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ATP5O — IRF6

Text-mined interactions from Literome

Vairo et al., J Cell Physiol 1992 : All three agents stimulated BMM protein synthesis ; TNF alpha and LPS , but not IFN gamma, stimulated BMM Na+/H+ exchange and Na+, K ( + ) -ATPase activities, as well as c-fos mRNA levels
Helmer et al., Ann Surg 2004 : LPS increased alpha- and beta-H/K-ATPase subunit mRNA expression ( Northern blot ) in the absence of PG compared with saline
Akopova et al., FiziolohichnyÄ­ zhurnal (Kiev, Ukraine : 1994) 2009 : The results obtained suggest that NOS- and cGMP dependent pathway takes part in Na+, ( + ) -ATPase activation by LPS and NG, but the enzyme inhibition by nitric oxide in vivo is not cGMP dependent and is determined by the activation of free-radical reactions and dramatic enhancement of nitrosylation level in rat aorta tissue
Yadav et al., Exp Eye Res 2010 : Further, LPS induced decrease in the expression of Na/K-ATPase in hNPECs was restored by AR inhibitors
Yao et al., Zhongguo Ying Yong Sheng Li Xue Za Zhi 2009 (Shock, Septic) : Single pretreatment with either AMG or BQ-123 did not attenuate the impairment of SR Ca2+ -ATPase induced by LPS ... But neither ET-1 nor NO participates in the impairment of SR Ca2+ -ATPase induced by LPS
Kang et al., J Histochem Cytochem 1990 : In the present work, the effects of LPS and CAM on Ca2 ( + ) -ATPase and intracellular Ca2+ in human NK cells were studied by a combined technique of immunogold electron microscopy and ultracytochemistry ... Ca2 ( + ) -ATPase was localized in the plasma membrane of NK cells, and its activity was suppressed by LPS but was enhanced by CAM ... The results indicate that CAM is capable of blocking or reversing the inhibitory effect of LPS on Ca2 ( + ) -ATPase , and suggest that in human NK cells the plasma membrane associated Ca2 ( + ) -ATPase is responsible for extrusion of intracellular Ca2+
Zhang et al., Basic Res Cardiol 2012 (Calcium Signaling...) : LPS induced reduction in Na/K-ATPase activity was prevented by inhibition of PI3K, Rac1 and NADPH oxidase using LY294002, a dominant negative Rac1 adenovirus ( Ad-Rac1N17 ) and apocynin, respectively