| First Author | Meares GP | Year | 2011 |
| Journal | Mol Cell Biol | Volume | 31 |
| Issue | 21 | Pages | 4286-97 |
| PubMed ID | 21896783 | Mgi Jnum | J:178323 |
| Mgi Id | MGI:5298146 | Doi | 10.1128/MCB.05668-11 |
| Citation | Meares GP, et al. (2011) IRE1-dependent activation of AMPK in response to nitric oxide. Mol Cell Biol 31(21):4286-97 |
| abstractText | While there can be detrimental consequences of nitric oxide production at pathological concentrations, eukaryotic cells have evolved protective mechanisms to defend themselves against this damage. The unfolded-protein response (UPR), activated by misfolded proteins and oxidative stress, is one adaptive mechanism that is employed to protect cells from stress. Nitric oxide is a potent activator of AMP-activated protein kinase (AMPK), and AMPK participates in the cellular defense against nitric oxide-mediated damage in pancreatic beta-cells. In this study, the mechanism of AMPK activation by nitric oxide was explored. The known AMPK kinases LKB1, CaMKK, and TAK1 are not required for the activation of AMPK by nitric oxide. Instead, this activation is dependent on the endoplasmic reticulum (ER) stress-activated protein IRE1. Nitric oxide-induced AMPK phosphorylation and subsequent signaling to AMPK substrates, including Raptor, acetyl coenzyme A carboxylase, and PGC-1alpha, is attenuated in IRE1alpha-deficient cells. The endoribonuclease activity of IRE1 appears to be required for AMPK activation in response to nitric oxide. In addition to nitric oxide, stimulation of IRE1 endoribonuclease activity with the flavonol quercetin leads to IRE1-dependent AMPK activation. These findings indicate that the RNase activity of IRE1 participates in AMPK activation and subsequent signaling through multiple AMPK-dependent pathways in response to nitrosative stress. |
