Literature DB >> 2458630

Dendritic development and preferential growth into synaptogenic fields: a quantitative study of Golgi-impregnated spinal motor neurons.

J E Vaughn1, R P Barber, T J Sims.   

Abstract

Branching patterns of dendrites may be modulated by the way in which dendritic growth cone filopodia come into initial synaptic relationships with afferent axons. This synaptotropic hypothesis of dendritic branching predicts that dendritic growth will be directed preferentially into regions containing numerous prospective presynaptic elements. The developing mouse spinal cord provides a natural experiment to test this prediction, because synapses are found exclusively within the marginal zones bordering the motor columns during the early (E11-14) period of synaptogenesis. During this time, therefore, most motor dendritic growth would be expected to be directed laterally or ventrally into the marginal zones, whereas internally directed growth should become more prevalent later, when synaptogenesis begins to take place within the intermediate zone, i.e., the motor columns proper. A computer-assisted three dimensional reconstruction system has been used to test these expectations in Golgi preparations of developing mouse (C57BL/6J) spinal cords ranging in age from E13 through P1. Mean dendritic lengths and branch densities are significantly greater for marginal zone dendrites than for intermediate zone dendrites at early ages (E13-14), but there are no significant differences in these measures at later stages of development (P0,1). These findings are interpreted as meaning that motor dendritic growth is initially biased into the marginal zone by synaptogenic afferents and that this preferential distribution is progressively lost as synapses develop within the intermediate zone to attract or to stabilize internally directed dendritic growth. Thus the findings of this study are consistent with predictions of the synaptotropic hypothesis of dendritic branching.

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Year:  1988        PMID: 2458630     DOI: 10.1002/syn.890020110

Source DB:  PubMed          Journal:  Synapse        ISSN: 0887-4476            Impact factor:   2.562


  24 in total

1.  N-cadherin-dependent neuron-neuron interaction is required for the maintenance of activity-induced dendrite growth.

Authors:  Zhu-Jun Tan; Yun Peng; He-Ling Song; Jing-Jing Zheng; Xiang Yu
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-10       Impact factor: 11.205

2.  The AMPA receptor subunit GluR1 regulates dendritic architecture of motor neurons.

Authors:  Fiona M Inglis; Richard Crockett; Sailaja Korada; Wickliffe C Abraham; Michael Hollmann; Robert G Kalb
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

3.  In vivo imaging reveals dendritic targeting of laminated afferents by zebrafish retinal ganglion cells.

Authors:  Jeff S Mumm; Philip R Williams; Leanne Godinho; Amy Koerber; Andrew J Pittman; Tobias Roeser; Chi-Bin Chien; Herwig Baier; Rachel O L Wong
Journal:  Neuron       Date:  2006-11-22       Impact factor: 17.173

Review 4.  The regulation of dendritic arbor development and plasticity by glutamatergic synaptic input: a review of the synaptotrophic hypothesis.

Authors:  Hollis Cline; Kurt Haas
Journal:  J Physiol       Date:  2008-01-17       Impact factor: 5.182

5.  Tactile stimulation during artificial rearing influences adult function and morphology in a sexually dimorphic neuromuscular system.

Authors:  Kathryn M Lenz; M Dean Graham; Mayte Parada; Alison S Fleming; Dale R Sengelaub; D Ashley Monks
Journal:  Dev Neurobiol       Date:  2008-03       Impact factor: 3.964

Review 6.  Key aspects of phrenic motoneuron and diaphragm muscle development during the perinatal period.

Authors:  Carlos B Mantilla; Gary C Sieck
Journal:  J Appl Physiol (1985)       Date:  2008-04-10

7.  Structure of the embryonic primate spinal cord at the closure of the first reflex arc.

Authors:  E Knyihar-Csillik; B Csillik; P Rakic
Journal:  Anat Embryol (Berl)       Date:  1995-06

Review 8.  Protocadherins branch out: Multiple roles in dendrite development.

Authors:  Austin B Keeler; Michael J Molumby; Joshua A Weiner
Journal:  Cell Adh Migr       Date:  2015-04-14       Impact factor: 3.405

9.  Optogenetic activation of cajal-retzius cells reveals their glutamatergic output and a novel feedforward circuit in the developing mouse hippocampus.

Authors:  Giulia Quattrocolo; Gianmaria Maccaferri
Journal:  J Neurosci       Date:  2014-09-24       Impact factor: 6.167

10.  Neurobeachin is required postsynaptically for electrical and chemical synapse formation.

Authors:  Adam C Miller; Lisa H Voelker; Arish N Shah; Cecilia B Moens
Journal:  Curr Biol       Date:  2014-12-04       Impact factor: 10.834

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