@article {136,
	title = {Influenza A Viral Replication Is Blocked by Inhibition of the Inositol-requiring Enzyme 1 (IRE1) Stress Pathway.},
	journal = {Journal of Biological Chemistry},
	volume = {287},
	year = {2012},
	note = {CAPLUS AN 2012:212308(Journal; Online Computer File)},
	month = {2012///},
	pages = {4679 - 4689},
	publisher = {American Society for Biochemistry and Molecular Biology},
	abstract = {Known therapies for influenza A virus infection are complicated by the frequent emergence of resistance.  A therapeutic strategy that may escape viral resistance is targeting host cellular mechanisms involved in viral replication and pathogenesis.  The endoplasmic reticulum (ER) stress response, also known as the unfolded protein response (UPR), is a primitive, evolutionary conserved mol. signaling cascade that has been implicated in multiple biol. phenomena including innate immunity and the pathogenesis of certain viral infections.  We investigated the effect of influenza A viral infection on ER stress pathways in lung epithelial cells.  Influenza A virus induced ER stress in a pathway-specific manner.  We showed that the virus activates the IRE1 pathway with little or no concomitant activation of the PERK and the ATF6 pathways.  When we examd. the effects of modulating the ER stress response on the virus, we found that the mol. chaperone tauroursodeoxycholic acid (TUDCA) significantly inhibits influenza A viral replication.  In addn., a specific inhibitor of the IRE1 pathway also blocked viral replication.  Our findings constitute the first evidence that ER stress plays a role in the pathogenesis of influenza A viral infection.  Decreasing viral replication by modulating the host ER stress response is a novel strategy that has important therapeutic implications. [on SciFinder(R)]},
	keywords = {influenza viral replication IRE1 stress pathway inhibition},
	isbn = {0021-9258},
	author = {Hassan, Ihab H. and Zhang, Michael S. and Powers, Linda S. and Shao, Jian Q. and Baltrusaitis, Jonas and Rutkowski, D. Thomas and Legge, Kevin and Monick, Martha M.}
}
