Literature DB >> 8889934

Restricted expression of R-cadherin by brain nuclei and neural circuits of the developing chicken brain.

K Arndt1, C Redies.   

Abstract

Cadherins are a family of Ca(2+)-dependent cell-cell adhesion molecules regulating morphogenesis by a preferentially homophilic binding mechanism. We have previously shown that the expression of R-cadherin in the early chicken forebrain (embryonic days E3-E6) is restricted to particular neuromeres or parts of neuromeres. R-cadherin-expressing neuroblasts born in these areas accumulate in the mantle zone and aggregate in particular (pro-) nuclei (Gänzler and Redies [1995] J. Neurosci. 15:4157-4172). In the present study, these findings are extended to later developmental stages (embryonic days E8, E11, and E15). By immunohistochemical and in situ hybridization techniques, we show that, at these stages of development, R-cadherin expression remains restricted to particular developing gray matter regions and fiber tracts. The R-cadherin-positive fiber tracts connect some of the R-cadherin-positive gray matter areas to form parts of particular neural circuits in the visual, auditory, somatosensory, and motor systems. Moreover, R-cadherin expression reflects the morphologic differentiation of gray matter regions. As brain nuclei become morphologically more distinct, the expression of R-cadherin shows a clearer demarcation of the nuclear boundaries. In addition, R-cadherin expression in some nuclei becomes restricted to particular subregions or to clusters of neurons. In the cerebellum, R-cadherin is expressed in parasagittal stripes. These results suggest that R-cadherin expression reflects the functional and morphologic maturation of gray matter structures and of information processing circuits in the embryonic chicken brain.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8889934     DOI: 10.1002/(SICI)1096-9861(19960923)373:3<373::AID-CNE5>3.0.CO;2-#

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


  8 in total

1.  Temporally distinct demands for classic cadherins in synapse formation and maturation.

Authors:  Ozlem Bozdagi; Martin Valcin; Kira Poskanzer; Hidekazu Tanaka; Deanna L Benson
Journal:  Mol Cell Neurosci       Date:  2004-12       Impact factor: 4.314

2.  Expression of classical cadherins in the cerebellar anlage: quantitative and functional aspects.

Authors:  Michael Gliem; Gunnar Weisheit; Kirsten D Mertz; Elmar Endl; John Oberdick; Karl Schilling
Journal:  Mol Cell Neurosci       Date:  2006-10-16       Impact factor: 4.314

3.  N-cadherin redistribution during synaptogenesis in hippocampal neurons.

Authors:  D L Benson; H Tanaka
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

4.  Blocking N-cadherin function disrupts the epithelial structure of differentiating neural tissue in the embryonic chicken brain.

Authors:  S I Gänzler-Odenthal; C Redies
Journal:  J Neurosci       Date:  1998-07-15       Impact factor: 6.167

Review 5.  The role of glycoproteins in neural development function, and disease.

Authors:  K C Breen; C M Coughlan; F D Hayes
Journal:  Mol Neurobiol       Date:  1998-04       Impact factor: 5.590

Review 6.  Cadherins in cerebellar development: translation of embryonic patterning into mature functional compartmentalization.

Authors:  Christoph Redies; Franziska Neudert; Juntang Lin
Journal:  Cerebellum       Date:  2011-09       Impact factor: 3.847

7.  Expression of a novel protocadherin, OL-protocadherin, in a subset of functional systems of the developing mouse brain.

Authors:  S Hirano; Q Yan; S T Suzuki
Journal:  J Neurosci       Date:  1999-02-01       Impact factor: 6.167

8.  Comparative analysis of protocadherin-11 X-linked expression among postnatal rodents, non-human primates, and songbirds suggests its possible involvement in brain evolution.

Authors:  Eiji Matsunaga; Sanae Nambu; Mariko Oka; Kazuo Okanoya; Atsushi Iriki
Journal:  PLoS One       Date:  2013-03-18       Impact factor: 3.240

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.