Axonal degeneration within the tympanal nerve of Schistocerca gregaria

Citation
K. Jacobs et R. Lakes-harlan, Axonal degeneration within the tympanal nerve of Schistocerca gregaria, CELL TIS RE, 298(1), 1999, pp. 167-178
Citations number
43
Categorie Soggetti
Cell & Developmental Biology
Journal title
CELL AND TISSUE RESEARCH
ISSN journal
0302766X → ACNP
Volume
298
Issue
1
Year of publication
1999
Pages
167 - 178
Database
ISI
SICI code
0302-766X(199910)298:1<167:ADWTTN>2.0.ZU;2-W
Abstract
This study describes time course and ultrastructural changes during axonal degeneration of different neurones within the tympanal nerve of the locust Schistocerca gregaria. The tympanal nerve innervates the tergit and pleurit of the first abdominal segment and contains the axons of both sensory and motor neurones. The majority of axons (approx. 97%) belong to several types of sensory neurones: mechano- and chemosensitive hair sensilla, multipolar neurones, campaniform sensilla and sensory cells of a scolopidial organ, t he auditory organ. Axons of campaniform sensilla, of auditory sensory cells and of motor neurones are wrapped by glial cell processes. In contrast, th e very small and numerous axons (diameter <1 mu m) of multipolar neurones a nd hair sensilla are not separated individually by glia sheets. Distal part s of sensory and motor axons show different reactions to axotomy: 1 week af ter separation from their somata, distal parts of motor axons are invaded b y glial cell processes. This results in fascicles of small axon bundles. In contrast, distal parts of most sensory axons degenerate rapidly after bein g lesioned. The time to onset of degeneration depends on distance from the lesion site and on the type of sensory neurone. In axons of auditory sensor y neurones, ultrastructural signs of degeneration can be found as soon as 2 days after lesion. After complete lysis of distal parts of axons, glial ce ll processes invade the space formerly occupied by sensory axons. The rapid degeneration of distal auditory axon parts allows it to be excluded that t hey provide a structure that leads regenerating axons to their targets. Pro ximal parts of severed axons do not degenerate.