CD4(+) T cells contribute to neurodegeneration in Lewy body dementia

However, the mechanism regulating T cell brain homing in LBD is unknown. Here, we observed T cells adjacent to Lewy bodies and dopaminergic neurons in postmortem LBD brains. Single-cell RNA sequencing of cerebrospinal fluid (CSF) identified up-regulated expression of C-X-C motif chemokine receptor 4...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2021-11, Vol.374 (6569), p.868-874
Hauptverfasser: Gate, David, Tapp, Emma, Leventhal, Olivia, Shahid, Marian, Nonninger, Tim J., Yang, Andrew C., Strempfl, Katharina, Unger, Michael S., Fehlmann, Tobias, Oh, Hamilton, Channappa, Divya, Henderson, Victor W., Keller, Andreas, Aigner, Ludwig, Galasko, Douglas R., Davis, Mark M., Poston, Kathleen L., Wyss-Coray, Tony
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Sprache:eng
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Zusammenfassung:However, the mechanism regulating T cell brain homing in LBD is unknown. Here, we observed T cells adjacent to Lewy bodies and dopaminergic neurons in postmortem LBD brains. Single-cell RNA sequencing of cerebrospinal fluid (CSF) identified up-regulated expression of C-X-C motif chemokine receptor 4 (CXCR4) in CD4(+) T cells in LBD. CSF protein levels of the CXCR4 ligand, C-X-C motif chemokine ligand 12 (CXCL12), were associated with neuroaxonal damage in LBD. Furthermore, we observed clonal expansion and up-regulated interleukin 17A expression by CD4(+) T cells stimulated with a phosphorylated a-synuclein epitope. Thus, CXCR4-CXCL12 signaling may represent a mechanistic target for inhibiting pathological interleukin-17-producing T cell trafficking in LBD.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.abf7266