Literature DB >> 1401258

Expression of s-laminin and laminin in the developing rat central nervous system.

D D Hunter1, R Llinas, M Ard, J P Merlie, J R Sanes.   

Abstract

The extracellular matrix component, s-laminin, is a homologue of the B1 subunit of laminin. S-laminin is concentrated in the synaptic cleft at the neuromuscular junction and contains a site that is adhesive for motor neurons, suggesting that it may influence neuromuscular development. To ascertain whether s-laminin may also play roles in the genesis of the central nervous system, we have examined its expression in the brain and spinal cord of embryonic and postnatal rats. S-laminin was not detectable in synapse-rich areas of adults. However, s-laminin was present in discrete subsets of three laminin-containing structures: (1) In the developing cerebral cortex, laminin and s-laminin were expressed in the subplate, a transient layer through which neuroblasts migrate and cortical afferents grow. Both laminin and s-laminin disappeared as embryogenesis proceeded; however, laminin was more widely distributed and present longer than s-laminin. (2) In the developing spinal cord, laminin was present throughout the pia. In contrast, s-laminin was concentrated in the pia that overlies the floor plate, a region in which extracellular cues have been postulated to guide growing axons. (3) In central capillaries, s-laminin appeared perinatally, an interval during which the blood-brain barrier matures. In contrast, laminin was present in capillary walls of both embryos and adults. To extend our immunohistochemical results, we used biochemical methods to characterize s-laminin in brain. We found that authentic s-laminin mRNA is present in the embryonic brain, but that brain-derived s-laminin differs (perhaps by a posttranslational modification) from that derived from nonneural tissues. We also used tissue culture methods to show that glia are capable of synthesizing "brain-like" s-laminin, and of assembling it into an extracellular matrix. Thus, glia may be one cellular source of s-laminin in brain. Together, these results demonstrate that s-laminin is present in the developing central nervous system, and raise the possibility that this molecule may influence developmental processes.

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Year:  1992        PMID: 1401258     DOI: 10.1002/cne.903230208

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


  25 in total

1.  Laminin expression in adult and developing retinae: evidence of two novel CNS laminins.

Authors:  R T Libby; M F Champliaud; T Claudepierre; Y Xu; E P Gibbons; M Koch; R E Burgeson; D D Hunter; W J Brunken
Journal:  J Neurosci       Date:  2000-09-01       Impact factor: 6.167

2.  Temporally restricted substrate interactions direct fate and specification of neural precursors derived from embryonic stem cells.

Authors:  A Katrin Goetz; Bjorn Scheffler; Huan-Xin Chen; Shanshan Wang; Oleg Suslov; Hui Xiang; Oliver Brüstle; Steve N Roper; Dennis A Steindler
Journal:  Proc Natl Acad Sci U S A       Date:  2006-07-10       Impact factor: 11.205

Review 3.  Role of laminin and integrin interactions in growth cone guidance.

Authors:  L McKerracher; M Chamoux; C O Arregui
Journal:  Mol Neurobiol       Date:  1996-04       Impact factor: 5.590

4.  Dual action of a carbohydrate epitope on afferent and efferent axons in cortical development.

Authors:  S Henke-Fahle; F Mann; M Götz; K Wild; J Bolz
Journal:  J Neurosci       Date:  1996-07-01       Impact factor: 6.167

5.  Ontogeny of four blood-brain barrier markers: an immunocytochemical comparison of pial and cerebral cortical microvessels.

Authors:  J P Cassella; J G Lawrenson; G Allt; J A Firth
Journal:  J Anat       Date:  1996-10       Impact factor: 2.610

Review 6.  Basement Membrane Changes in Ischemic Stroke.

Authors:  Minkyung Kang; Yao Yao
Journal:  Stroke       Date:  2020-03-03       Impact factor: 7.914

7.  Retroviral transfer of antisense integrin alpha6 or alpha8 sequences results in laminar redistribution or clonal cell death in developing brain.

Authors:  Z Zhang; D S Galileo
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

8.  Tissue distribution of the laminin beta1 and beta2 chain during embryonic and fetal human development.

Authors:  Matthias Roediger; Nicolai Miosge; Nikolaus Gersdorff
Journal:  J Mol Histol       Date:  2010-06-15       Impact factor: 2.611

Review 9.  The role of laminins in the organization and function of neuromuscular junctions.

Authors:  Robert S Rogers; Hiroshi Nishimune
Journal:  Matrix Biol       Date:  2016-09-07       Impact factor: 11.583

10.  G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivo.

Authors:  Melissa P Wu; Jamie R Doyle; Brenda Barry; Ariane Beauvais; Anete Rozkalne; Xianhua Piao; Michael W Lawlor; Alan S Kopin; Christopher A Walsh; Emanuela Gussoni
Journal:  FEBS J       Date:  2013-10-08       Impact factor: 5.542

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