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The expression of B-50/GAP-43 in Schwann cells is upregulated in degenerating peripheral nerve stumps following nerve injury

Identifieur interne : 004606 ( Main/Exploration ); précédent : 004605; suivant : 004607

The expression of B-50/GAP-43 in Schwann cells is upregulated in degenerating peripheral nerve stumps following nerve injury

Auteurs : L. C. Plantinga [Pays-Bas] ; J. Verhaagen [Pays-Bas] ; P. M. Edwards [Royaume-Uni] ; E. M. Hol [Pays-Bas] ; P. R. B R [Pays-Bas] ; W. H. Gispen [Pays-Bas]

Source :

RBID : ISTEX:E3E9D6A33CF51AA3E238C3D87C57D408D088F2F4

English descriptors

Abstract

Abstract: We have detected mRNA for B-50 (GAP-43, pp46, F1, neuromodulin), which was originally believed to be a neuron-specific protein, in non-neuronal cells in the rat sciatic nerve. In control rats, the level of B-50 mRNA in sciatic nerve tissue was much lower than in dorsal root ganglia. Following nerve crush or transection, the expression of B-50 mRNA in the distal nerve stump increased dramatically between 1 and 2 days post-injury. The B-50 mRNA levels in the distal stump of crushed nerves remained elevated for up tp 4 weeks and subsequently returned to control levels after 7 weeks. In contrast, after nerve transection B-50 mRNA levels in the distal nerve portion continued to increase up to 7 weeks post-lesion. No changes in the levels of the B-50 transcript were observed in the proximal portion of either crush-lesioned or transected sciatic nerves. In situ hybridization demonstrated B-50 mRNA associated with Schwann cells in the distal nerve stump. The observation that Schwann cells are capable of producing B-50 mRNA was confirmed by Northern blot analysis of total RNA isolated from primary Schwann cell cultures. Taken together, these data show the expression of B-50 mRNA by Schwann cells and the up-regulation of B-50 mRNA in reactive Schwann cells upon loss of axonal contact.

Url:
DOI: 10.1016/0006-8993(93)90243-G


Affiliations:


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Le document en format XML

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<term>Axotomy</term>
<term>B-50</term>
<term>GAP-43</term>
<term>Peripheral nerve regeneration</term>
<term>Schwann cell</term>
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<term>Agarose</term>
<term>Axon</term>
<term>Axonal</term>
<term>Axonal regeneration</term>
<term>Biol</term>
<term>Cdna</term>
<term>Cdna probe</term>
<term>Cell contact</term>
<term>Control nerves</term>
<term>Control rats</term>
<term>Crush</term>
<term>Crush injury</term>
<term>Distal nerve portion</term>
<term>Distal nerve stump</term>
<term>Distal portion</term>
<term>Dorsal</term>
<term>Dorsal root ganglia</term>
<term>Ethidium bromide</term>
<term>Fibroblast</term>
<term>Ganglion</term>
<term>Gene expression</term>
<term>Gispen</term>
<term>Growth cones</term>
<term>Hybridization</term>
<term>Hybridized</term>
<term>Immunoreactivity</term>
<term>Intact sciatic nerve</term>
<term>Lower panel</term>
<term>Mrna</term>
<term>Mrna expression</term>
<term>Nerve</term>
<term>Nerve crush</term>
<term>Nerve injury</term>
<term>Nerve transection</term>
<term>Neuron</term>
<term>Neuronal</term>
<term>Neurosci</term>
<term>Northern blot analysis</term>
<term>Oestreicher</term>
<term>Peritraumatic</term>
<term>Polymerase</term>
<term>Polymerase chain reaction</term>
<term>Primer</term>
<term>Protein kinase</term>
<term>Proximal</term>
<term>Proximal portion</term>
<term>Reactive schwann cells</term>
<term>Regeneration</term>
<term>Rinsed</term>
<term>Schwann</term>
<term>Schwann cells</term>
<term>Sciatic</term>
<term>Sciatic nerve</term>
<term>Sciatic nerve crush</term>
<term>Sciatic nerves</term>
<term>Spinal cord</term>
<term>Stump</term>
<term>Transected</term>
<term>Transected sciatic nerves</term>
<term>Transection</term>
<term>Upper panel</term>
<term>Verhaagen</term>
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<div type="abstract" xml:lang="en">Abstract: We have detected mRNA for B-50 (GAP-43, pp46, F1, neuromodulin), which was originally believed to be a neuron-specific protein, in non-neuronal cells in the rat sciatic nerve. In control rats, the level of B-50 mRNA in sciatic nerve tissue was much lower than in dorsal root ganglia. Following nerve crush or transection, the expression of B-50 mRNA in the distal nerve stump increased dramatically between 1 and 2 days post-injury. The B-50 mRNA levels in the distal stump of crushed nerves remained elevated for up tp 4 weeks and subsequently returned to control levels after 7 weeks. In contrast, after nerve transection B-50 mRNA levels in the distal nerve portion continued to increase up to 7 weeks post-lesion. No changes in the levels of the B-50 transcript were observed in the proximal portion of either crush-lesioned or transected sciatic nerves. In situ hybridization demonstrated B-50 mRNA associated with Schwann cells in the distal nerve stump. The observation that Schwann cells are capable of producing B-50 mRNA was confirmed by Northern blot analysis of total RNA isolated from primary Schwann cell cultures. Taken together, these data show the expression of B-50 mRNA by Schwann cells and the up-regulation of B-50 mRNA in reactive Schwann cells upon loss of axonal contact.</div>
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