Literature DB >> 11306627

Cortical axon guidance by the glial wedge during the development of the corpus callosum.

T Shu1, L J Richards.   

Abstract

Growing axons are often guided to their final destination by intermediate targets. In the developing spinal cord and optic nerve, specialized cells at the embryonic midline act as intermediate targets for guiding commissural axons. Here we investigate whether similar intermediate targets may play a role in guiding cortical axons in the developing brain. During the development of the corpus callosum, cortical axons from one cerebral hemisphere cross the midline to reach their targets in the opposite cortical hemisphere. We have identified two early differentiating populations of midline glial cells that may act as intermediate guideposts for callosal axons. The first differentiates directly below the corpus callosum forming a wedge shaped structure (the glial wedge) and the second differentiates directly above the corpus callosum within the indusium griseum. Axons of the corpus callosum avoid both of these populations in vivo. This finding is recapitulated in vitro in three-dimensional collagen gels. In addition, experimental manipulations in organotypic slices show that callosal axons require the presence and correct orientation of these populations to turn toward the midline. We have also identified one possible candidate for this activity because both glial populations express the chemorepellent molecule slit-2, and cortical axons express the slit-2 receptors robo-1 and robo-2. Furthermore, slit-2 repels-suppresses cortical axon growth in three-dimensional collagen gel cocultures.

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Year:  2001        PMID: 11306627      PMCID: PMC6762517     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  53 in total

1.  Cellular and molecular guidance of GABAergic neuronal migration from an extracortical origin to the neocortex.

Authors:  Y Zhu; H Li; L Zhou; J Y Wu; Y Rao
Journal:  Neuron       Date:  1999-07       Impact factor: 17.173

2.  Monoclonal antibody R2D5 reveals midsagittal radial glial system in postnatally developing and adult brainstem.

Authors:  K Mori; J Ikeda; O Hayaishi
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

Review 3.  Glial cell extracellular matrix: boundaries for axon growth in development and regeneration.

Authors:  M T Fitch; J Silver
Journal:  Cell Tissue Res       Date:  1997-11       Impact factor: 5.249

4.  Embryonic development of axon pathways in the Drosophila CNS. I. A glial scaffold appears before the first growth cones.

Authors:  J R Jacobs; C S Goodman
Journal:  J Neurosci       Date:  1989-07       Impact factor: 6.167

5.  Development of intersecting CNS fiber tracts: the corpus callosum and its perforating fiber pathway.

Authors:  M H Hankin; J Silver
Journal:  J Comp Neurol       Date:  1988-06-08       Impact factor: 3.215

6.  Transient midline raphe glial structure in the developing rat.

Authors:  C Van Hartesveldt; B Moore; B K Hartman
Journal:  J Comp Neurol       Date:  1986-11-08       Impact factor: 3.215

7.  Directed growth of early cortical axons is influenced by a chemoattractant released from an intermediate target.

Authors:  L J Richards; S E Koester; R Tuttle; D D O'Leary
Journal:  J Neurosci       Date:  1997-04-01       Impact factor: 6.167

8.  Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance.

Authors:  K Brose; K S Bland; K H Wang; D Arnott; W Henzel; C S Goodman; M Tessier-Lavigne; T Kidd
Journal:  Cell       Date:  1999-03-19       Impact factor: 41.582

9.  Immunoperoxidase localization of glial fibrillary acidic protein in radial glial cells and astrocytes of the developing rhesus monkey brain.

Authors:  P Levitt; P Rakic
Journal:  J Comp Neurol       Date:  1980-10-01       Impact factor: 3.215

10.  Defects in thalamocortical axon pathfinding correlate with altered cell domains in Mash-1-deficient mice.

Authors:  R Tuttle; Y Nakagawa; J E Johnson; D D O'Leary
Journal:  Development       Date:  1999-05       Impact factor: 6.868

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  82 in total

1.  The glial sling is a migratory population of developing neurons.

Authors:  Tianzhi Shu; Ying Li; Asaf Keller; Linda J Richards
Journal:  Development       Date:  2003-07       Impact factor: 6.868

2.  Slit2 guides both precrossing and postcrossing callosal axons at the midline in vivo.

Authors:  Tianzhi Shu; Vasi Sundaresan; Margaret M McCarthy; Linda J Richards
Journal:  J Neurosci       Date:  2003-09-03       Impact factor: 6.167

3.  Temporally defined neocortical translation and polysome assembly are determined by the RNA-binding protein Hu antigen R.

Authors:  Matthew L Kraushar; Kevin Thompson; H R Sagara Wijeratne; Barbara Viljetic; Kristina Sakers; Justin W Marson; Dimitris L Kontoyiannis; Steven Buyske; Ronald P Hart; Mladen-Roko Rasin
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-25       Impact factor: 11.205

4.  A positive autoregulatory loop of Jak-STAT signaling controls the onset of astrogliogenesis.

Authors:  Fei He; Weihong Ge; Keri Martinowich; Sara Becker-Catania; Volkan Coskun; Wenyu Zhu; Hao Wu; Diogo Castro; Francois Guillemot; Guoping Fan; Jean de Vellis; Yi E Sun
Journal:  Nat Neurosci       Date:  2005-04-24       Impact factor: 24.884

Review 5.  Slit-Robo interactions during cortical development.

Authors:  William D Andrews; Melissa Barber; John G Parnavelas
Journal:  J Anat       Date:  2007-06-06       Impact factor: 2.610

6.  The transcription factor Zfp423/OAZ is required for cerebellar development and CNS midline patterning.

Authors:  Li E Cheng; Jiangyang Zhang; Randall R Reed
Journal:  Dev Biol       Date:  2007-04-12       Impact factor: 3.582

7.  Axon position within the corpus callosum determines contralateral cortical projection.

Authors:  Jing Zhou; Yunqing Wen; Liang She; Ya-Nan Sui; Lu Liu; Linda J Richards; Mu-Ming Poo
Journal:  Proc Natl Acad Sci U S A       Date:  2013-06-28       Impact factor: 11.205

8.  Growth-associated protein-43 is required for commissural axon guidance in the developing vertebrate nervous system.

Authors:  Yiping Shen; Shyamala Mani; Stacy L Donovan; James E Schwob; Karina F Meiri
Journal:  J Neurosci       Date:  2002-01-01       Impact factor: 6.167

9.  MARCKS Is Necessary for Netrin-DCC Signaling and Corpus Callosum Formation.

Authors:  J J Brudvig; J T Cain; G G Schmidt-Grimminger; D J Stumpo; K J Roux; P J Blackshear; J M Weimer
Journal:  Mol Neurobiol       Date:  2018-03-15       Impact factor: 5.590

10.  Ephrin-B1 regulates axon guidance by reverse signaling through a PDZ-dependent mechanism.

Authors:  Jeffrey O Bush; Philippe Soriano
Journal:  Genes Dev       Date:  2009-06-10       Impact factor: 11.361

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