Phosphatidylinositol 4-phosphate 5-kinase alpha negatively regulates nerve growth factor-induced neurite outgrowth in PC12 cells.
- Author:
Tian LIU
1
;
Sang Yoon LEE
Author Information
1. Neuroscience Graduate Program, Ajou University School of Medicine, Suwon, Korea. sangyoon@ajou.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Akt;
nerve growth factor;
neurite outgrowth;
PI3K;
phosphatidylinositol 4;
1-phosphatidylinositol-4-phosphate 5-kinase;
5-bisphosphate
- MeSH:
Animals;
Enzyme Activation/drug effects;
Gene Knockdown Techniques;
Mice;
Nerve Growth Factor/*pharmacology;
Neurites/drug effects/*enzymology;
PC12 Cells;
Phosphatidylinositol 3-Kinases/metabolism;
Phosphatidylinositol 4,5-Diphosphate/metabolism;
Phosphorylation/drug effects;
Phosphotransferases (Alcohol Group Acceptor)/*metabolism;
Proto-Oncogene Proteins c-akt/metabolism;
Rats;
Reactive Oxygen Species/metabolism;
Signal Transduction/drug effects
- From:Experimental & Molecular Medicine
2013;45(3):e16-
- CountryRepublic of Korea
- Language:English
-
Abstract:
Neurite outgrowth, a cell differentiation process involving membrane morphological changes, is critical for neuronal network and development. The membrane lipid, phosphatidylinositol (PI) 4,5-bisphosphate (PIP2), is a key regulator of many important cell surface events of membrane signaling, trafficking and dynamics. This lipid is produced mainly by the type I PI 4-phosphate 5-kinase (PIP5K) family members. In this study, we addressed whether PIP5Kalpha, an isoform of PIP5K, could have a role in neurite outgrowth induced by nerve growth factor (NGF). For this purpose, we knocked down PIP5Kalpha in PC12 rat pheochromocytoma cells by stable expression of PIP5Kalpha microRNA that significantly reduced PIP5Kalpha expression and PIP2 level. Interestingly, NGF-induced neurite outgrowth was more prominent in PIP5Kalpha-knockdown (KD) cells than in control cells. Conversely, add-back of PIP5Kalpha into PIP5Kalpha KD cells abrogated the effect of NGF on neurite outgrowth. NGF treatment activated PI 3-kinase (PI3K)/Akt pathway, which seemed to be associated with reactive oxygen species generation. Similar to the changes in neurite outgrowth, the PI3K/Akt activation by NGF was potentiated by PIP5Kalpha KD, but was attenuated by the reintroduction of PIP5Kalpha. Moreover, exogenously applied PIP2 to PIP5Kalpha KD cells also suppressed Akt activation by NGF. Together, our results suggest that PIP5Kalpha acts as a negative regulator of NGF-induced neurite outgrowth by inhibiting PI3K/Akt signaling pathway in PC12 cells.
