Literature DB >> 15803510

L1 CAM expression in the superficial dorsal horn is derived from the dorsal root ganglion.

Stephen A Runyan1, Roland Roy, Hui Zhong, Patricia E Phelps.   

Abstract

The cell adhesion molecule L1 is highly expressed on embryonic axons and may play a role in axonal outgrowth and fasciculation. Generally only low levels of L1 are found in adult spinal cord except for intense labeling in Lissauer's tract, in laminae I-II, and on dorsolateral funicular axons. In this study we determine the source of L1 immunoreactivity in the dorsal spinal cord, the presence of L1 expression on sprouting axons, and the effect of exercise on L1 expression. We determined the source of L1 immunoreactivity in the superficial dorsal horn by performing acute unilateral rhizotomies (T12-L4) in adult rats. This resulted in a marked decrease in L1 expression in Lissauer's tract and laminae I-II on the deafferented side. The peptidergic and nonpeptidergic small-diameter primary afferent markers, calcitonin gene-related peptide (CGRP) and the lectin IB4 respectively, closely correlated with L1 expression and also decreased dramatically after rhizotomy. Considering its developmental role, we asked whether L1 was expressed on sprouting axons following chronic rhizotomy. L1 and CGRP, but not IB4, were detected on sprouting axons. Lastly, we investigated the effect of exercise on L1 expression by giving animals with chronic rhizotomies free access to an exercise wheel. After extensive exercise, L1, CGRP, and IB4 expression levels were unchanged compared with those of sedentary chronic animals. Combined, these data demonstrate that the dorsal root ganglia is a major source of L1-positive axons in the superficial dorsal horn, that both L1 and CGRP identify sprouting axons following rhizotomy, and that exercise does not upregulate L1 expression. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15803510     DOI: 10.1002/cne.20479

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  9 in total

1.  L1 cell adhesion molecule is not required for small-diameter primary afferent sprouting after deafferentation.

Authors:  S A Runyan; R R Roy; H Zhong; P E Phelps
Journal:  Neuroscience       Date:  2007-10-18       Impact factor: 3.590

2.  Analysis of human embryonic stem cells with regulatable expression of the cell adhesion molecule l1 in regeneration after spinal cord injury.

Authors:  Myungsik Yoo; Gunho Anthony Lee; Christopher Park; Rick I Cohen; Melitta Schachner
Journal:  J Neurotrauma       Date:  2014-03-15       Impact factor: 5.269

Review 3.  Biological roles of olfactory ensheathing cells in facilitating neural regeneration: a systematic review.

Authors:  Hao Yang; Bao-Rong He; Ding-Jun Hao
Journal:  Mol Neurobiol       Date:  2014-03-11       Impact factor: 5.590

4.  Olfactory ensheathing glia express aquaporin 1.

Authors:  Shannon D Shields; Katherine D Moore; Patricia E Phelps; Allan I Basbaum
Journal:  J Comp Neurol       Date:  2010-11-01       Impact factor: 3.215

5.  Modulating Sema3A signal with a L1 mimetic peptide is not sufficient to promote motor recovery and axon regeneration after spinal cord injury.

Authors:  Erik Mire; Nicole Thomasset; Lyn B Jakeman; Geneviève Rougon
Journal:  Mol Cell Neurosci       Date:  2007-10-03       Impact factor: 4.314

6.  L1 cell adhesion molecule is essential for the maintenance of hyperalgesia after spinal cord injury.

Authors:  Emily L Hoschouer; Feng Qin Yin; Lyn B Jakeman
Journal:  Exp Neurol       Date:  2008-11-13       Impact factor: 5.330

7.  Mouse olfactory ensheathing glia enhance axon outgrowth on a myelin substrate in vitro.

Authors:  Stephen A Runyan; Patricia E Phelps
Journal:  Exp Neurol       Date:  2008-12-03       Impact factor: 5.330

8.  Alteration of the cell adhesion molecule L1 expression in a specific subset of primary afferent neurons contributes to neuropathic pain.

Authors:  Hiroki Yamanaka; Koichi Obata; Kimiko Kobayashi; Yi Dai; Tetsuo Fukuoka; Koichi Noguchi
Journal:  Eur J Neurosci       Date:  2007-02       Impact factor: 3.386

9.  CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro.

Authors:  Daniel Terheyden-Keighley; Xiaoqing Zhang; Beate Brand-Saberi; Carsten Theiss
Journal:  Biol Open       Date:  2018-09-19       Impact factor: 2.422

  9 in total

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