iNOS (NOS2) at a glance

Nitric oxide (NO) is an effector of the innate immune system. The innate immune system is a set of rapid host responses to pathogens. Cells of the innate immune system - macrophages, neutrophils and natural killer cells - use pattern recognition receptors to recognize molecular patterns associated with pathogens (Medzhitov, 2001). Activated macrophages then inhibit pathogen replication by releasing a variety of effector molecules, including NO.Resting immune cells lack the inducible NO synthase (iNOS or NOS2), the enzyme that synthesizes NO. However, a variety of extracellular stimuli can activate distinct signaling pathways that converge to initiate expression of NOS2. Cell wall components of bacteria and fungi can trigger the innate immune signaling cascade, leading to expression of NOS2. For example, lipopolysaccharide (LPS), a component of the wall of Gram-negative bacteria, can bind to LPS-binding protein (LBP), which delivers LPS to CD14, a high-affinity LPS receptor. Toll-like receptor 4 (TLR4) in conjunction with the small extracellular protein MD-2 interacts with the CD14-LPS complex, and then activates an intracellular signaling cascade via adaptors that include IRAK and MyD88, which in turn activate downstream molecules including TRAF6. The innate immune pathway then activates signaling pathways including the mitogen-activated protein kinase (MAPK) pathway and the nuclear factor κB (NF-κB) pathway. These pathways converge to activate NOS2 transcription.FIG1Cytokines released from infected host cells can also activate NO production, including tumor necrosis factor α (TNF-α) and interleukin 1β (IL-1β). Interferon γ (IFN-γ) produced by activated immune cells can activate NOS2 expression, and can synergistically activate NOS2 expression in combination with other agents such as LPS. IFN-γ interacts with the interferon receptor 1 (IFNR1) and IFNR2 complex, which activates kinases of the Jak family and signal transducers and activators of transcription (STAT) pathways (Darnell et al., 1994). The interferon signaling pathway can also activate NOS2 transcription.LPS-mediated activation of the innate immune pattern recognition receptors stimulates NOS2 mRNA transcription within 2-4 hours, and NOS2 translation within 6 hours. LPS activation of TLR4 leads to phosphorylation of inhibitor of NF-κB kinase (IKK), which phosphorylates the inhibitor of NF-κB (IκB), which releases the transcription factor NF-κB. NF-κB translocates from the cytoplasm to the nucleus, where it interacts with κB elements in the NOS2 5′ flanking region, triggering NOS2 transcription (Xie et al., 1994). IFN-γ triggers NOS2 transcription by activating the JAK/STAT pathway, leading to synthesis of the transcription factor interferon response factor 1 (IRF-1), which stimulates NOS2 transcription (Kamijo et al., 1994). IFN-γ also provides a synergistic boost to LPS induction of NOS2 transcription because IRF-1 interacts with NF-κB, altering the conformation of the NOS2 promoter (Saura et al., 1999a). Scaffolding proteins such as HMG-Y(I) and transcriptional activators such as CBP interact with IRF-1 and NF-κB, forming a multi-subunit complex that increases NOS2 transcription (Perrella et al., 1999). Other transcription factors, including Stat1α and hypoxia inducible factor-1 (HIF-1), can also regulate NOS2 expression.The 3′ untranslated region of NOS2 mRNA contains multiple AUUUA elements, which mediate stability of mRNAs of cytokines. The RNA-binding protein HuR interacts stabilizing NOS2 mRNA with the AUUUA elements of the NOS2 mRNA, (Rodriguez-Pascual et al., 2000). Lack of HuR leads to destabilization of NOS2 mRNA and decreased NOS2 expression.NOS2 does not synthesize NO until it forms homodimers. A set of proteins can inhibit NOS2 activity by preventing NOS2 homodimerization. For example, NOS-associated protein 110 kDa (NAP110) interacts with the N-terminus of NOS2, forming NOS2-NAP110 heterodimers, and blocking the formation of NOS2-NOS2 dimers (Ratovitski et al., 1999). Although NOS2 is ubiquitylated and phosphorylated, the significance of these post-translational modifications is unknown.Transforming growth factor β (TGF-β) inhibits NOS2 expression through transcriptional, post-transcriptional and post-translational mechanisms (Vodovotz et al., 1993). TGF-β inhibits NOS2 transcription