Y-27632 Induces Neurite Outgrowth by Activating the NOX1-Mediated AKT and PAK1 Phosphorylation Cascades in PC12 Cells
- Int J Mol Sci. 2020 Oct 16;21(20):7679. doi: 10.3390/ijms21207679.
- 1. Department of Oral Biology, Yonsei University College of Dentistry, Seoul 03722, Korea.
- 2. Department of Molecular Bioscience, School of Bioscience and Biotechnology, Kangwon National University, Chuncheon 24341, Korea.
Y-27632 is known as a selective Rho-associated coiled coil-forming kinase (ROCK) inhibitor. Y-27632 has been shown to induce neurite outgrowth in several neuronal cells. However, the precise molecular mechanisms linking neurite outgrowth to Y-27632 are not completely understood. In this study, we examined the ability of Y-27632 to induce neurite outgrowth in PC12 cells and evaluated the signaling cascade. The effect of Y-27632 on the neurite outgrowth was inhibited by Reactive Oxygen Species (ROS) scavengers such as N-acetyl cysteine (NAC) and trolox. Furthermore, Y-27632-induced neurite outgrowth was not triggered by NADPH Oxidase 1 (NOX1) knockdown or diphenyleneiodonium (DPI), a NOX inhibitor. Suppression of the Rho-family GTPase Rac1, which is under the negative control of ROCK, with expression of the dominant negative Rac1 mutant (Rac1N17) prevented Y-27632-induced neurite outgrowth. Moreover, the Rac1 inhibitor NSC23766 prevented Y-27632-induced Akt and p21-Activated Kinase 1 (PAK1) activation. Akt inhibition with MK2206 suppressed Y-27632-induced PAK1 phosphorylation and neurite outgrowth. In conclusion, our results suggest that Rac1/NOX1-dependent ROS generation and subsequent activation of the Akt/PAK1 cascade contribute to Y-27632-induced neurite outgrowth in PC12 cells.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: ROCK; NF-κB; Apoptosis; Autophagy; Akt; mTOR; NADPH Oxidase; Reactive Oxygen Species (ROS); PAK; Ras
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target: ROCK; Akt; PAK; Autophagy; mTOR; NF-κB; Reference Standards; Reactive Oxygen Species (ROS); NADPH Oxidase; Apoptosis; RasResearch Areas: Cancer