Literature DB >> 12756176

The glial sling is a migratory population of developing neurons.

Tianzhi Shu1, Ying Li, Asaf Keller, Linda J Richards.   

Abstract

For two decades the glial sling has been hypothesized to act as a guidance substratum for developing callosal axons. However, neither the cellular nature of the sling nor its guidance properties have ever been clearly identified. Although originally thought to be glioblasts, we show here that the subventricular zone cells forming the sling are in fact neurons. Sling cells label with a number of neuronal markers and display electrophysiological properties characteristic of neurons and not glia. Furthermore, sling cells are continuously generated until early postnatal stages and do not appear to undergo widespread cell death. These data indicate that the sling may be a source of, or migratory pathway for, developing neurons in the rostral forebrain, suggesting additional functions for the sling independent of callosal axon guidance.

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Year:  2003        PMID: 12756176      PMCID: PMC2810520          DOI: 10.1242/dev.00514

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  48 in total

1.  An immunocytochemical analysis of the ontogeny of the microtubule-associated proteins MAP-2 and Tau in the nervous system of the rat.

Authors:  A Ferreira; J Busciglio; A Cáceres
Journal:  Brain Res       Date:  1987-07       Impact factor: 3.252

2.  Death of the subcallosal glial sling is correlated with formation of the cavum septi pellucidi.

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

3.  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

4.  Post-natal development of electrophysiological properties of rat cerebral cortical pyramidal neurones.

Authors:  D A McCormick; D A Prince
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

5.  Postnatally induced formation of the corpus callosum in acallosal mice on glia-coated cellulose bridges.

Authors:  J Silver; M Y Ogawa
Journal:  Science       Date:  1983-06-03       Impact factor: 47.728

6.  Ontophyletics of the nervous system: development of the corpus callosum and evolution of axon tracts.

Authors:  M J Katz; R J Lasek; J Silver
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

7.  Changing role of forebrain astrocytes during development, regenerative failure, and induced regeneration upon transplantation.

Authors:  G M Smith; R H Miller; J Silver
Journal:  J Comp Neurol       Date:  1986-09-01       Impact factor: 3.215

8.  The morphology and phased outgrowth of callosal axons in the fetal rat.

Authors:  M K Floeter; E G Jones
Journal:  Brain Res       Date:  1985-09       Impact factor: 3.252

9.  Growth-associated protein, GAP-43, a polypeptide that is induced when neurons extend axons, is a component of growth cones and corresponds to pp46, a major polypeptide of a subcellular fraction enriched in growth cones.

Authors:  K F Meiri; K H Pfenninger; M B Willard
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

10.  Characterization of microtubule-associated protein 2 from mouse brain and its localization in the cerebellar cortex.

Authors:  M Niinobe; N Maeda; H Ino; K Mikoshiba
Journal:  J Neurochem       Date:  1988-10       Impact factor: 5.372

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  25 in total

1.  Protooncogene Ski cooperates with the chromatin-remodeling factor Satb2 in specifying callosal neurons.

Authors:  Constanze Baranek; Manuela Dittrich; Srinivas Parthasarathy; Carine Gaiser Bonnon; Olga Britanova; Dmitriy Lanshakov; Fatiha Boukhtouche; Julia E Sommer; Clemencia Colmenares; Victor Tarabykin; Suzana Atanasoski
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-14       Impact factor: 11.205

Review 2.  Integrative mechanisms of oriented neuronal migration in the developing brain.

Authors:  Irina Evsyukova; Charlotte Plestant; E S Anton
Journal:  Annu Rev Cell Dev Biol       Date:  2013-08-07       Impact factor: 13.827

Review 3.  Guiding neuronal cell migrations.

Authors:  Oscar Marín; Manuel Valiente; Xuecai Ge; Li-Huei Tsai
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-02       Impact factor: 10.005

Review 4.  Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.

Authors:  Timothy J Edwards; Elliott H Sherr; A James Barkovich; Linda J Richards
Journal:  Brain       Date:  2014-01-28       Impact factor: 13.501

5.  Patterns of cell death in the perinatal mouse forebrain.

Authors:  Morgan Mosley; Charisma Shah; Kiriana A Morse; Stephen A Miloro; Melissa M Holmes; Todd H Ahern; Nancy G Forger
Journal:  J Comp Neurol       Date:  2016-06-13       Impact factor: 3.215

Review 6.  Development, specification, and diversity of callosal projection neurons.

Authors:  Ryann M Fame; Jessica L MacDonald; Jeffrey D Macklis
Journal:  Trends Neurosci       Date:  2010-12-02       Impact factor: 13.837

7.  The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformation.

Authors:  Charles Raybaud
Journal:  Neuroradiology       Date:  2010-04-27       Impact factor: 2.804

8.  Nuclear factor one transcription factors in CNS development.

Authors:  Sharon Mason; Michael Piper; Richard M Gronostajski; Linda J Richards
Journal:  Mol Neurobiol       Date:  2008-12-05       Impact factor: 5.590

9.  Transient neuronal populations are required to guide callosal axons: a role for semaphorin 3C.

Authors:  Mathieu Niquille; Sonia Garel; Fanny Mann; Jean-Pierre Hornung; Belkacem Otsmane; Sébastien Chevalley; Carlos Parras; Francois Guillemot; Patricia Gaspar; Yuchio Yanagawa; Cécile Lebrand
Journal:  PLoS Biol       Date:  2009-10-27       Impact factor: 8.029

10.  Multiple non-cell-autonomous defects underlie neocortical callosal dysgenesis in Nfib-deficient mice.

Authors:  Michael Piper; Randal X Moldrich; Charlotta Lindwall; Erica Little; Guy Barry; Sharon Mason; Nana Sunn; Nyoman Dana Kurniawan; Richard M Gronostajski; Linda J Richards
Journal:  Neural Dev       Date:  2009-12-04       Impact factor: 3.842

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