Proteomics analysis of the expression of neurogranin in murine neuroblastoma (Neuro-2a) cells reveals its involvement for cell differentiation

• Published in: International journal of biological sciences 2007-04, Vol.3 (5), p.263-273
• Main Authors: Han, Nian-Lin Reena, Wen, Jing, Lin, Qingsong, Tan, Pei Ling, Liou, Yih-Cherng, Sheu, Fwu-Shan
• Format: Article
• Language: English
• Subjects: Animals; Blotting, Western; Cell Differentiation - physiology; Cell Line, Tumor; Chromatography, Liquid; Cytoskeletal Proteins - metabolism; Extracellular Signal-Regulated MAP Kinases - metabolism; Gene Expression; Gene Expression Profiling; Humans; Isotope Labeling; Mice; Neuroblastoma; Neurogranin - metabolism; Neurogranin - physiology; Neurons - cytology; Phosphorylation; Protein Kinase C - metabolism; Proteomics; Research Paper; Tandem Mass Spectrometry; Up-Regulation
• ISSN: 1449-2288; 1449-2288
• DOI: 10.7150/ijbs.3.263

Neurogranin (Ng) is a neural-specific, calmodulin (CaM)-binding protein that is phosphorylated by protein kinase C (PKC). Although its biochemical property has been well characterized, the physiological function of Ng needs to be elucidated. In the present study, we performed proteomics analysis of the induced compositional changes due to the expression of Ng in murine neuroblastoma (Neuro-2a) cells using isotope coded affinity tags (ICAT) combined with 2-dimensional liquid chromatography/tandem mass spectrometry (2D-LC/MS/MS). We found that 40% of identified proteins were down-regulated and most of these proteins are microtubule components and associated proteins that mediated neurite outgrowth. Western blot experiments confirmed the expression of alpha-tubulin and microtubule- associated protein 1B (MAP 1B) was dramatically reduced in Neuro-2a-Ng cells compared to control. Cell morphology of Neuro-2a-Ng showed far less neurites than the control. Serum deprivation induced the extension of only one or two long neurites per cell in Neuro-2a-Ng, contrasting to the extension of multiple neurites per control cell. Ng may be linked to neurite formation by affecting expression of several microtubule related proteins. Furthermore, the PKC activator (PMA) induced an enhanced ERK1/2 activity in the cells that expressed Ng. The mutation of Ng at S36A caused sustained increase of ERK1/2 activity, whereas the ERK1/2 activity in mutation at I33Q showed no difference compared to wild type Ng, suggesting the phosphorylation of Ng but not the CaM /Ng interaction plays an important role in ERK activation. Ng may be involved in neuronal growth and differentiation via PKC and ERK1/2 signaling pathways.