Literature DB >> 1700811

Enhanced expression of the extracellular matrix molecule J1/tenascin in the regenerating adult mouse sciatic nerve.

R Martini1, M Schachner, A Faissner.   

Abstract

We have investigated the expression of J1/tenascin in the sciatic nerve of the adult mouse under normal and regenerating conditions by immunocytological and immunochemical methods. In the normal nerve, J1/tenascin expression was confined to the extracellular matrix at the node of Ranvier and in the perineurium. At 2 days after nerve transection, J1/tenascin was detectable in the fibroblast-containing caps of the distal and proximal nerve stumps, in the distal nerve stump along its entire length and in the distal end of the proximal nerve stump. In the nerve stumps immunoreactivity was predominantly associated with extracellular matrix consisting of collagen fibrils and Schwann cell basal laminae. Approximately 7 days after transection, the caps of the nerve stumps had usually grown together forming a bridge. This bridge consisted of a J1/tenascin-negative perineurium-like structure and an inner part of predominantly fibroblasts, endothelial cells and macrophages. All cell types in this inner part were embedded in a J1/tenascin-positive matrix of collagen fibrils indicating the prospective direction of growth of neural elements. A few days later, J1/tenascin in the bridge was confined to the extracellular matrix around small Schwann cell-containing nerve fascicles. In nerves chronically denervated for 19 days, J1/tenascin was poorly detectable in the cap of the distal stump, although Schwann cells had infiltrated this cap. Approximately 19 days after the lesion, J1/tenascin expression returned to control levels in the proximal nerve stump. In the distal nerve stump, J1/tenascin immunoreactivity reached a peak at approximately 14 days after nerve transection and vanished only at approximately 35 days, thus correlating with the time of active regrowth of axons into the distal nerve stump. This reduction was prevented by chronic denervation, suggesting that reinnervation of target structures may be related to the down-regulation of J1/tenascin. These combined observations suggest that J1/tenascin is differentially regulated in the individual parts of the regenerating nerve, possibly triggered by different cellular and molecular signals.

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Year:  1990        PMID: 1700811     DOI: 10.1007/bf01257247

Source DB:  PubMed          Journal:  J Neurocytol        ISSN: 0300-4864


  23 in total

1.  Deposition of the NG2 proteoglycan at nodes of Ranvier in the peripheral nervous system.

Authors:  S Martin; A K Levine; Z J Chen; Y Ughrin; J M Levine
Journal:  J Neurosci       Date:  2001-10-15       Impact factor: 6.167

2.  Comparison of neurite outgrowth induced by intact and injured sciatic nerves: a confocal and functional analysis.

Authors:  E Agius; P Cochard
Journal:  J Neurosci       Date:  1998-01-01       Impact factor: 6.167

Review 3.  Molecules inhibiting neurite growth: a minireview.

Authors:  M E Schwab
Journal:  Neurochem Res       Date:  1996-07       Impact factor: 3.996

Review 4.  The cellular and molecular basis of peripheral nerve regeneration.

Authors:  S Y Fu; T Gordon
Journal:  Mol Neurobiol       Date:  1997 Feb-Apr       Impact factor: 5.590

5.  Microtubule reorganization is obligatory for growth cone turning.

Authors:  T Williamson; P R Gordon-Weeks; M Schachner; J Taylor
Journal:  Proc Natl Acad Sci U S A       Date:  1996-12-24       Impact factor: 11.205

Review 6.  Axonal regeneration through acellular muscle grafts.

Authors:  S Hall
Journal:  J Anat       Date:  1997-01       Impact factor: 2.610

7.  The AN2 protein is a novel marker for the Schwann cell lineage expressed by immature and nonmyelinating Schwann cells.

Authors:  S Schneider; F Bosse; D D'Urso; H Muller; M W Sereda; K Nave; A Niehaus; T Kempf; M Schnolzer; J Trotter
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

8.  The influence of predegenerated nerve grafts on axonal regeneration from prelesioned peripheral nerves.

Authors:  N A Hasan; M M Neumann; M A de Souky; K F So; K S Bedi
Journal:  J Anat       Date:  1996-10       Impact factor: 2.610

9.  Glial growth factor 2, a soluble neuregulin, directly increases Schwann cell motility and indirectly promotes neurite outgrowth.

Authors:  N K Mahanthappa; E S Anton; W D Matthew
Journal:  J Neurosci       Date:  1996-08-01       Impact factor: 6.167

10.  Adaptation of a non-radioactive in situ hybridization method to electron microscopy: detection of tenascin mRNAs in mouse cerebellum with digoxigenin-labelled probes and gold-labelled antibodies.

Authors:  U Dörries; U Bartsch; C Nolte; J Roth; M Schachner
Journal:  Histochemistry       Date:  1993-03
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