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507894 
Journal Article 
Kynurenine pathway metabolism in human blood-brain-barrier cells: implications for immune tolerance & neurotoxicity 
Owe-Young, R; Webster, NL; Mukhtar, M; Pomerantz, RJ; Smythe, G; Walker, D; Armati, PJ; Crowe, SM; Brew, BJ 
2008 
Yes 
Journal of Neurochemistry
ISSN: 0022-3042
EISSN: 1471-4159 
105 
4 
1346-1357 
English 
The catabolic pathway of L-tryptophan (L-trp), known as the kynurenine pathway (KP), has been implicated in the pathogenesis of a wide range of brain diseases through its ability to lead to immune tolerance and neurotoxicity. As endothelial cells (ECs) and pericytes of the blood-brain-barrier (BBB) are among the first brain-associated cells that a blood-borne pathogen would encounter, we sought to determine their expression of the KP. Using RT-PCR and HPLC/GC-MS, we show that BBB ECs and pericytes constitutively express components of the KP. BBB ECs constitutively synthesized kynurenic acid, and after immune activation, kynurenine (KYN), which is secreted basolaterally. BBB pericytes produced small amounts of picolinic acid and after immune activation, KYN. These results have significant implications for the pathogenesis of inflammatory brain diseases in general, particularly human immunodeficiency virus (HIV)-related brain disease. Kynurenine pathway activation at the BBB results in local immune tolerance and neurotoxicity: the basolateral secretion of excess KYN can be further metabolized by perivascular macrophages and microglia with synthesis of quinolinic acid. The results point to a mechanism whereby a systemic inflammatory signal can be transduced across an intact BBB to cause local neurotoxicity. 
blood-brain barrier; IDO; immune tolerance; neurotoxicity; quinolinic; acid; tryptophan metabolism; microvascular endothelial-cells; indoleamine 2,3-dioxygenase activity; mycobacterium-avium complex; quinolinic acid; picolinic-acid; t-cell; interferon-gamma; 3-hydroxyanthranilic acid; cerebrospinal-fluid; dendritic cells