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Molecular and Cellular Biology, January 2005, p. 830-846, Vol. 25, No. 2
0270-7306/05/$08.00+0     doi:10.1128/MCB.25.2.830-846.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Rit Contributes to Nerve Growth Factor-Induced Neuronal Differentiation via Activation of B-Raf-Extracellular Signal-Regulated Kinase and p38 Mitogen-Activated Protein Kinase Cascades

Geng-Xian Shi and Douglas A. Andres*

Department of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, Kentucky

Received 24 August 2004/ Returned for modification 22 September 2004/ Accepted 17 October 2004

Rit is one of the original members of a novel Ras GTPase subfamily that uses distinct effector pathways to transform NIH 3T3 cells and induce pheochromocytoma cell (PC6) differentiation. In this study, we find that stimulation of PC6 cells by growth factors, including nerve growth factor (NGF), results in rapid and prolonged Rit activation. Ectopic expression of active Rit promotes PC6 neurite outgrowth that is morphologically distinct from that promoted by oncogenic Ras (evidenced by increased neurite branching) and stimulates activation of both the extracellular signal-regulated kinase (ERK) and p38 mitogen-activated protein (MAP) kinase signaling pathways. Furthermore, Rit-induced differentiation is dependent upon both MAP kinase cascades, since MEK inhibition blocked Rit-induced neurite outgrowth, while p38 blockade inhibited neurite elongation and branching but not neurite initiation. Surprisingly, while Rit was unable to stimulate ERK activity in NIH 3T3 cells, it potently activated ERK in PC6 cells. This cell type specificity is explained by the finding that Rit was unable to activate C-Raf, while it bound and stimulated the neuronal Raf isoform, B-Raf. Importantly, selective down-regulation of Rit gene expression in PC6 cells significantly altered NGF-dependent MAP kinase cascade responses, inhibiting both p38 and ERK kinase activation. Moreover, the ability of NGF to promote neuronal differentiation was attenuated by Rit knockdown. Thus, Rit is implicated in a novel pathway of neuronal development and regeneration by coupling specific trophic factor signals to sustained activation of the B-Raf/ERK and p38 MAP kinase cascades.

* Corresponding author. Mailing address: Department of Molecular and Cellular Biochemistry, Room MS639, Chandler Medical Center, University of Kentucky College of Medicine, 800 Rose St., Lexington, KY 40536-0298. Phone: (859) 257-6775. Fax: (859) 323-1037. E-mail: dandres{at}pop.uky.edu.

Molecular and Cellular Biology, January 2005, p. 830-846, Vol. 25, No. 2
0022-538X/05/$08.00+0     doi:10.1128/MCB.25.2.830-846.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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