Medical Journals

Brain-derived Neurotrophic Factor Activates Erk5 in Cortical Neurons Via a Rap1-mekk2 Signaling Cascade.

Authors:
  • Wang Yupeng
  • Su Bing
  • Xia Zhengui

From: Toxicology Program, Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington 98195-7234, USA.

The Journal of biological chemistry

  • Publish Date: Nov 2006
  • ISSN: 0021-9258
  • Volume: 281
  • Issue: 47
  • Pages: 35965-74
  • Medium: Print
  • Language: English
  • Citation (JAMA): Wang Yupeng, Su Bing, Xia Zhengui, et al. Brain-derived Neurotrophic Factor Activates Erk5 in Cortical Neurons Via a Rap1-mekk2 Signaling Cascade.. J. Biol. Chem. Nov 2006;281:35965-74

Abstract

The extracellular signal-regulated kinase 5 (ERK5) is activated in neurons of the central nervous system by neurotrophins including brain-derived neurotrophic factor (BDNF). Although MEK5 is known to mediate BDNF stimulation of ERK5 in central nervous system neurons, other upstream signaling components have not been identified. Here, we report that BDNF induces a sustained activation of ERK5 in rat cortical neurons and activates Rap1, a small GTPase, as well as MEKK2, a MEK5 kinase. Our data indicate that activation of Rap1 or MEKK2 is sufficient to stimulate ERK5, whereas inhibition of either Rap1 or MEKK2 attenuates BDNF activation of ERK5. Furthermore, BDNF stimulation of MEKK2 is regulated by Rap1. Our evidence also indicates that Ras and MEKK3, a MEK5 kinase in non-neuronal cells, do not play a significant role in BDNF activation of ERK5. This study identifies Rap1 and MEKK2 as critical upstream signaling molecules mediating BDNF stimulation of ERK5 in central nervous system neurons.

Mesh Headings (Keywords): Animals, Apoptosis, Brain, Brain-Derived Neurotrophic Factor, Central Nervous System, Enzyme Activation, MAP Kinase Kinase Kinase 2, Mice, Mitogen-Activated Protein Kinase 7, Models, Biological, Neurons, Rats, Rats, Sprague-Dawley, Signal Transduction, rap1 GTP-Binding Proteins


Check for Full Text / PubMed Unique Identifier (PMID): 17003042


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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