Effector T-cell trafficking between the leptomeninges and the cerebrospinal fluid

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Christian Schläger - , University of Göttingen (Author)
  • Henrike Körner - , University of Göttingen (Author)
  • Martin Krueger - , Leipzig University (Author)
  • Stefano Vidoli - , University of Rome La Sapienza (Author)
  • Michael Haberl - , University of Göttingen (Author)
  • Dorothee Mielke - , University of Göttingen (Author)
  • Elke Brylla - , Leipzig University (Author)
  • Thomas Issekutz - , Dalhousie University (Author)
  • Carlos Cabanãs - , Spanish National Research Council (Author)
  • Peter J. Nelson - , Ludwig Maximilian University of Munich (Author)
  • Tjalf Ziemssen - , Department of Neurology (Author)
  • Veit Rohde - , University of Göttingen (Author)
  • Ingo Bechmann - , Leipzig University (Author)
  • Dmitri Lodygin - , University of Göttingen (Author)
  • Francesca Odoardi - , University of Göttingen (Author)
  • Alexander Flügel - , University of Göttingen, Max Planck Institute of Experimental Medicine (Author)

Abstract

In multiple sclerosis, brain-reactive T cells invade the central nervous system (CNS) and induce a self-destructive inflammatory process. T-cell infiltrates are not only found within the parenchyma and the meninges, but also in the cerebrospinal fluid (CSF) that bathes the entire CNS tissue. How the T cells reach the CSF, their functionality, and whether they traffic between the CSF and other CNS compartments remains hypothetical. Here we show that effector T cells enter the CSF from the leptomeninges during Lewis rat experimental autoimmune encephalomyelitis (EAE), a model of multiple sclerosis. While moving through the three-dimensional leptomeningeal network of collagen fibres in a random Brownian walk, T cells were flushed from the surface by the flow of the CSF. The detached cells displayed significantly lower activation levels compared to T cells from the leptomeninges and CNS parenchyma. However, they did not represent a specialized non-pathogenic cellular sub-fraction, as their gene expression profile strongly resembled that of tissue-derived T cells and they fully retained their encephalitogenic potential. T-cell detachment from the leptomeninges was counteracted by integrins VLA-4 and LFA-1 binding to their respective ligands produced by resident macrophages. Chemokine signalling via CCR5/CXCR3 and antigenic stimulation of T cells in contact with the leptomeningeal macrophages enforced their adhesiveness. T cells floating in the CSF were able to reattach to the leptomeninges through steps reminiscent of vascular adhesion in CNS blood vessels, and invade the parenchyma. The molecular/cellular conditions for T-cell reattachment were the same as the requirements for detachment from the leptomeningeal milieu. Our data indicate that the leptomeninges represent a checkpoint at which activated T cells are licensed to enter the CNS parenchyma and non-activated T cells are preferentially released into the CSF, from where they can reach areas of antigen availability and tissue damage.

Details

Original languageEnglish
Pages (from-to)349-353
Number of pages5
JournalNature
Volume530
Issue number7590
Publication statusPublished - 18 Feb 2016
Peer-reviewedYes

External IDs

PubMed 26863192

Keywords

ASJC Scopus subject areas