Timing-Dependent Actions of NGF Required for Cell Differentiation

被引:39
作者
Chung, Jaehoon [1 ]
Kubota, Hiroyuki [1 ]
Ozaki, Yu-ichi [1 ]
Uda, Shinsuke [1 ]
Kuroda, Shinya [1 ]
机构
[1] Univ Tokyo, Dept Biophys & Biochem, Grad Sch Sci, CREST,Japan Sci & Technol Agcy, Tokyo 113, Japan
关键词
NERVE GROWTH-FACTOR; PLASMINOGEN-ACTIVATOR RECEPTOR; PC12 PHEOCHROMOCYTOMA CELLS; 2 DISTINCT PHASES; NEURONAL DIFFERENTIATION; NEURITE OUTGROWTH; PHOSPHATIDYLINOSITOL-3; KINASE; SIGNAL-TRANSDUCTION; ERK ACTIVATION; EXPRESSION;
D O I
10.1371/journal.pone.0009011
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Continuous NGF stimulation induces PC12 cell differentiation. However, why continuous NGF stimulation is required for differentiation is unclear. In this study, we investigated the underlying mechanisms of the timing-dependent requirement of NGF action for cell differentiation. Methodology/Principal Findings: To address the timing-dependency of the NGF action, we performed a discontinuous stimulation assay consisting of a first transient stimulation followed by an interval and then a second sustained stimulation and quantified the neurite extension level. Consequently, we observed a timing-dependent action of NGF on cell differentiation, and discontinuous NGF stimulation similarly induced differentiation. The first stimulation did not induce neurite extension, whereas the second stimulation induced fast neurite extension; therefore, the first stimulation is likely required as a prerequisite condition. These observations indicate that the action of NGF can be divided into two processes: an initial stimulation-driven latent process and a second stimulation-driven extension process. The latent process appears to require the activities of ERK and transcription, but not PI3K, whereas the extension-process requires the activities of ERK and PI3K, but not transcription. We also found that during the first stimulation, the activity of NGF can be replaced by PACAP, but not by insulin, EGF, bFGF or forskolin; during the second stimulation, however, the activity of NGF cannot be replaced by any of these stimulants. These findings allowed us to identify potential genes specifically involved in the latent process, rather than in other processes, using a microarray. Conclusions/Significance: These results demonstrate that NGF induces the differentiation of PC12 cells via mechanically distinct processes: an ERK-driven and transcription-dependent latent process, and an ERK- and PI3K-driven and transcription-independent extension process.
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页数:14
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