Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-42320
Cell Physiol Biochem 2010 Jan 01;264-5:587-96. doi: 10.1159/000322326.
Show Gene links Show Anatomy links

60kDa lysophospholipase, a new Sgk1 molecular partner involved in the regulation of ENaC.

Menniti M , Iuliano R , Föller M , Sopjani M , Alesutan I , Mariggiò S , Nofziger C , Perri AM , Amato R , Blazer-Yost B , Corda D , Lang F , Perrotti N .


???displayArticle.abstract???
The serum- and glucocorticoid-regulated kinase (Sgk1) is essential for hormonal regulation of ENaC-mediated sodium transport and is involved in the transduction of growth-factor-dependent cell survival and proliferation. The identification of molecular partners for Sgk1 is crucial for the understanding of its mechanisms of action. We performed a yeast two-hybrid screening based on a human kidney cDNA library to identify molecular partners of Sgk1. As a result the screening revealed a specific interaction between Sgk1 and a 60 kDa Lysophospholipase (LysoLP). LysoLP is a poorly characterized enzyme that, based on sequence analysis, might possess lysophospholipase and asparaginase activities. We demonstrate that LysoLP has indeed a lysophospholipase activity and affects metabolic functions related to cell proliferation and regulation of membrane channels. Moreover we demonstrate in the Xenopus oocyte expression system that LysoLP downregulates basal and Sgk1-dependent ENaC activity. In conclusion LysoLP may represent a new player in the regulation of ENaC and Sgk1-dependent signaling.

???displayArticle.pubmedLink??? 21063096
???displayArticle.link??? Cell Physiol Biochem


Species referenced: Xenopus
Genes referenced: sgk1