PrP Expression and Replication by Schwann Cells: Implications in Prion Spreading

Author:

Follet Jérôme12,Lemaire-Vieille Catherine12,Blanquet-Grossard Françoise12,Podevin-Dimster Valérie1,Lehmann Sylvain,Chauvin Jean-Paul3,Decavel Jean-Pierre1,Varea Ruth4,Grassi Jacques5,Fontès Michel6,Cesbron Jean-Yves12

Affiliation:

1. Laboratoire de Physiopathologie des Encéphalopathies Spongiformes Transmissibles, C.N.R.S. IFR3-Institut de Biologie de Lille-Institut Pasteur de Lille, 59021 Lille Cedex

2. UFR de Médecine de Grenoble, Université Joseph Fourier, 38706 La Tronche Cedex

3. UMR-6545, Laboratoire de Génétique et de Physiologie du Développement, IBDM-CNRS-INSERM, Université de la Méditerranée, Campus Luminy, 13288 Marseille Cedex 09

4. Departamento de Patologia Animal, Facultad de Veterinaria, 50013 Zaragoza, Spain

5. Service de Pharmacologie et d'Immunologie, CEA-Saclay, 91191 Gif/Yvette

6. INSERM-U491 Génétique médicale et développement, Faculté de Médecine de la Timone, 13358 Marseille, France

Abstract

ABSTRACT Prion infection relies on a continuous chain of PrP c -expressing tissues to spread from peripheral sites to the central nervous system (CNS). Direct neuroinvasion via peripheral nerves has long been considered likely. However, the speed of axonal flow is incompatible with the lengthy delay prior to the detection of PrP Sc in the brain. We hypothesized that Schwann cells could be the candidate implicated in this mechanism; for that, it has to express PrP c and to allow PrP Sc conversion. We investigated in vivo localization of PrP c in sciatic nerve samples from different strains of mice. We demonstrated that PrP c is mainly localized at the cell membrane of the Schwann cell. We also studied in vitro expression of PrP c in the Schwann cell line MSC-80 and demonstrated that it expresses PrP c at the same location. More specifically, we demonstrated that this glial cell line, when infected in vitro with the mouse Chandler prion strain, both produces the PrP Sc till after 18 passages and is able to transmit disease to mice, which then develop the typical signs of prion diseases. It is the first time that infection and replication of PrP Sc are shown in a peripheral glial cell line.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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