Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2202-14-153
Title: C-Jun N-terminal kinase in synergistic neurite outgrowth in PC12 cells mediated through P90RSK
Authors: Seow, K.H.
Zhou, L. 
Stephanopoulos, G.
Too, H.-P.
Keywords: EGF
FGFb
JNK
Neurite outgrowth
NGF
P90RSK
PACAP
PC12
Synergistic
Issue Date: 12-Dec-2013
Citation: Seow, K.H., Zhou, L., Stephanopoulos, G., Too, H.-P. (2013-12-12). C-Jun N-terminal kinase in synergistic neurite outgrowth in PC12 cells mediated through P90RSK. BMC Neuroscience 14 : -. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2202-14-153
Abstract: Background: Synergistic multi-ligand treatments that can induce neuronal differentiation offer valuable strategies to regulate and modulate neurite outgrowth. Whereas the signaling pathways mediating single ligand-induced neurite outgrowth, such as Akt, extracellular signal-regulated kinase (Erk), c-Jun N-terminal kinase (JNK), and p38 mitogen-activated protein kinase (P38), have been extensively studied, the mechanisms underlying multi-ligand synergistic neurite outgrowth are poorly understood. In an attempt to gain insight into synergistic neurite outgrowth, PC12 cells were treated with one of three combinations: pituitary adenylate cyclase-activating peptide (PACAP) with epidermal growth factor (EP), basic fibroblast growth factor (FP), or nerve growth factor (NP) and then challenged with the appropriate kinase inhibitors to assess the signaling pathways involved in the process.Results: Response surface analyses indicated that synergistic neurite outgrowth was regulated by distinct pathways in these systems. Synergistic increases in the phosphorylation of Erk and JNK, but not Akt or P38, were observed with the three growth factor-PACAP combinations. Unexpectedly, we identified a synergistic increase in JNK phosphorylation, which was involved in neurite outgrowth in the NP and FP, but not EP, systems. Inhibition of JNK using the SP600125 inhibitor reduced phosphorylation of 90 kDa ribosomal S6 kinase (P90RSK) in the NP and FP, but not EP, systems. This suggested the involvement of P90RSK in mediating the differential effects of JNK in synergistic neurite outgrowth.Conclusions: Taken together, these findings reveal the involvement of distinct signaling pathways in regulating neurite outgrowth in response to different synergistic growth factor-PACAP treatments. Our findings demonstrate a hitherto unrecognized mechanism of JNK-P90RSK in mediating synergistic neurite outgrowth induced by the co-treatment of growth factors and PACAP. © 2013 Seow et al.; licensee BioMed Central Ltd.
Source Title: BMC Neuroscience
URI: http://scholarbank.nus.edu.sg/handle/10635/114630
ISSN: 14712202
DOI: 10.1186/1471-2202-14-153
Appears in Collections:Staff Publications
Elements

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
2013-c_jun_n_terminal_kinase-published.pdf3.18 MBAdobe PDF

OPEN

PublishedView/Download

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.