Literature DB >> 12534965

The expression of vesicular glutamate transporters VGLUT1 and VGLUT2 in neurochemically defined axonal populations in the rat spinal cord with emphasis on the dorsal horn.

A J Todd1, D I Hughes, E Polgár, G G Nagy, M Mackie, O P Ottersen, D J Maxwell.   

Abstract

Two vesicular glutamate transporters, VGLUT1 and VGLUT2, have recently been identified, and it has been reported that they are expressed by largely nonoverlapping populations of glutamatergic neurons in the brain. We have used immunocytochemistry with antibodies against both transporters, together with markers for various populations of spinal neurons, in an attempt to identify glutamatergic interneurons in the dorsal horn of the mid-lumbar spinal cord of the rat. The great majority (94-100%) of nonprimary axonal boutons that contained somatostatin, substance P or neurotensin, as well as 85% of those that contained enkephalin, were VGLUT2-immunoreactive, which suggests that most dorsal horn neurons that synthesize these peptides are glutamatergic. In support of this, we found that most somatostatin- and enkephalin-containing boutons (including somatostatin-immunoreactive boutons that lacked calcitonin gene-related peptide and were therefore probably derived from local interneurons) formed synapses at which AMPA receptors were present. We also investigated VGLUT expression in central terminals of primary afferents. Myelinated afferents were identified with cholera toxin B subunit; most of those in lamina I were VGLUT2-immunoreactive, whereas all those in deeper laminae were VGLUT1-immunoreactive, and some (in laminae III-VI) appeared to contain both transporters. However, peptidergic primary afferents that contained substance P or somatostatin (most of which are unmyelinated), as well as nonpeptidergic C fibres (identified with Bandeiraea simplicifolia isolectin B4) showed low levels of VGLUT2-immunoreactivity, or were not immunoreactive with either VGLUT antibody. As all primary afferents are thought to be glutamatergic, this raises the possibility that unmyelinated afferents, most of which are nociceptors, express a different vesicular glutamate transporter.

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Year:  2003        PMID: 12534965     DOI: 10.1046/j.1460-9568.2003.02406.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  175 in total

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2.  Permanent reorganization of Ia afferent synapses on motoneurons after peripheral nerve injuries.

Authors:  Francisco J Alvarez; Katie L Bullinger; Haley E Titus; Paul Nardelli; Timothy C Cope
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3.  Networks of inhibitory and excitatory commissural interneurons mediating crossed reticulospinal actions.

Authors:  B Anne Bannatyne; Stephen A Edgley; Ingela Hammar; Elzbieta Jankowska; David J Maxwell
Journal:  Eur J Neurosci       Date:  2003-10       Impact factor: 3.386

4.  Distribution and injury-induced plasticity of cadherins in relationship to identified synaptic circuitry in adult rat spinal cord.

Authors:  John H Brock; Alice Elste; George W Huntley
Journal:  J Neurosci       Date:  2004-10-06       Impact factor: 6.167

5.  Properties of axon terminals contacting intermediate zone excitatory and inhibitory premotor interneurons with monosynaptic input from group I and II muscle afferents.

Authors:  Ting Ting Liu; B Anne Bannatyne; Elzbieta Jankowska; David J Maxwell
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Review 6.  Glutamate receptor phosphorylation and trafficking in pain plasticity in spinal cord dorsal horn.

Authors:  Xue Jun Liu; Michael W Salter
Journal:  Eur J Neurosci       Date:  2010-07-11       Impact factor: 3.386

7.  Ectopic myelinating oligodendrocytes in the dorsal spinal cord as a consequence of altered semaphorin 6D signaling inhibit synapse formation.

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Review 8.  Transmitting pain and itch messages: a contemporary view of the spinal cord circuits that generate gate control.

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Journal:  Neuron       Date:  2014-05-07       Impact factor: 17.173

9.  Roles of glutamate, substance P, and gastrin-releasing peptide as spinal neurotransmitters of histaminergic and nonhistaminergic itch.

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Journal:  Pain       Date:  2013-09-13       Impact factor: 6.961

10.  Circuits for grasping: spinal dI3 interneurons mediate cutaneous control of motor behavior.

Authors:  Tuan V Bui; Turgay Akay; Osama Loubani; Thomas S Hnasko; Thomas M Jessell; Robert M Brownstone
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