Author
Listed:
- Dmitri Lodygin
(University Medical Center Göttingen)
- Moritz Hermann
(University Medical Center Göttingen)
- Nils Schweingruber
(University Medical Center Göttingen)
- Cassandra Flügel-Koch
(Friedrich-Alexander-University Erlangen-Nürnberg)
- Takashi Watanabe
(Biomedizinische NMR, Max-Planck-Institut für biophysikalische Chemie)
- Corinna Schlosser
(University Medical Center Göttingen)
- Arianna Merlini
(University Medical Center Göttingen)
- Henrike Körner
(University Medical Center Göttingen)
- Hsin-Fang Chang
(University Medical Center Göttingen)
- Henrike J. Fischer
(University Medical Center Göttingen)
- Holger M. Reichardt
(University Medical Center Göttingen)
- Marta Zagrebelsky
(Technical University Braunschweig)
- Brit Mollenhauer
(Paracelsus-Elena-Klinik Kassel
University Medical Center Göttingen)
- Sebastian Kügler
(University Medical Center Göttingen)
- Dirk Fitzner
(University Medical Center Göttingen)
- Jens Frahm
(Biomedizinische NMR, Max-Planck-Institut für biophysikalische Chemie)
- Christine Stadelmann
(University Medical Center Göttingen)
- Michael Haberl
(University Medical Center Göttingen)
- Francesca Odoardi
(University Medical Center Göttingen
Center for Biostructural Imaging of Neurodegeneration)
- Alexander Flügel
(University Medical Center Göttingen)
Abstract
The grey matter is a central target of pathological processes in neurodegenerative disorders such as Parkinson’s and Alzheimer’s diseases. The grey matter is often also affected in multiple sclerosis, an autoimmune disease of the central nervous system. The mechanisms that underlie grey matter inflammation and degeneration in multiple sclerosis are not well understood. Here we show that, in Lewis rats, T cells directed against the neuronal protein β-synuclein specifically invade the grey matter and that this is accompanied by the presentation of multifaceted clinical disease. The expression pattern of β-synuclein induces the local activation of these T cells and, therefore, determined inflammatory priming of the tissue and targeted recruitment of immune cells. The resulting inflammation led to significant changes in the grey matter, which ranged from gliosis and neuronal destruction to brain atrophy. In humans, β-synuclein-specific T cells were enriched in patients with chronic-progressive multiple sclerosis. These findings reveal a previously unrecognized role of β-synuclein in provoking T-cell-mediated pathology of the central nervous system.
Suggested Citation
Dmitri Lodygin & Moritz Hermann & Nils Schweingruber & Cassandra Flügel-Koch & Takashi Watanabe & Corinna Schlosser & Arianna Merlini & Henrike Körner & Hsin-Fang Chang & Henrike J. Fischer & Holger M, 2019.
"β-Synuclein-reactive T cells induce autoimmune CNS grey matter degeneration,"
Nature, Nature, vol. 566(7745), pages 503-508, February.
Handle:
RePEc:nat:nature:v:566:y:2019:i:7745:d:10.1038_s41586-019-0964-2
DOI: 10.1038/s41586-019-0964-2
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