Neurons are MHC Class I-Dependent Targets for CD8 T Cells upon Neurotropic Viral Infection

PLoS Pathogens

Roland Liblau¹  Elsa Suberbielle¹  Guillaume Martin-Blondel¹  Gwendal Le Masson²  Grégoire Chevalier²  Valérie Duplan²  Céline Monnet³  Fanny Farrugia³  Daniel Gonzalez-Dunia³ 

[1] CNRS, U5282, Toulouse, France;Inserm, U1043, Toulouse, France;Université de Toulouse, UPS, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse, France

关键词: Neurons;    T cells;    Cytotoxic T cells;    Major histocompatibility complex;    Cytokines;    Apoptosis;    Central nervous system;    Neural networks;   

DOI  :  10.1371/journal.ppat.1002393

学科分类：生物科学（综合）

来源: Public Library of Science

【 摘 要 】

Following infection of the central nervous system (CNS), the immune system is faced with the challenge of eliminating the pathogen without causing significant damage to neurons, which have limited capacities of renewal. In particular, it was thought that neurons were protected from direct attack by cytotoxic T lymphocytes (CTL) because they do not express major histocompatibility class I (MHC I) molecules, at least at steady state. To date, most of our current knowledge on the specifics of neuron-CTL interaction is based on studies artificially inducing MHC I expression on neurons, loading them with exogenous peptide and applying CTL clones or lines often differentiated in culture. Thus, much remains to be uncovered regarding the modalities of the interaction between infected neurons and antiviral CD8 T cells in the course of a natural disease. Here, we used the model of neuroinflammation caused by neurotropic Borna disease virus (BDV), in which virus-specific CTL have been demonstrated as the main immune effectors triggering disease. We tested the pathogenic properties of brain-isolated CD8 T cells against pure neuronal cultures infected with BDV. We observed that BDV infection of cortical neurons triggered a significant up regulation of MHC I molecules, rendering them susceptible to recognition by antiviral CTL, freshly isolated from the brains of acutely infected rats. Using real-time imaging, we analyzed the spatio-temporal relationships between neurons and CTL. Brain-isolated CTL exhibited a reduced mobility and established stable contacts with BDV-infected neurons, in an antigen- and MHC-dependent manner. This interaction induced rapid morphological changes of the neurons, without immediate killing or impairment of electrical activity. Early signs of neuronal apoptosis were detected only hours after this initial contact. Thus, our results show that infected neurons can be recognized efficiently by brain-isolated antiviral CD8 T cells and uncover the unusual modalities of CTL-induced neuronal damage.

【 授权许可】

CC BY