Literature DB >> 3680638

Organization of radial glial cells during the development of the rat dentate gyrus.

M Rickmann1, D G Amaral, W M Cowan.   

Abstract

The temporal and spatial patterns of development of radial glial processes in the rat dentate gyrus have been studied in immunohistochemical preparations stained for the presence of either the glial fibrillary acidic protein (GFAP) or the vimentin-associated antigen R4. Additional electron microscopic (EM) observations were made from material prepared either immunohistochemically or by the Golgi method. R4 immunoreactive radial fibers were observed in the incipient dentate gyrus as early as E13 and by E14 the density of stained fibers was clearly higher in the anlage of the dentate gyrus than in the adjacent hippocampus. By E15 it was possible to identify in the EM the endfeet of radial glial cells that contained numerous glycogen particles. GFAP-positive radial processes were first observed on E17; these processes tended to be of larger diameter than those stained with the R4 antibody, suggesting that they were among the more mature processes. The orientation of both the R4- and GFAP-positive glial processes changed throughout the last week of embryonic life and by the end of the first postnatal week they formed a complex meshwork of intertwined processes. The distribution of their cell bodies also changed with time; initially their perikarya were located in the neuroepithelium at the lateral margin of the hippocampal primordium; later they were found mainly beneath the granule cell layer. Dividing cells that contained GFAP were observed along the trajectory of the migrating granule cell precursors and in the hilus of the dentate gyrus; at later stages some GFAP-positive mitotic figures were seen within and immediately below the granule cell layer. On the basis of these observations, we have attempted to reconstruct the role that radial glial processes play in the morphogenesis of the dentate gyrus. First, radial processes extend from the neuroepithelium to the pial surface prior to the migration of neurons that will form the dentate gyrus. These early generated glia appear to form the boundaries of the developing dentate gyrus and provide an internal lattice that may guide the initial wave of migrating progenitor cells. As the dentate gyrus enlarges, these early formed processes maintain their contacts along the hippocampal fissure and along the pial surface of the dentate anlage. Thus, with time they become increasingly distorted and are ultimately compressed into two bundles; one lies deep to the hippocampal fissure parallel to the granule cell layer and the other is located at the fimbriodentate juncture.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Year:  1987        PMID: 3680638     DOI: 10.1002/cne.902640403

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


  59 in total

1.  Distribution patterns of vimentin-immunoreactive structures in the human prosencephalon during the second half of gestation.

Authors:  N Ulfig; F Neudörfer; J Bohl
Journal:  J Anat       Date:  1999-07       Impact factor: 2.610

2.  Unique expression patterns of cell fate molecules delineate sequential stages of dentate gyrus development.

Authors:  S J Pleasure; A E Collins; D H Lowenstein
Journal:  J Neurosci       Date:  2000-08-15       Impact factor: 6.167

3.  Clonal architecture of the mouse hippocampus.

Authors:  Loren A Martin; Seong-Seng Tan; Dan Goldowitz
Journal:  J Neurosci       Date:  2002-05-01       Impact factor: 6.167

4.  The human brain at stages 21-23, with particular reference to the cerebral cortical plate and to the development of the cerebellum.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1990

5.  Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy.

Authors:  M Liu; S J Pleasure; A E Collins; J L Noebels; F J Naya; M J Tsai; D H Lowenstein
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-18       Impact factor: 11.205

6.  Reelin, Disabled 1, and beta 1 integrins are required for the formation of the radial glial scaffold in the hippocampus.

Authors:  Eckart Förster; Albrecht Tielsch; Barbara Saum; Karl Heinz Weiss; Celine Johanssen; Diana Graus-Porta; Ulrich Müller; Michael Frotscher
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-20       Impact factor: 11.205

7.  Glial cell differentiation in neuron-free and neuron-rich regions. I. Selective appearance of S-100 protein in radial glial cells of the hippocampal fimbria in human fetuses.

Authors:  M Stagaard Janas; R S Nowakowski; O B Terkelsen; K Møllgård
Journal:  Anat Embryol (Berl)       Date:  1991

8.  Lhx2 selector activity specifies cortical identity and suppresses hippocampal organizer fate.

Authors:  Vishakha S Mangale; Karla E Hirokawa; Prasad R V Satyaki; Nandini Gokulchandran; Satyadeep Chikbire; Lakshmi Subramanian; Ashwin S Shetty; Ben Martynoga; Jolly Paul; Mark V Mai; Yuqing Li; Lisa A Flanagan; Shubha Tole; Edwin S Monuki
Journal:  Science       Date:  2008-01-18       Impact factor: 47.728

9.  Fibroblast growth factor receptor 1 is required for the proliferation of hippocampal progenitor cells and for hippocampal growth in mouse.

Authors:  Yasushi Ohkubo; Ayumi O Uchida; Dana Shin; Juha Partanen; Flora M Vaccarino
Journal:  J Neurosci       Date:  2004-07-07       Impact factor: 6.167

Review 10.  The role of BETA2/NeuroD1 in the development of the nervous system.

Authors:  Jang-Hyeon Cho; Ming-Jer Tsai
Journal:  Mol Neurobiol       Date:  2004-08       Impact factor: 5.590

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.