Literature DB >> 6185644

Changes in sciatic nerve cathepsin D after ligation or exposure to neurotoxins.

J N Whitaker, S P Dodd, Z Sahenk, J R Mendell.   

Abstract

The content and distribution of cathepsin D, a lysosomal acidic endopeptidase, were determined by immunochemical methods in rat sciatic nerve near the site of a ligature or after exposure of animals to neurotoxins. In normal sciatic nerve, cathepsin D was localized predominantly in the perinuclear regions of Schwann cells. In ligated nerve, cathepsin D increased equally in both the proximal and distal nerve segments adjacent to the ligature. Although orthograde and retrograde axonal transport of cathepsin D may have contributed to this increase, immunocytochemical methods indicated that Schwann cells or other phagocytic cells accounted for the bulk of the increased cathepsin D content of nerve. Axonal function was nontraumatically altered by the administration of 2,5-hexanedione, acrylamide, B,B'-iminodipropionitrile or zinc pyridinethione. Exposure to any of these neurotoxins raised cathepsin D content throughout the sciatic nerve twofold or more, and greater amounts of immunoreactive cathepsin D in the cytoplasm of Schwann cells could be demonstrated immunocytochemically. These results indicate that changes in cathepsin D content of Schwann cells may be a reflection of their catabolic activity. The increased Schwann cell cathepsin D content in toxic axonopathies is further proof for an enhanced Schwann cell role as a phagocyte resulting from axonal injury.

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Year:  1983        PMID: 6185644     DOI: 10.1097/00005072-198301000-00008

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  3 in total

Review 1.  Proteinases in inflammatory demyelinating disease.

Authors:  C T Bever; J N Whitaker
Journal:  Springer Semin Immunopathol       Date:  1985

2.  Proteolysis of peripheral nerve myelin in acute experimental allergic neuritis.

Authors:  K Schott; M Schabet; A Stevens; R Bühler; H Wiethölter
Journal:  Neurochem Res       Date:  1990-09       Impact factor: 3.996

3.  Degradation of bovine P2 protein by bovine brain cathepsin D.

Authors:  J N Whitaker; J M Seyer
Journal:  Neurochem Res       Date:  1984-10       Impact factor: 3.996

  3 in total

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