Literature DB >> 7648632

Compensatory responses and development of the nodose ganglion following ablation of placodal precursors in the embryonic chick (Gallus domesticus).

T A Harrison1, H A Stadt, D Kumiski, M L Kirby.   

Abstract

The nodose ganglion is the distal cranial ganglion of the vagus nerve which provides sensory innervation to the heart and other viscera. In this study, removal of the neuronal precursors which normally populate the right nodose ganglion was accomplished by ablating the right nodose placode in stage 9 chick embryos. Subsequent histological evaluation showed that in 54% of lesioned embryos surviving to day 6, the right ganglion was absent. Most embryos surviving to day 12, however, had identifiable right ganglia. In day 12 embryos, the right ganglion which developed was abnormal, with ganglion volume and ganglion cell diameter reduced by 50% and 20%, respectively, compared to control ganglia. To investigate the source of the neuron population in the regenerated ganglion, we combined nodose placode ablation with bilateral replacement of chick with quail "cardiac" neural crest (from mid-otic placode to somite 3). These cells normally provide only non-neuronal cells to the nodose ganglion, but produce neurons in other regions. At day 9, quail-derived neurons were identified in the right nodose ganglia of these chimeras, indicating that cardiac neural crest cells can generate neurons in the ganglion when placode-derived neurons are absent or reduced in number. On the other hand, we found that "sympathetic" neural crest (from somites 10 to 20) does not support ganglion development, suggesting that only neural crest cells normally present in the ganglion participate in reconstituting its neuronal population. Our previous work has shown that right nodose placode ablation produces abnormal cardiac function, which mimics a life-threatening human heart condition known as long QT syndrome. The present results suggest that the presence of neural crest-derived neurons in the developing right nodose ganglion may contribute to the functional abnormality in long QT syndrome.

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Year:  1995        PMID: 7648632     DOI: 10.1007/bf00583407

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  16 in total

Review 1.  Pathogenesis and therapy of the idiopathic long QT syndrome.

Authors:  P J Schwartz; O Bonazzi; E Locati; C Napolitano; S Sala
Journal:  Ann N Y Acad Sci       Date:  1992-01-27       Impact factor: 5.691

2.  Experimental analysis of the dual origin of the trigeminal ganglion in the chick embryo.

Authors:  V HAMBURGER
Journal:  J Exp Zool       Date:  1961-11

3.  A series of normal stages in the development of the chick embryo.

Authors:  V HAMBURGER; H L HAMILTON
Journal:  J Morphol       Date:  1951-01       Impact factor: 1.804

4.  Increase in the cholinergic cardiac plexus in sympathetically aneural chick hearts.

Authors:  M L Kirby; D C Conrad; D E Stewart
Journal:  Cell Tissue Res       Date:  1987-03       Impact factor: 5.249

5.  Adrenergic innervation of the developing chick heart: neural crest ablations to produce sympathetically aneural hearts.

Authors:  M Kirby; D Stewart
Journal:  Am J Anat       Date:  1984-11

6.  Neural crest cells contribute to normal aorticopulmonary septation.

Authors:  M L Kirby; T F Gale; D E Stewart
Journal:  Science       Date:  1983-06-03       Impact factor: 47.728

7.  Characterization of conotruncal malformations following ablation of "cardiac" neural crest.

Authors:  M L Kirby; K L Turnage; B M Hays
Journal:  Anat Rec       Date:  1985-09

8.  Temporal patterns of neurogenesis in avian cranial sensory and autonomic ganglia.

Authors:  A D'Amico-Martel
Journal:  Am J Anat       Date:  1982-04

9.  Parasympathetic, sympathetic, and sensory interactions in the iris: nerve growth factor regulates cholinergic ciliary ganglion innervation in vivo.

Authors:  J A Kessler
Journal:  J Neurosci       Date:  1985-10       Impact factor: 6.167

10.  Plasticity and predetermination of mesencephalic and trunk neural crest transplanted into the region of the cardiac neural crest.

Authors:  M L Kirby
Journal:  Dev Biol       Date:  1989-08       Impact factor: 3.582

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  5 in total

1.  FGF-8 in the ventral pharynx alters development of myocardial calcium transients after neural crest ablation.

Authors:  M J Farrell; J L Burch; K Wallis; L Rowley; D Kumiski; H Stadt; R E Godt; T L Creazzo; M L Kirby
Journal:  J Clin Invest       Date:  2001-06       Impact factor: 14.808

2.  Brain-derived neurotrophic factor, neurotrophin-3, and neurotrophin-4 complement and cooperate with each other sequentially during visceral neuron development.

Authors:  W M ElShamy; P Ernfors
Journal:  J Neurosci       Date:  1997-11-15       Impact factor: 6.167

3.  Embryonic origin of gustatory cranial sensory neurons.

Authors:  Danielle E Harlow; Linda A Barlow
Journal:  Dev Biol       Date:  2007-08-15       Impact factor: 3.582

4.  Reprogramming Axial Level Identity to Rescue Neural-Crest-Related Congenital Heart Defects.

Authors:  Shashank Gandhi; Max Ezin; Marianne E Bronner
Journal:  Dev Cell       Date:  2020-05-04       Impact factor: 12.270

5.  The transcription factor six1 inhibits neuronal and promotes hair cell fate in the developing zebrafish (Danio rerio) inner ear.

Authors:  Olivier Bricaud; Andres Collazo
Journal:  J Neurosci       Date:  2006-10-11       Impact factor: 6.167

  5 in total

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