Literature DB >> 2352935

Central nervous system neurons migrate on astroglial fibers from heterotypic brain regions in vitro.

U E Gasser1, M E Hatten.   

Abstract

In different regions of the developing mammalian brain, neurons follow the processes of radial glial cells over very different trajectories to reach their destinations in specific neuronal layers. To investigate whether the movement of neurons along glial fibers is specified by glia in a given region or whether glia provide a permissive substrate for migration in different brain regions, we purified neurons and astroglial cells from developing cerebellum and hippocampus and analyzed neuronal migration on heterotypic glial fibers with time-lapse, video-enhanced differential interference microscopy in vitro. Granule neurons purified from early postnatal rat cerebellum migrated on astroglial processes of glia purified from late embryonic or early postnatal rat hippocampus with a cytology, neuron-glial relationship, and dynamics of movement that were indistinguishable from those of mouse granule cells migrating on cerebellar astroglial processes in vitro [Edmondson, J. C. & Hatten, M. E. (1987) J. Neurosci. 7, 1928-1934]. In the reciprocal combination, hippocampal neurons migrated on cerebellar glial processes in a manner that was also remarkably similar to migration along homotypic, hippocampal glial fibers [Gasser, U. E. & Hatten, M. E. (1990) J. Neurosci. 10, 1276-1285]. In all cases, migrating neurons had a characteristic appearance, apposing their cell soma against the glial fiber and extending in the direction of migration a motile, leading process that enfolded the glial fiber with short filopodia and lamellipodia. As seen by video microscopy, neurons moved along homotypic and heterotypic glial processes by translocation of the soma and were not "pulled" forward by the leading process. As the neuron moved, the nucleus remained in the posterior portion of the cell and cytoplasmic vesicles moved forward from the soma into the leading process. The dynamics of the movement of neurons along heterotypic glial substrates, including the speed and periodicity of motion, was identical to that of neurons migrating along homotypic glial substrates. These experiments suggest that the mechanism of movement of neurons along glial fibers is conserved in these two brain regions during development.

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Year:  1990        PMID: 2352935      PMCID: PMC54152          DOI: 10.1073/pnas.87.12.4543

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  32 in total

1.  Cytology and neuron-glial apposition of migrating cerebellar granule cells in vitro.

Authors:  W A Gregory; J C Edmondson; M E Hatten; C A Mason
Journal:  J Neurosci       Date:  1988-05       Impact factor: 6.167

2.  Neuron-glia interactions of rat hippocampal cells in vitro: glial-guided neuronal migration and neuronal regulation of glial differentiation.

Authors:  U E Gasser; M E Hatten
Journal:  J Neurosci       Date:  1990-04       Impact factor: 6.167

3.  Neuron-glia relationship during granule cell migration in developing cerebellar cortex. A Golgi and electronmicroscopic study in Macacus Rhesus.

Authors:  P Rakic
Journal:  J Comp Neurol       Date:  1971-03       Impact factor: 3.215

4.  Time of neuron origin in the hippocampus and dentate gyrus of normal and reeler mutant mice: an autoradiographic analysis.

Authors:  V S Caviness
Journal:  J Comp Neurol       Date:  1973-09-15       Impact factor: 3.215

5.  Glial-guided granule neuron migration in vitro: a high-resolution time-lapse video microscopic study.

Authors:  J C Edmondson; M E Hatten
Journal:  J Neurosci       Date:  1987-06       Impact factor: 6.167

6.  Fates of visual cortical neurons in the ferret after isochronic and heterochronic transplantation.

Authors:  S K McConnell
Journal:  J Neurosci       Date:  1988-03       Impact factor: 6.167

Review 7.  Neuronal migration, with special reference to developing human brain: a review.

Authors:  R L Sidman; P Rakic
Journal:  Brain Res       Date:  1973-11-09       Impact factor: 3.252

8.  Mode of cell migration to the superficial layers of fetal monkey neocortex.

Authors:  P Rakic
Journal:  J Comp Neurol       Date:  1972-05       Impact factor: 3.215

9.  Weaver mutant mouse cerebellum: defective neuronal migration secondary to abnormality of Bergmann glia.

Authors:  P Rakic; R L Sidman
Journal:  Proc Natl Acad Sci U S A       Date:  1973-01       Impact factor: 11.205

10.  Neuronal inhibition of astroglial cell proliferation is membrane mediated.

Authors:  M E Hatten
Journal:  J Cell Biol       Date:  1987-05       Impact factor: 10.539

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  12 in total

1.  Cell coupling and uncoupling in the ventricular zone of developing neocortex.

Authors:  K Bittman; D F Owens; A R Kriegstein; J J LoTurco
Journal:  J Neurosci       Date:  1997-09-15       Impact factor: 6.167

Review 2.  Mechanisms of glial-guided neuronal migration in vitro and in vivo.

Authors:  M E Hatten; C A Mason
Journal:  Experientia       Date:  1990-09-15

3.  Blood vessels form a scaffold for neuroblast migration in the adult olfactory bulb.

Authors:  Serena Bovetti; Yi-Chun Hsieh; Patrizia Bovolin; Isabelle Perroteau; Toida Kazunori; Adam C Puche
Journal:  J Neurosci       Date:  2007-05-30       Impact factor: 6.167

Review 4.  The role of Rho GTPase proteins in CNS neuronal migration.

Authors:  Eve-Ellen Govek; Mary E Hatten; Linda Van Aelst
Journal:  Dev Neurobiol       Date:  2011-06       Impact factor: 3.964

5.  Two distal downstream enhancers direct expression of the human apolipoprotein E gene to astrocytes in the brain.

Authors:  S Grehan; E Tse; J M Taylor
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

6.  A short-range signal restricts cell movement between telencephalic proliferative zones.

Authors:  C Neyt; M Welch; A Langston; J Kohtz; G Fishell
Journal:  J Neurosci       Date:  1997-12-01       Impact factor: 6.167

7.  Neuroglobin overexpression inhibits oxygen-glucose deprivation-induced mitochondrial permeability transition pore opening in primary cultured mouse cortical neurons.

Authors:  Zhanyang Yu; Ning Liu; Yadan Li; Jianfeng Xu; Xiaoying Wang
Journal:  Neurobiol Dis       Date:  2013-04-29       Impact factor: 5.996

8.  The actin cross-linking protein AFAP120 regulates axon elongation in a tyrosine phosphorylation-dependent manner.

Authors:  Jennifer Harder; Xiaohua Xu; Paul Letourneau; Lorene M Lanier
Journal:  Neurosci Lett       Date:  2008-08-15       Impact factor: 3.046

9.  Impaired motor coordination and disrupted cerebellar architecture in Fgfr1 and Fgfr2 double knockout mice.

Authors:  Karen Müller Smith; Theresa L Williamson; Michael L Schwartz; Flora M Vaccarino
Journal:  Brain Res       Date:  2012-04-11       Impact factor: 3.252

10.  Endocytosis regulates cell soma translocation and the distribution of adhesion proteins in migrating neurons.

Authors:  Jennifer C Shieh; Bruce T Schaar; Karpagam Srinivasan; Frances M Brodsky; Susan K McConnell
Journal:  PLoS One       Date:  2011-03-22       Impact factor: 3.240

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