Literature DB >> 8245215

Cytoarchitecture of spinal-projecting neurons in the brain of the larval sea lamprey.

G P Swain1, J A Snedeker, J Ayers, M E Selzer.   

Abstract

The descending spinal projecting system of the lamprey is of interest because it includes axons that activate swimming pattern generators and because regeneration of this system is involved in the behavioral recovery of lampreys following spinal transection. However, little is known about the true size of this projection and of the distribution of its terminations along the spinal cord. Brain neurons with spinal projections were studied in larval sea lampreys by using wholemount preparations labeled retrogradely with horseradish peroxidase (HRP) from spinal injections at 10%, 15%, 25%, 50%, 70%, and 75% of body length from the anterior end. Neurons projecting to different levels of the spinal cord were mapped. A large number of descending axons terminated within nine segments caudal to the last gill. The spinal projection system was divided into 10 bilateral groups based on cytoarchitectural landmarks. All of the lateral nuclear groups had contralateral spinal projections. In addition to the 12 pairs of Müller cells, the pair of Mauthner cells, and the pair of auxiliary Mauthner cells described by previous authors, the study revealed four pairs of smaller neurons that were individually identifiable.

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Year:  1993        PMID: 8245215     DOI: 10.1002/cne.903360204

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


  19 in total

1.  Magnetic resonance microimaging of intraaxonal water diffusion in live excised lamprey spinal cord.

Authors:  Masaya Takahashi; David B Hackney; Guixin Zhang; Suzanne L Wehrli; Alex C Wright; William T O'Brien; Hidemasa Uematsu; Felix W Wehrli; Michael E Selzer
Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-25       Impact factor: 11.205

2.  Conditioning lesions enhance axonal regeneration of descending brain neurons in spinal-cord-transected larval lamprey.

Authors:  Lei Zhang; Ryan Palmer; Andrew D McClellan
Journal:  J Comp Neurol       Date:  2004-10-25       Impact factor: 3.215

3.  Activated caspase detection in living tissue combined with subsequent retrograde labeling, immunohistochemistry or in situ hybridization in whole-mounted lamprey brains.

Authors:  Jianli Hu; Guixin Zhang; Michael E Selzer
Journal:  J Neurosci Methods       Date:  2013-09-08       Impact factor: 2.390

Review 4.  The spinobulbar system in lamprey.

Authors:  James T Buchanan; James F Einum
Journal:  Brain Res Rev       Date:  2007-08-06

5.  Spinal locomotor inputs to individually identified reticulospinal neurons in the lamprey.

Authors:  James T Buchanan
Journal:  J Neurophysiol       Date:  2011-08-10       Impact factor: 2.714

Review 6.  Flexibility in the patterning and control of axial locomotor networks in lamprey.

Authors:  James T Buchanan
Journal:  Integr Comp Biol       Date:  2011-07-09       Impact factor: 3.326

7.  Recovery of neurofilament expression selectively in regenerating reticulospinal neurons.

Authors:  A J Jacobs; G P Swain; J A Snedeker; D S Pijak; L J Gladstone; M E Selzer
Journal:  J Neurosci       Date:  1997-07-01       Impact factor: 6.167

8.  Regeneration in the era of functional genomics and gene network analysis.

Authors:  Joel Smith; Jennifer R Morgan; Steven J Zottoli; Peter J Smith; Joseph D Buxbaum; Ona E Bloom
Journal:  Biol Bull       Date:  2011-08       Impact factor: 1.818

9.  The role of RhoA in retrograde neuronal death and axon regeneration after spinal cord injury.

Authors:  Jianli Hu; Guixin Zhang; William Rodemer; Li-Qing Jin; Michael Shifman; Michael E Selzer
Journal:  Neurobiol Dis       Date:  2016-11-22       Impact factor: 5.996

10.  Expression of the repulsive guidance molecule RGM and its receptor neogenin after spinal cord injury in sea lamprey.

Authors:  Michael I Shifman; Rae Eden Yumul; Cindy Laramore; Michael E Selzer
Journal:  Exp Neurol       Date:  2009-03-05       Impact factor: 5.330

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