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Llovera, G.* ; Benakis, C.* ; Enzmann, G.* ; Cai, R.* ; Arzberger, T.* ; Ghasemigharagoz, A.* ; Mao, X.* ; Malik, R.* ; Lazarevic, I.* ; Liebscher, S.* ; Ertürk, A. ; Meissner, L.* ; Vivien, D.* ; Haffner, C.* ; Plesnila, N.* ; Montaner, J.* ; Engelhardt, B.* ; Liesz, A.*

The choroid plexus is a key cerebral invasion route for T cells after stroke.

Acta Neuropathol. 134, 851-868 (2017)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Neuroinflammation contributes substantially to stroke pathophysiology. Cerebral invasion of peripheral leukocytes-particularly T cells-has been shown to be a key event promoting inflammatory tissue damage after stroke. While previous research has focused on the vascular invasion of T cells into the ischemic brain, the choroid plexus (ChP) as an alternative cerebral T-cell invasion route after stroke has not been investigated. We here report specific accumulation of T cells in the peri-infarct cortex and detection of T cells as the predominant population in the ipsilateral ChP in mice as well as in human post-stroke autopsy samples. T-cell migration from the ChP to the peri-infarct cortex was confirmed by in vivo cell tracking of photoactivated T cells. In turn, significantly less T cells invaded the ischemic brain after photothrombotic lesion of the ipsilateral ChP and in a stroke model encompassing ChP ischemia. We detected a gradient of CCR2 ligands as the potential driving force and characterized the neuroanatomical pathway for the intracerebral migration. In summary, our study demonstrates that the ChP is a key invasion route for post-stroke cerebral T-cell invasion and describes a CCR2-ligand gradient between cortex and ChP as the potential driving mechanism for this invasion route.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
ISSN (print) / ISBN 0001-6322
e-ISSN 1432-0533
Quellenangaben Volume: 134, Issue: 6, Pages: 851-868 Article Number: , Supplement: ,
Publisher Springer
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute for Tissue Engineering and Regenerative Medicine (ITERM)