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60kDa溶血磷脂酶,一种参与上皮钠通道(ENaC)调节的新型血清糖皮质激素诱导激酶1(Sgk1)分子伴侣。

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

作者信息

Menniti Miranda, Iuliano Rodolfo, Föller Michael, Sopjani Mentor, Alesutan Ioana, Mariggiò Stefania, Nofziger Charity, Perri Angela M, Amato Rosario, Blazer-Yost Bonnie, Corda Daniela, Lang Florian, Perrotti Nicola

机构信息

Dipartimento di Medicina Sperimentale e Clinica G. Salvatore, Università Magna Graecia, Catanzaro, Italy.

出版信息

Cell Physiol Biochem. 2010;26(4-5):587-96. doi: 10.1159/000322326. Epub 2010 Oct 29.

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.

摘要

血清和糖皮质激素调节激酶(Sgk1)对于ENaC介导的钠转运的激素调节至关重要,并参与生长因子依赖性细胞存活和增殖的转导。鉴定Sgk1的分子伴侣对于理解其作用机制至关重要。我们基于人肾cDNA文库进行了酵母双杂交筛选,以鉴定Sgk1的分子伴侣。结果显示,筛选揭示了Sgk1与一种60 kDa溶血磷脂酶(LysoLP)之间的特异性相互作用。LysoLP是一种特征不明确的酶,基于序列分析,可能具有溶血磷脂酶和天冬酰胺酶活性。我们证明LysoLP确实具有溶血磷脂酶活性,并影响与细胞增殖和膜通道调节相关的代谢功能。此外,我们在非洲爪蟾卵母细胞表达系统中证明,LysoLP下调基础和Sgk1依赖性ENaC活性。总之,LysoLP可能是ENaC和Sgk1依赖性信号调节中的一个新参与者。

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