J Physiol Society Membership
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 416 pp 183-213
Copyright © 1989 by The Physiological Society
This Article
Right arrow Full Text (PDF)
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Friedlander, M J
Right arrow Articles by Martin, K A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Friedlander, M J
Right arrow Articles by Martin, K A

Development of Y-axon innervation of cortical area 18 in the cat.

M J Friedlander and K A Martin

Neurobiology Research Center, University of Alabama, Birmingham 35294.

1. Geniculocortical Y-axons (n = 38) in the optic radiations of 4-5-week-old kittens (n = 20) and adult cats (n = 18) were studied both physiologically and morphologically. Axons were recorded from intracellularly and subsequently filled ionophoretically with horseradish peroxidase (HRP). The HRP filled the axons' terminal arborizations in visual cortex (particularly well for those innervating area 18). Fourteen axons appeared to be completely filled with HRP (n = 8 in kitten, n = 6 in adult) and served as the basis for the quantitative analysis of the terminal arborizations reported in this study. 2. The distribution and correspondence of the axonal boutons to presynaptic elements in cortical layer 4A was analysed at both the light and electron microscope level using computerized three-dimensional analysis and serial section reconstruction, respectively. Compared to adult axons, the boutons of the kitten axons were smaller (means = 0.75 vs. 1.75 microns length, P less than 0.001) and more densely spaced both along individual axon branches (means = 6.60 vs. 11.20 microns interbouton interval, P less than 0.001) and between neighbouring branches of the same axon (means = 4.7 vs. 6.4 microns nearest-neighbour distance, P less than 0.01). 3. Most kitten boutons made a single Gray's type 1 synapse on a cortical neurone, unlike adult boutons which usually contacted two or more postsynaptic targets. Both kitten and adult axons had dendritic spines as their major target. Occasionally, HRP reaction-product was observed in cortical neurones postsynaptic to the labelled geniculocortical axon, which gave some estimate of the number of synaptic contacts between a single geniculocortical axon and target cell (about five). 4. The kitten Y-axons innervated the visual cortex in a pattern similar to that of the adult, with the richest terminal branching and bouton density in layer 4A with some additional boutons distributed in layers 3, 4B and 6. The extent of the terminal arborizations primarily in layer 4A (as measured in surface views) of kitten Y-axons in area 18 was significantly less than that of adult Y-axons in area 18 (means = 0.9 mm2 vs. means = 1.2 mm2, P = 0.04). 5. We conclude that between 4 and 5 postnatal weeks and 1 year, geniculocortical Y-axons projecting to cortical area 18 undergo four major changes. These include a reduction in synaptic bouton density (both in three-dimensional space and along individual branches), a concomitant moderate expansion in the surface area of cortex innervated, an increase in bouton size and an increase in the number of synaptic contacts made by each bouton. A general proportional growth of the individual axons' terminal arborization together with fusion and/or separation of neighbouring boutons is sufficient to explain this development.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
L. A. Schrader, S. P. Perrett, L. Ye, and M. J. Friedlander
Substrates for Coincidence Detection and Calcium Signaling for Induction of Synaptic Potentiation in the Neonatal Visual Cortex
J Neurophysiol, June 1, 2004; 91(6): 2747 - 2764.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. Erisir and J. L. Harris
Decline of the Critical Period of Visual Plasticity Is Concurrent with the Reduction of NR2B Subunit of the Synaptic NMDA Receptor in Layer 4
J. Neurosci., June 15, 2003; 23(12): 5208 - 5218.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. P. Perrett, S. M. Dudek, D. Eagleman, P. R. Montague, and M. J. Friedlander
LTD Induction in Adult Visual Cortex: Role of Stimulus Timing and Inhibition
J. Neurosci., April 1, 2001; 21(7): 2308 - 2319.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
K. M. Murphy, K. R. Duffy, D. G. Jones, and D. E. Mitchell
Development of Cytochrome Oxidase Blobs in Visual Cortex of Normal and Visually Deprived Cats
Cereb Cortex, February 1, 2001; 11(2): 122 - 135.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. A. Silver and M. P. Stryker
Synaptic Density in Geniculocortical Afferents Remains Constant after Monocular Deprivation in the Cat
J. Neurosci., December 15, 1999; 19(24): 10829 - 10842.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. Harsanyi and M. J. Friedlander
Transient Synaptic Potentiation in the Visual Cortex. I. Cellular Mechanisms
J Neurophysiol, March 1, 1997; 77(3): 1269 - 1283.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. Harsanyi and M. J. Friedlander
Transient Synaptic Potentiation in the Visual Cortex. II. Developmental Regulation
J Neurophysiol, March 1, 1997; 77(3): 1284 - 1293.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
E. S. Ruthazer and M. P. Stryker
The Role of Activity in the Development of Long-Range Horizontal Connections in Area 17 of the Ferret
J. Neurosci., November 15, 1996; 16(22): 7253 - 7269.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1989 The Physiological Society.