Nitric oxide and thiol redox regulation of Janus kinase activity

• DOI: 10.1073/pnas.95.1.126
• Publication Date: 2002-07-26T14:40:11Z
• Authors: Roy J. Duhé; Gerald A. Evans; Rebecca A. Erwin; Robert A. Kirken; George W. Cox; William L. Farrar
• Keywords: 0301 basic medicine; Sulfhydryl Reagents; Janus Kinase 3; Janus Kinase 1; Janus Kinase 2; Protein-Tyrosine Kinases; Spodoptera; Nitric Oxide; Rats; Enzyme Activation; Dithiothreitol; Mice; 03 medical and health sciences; Proto-Oncogene Proteins; Animals; Humans; Iodobenzoates; Enzyme Inhibitors; Baculoviridae; Oxidation-Reduction; Cells, Cultured

The activation of Janus kinases (JAKs) is crucial for propagation of the proliferative response initiated by many cytokines. The proliferation of various cell lines, particularly those of hematopoietic origin, is also modulated by mediators of oxidative stress such as nitric oxide and thiol redox reagents. Herein we demonstrate that nitric oxide and other thiol oxidants can inhibit the autokinase activity of rat JAK2in vitro, presumably through oxidation of crucial dithiols to disulfides within JAK2. The reduced form of JAK2 is the most active form, and the oxidized JAK2 form is inactive. Nitric oxide pretreatment of quiescent Ba/F3 cells also inhibits the interleukin 3-triggeredin vivoactivation of JAK2, a phenomenon that correlates with inhibited proliferation. Furthermore, we observed that the autokinase activity of JAK3 responds in a similar fashion to thiol redox reagentsin vitroand to nitric oxide donorsin vivo. We suggest that the thiol redox regulation of JAKs may partially explain the generally immunosuppressive effects of nitric oxide and of other thiol oxidants.