Literature DB >> 19189712

Origin of spinal cord axons in the lizard regenerated tail: supernormal projections from local spinal neurons.

M T Duffy1, S B Simpson, D R Liebich, B M Davis.   

Abstract

During tail regeneration most lizards also regenerate the tail spinal cord. The regenerated spinal cord primarily contains neuroepithelium (i.e., the ependymal tube which forms the central canal) and descending axons. The present experiments identify the source of the axons in the regenerated spinal cord. Application of HRP to normal tail spinal cord resulted in labeled cells in the nucleus paraventricularis, the interstitial nucleus of the fasciculus longitudinalis medialis, the nucleus ruber, the medullary reticular formation (including raphe nuclei), as well as in vestibular nuclei. HRP applied to the regenerated spinal cord labeled only 4% of the cells seen in normal animals, and these were confined to rhombencephalic nuclei. The lack of labeling of more rostral nuclei was not due to the death of descending neurons. Application of HRP immediately rostral to the regenerated spinal cord resulted in the labeling of a normal, and in some cases, greater than normal, number of neurons. To quantify the origin of axons in the regenerated spinal cord, electron microscopic montages of the regenerated spinal cord were made and the number of axons counted, before and after various spinal lesions. Only lesions within one spinal segment of the regenerated spinal cord had a significant effect on the number of axons in the regenerated tail spinal cord. This indicated that most of the regenerated axons were of local spinal origin. A significant increase in the number of labeled local spinal neurons was revealed following application of HRP to a regenerated tail spinal cord. These results suggest that while various portions of the lizard central nervous system can grow axons into the regenerating tail spinal cord, the great majority of axons in the regenerate are of local origin and that some of these arise from neurons that do not normally possess descending projections. Finally, to test whether new neurons were participating in the regeneration process, 3H-thymidine was injected during the regrowth of the tail. No labeled spinal cord cells were conclusively identified as neurons. Thus, the regenerating lizard tail spinal cord exhibits robust axonal sprouting from neurons near the site of a spinal transection in a manner reminiscent of sprouting in the mammalian CNS. This sprouting can develop into descending spinal projections that extend for significant distances into the regenerated tail spinal cord and provides a unique model for exploring the requirements for successful axon growth in an adult vertebrate CNS.

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Year:  1990        PMID: 19189712     DOI: 10.1002/cne.902930205

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


  12 in total

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Authors:  R Grill; K Murai; A Blesch; F H Gage; M H Tuszynski
Journal:  J Neurosci       Date:  1997-07-15       Impact factor: 6.167

2.  Reinnervation accuracy of the rat femoral nerve by motor and sensory neurons.

Authors:  R D Madison; S J Archibald; T M Brushart
Journal:  J Neurosci       Date:  1996-09-15       Impact factor: 6.167

3.  Developmental and adult-specific processes contribute to de novo neuromuscular regeneration in the lizard tail.

Authors:  Minami A Tokuyama; Cindy Xu; Rebecca E Fisher; Jeanne Wilson-Rawls; Kenro Kusumi; Jason M Newbern
Journal:  Dev Biol       Date:  2017-12-25       Impact factor: 3.582

4.  Recovery of supraspinal control of stepping via indirect propriospinal relay connections after spinal cord injury.

Authors:  Gregoire Courtine; Bingbing Song; Roland R Roy; Hui Zhong; Julia E Herrmann; Yan Ao; Jingwei Qi; V Reggie Edgerton; Michael V Sofroniew
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5.  A novel amniote model of epimorphic regeneration: the leopard gecko, Eublepharis macularius.

Authors:  Katherine E McLean; Matthew K Vickaryous
Journal:  BMC Dev Biol       Date:  2011-08-16       Impact factor: 1.978

6.  Transcriptomic analysis of tail regeneration in the lizard Anolis carolinensis reveals activation of conserved vertebrate developmental and repair mechanisms.

Authors:  Elizabeth D Hutchins; Glenn J Markov; Walter L Eckalbar; Rajani M George; Jesse M King; Minami A Tokuyama; Lauren A Geiger; Nataliya Emmert; Michael J Ammar; April N Allen; Ashley L Siniard; Jason J Corneveaux; Rebecca E Fisher; Juli Wade; Dale F DeNardo; J Alan Rawls; Matthew J Huentelman; Jeanne Wilson-Rawls; Kenro Kusumi
Journal:  PLoS One       Date:  2014-08-20       Impact factor: 3.240

Review 7.  The regeneration blastema of lizards: an amniote model for the study of appendage replacement.

Authors:  E A B Gilbert; S L Delorme; M K Vickaryous
Journal:  Regeneration (Oxf)       Date:  2015-05-11

8.  Anatomical recovery of the spinal glutamatergic system following a complete spinal cord injury in lampreys.

Authors:  Blanca Fernández-López; Antón Barreiro-Iglesias; María Celina Rodicio
Journal:  Sci Rep       Date:  2016-11-25       Impact factor: 4.379

9.  The cloning and characterization of the enolase2 gene of Gekko japonicus and its polyclonal antibody preparation.

Authors:  Jing Li; Ronghua Wu; Haijiao Chen; Youlang Zhou; Yan Li; Yongjun Wang; Yan Liu; Mei Liu
Journal:  Int J Mol Sci       Date:  2013-04-24       Impact factor: 5.923

10.  Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors.

Authors:  Anneke Dixie Kakebeen; Alexander Daniel Chitsazan; Madison Corinne Williams; Lauren M Saunders; Andrea Elizabeth Wills
Journal:  Elife       Date:  2020-04-27       Impact factor: 8.140

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