Literature DB >> 7757257

Initial tract formation in the brain of the chick embryo: selective expression of the BEN/SC1/DM-GRASP cell adhesion molecule.

A Chédotal1, O Pourquié, C Sotelo.   

Abstract

This study reports the spatio-temporal pattern of BEN expression (a molecule of the immunoglobulin superfamily) during early stages of the first axonal tract formation, in the fore- and midbrain of chick embryos [Hamburger and Hamilton (HH) stages 12-22]. The expression of BEN has been analysed using immunohistochemistry and non-radioactive in situ hybridization. Furthermore, double labelling experiments (combining anti-class III beta-tubulin, a pan-neuronal marker, and anti-BEN antibodies) have been carried out to determine whether BEN is expressed by all first axonal tracts. The first neurons expressing BEN appear around stage HH13-14, in the caudal diencephalon. They belong to the interstitial nucleus of Cajal, and their axons are the first components of the medial longitudinal fasciculus. By HH14, two other early axonal tracts appear: the tract of the postoptic commissure and the descending root of the mesencephalic nucleus of the trigeminal nerve. Only the latter expresses BEN. At later stages of development numerous new axonal tracts appear in the telencephalic, diencephalic and mesencephalic domains. Only a few of them (the fourth nerve, the lemniscus lateralis, the tectobulbar and habenulopeduncular tracts) express BEN. In all BEN positive systems, the cell bodies, axons and growth cones are uniformly labelled by the antibody. We have found that none of the early axonal tracts grows preferentially at interneuromeric boundaries. Moreover, each tract is formed by several thin fascicles rather than a single one. The expression of BEN is transient and disappears shortly before hatching. These results suggest that BEN may serve to promote axonal outgrowth of precise neuronal systems involved in 'axonal scaffolding'.

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Year:  1995        PMID: 7757257     DOI: 10.1111/j.1460-9568.1995.tb01056.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  27 in total

1.  DM-GRASP is necessary for nonradial cell migration during chick diencephalic development.

Authors:  D S Heffron; J A Golden
Journal:  J Neurosci       Date:  2000-03-15       Impact factor: 6.167

2.  Roles of the telencephalic cells and their chondroitin sulfate proteoglycans in delimiting an anterior border of the retinal pathway.

Authors:  H Ichijo; I Kawabata
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

Review 3.  Proteoglycans as cues for axonal guidance in formation of retinotectal or retinocollicular projections.

Authors:  Hiroyuki Ichijo
Journal:  Mol Neurobiol       Date:  2004-08       Impact factor: 5.590

4.  Tlx-1 and Tlx-3 homeobox gene expression in cranial sensory ganglia and hindbrain of the chick embryo: markers of patterned connectivity.

Authors:  C Logan; R J Wingate; I J McKay; A Lumsden
Journal:  J Neurosci       Date:  1998-07-15       Impact factor: 6.167

Review 5.  Longitudinal axons are guided by Slit/Robo signals from the floor plate.

Authors:  Grant S Mastick; W Todd Farmer; Amy L Altick; Hikmet Feyza Nural; James P Dugan; Thomas Kidd; Frederic Charron
Journal:  Cell Adh Migr       Date:  2010-07-18       Impact factor: 3.405

6.  Development of the early axon scaffold in the rostral brain of the chick embryo.

Authors:  Michelle Ware; Frank R Schubert
Journal:  J Anat       Date:  2011-05-22       Impact factor: 2.610

7.  Control of somite patterning by signals from the lateral plate.

Authors:  O Pourquié; M Coltey; C Bréant; N M Le Douarin
Journal:  Proc Natl Acad Sci U S A       Date:  1995-04-11       Impact factor: 11.205

8.  Netrin-DCC, Robo-Slit, and heparan sulfate proteoglycans coordinate lateral positioning of longitudinal dopaminergic diencephalospinal axons.

Authors:  Edda Kastenhuber; Ursula Kern; Joshua L Bonkowsky; Chi-Bin Chien; Wolfgang Driever; Joern Schweitzer
Journal:  J Neurosci       Date:  2009-07-15       Impact factor: 6.167

9.  Slit and Netrin-1 guide cranial motor axon pathfinding via Rho-kinase, myosin light chain kinase and myosin II.

Authors:  Ailish Murray; Arifa Naeem; Sarah H Barnes; Uwe Drescher; Sarah Guthrie
Journal:  Neural Dev       Date:  2010-06-22       Impact factor: 3.842

10.  BEN as a presumptive target recognition molecule during the development of the olivocerebellar system.

Authors:  A Chédotal; O Pourquié; F Ezan; H San Clemente; C Sotelo
Journal:  J Neurosci       Date:  1996-05-15       Impact factor: 6.167

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