| Literature DB >> 14977878 |
Kenichiro Yamashita1, James McDaid, Robert Ollinger, Tung-Yu Tsui, Pascal O Berberat, Anny Usheva, Eva Csizmadia, R Neal Smith, Miguel P Soares, Fritz H Bach.
Abstract
Biliverdin, a product of heme oxygenase-1 (HO-1) enzymatic action, is converted into bilirubin, which has been considered a waste product in the past. We now show that administration of biliverdin has a salutary effect in organ transplantation. A brief course of treatment with biliverdin leads to long-term survival of H-2 incompatible heart allografts. Furthermore, those recipients harboring long-surviving (>100 days) allografts were tolerant to donor antigens indicated by the acceptance of second donor strain hearts but not third-party grafts. Treatment with biliverdin decreased intragraft leukocyte infiltration and inhibited T cell proliferation. Likely related to tolerance induction, biliverdin interferes with T cell signaling by inhibiting activation of nuclear factor of activated T cells (NFAT) and nuclear factor kappaB (NF-kappaB), two transcription factors involved in interleukin-2 (IL-2) transcription and T cell proliferation, as well as suppressing Th1 interferon-gamma (IFN-gamma) production in vitro. These findings support the potential use of biliverdin, a natural product, in transplantation and other T cell mediated immune disorders.Entities:
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Year: 2004 PMID: 14977878 DOI: 10.1096/fj.03-0839fje
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191