CD40 can participate in inflammatory processes after binding its cognate Li
gand (CD40L). We found that fetal human astrocytes constitutively express C
D40 mRNA and protein. Upon incubating cultures with proinflammatory cytokin
es (TNF-alpha, IL-1 beta and IFN-gamma) or with lipopolysaccharide (LPS), C
D40 expression was increased. No change in CD40 expression was noted in ast
rocyte cultures incubated with IL-6, HIV or gp41. Astrocytes also showed in
creased release of proinflammatory cytokines TNF-alpha, IL-1 beta and IL-6
after incubation with CD40L peptide. These observations suggest a role for
CD40 in central nervous system (CNS) inflammation and that CD40/CD40L autoc
rine or paracrine pathways may mediate this role. (C) 1999 Elsevier Science
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