in part by blocking expression of the scaffolding protein HMG-I(Y). A variety of other signaling molecules, including IL-4, IL-10, IL-13 and macrophage deactivation factor, inhibit NOS2 expression by unknown mechanisms.NOS2 contains a C-terminal reductase domain, which binds NADPH and transfers electrons from NADPH to FAD and then to FMN, and an N-terminal oxygenase domain, which contains a heme and binding sites for arginine, tetrahydrobiopterin and calmodulin. NOS2 utilizes oxygen and electrons from NADPH to oxidize the substrate L-arginine into the intermediate OH-L-arginine, which is then oxidized into NO and L-citrulline.In contrast to the other NOS isoforms NOS1 and NOS3, dimeric NOS2 is always active when expressed. Although NOS2 binds calmodulin, NOS2 is independent of intracellular calcium levels, whereas calcium regulates NOS1 and NOS3 activity (Cho et al., 1992). The Vmax of NOS2 is approximately 10-fold greater than the other NOS isoforms; so NOS2 is a high-output NOS compared with the low-output isoforms NOS1 and NOS3.NO and superoxide (O2-) are radical effectors of the innate immune system that can directly inhibit pathogen replication (Nathan and Shiloh, 2000). Derivatives of NO can also block infections. NO can combine with O2- to form peroxynitrite anion (ONOO-). NO can also form nitrosothiols, nitrogen dioxide (NO2) and other nitrosating species. Superoxide can form hydrogen peroxide, which in turn can form hypochlorous acid and other oxidants. These reactive nitrogen intermediates and reactive oxygen intermediates can cross bacterial and fungal walls with differing facility, and react with specific pathogen targets (Fang, 1997).NO is an anti-bacterial effector of the innate immune system (Fang, 1997). NO can inhibit bacterial DNA synthesis by inhibiting bacterial ribonucleotide reductase. NO can also cause double-stranded breaks (DSBs) in bacterial DNA. NO can modify cysteine residues in bacterial proteins, oxidize bacterial lipids, and interact with heme iron and iron-sulfur clusters in bacterial enzymes. However, it is unclear whether modification of these bacterial targets contributes to the anti-bacterial effects of NO. NO mobilizes zinc in bacteria, which suggests that DNA-binding proteins containing zinc are targets of NO (Schapiro et al., 2003). It can also can increase the susceptibility of bacteria to oxidative DNA damage by blocking respiration (Woodmansee and Imlay, 2003). Peroxynitrite can oxidize bacterial lipids and produce nitrotyrosine of bacterial polypeptides, but the biological significance of these modifications is also unclear.Oxidants activate bacterial defenses. The bacterial protein SoxRS serves as a sensor for NO, and can activate transcription of a set of bacterial genes whose products defend the pathogen from oxidant damage - for example, bacterial superoxide dismutase (SOD). The bacterial protein OxyR can be modified and activated by hydrogen peroxide or NO, and directs the transcription of bacterial genes such as alkyl hydroperoxide reductase (AHP), which confers resistance to peroxynitrite, and catalase (CAT), which deactivates hydrogen peroxide (Bryk et al., 2000; Hausladen et al., 1996). The bacterial protein ferric uptake regulatory protein (Fur) also serves as an NO sensor. Fur is an iron-containing bacterial transcription factor that normally represses a set of nitrosative stress response genes. NO inactivates Fur by interacting with its iron cofactor, permitting expression of genes protective against oxidative stress (Crawford and Goldberg, 1998; D'Autreaux et al., 2002). One bacterial gene regulated by Fur encodes a flavohemoglobin that can detoxify NO, protecting pathogens from NO (Gardner et al., 1998; Hausladen et al., 2001). Thus multiple signaling pathways defend bacteria against NO.NO is an anti-viral effector of the innate immune system. It can inhibit replication of a variety of viruses, including Herpesviruses, Picornaviruses, Flaviviruses and Coronaviruses. Viral proteases are a target of NO. Many RNA viruses depend on viral proteases to cleave large viral polyproteins into smaller viral polypeptides. NO can nitrosylate the cysteine protease 3Cpro of Picornaviruses, inhibiting viral protease cleavage of the viral polyprotein, and thus blocking viral replication (Saura et al., 1999b; Zaragoza et al., 1998).