pasteur.archives-ouvertes.fr/pasteur-00363900
(19008946)
Alteration of blood-brain barrier integrity by retroviral infection.
Philippe V. Afonso1, Simona Ozden1, Marie-Christine Cumont2, Danielle Seilhean3, Luis Cartier4, Payam Rezaie5, Sarah Mason5, Sophie Lambert6, Michel Huerre2, Antoine Gessain1, Pierre-Olivier Couraud6, Claudine Pique6, Pierre-Emmanuel Ceccaldi () 1, Ignacio A. Romero () 1, 5
1 :  Epidémiologie et Physiopathologie des Virus Oncogènes
Institut Pasteur de Paris – CNRS : URA3015
25-28 rue du Docteur Roux F-75724 Paris Cedex 15
France
2 :  Histotechnologie et Pathologie
Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
3 :  Laboratoire de Neuropathologie Raymond Escourolle
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital Pitié-Salpêtrière – Université Pierre et Marie Curie [UPMC] - Paris VI
47-83, boulevard de l'Hôpital 75651 PARIS Cedex 13
France
4 :  Facultad de Medicina
Universidad de Chile
Santiago de Chile
Chili
5 :  Department of Life Sciences
The Open University
Milton Keynes
Royaume-Uni
6 :  IC - Institut Cochin
http://www.cochin.inserm.fr
CNRS : UMR8104 – INSERM : U567 – Université Paris V - Paris Descartes
Direction,services Communs,plateformes Bâtiment MECHAIN 22 rue Méchain 75014 PARIS
France
The blood-brain barrier (BBB), which forms the interface between the blood and the cerebral parenchyma, has been shown to be disrupted during retroviral-associated neuromyelopathies. Human T Lymphotropic Virus (HTLV-1) Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP) is a slowly progressive neurodegenerative disease associated with BBB breakdown. The BBB is composed of three cell types: endothelial cells, pericytes and astrocytes. Although astrocytes have been shown to be infected by HTLV-1, until now, little was known about the susceptibility of BBB endothelial cells to HTLV-1 infection and the impact of such an infection on BBB function. We first demonstrated that human cerebral endothelial cells express the receptors for HTLV-1 (GLUT-1, Neuropilin-1 and heparan sulfate proteoglycans), both in vitro, in a human cerebral endothelial cell line, and ex vivo, on spinal cord autopsy sections from HAM/TSP and non-infected control cases. In situ hybridization revealed HTLV-1 transcripts associated with the vasculature in HAM/TSP. We were able to confirm that the endothelial cells could be productively infected in vitro by HTLV-1 and that blocking of either HSPGs, Neuropilin 1 or Glut1 inhibits this process. The expression of the tight-junction proteins within the HTLV-1 infected endothelial cells was altered. These cells were no longer able to form a functional barrier, since BBB permeability and lymphocyte passage through the monolayer of endothelial cells were increased. This work constitutes the first report of susceptibility of human cerebral endothelial cells to HTLV-1 infection, with implications for HTLV-1 passage through the BBB and subsequent deregulation of the central nervous system homeostasis. We propose that the susceptibility of cerebral endothelial cells to retroviral infection and subsequent BBB dysfunction is an important aspect of HAM/TSP pathogenesis and should be considered in the design of future therapeutics strategies.
Sciences du Vivant/Microbiologie et Parasitologie
Anglais
1553-7366

Articles dans des revues avec comité de lecture
10.1371/journal.ppat.1000205
PLoS Pathogens
Publisher Public Library of Science
ISSN 1553-7366 (eISSN : 1553-7374)
internationale
11/2008
4
11
e1000205

Autopsy – Blood-Brain Barrier – Cell Line – Endothelial Cells – Human T-lymphotropic virus 1 – Humans – Paraparesis – Tropical Spastic – Receptors – Virus – Retroviridae Infections – Spinal Cord – Tight Junctions
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