Abstract:
:Extracellular matrix (ECM) proteins secreted by blood-brain barrier (BBB) endothelial cells (ECs) are implicated in cell trafficking. We discovered that the expression of ECM epidermal growth factor-like protein 7 (EGFL7) is increased in the CNS vasculature of patients with multiple sclerosis (MS), and in mice with experimental autoimmune encephalomyelitis (EAE). Perivascular CD4 T lymphocytes colocalize with ECM-bound EGFL7 in MS lesions. Human and mouse activated T cells upregulate EGFL7 ligand αvβ3 integrin and can adhere to EGFL7 through integrin αvβ3. EGFL7-knockout (KO) mice show earlier onset of EAE and increased brain and spinal cord parenchymal infiltration of T lymphocytes. Importantly, EC-restricted EGFL7-KO is associated with a similar EAE worsening. Finally, treatment with recombinant EGFL7 improves EAE, reduces MCAM expression, and tightens the BBB in mouse. Our data demonstrate that EGFL7 can limit CNS immune infiltration and may represent a novel therapeutic avenue in MS.
journal_name
Nat Communjournal_title
Nature communicationsauthors
Larochelle C,Uphaus T,Broux B,Gowing E,Paterka M,Michel L,Dudvarski Stankovic N,Bicker F,Lemaître F,Prat A,Schmidt MHH,Zipp Fdoi
10.1038/s41467-018-03186-zsubject
Has Abstractpub_date
2018-02-26 00:00:00pages
819issue
1issn
2041-1723pii
10.1038/s41467-018-03186-zjournal_volume
9pub_type
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