Literature DB >> 12062045

Visually driven modulation of glutamatergic synaptic transmission is mediated by the regulation of intracellular polyamines.

Carlos D Aizenman1, Guillermo Muñoz-Elías, Hollis T Cline.   

Abstract

Ca2+-permeable AMPARs are inwardly rectifying due to block by intracellular polyamines. Neuronal activity regulates polyamine synthesis, yet whether this affects Ca2+-AMPAR-mediated synaptic transmission is unknown. We test whether 4 hr of increased visual stimulation regulates glutamatergic retino-tectal synapses in Xenopus tadpoles. Tectal neurons containing Ca2+-AMPARs form a gradient along the rostro-caudal developmental axis. These neurons had inwardly rectifying AMPAR-mediated EPSCs. Four hours of visual stimulation or addition of intracellular spermine increased rectification in immature neurons. Polyamine synthesis inhibitors blocked the effect of visual stimulation, suggesting that visual activity regulates AMPARs via the polyamine synthesis pathway. This modulation resulted in changes in the integrative properties of tectal neurons. Regulation of polyamine synthesis by physiological stimuli is a novel form of modulation of synaptic transmission important for understanding the short-term effects of enhanced sensory experience during development.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12062045     DOI: 10.1016/s0896-6273(02)00674-8

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  42 in total

Review 1.  Glutamate receptor ion channels: structure, regulation, and function.

Authors:  Stephen F Traynelis; Lonnie P Wollmuth; Chris J McBain; Frank S Menniti; Katie M Vance; Kevin K Ogden; Kasper B Hansen; Hongjie Yuan; Scott J Myers; Ray Dingledine
Journal:  Pharmacol Rev       Date:  2010-09       Impact factor: 25.468

2.  AMPA receptor inhibition by synaptically released zinc.

Authors:  Bopanna I Kalappa; Charles T Anderson; Jacob M Goldberg; Stephen J Lippard; Thanos Tzounopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-08       Impact factor: 11.205

3.  Transport of polyamines in Drosophila S2 cells: kinetics, pharmacology and dependence on the plasma membrane proton gradient.

Authors:  Rafael Romero-Calderón; David E Krantz
Journal:  Biochem J       Date:  2006-01-15       Impact factor: 3.857

4.  Homeostatic regulation of intrinsic excitability and synaptic transmission in a developing visual circuit.

Authors:  Kara G Pratt; Carlos D Aizenman
Journal:  J Neurosci       Date:  2007-08-01       Impact factor: 6.167

Review 5.  The regulation of dendritic arbor development and plasticity by glutamatergic synaptic input: a review of the synaptotrophic hypothesis.

Authors:  Hollis Cline; Kurt Haas
Journal:  J Physiol       Date:  2008-01-17       Impact factor: 5.182

Review 6.  Roles of distinct glutamate receptors in induction of anti-Hebbian long-term potentiation.

Authors:  Dimitri M Kullmann; Karri Lamsa
Journal:  J Physiol       Date:  2008-01-10       Impact factor: 5.182

Review 7.  Ca(2+) permeable AMPA receptors switch allegiances: mechanisms and consequences.

Authors:  Siqiong June Liu; Iaroslav Savtchouk
Journal:  J Physiol       Date:  2011-09-05       Impact factor: 5.182

8.  Acute synthesis of CPEB is required for plasticity of visual avoidance behavior in Xenopus.

Authors:  Wanhua Shen; Han-Hsuan Liu; Lucio Schiapparelli; Daniel McClatchy; Hai-Yan He; John R Yates; Hollis T Cline
Journal:  Cell Rep       Date:  2014-02-13       Impact factor: 9.423

9.  Stargazin attenuates intracellular polyamine block of calcium-permeable AMPA receptors.

Authors:  David Soto; Ian D Coombs; Leah Kelly; Mark Farrant; Stuart G Cull-Candy
Journal:  Nat Neurosci       Date:  2007-09-16       Impact factor: 24.884

10.  Inward-rectifying potassium (Kir) channels regulate pacemaker activity in spinal nociceptive circuits during early life.

Authors:  Jie Li; Meredith L Blankenship; Mark L Baccei
Journal:  J Neurosci       Date:  2013-02-20       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.