Literature DB >> 3305598

Morphology and quantitative changes of transient NPY-ir neuronal populations during early postnatal development of the cat visual cortex.

P Wahle, G Meyer.   

Abstract

The early postnatal development of neuropeptide Y-containing neurons in the visual cortex of the cat was analyzed. Immunohistochemistry reveals several stages of morphological differentiation and degeneration. Completely undifferentiated neurons have very small somata with nuclei surrounded by a thin rim of cytoplasm and processes unclearly differentiated into dendrites and axons. Processes bear growth cones. Differentiating neurons show an increase in soma size and complexity of processes. Axons are recognizable. Fully differentiated neurons have well-defined axonal and dendritic patterns. Degenerating neurons are identified by thick, heavily beaded processes covered by hairy appendages and vacuolar inclusions in the somata. Cell death is expressed by shrunken somata and lysed, fragmented processes. According to their postnatal time course of differentiation and/or degeneration, NPY-immunoreactive neurons, which form several morphologically distinct cell types, are grouped into 3 neuronal populations. (1) Pseudopyramidal cells, bitufted "rectangular" cells with wide dendritic fields, unitufted cells, and small multipolar cells are located in the gray matter and have a rather primitive morphology resembling cell types found in lower vertebrate cortex and tectum. They constitute a first transient neuronal population, because all neurons are fully differentiated at birth and become largely eliminated by postnatal day (P) 12. (2) Axonal loop cells are mainly located in the white matter. Their most prominent feature is an often long hairpin loop formed by either the main axon itself or by a major collateral. The axonal branches pass through the cortex to connect the white matter and layer I. Axons do not form local plexusses and terminal elements in the gray matter. Neurons differentiate perinatally, form a first peak from P6 to P10, followed by a decrease in cell number and innervation density at P12, followed by a second peak from P15 to P20. After P20 the number of axonal loop cells steadily decreases, and they become eliminated by P48. (3) A third population consists of neurons with a higher degree of axonal ramification and a variety of axonal patterns. Early members are located mainly at the layer VI/white matter border, differentiate during the first postnatal week, and give rise to a diffuse innervation of the gray matter without forming specific terminal elements. Some of the early axonal patterns persist into adulthood, whereas others are not found in the adult brain.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3305598     DOI: 10.1002/cne.902610202

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


  22 in total

1.  Subplate neurons: a missing link among neurotrophins, activity, and ocular dominance plasticity?

Authors:  A K McAllister
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-23       Impact factor: 11.205

2.  Unique morphological features of the proliferative zones and postmitotic compartments of the neural epithelium giving rise to striate and extrastriate cortex in the monkey.

Authors:  Iain H M Smart; Colette Dehay; Pascale Giroud; Michel Berland; Henry Kennedy
Journal:  Cereb Cortex       Date:  2002-01       Impact factor: 5.357

Review 3.  The specification of neuronal identity in the mammalian cerebral cortex.

Authors:  S K McConnell
Journal:  Experientia       Date:  1990-09-15

Review 4.  Early history of subplate and interstitial neurons: from Theodor Meynert (1867) to the discovery of the subplate zone (1974).

Authors:  Miloš Judaš; Goran Sedmak; Mihovil Pletikos
Journal:  J Anat       Date:  2010-10       Impact factor: 2.610

5.  Synaptogenesis in purified cortical subplate neurons.

Authors:  Claire E McKellar; Carla J Shatz
Journal:  Cereb Cortex       Date:  2008-11-21       Impact factor: 5.357

6.  GABAA receptor immunoreactivity in adult and developing monkey sensory-motor cortex.

Authors:  G W Huntley; A L de Blas; E G Jones
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

7.  Differential survival of Cajal-Retzius cells in organotypic cultures of hippocampus and neocortex.

Authors:  J A Del Río; B Heimrich; H Supèr; V Borrell; M Frotscher; E Soriano
Journal:  J Neurosci       Date:  1996-11-01       Impact factor: 6.167

8.  Transient expression of neuropeptide Y (NPY) immunoreactivity in the developing hamster paraventricular thalamic area is due to apoptosis.

Authors:  G I Botchkina; S Lyubsky; N G Hagag
Journal:  Cell Mol Neurobiol       Date:  1996-12       Impact factor: 5.046

9.  Functional synaptic projections onto subplate neurons in neonatal rat somatosensory cortex.

Authors:  Ileana L Hanganu; Werner Kilb; Heiko J Luhmann
Journal:  J Neurosci       Date:  2002-08-15       Impact factor: 6.167

10.  Morphology of neurons in the white matter of the adult human neocortex.

Authors:  G Meyer; P Wahle; A Castaneyra-Perdomo; R Ferres-Torres
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.