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. 2011 Oct;31(10):753–768. doi: 10.1089/jir.2011.0052

Table 1.

Characteristics of Cells Potentially Contributing to Disease Pathogenesis in Multiple Sclerosis and Experimental Autoimmune Encephalomyelitis

Cell type Characteristic features Potential contribution to MS/EAE
Parenchymal microglia MHC class II, PRRs, co-stimulatory molecules, immunoproteasome machinery, pro-inflammatory cytokines APC, disease initiation
Peripheral microglia/macrophages MHC class II, PRRs, co-stimulatory molecules, immunoproteasome machinery, pro-inflammatory cytokines APC, disease initiation or progression
Myeloid-derived DCs MHC class II, PRRs, co-stimulatory molecules, immunoproteasome machinery, pro-inflammatory cytokines APC, disease progression
Plasmacytoid DCs MHC II (inducible), PRRs, pro-inflammatory cytokines APC, immunoregulation
 neurons PRRs, pro-inflammatory cytokines Immunoregulation
Astrocytes MHC class II (inducible), PRRs (TLR3 only), pro-inflammatory cytokines Immunoregulation
Vascular endothelial cells MHC class II (inducible), co-stimulatory molecules (inducible) Immunoregulation

DC, dendritic cell; MS, multiple sclerosis; EAE, experimental autoimmune encephalomyelitis; TLR3, toll-like receptor 3; APC, antigen presenting cell; MHC, major histocompatibility complex; PRR, pattern recognition receptor.