Literature DB >> 23979837

Kainate receptor RNA editing is markedly altered by acute spinal cord injury.

Luca Caracciolo1, Fabio Fumagalli, Stephana Carelli, Laura Madaschi, Luca La Via, Daniela Bonini, Chiara Fiorentini, Sergio Barlati, Alfredo Gorio, Alessandro Barbon.   

Abstract

We have previously observed changes in the RNA editing of AMPA receptors after acute spinal cord injury (SCI); this implies that post-transcriptional modifications are capable of affecting the physiological properties of glutamate receptor channels and related signal transduction in this neurodegenerative condition. Here, we report that the editing of the ionotropic KAR is markedly decreased at both GluK1 and GluK2 Q/R sites in the epicenter of the lesion and with distinct magnitude and kinetics also in the caudal and rostral portions of the injured cord. These effects are persistent, being observed as late as 30 days after lesioning. In addition, also the I/V and Y/C sites of GluK2 were severely affected after SCI. These findings add novel information to the relevance of editing of glutamate receptors following acute SCI, thus expanding the recently emerged role of post-transcriptional mechanisms under these experimental conditions.

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Year:  2013        PMID: 23979837     DOI: 10.1007/s12031-013-0098-1

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  41 in total

1.  Presynaptic kainate receptors regulate spinal sensory transmission.

Authors:  G A Kerchner; T J Wilding; P Li; M Zhuo; J E Huettner
Journal:  J Neurosci       Date:  2001-01-01       Impact factor: 6.167

2.  Kainate receptors in primary afferents to the rat gracile nucleus.

Authors:  S J Hwang; A Rustioni; J G Valtschanoff
Journal:  Neurosci Lett       Date:  2001-10-26       Impact factor: 3.046

3.  Q/R editing of the rat GluR5 and GluR6 kainate receptors in vivo and in vitro: evidence for independent developmental, pathological and cellular regulation.

Authors:  A Bernard; L Ferhat; F Dessi; G Charton; A Represa; Y Ben-Ari; M Khrestchatisky
Journal:  Eur J Neurosci       Date:  1999-02       Impact factor: 3.386

Review 4.  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

5.  Developmental changes of RNA editing of glutamate receptor subunits GluR5 and GluR6: in vivo versus in vitro.

Authors:  W Paschen; J Schmitt; C Gissel; E Dux
Journal:  Brain Res Dev Brain Res       Date:  1997-02-20

6.  The differential expression of 16 NMDA and non-NMDA receptor subunits in the rat spinal cord and in periaqueductal gray.

Authors:  T R Tölle; A Berthele; W Zieglgänsberger; P H Seeburg; W Wisden
Journal:  J Neurosci       Date:  1993-12       Impact factor: 6.167

7.  Low editing efficiency of GluR2 mRNA is associated with a low relative abundance of ADAR2 mRNA in white matter of normal human brain.

Authors:  Yukio Kawahara; Kyoko Ito; Hui Sun; Ichiro Kanazawa; Shin Kwak
Journal:  Eur J Neurosci       Date:  2003-07       Impact factor: 3.386

8.  Glutamate receptor subunit expression after spinal cord injury in young rats.

Authors:  Kwame M Brown; Jean R Wrathall; Robert P Yasuda; Barry B Wolfe
Journal:  Brain Res Dev Brain Res       Date:  2004-08-18

9.  Fractional calcium currents through recombinant GluR channels of the NMDA, AMPA and kainate receptor subtypes.

Authors:  N Burnashev; Z Zhou; E Neher; B Sakmann
Journal:  J Physiol       Date:  1995-06-01       Impact factor: 5.182

10.  RNA editing of the glutamate receptor subunits GluR2 and GluR6 in human brain tissue.

Authors:  W Paschen; J C Hedreen; C A Ross
Journal:  J Neurochem       Date:  1994-11       Impact factor: 5.372

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