WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience MBF Bioscience Autoneuron
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (28)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kuroda, S.
Right arrow Articles by Kawato, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kuroda, S.
Right arrow Articles by Kawato, M.

 Previous Article  |  Next Article 

The Journal of Neuroscience, August 1, 2001, 21(15):5693-5702

Exploration of Signal Transduction Pathways in Cerebellar Long-Term Depression by Kinetic Simulation

Shinya Kuroda1, 2, Nicolas Schweighofer1, and Mitsuo Kawato1, 3

1 Kawato Dynamic Brain Project, ERATO, Japan Science and Technology, Kyoto 619-0288, Japan, 2 Division of Signal Transduction, Nara Institute of Science and Technology, Ikoma 630-0101, Japan, and 3 ATR, Kyoto 619-0288, Japan

Because multiple molecular signal transduction pathways regulate cerebellar long-term depression (LTD), which is thought to be a possible molecular and cellular basis of cerebellar learning, the systematic relationship between cerebellar LTD and the currently known signal transduction pathways remains obscure. To address this issue, we built a new diagram of signal transduction pathways and developed a computational model of kinetic simulation for the phosphorylation of AMPA receptors, known as a key step for expressing cerebellar LTD. The phosphorylation of AMPA receptors in this model consists of an initial phase and an intermediate phase. We show that the initial phase is mediated by the activation of linear cascades of protein kinase C (PKC), whereas the intermediate phase is mediated by a mitogen-activated protein (MAP) kinase-dependent positive feedback loop pathway that is responsible for the transition from the transient phosphorylation of the AMPA receptors to the stable phosphorylation of the AMPA receptors. These phases are dually regulated by the PKC and protein phosphatase pathways. Both phases also require nitric oxide (NO), although NO per se does not show any ability to induce LTD; this is consistent with a permissive role as reported experimentally (Lev-Ram et al., 1997). Therefore, the kinetic simulation is a powerful tool for understanding and exploring the behaviors of complex signal transduction pathways involved in cerebellar LTD.

Key words: cerebellar long-term depression; kinetics; simulation; signal transduction; positive feedback loop; phosphorylation


Copyright © 2001 Society for Neuroscience  0270-6474/01/21155693-10$05.00/0


This article has been cited by other articles:


Home page
J. Neurosci.Home page
H. Urakubo, M. Honda, R. C. Froemke, and S. Kuroda
Requirement of an Allosteric Kinetics of NMDA Receptors for Spike Timing-Dependent Plasticity
J. Neurosci., March 26, 2008; 28(13): 3310 - 3323.
[Abstract] [Full Text] [PDF]


Home page
PhysiologyHome page
S. M. Ajay and U. S. Bhalla
Synaptic plasticity in vitro and in silico: insights into an intracellular signaling maze.
Physiology, August 1, 2006; 21: 289 - 296.
[Abstract] [Full Text] [PDF]


Home page
Pharmacol. Rev.Home page
C. L. Palmer, L. Cotton, and J. M. Henley
The Molecular Pharmacology and Cell Biology of {alpha}-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Receptors
Pharmacol. Rev., June 1, 2005; 57(2): 253 - 277.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. Doi, S. Kuroda, T. Michikawa, and M. Kawato
Inositol 1,4,5-Trisphosphate-Dependent Ca2+ Threshold Dynamics Detect Spike Timing in Cerebellar Purkinje Cells
J. Neurosci., January 26, 2005; 25(4): 950 - 961.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
H. G. Serra, C. E. Byam, J. D. Lande, S. K. Tousey, H. Y. Zoghbi, and H. T. Orr
Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice
Hum. Mol. Genet., October 1, 2004; 13(20): 2535 - 2543.
[Abstract] [Full Text] [PDF]


Home page
Sci SignalHome page
S. J. Vayttaden and U. S. Bhalla
Developing Complex Signaling Models Using GENESIS/Kinetikit
Sci. Signal., February 10, 2004; 2004(219): pl4 - pl4.
[Abstract] [Full Text] [PDF]


Home page
Ann. N. Y. Acad. Sci.Home page
M. ITO
Historical Review of the Significance of the Cerebellum and the Role of Purkinje Cells in Motor Learning
Ann. N.Y. Acad. Sci., December 1, 2002; 978(1): 273 - 288.
[Abstract] [Full Text] [PDF]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2008 by Society for Neuroscience ONLINE ISSN: 1529-2401
-