Literature DB >> 75755

Characterization of an antiserum to synaptic glomeruli from rat cerebellum.

C Goridis, J Martin, M Schachner.   

Abstract

Rabbit anti-rat cerebellar synaptic glomeruli antiserum when absorbed with non-neural tissues reacts only with neural tissues when tested by indirect immunofluorescence on tissue sections. Further absorption with forebrain results in the antiserum which detectably reacts only with synaptic glomeruli and soma of Purkinje cells of both rat and mouse. The developmental expression of the synaptic glomeruli antigen(s) parallels the formation of synapses between mossy fibers and granule cells. Immature synaptic contacts do not contain recognizable antigen(s), whereas only at postnatal Day 15 glomeruli become antigen-positive. At this stage antigen in Purkinje cells is no longer carried in their dendrites, but becomes confined to the cell soma. Staggerer mutant mice still express the immature pattern of antigen distribution on postnatal Day 18.

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Year:  1978        PMID: 75755     DOI: 10.1016/0361-9230(78)90060-6

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  11 in total

1.  Immunocytochemical localization of cell type-specific markers in reaggregating cell cultures of mouse cerebellum.

Authors:  J Lindner; M Schachner
Journal:  Cell Tissue Res       Date:  1982       Impact factor: 5.249

2.  Development and expression of cytoplasmic antigens in Purkinje cells recognized by monoclonal antibodies. Studies in neurologically mutant mice.

Authors:  A Weber; M Schachner
Journal:  Cell Tissue Res       Date:  1982       Impact factor: 5.249

3.  Interstitial and parenchymal cells in the pineal gland of the golden hamster. A combined thin-section, freeze-fracture and immunofluorescence study.

Authors:  S K Huang; R Nobiling; M Schachner; R Taugner
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

4.  Glial cells in the pineal gland of mice and rats. A combined immunofluorescence and electron-microscopic study.

Authors:  M Schachner; S K Huang; P Ziegelmüller; B Bizzini; R Taugner
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

5.  J1-160 and J1-180 are oligodendrocyte-secreted nonpermissive substrates for cell adhesion.

Authors:  P Pesheva; E Spiess; M Schachner
Journal:  J Cell Biol       Date:  1989-10       Impact factor: 10.539

6.  Immunocytological and biochemical characterization of a new neuronal cell surface component (L1 antigen) which is involved in cell adhesion.

Authors:  F G Rathjen; M Schachner
Journal:  EMBO J       Date:  1984-01       Impact factor: 11.598

7.  Comparison of two cell surface molecules involved in neural cell adhesion.

Authors:  F G Rathjen; U Rutishauser
Journal:  EMBO J       Date:  1984-02       Impact factor: 11.598

8.  Immunoelectron microscopic localization of neural cell adhesion molecules (L1, N-CAM, and myelin-associated glycoprotein) in regenerating adult mouse sciatic nerve.

Authors:  R Martini; M Schachner
Journal:  J Cell Biol       Date:  1988-05       Impact factor: 10.539

9.  Biochemical and functional characterization of a novel neuron-glia adhesion molecule that is involved in neuronal migration.

Authors:  H Antonicek; E Persohn; M Schachner
Journal:  J Cell Biol       Date:  1987-06       Impact factor: 10.539

10.  Immunocytochemical demonstration of vimentin in astrocytes and ependymal cells of developing and adult mouse nervous system.

Authors:  J Schnitzer; W W Franke; M Schachner
Journal:  J Cell Biol       Date:  1981-08       Impact factor: 10.539

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