Regular Article
Leukotriene B4: Metabolism and Signal Transduction

https://doi.org/10.1006/abbi.2000.2168Get rights and content

Abstract

Leukotriene B4 (LTB4) is known as one of the most potent chemoattractants and activators of leukocytes and is involved in inflammatory diseases. Enzymes involved in the biosynthesis and metabolism of LTB4 have been cloned, and their properties are well understood. Two G-protein-coupled receptors (BLT1 and BLT2) have been cloned and characterized. BLT1 and BLT2 are high- and low-affinity LTB4 receptors, respectively, and form a gene cluster in human and mouse. In this article recent findings on the metabolism of and the receptors for LTB4 are reviewed. We also discuss briefly a coreceptor role of BLT in HIV infection, and ion channel modification by LTB4.

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      Leukotriene A4 (LTA4, Scheme 7) is an epoxide metabolite known as an electrophilic species highly reactive to nucleophiles. The epoxide product can be transformed to the corresponding diol (leukotriene B4, LTB4) and glutathione conjugate (leukotriene C4, LTC4) catalyzed by epoxide hydrolase and glutathione S-transferase, respectively [88–91]. Reiber and co-workers first demonstrated significant reactivity of LTA4 to isolated nucleosides and nucleotides of RNAs in an alkaline solution [92].

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    1

    To whom correspondence should be addressed. E-mail: [email protected].

    2

    Present address: Department of Biochemistry, Faculty of Medicine, Gunma University, Showamachi 3-39-22, Maebashi, Gunma 371-8511, Japan.

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