Abstract
Indoleamine 2,3-dioxygenase (IDO) is one of the initial and rate-limiting enzymes involved in the catabolism of the essential amino acid tryptophan. In cultured cells, the induction of IDO leads to depletion of tryptophan and tryptophan starvation. Recent studies suggest that modulation of tryptophan concentration via IDO plays a fundamental role in innate immune responses. Induction of IDO by interferon-γ in macrophages and dendritic cells results in tryptophan depletion and suppresses the immune-mediated activation of fibroblasts and T, B, and natural killer cells. To assess the role of IDO in collagen-induced arthritis (CIA), a model of rheumatoid arthritis characterized by a primarily Th1-like immune response, activity of IDO was inhibited by 1-methyl-tryptophan (1-MT) in vivo. The results showed significantly increased incidence and severity of CIA in mice treated with 1-MT. Activity of IDO, as determined by measuring the levels of kynurenine/tryptophan ratio in the sera, was increased in the acute phase of arthritis and was higher in collagen-immunized mice that did not develop arthritis. Treatment with 1-MT resulted in an enhanced cellular and humoral immune response and a more dominant polarization to Th1 in mice with arthritis compared with vehicle-treated arthritic mice. The results demonstrated that development of CIA was associated with increased IDO activity and enhanced tryptophan catabolism in mice. Blocking IDO with 1-MT aggravated the severity of arthritis and enhanced the immune responses. These findings suggest that IDO may play an important and novel role in the negative feedback of CIA and possibly in the pathogenesis of rheumatoid arthritis.
Highlights
Produced proinflammatory cytokines such as tumor necrosis factor-α, interleukin (IL)-1, and IL-6 play a pivotal role in the pathology of rheumatoid arthritis (RA)
The results demonstrated that development of collagen-induced arthritis (CIA) was associated with increased IDO activity and enhanced tryptophan catabolism in mice
Histological analysis of the ankle, metatarsophalangeal, and interphalangeal joints of 1MT-treated and vehicle-treated mice showed typical arthritis characterized by extensive leukocyte infiltration, synovial proliferation, pannus formation, and erosions
Summary
Produced proinflammatory cytokines such as tumor necrosis factor-α, interleukin (IL)-1, and IL-6 play a pivotal role in the pathology of rheumatoid arthritis (RA). These cytokines, by upregulation of several genes, are responsible both for the recruitment and continuous activation of the inflammatory cells and for inducing production of the enzymes that destroy bone and cartilage. Recent studies have established an entirely novel important biological function for IDO. These studies indicate that IDO-mediated tryptophan depletion in vitro results in inhibition of matrix-degrading metalloproteinase enzyme production, suppression of inflammatory responses, and
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