Association between TLR4 and PTEN Involved in LPS-TLR4 Signaling Response. (2nd August 2016)

• Record Type: Journal Article
• Authors: Yin, Huahua; Tan, Yan; Wu, Xiaofeng; Yan, Hong; Liu, Feng; Yao, Yuanzhang; Jiang, Jianxin; Wan, Qi; Li, Lei
• Other Names: Hisaeda Hajime Academic Editor.
• Is Part Of: BioMed research international. Volume 2016(2016)
• Publication Date: 2016-08-02
• Subjects: Medicine -- Periodicals; Biology -- Periodicals; Biotechnology -- Periodicals; Life sciences -- Periodicals; 610.5
• DOI: 10.1155/2016/6083178
• Languages: English
• ISSNs: 2314-6133

Abstract

Abstract : In this study, we explored the potential mechanisms of how PTEN regulating LPS induced TLR4 signaling pathway. The initial findings from ELISA demonstrate that PTEN influences TNF- α secretion by its lipid phosphatase activity. Subsequently, western blot, immunoprecipitation assay, and immunofluorescence were performed to explore the activation process of PTEN by stimulation with LPS. As early as 20 minutes after LPS stimulation, reduced phosphorylation of PTEN was found obviously. Accordingly, the whole cell-scattered PTEN translocated towards the cell membrane 20 minutes after stimulating with LPS. Moreover, the weak physical association between PTEN and TLR4 in resting RAW264.7 cells increased gradually after the stimulation of LPS. Furthermore, our study showed PTEN decreased LPS-induced Akt activity and upregulated NF-κ B-dependent gene transcription, identifying indirectly that the PTEN could regulate the activation of NF-κ B by its downstream Akt kinase. In summary, our study illustrates the potential signal transduction process of PTEN while stimulated by LPS: by increasing the association of TLR4, PTEN recruits to its phosphoinositide substrate PI(3, 4, 5)P3 located on the cell membrane and exerts its dephosphorylated function and subsequently depresses the activity of downstream molecule Akt and results in activation of NF-κ B, followed by the secretion of inflammatory mediators TNF- α .