Circulating Ly-6C+ myeloid precursors migrate to the CNS and play a pathogenic role during autoimmune demyelinating disease

IL King, TL Dickendesher… - Blood, The Journal of the …, 2009 - ashpublications.org
IL King, TL Dickendesher, BM Segal
Blood, The Journal of the American Society of Hematology, 2009ashpublications.org
Mature myeloid cells (macrophages and CD11b+ dendritic cells) form a prominent
component of neuroinflammatory infiltrates in multiple sclerosis and experimental
autoimmune encephalomyelitis (EAE). The mechanism by which these cells are replenished
during relapsing and chronic neuroinflammation is poorly understood. Here we demonstrate
that CD11b+ CD62L+ Ly6Chi monocytes with colony-forming potential are mobilized into
the bloodstream by a granulocyte-macrophage colony-stimulating factor-dependent …
Abstract
Mature myeloid cells (macrophages and CD11b+ dendritic cells) form a prominent component of neuroinflammatory infiltrates in multiple sclerosis and experimental autoimmune encephalomyelitis (EAE). The mechanism by which these cells are replenished during relapsing and chronic neuroinflammation is poorly understood. Here we demonstrate that CD11b+CD62L+Ly6Chi monocytes with colony-forming potential are mobilized into the bloodstream by a granulocyte-macrophage colony-stimulating factor-dependent pathway immediately before EAE relapses. Circulating Ly6Chi monocytes traffic across the blood-brain barrier, up-regulate proinflammatory molecules, and differentiate into central nervous system dendritic cells and macrophages. Enrichment of Ly6Chi monocytes in the circulating pool is associated with an earlier onset and increased severity of clinical EAE. Our studies indicate that granulocyte-macrophage colony-stimulating factor–driven release of Ly6Chi precursors from the bone marrow prevents exhaustion of central nervous system myeloid populations during relapsing or chronic autoimmune demyelination, suggesting a novel pathway for therapeutic targeting.
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