Light and electron microscopic localization of GABAA-receptors on cultured cerebellar granule cells and astrocytes using immunohistochemical techniques

Gert Helge Hansen; E Hösli; B Belhage; A Schousboe; L Hösli

Light and electron microscopic localization of GABAA-receptors on cultured cerebellar granule cells and astrocytes using immunohistochemical techniques

Gert Helge Hansen, E Hösli, B Belhage, A Schousboe, L Hösli

Institut for Cellulær og Molekylær Medicin

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

16 Citationer (Scopus)

Abstract

Udgivelsesdato: 1991-Mar

Originalsprog	Engelsk
Tidsskrift	Neurochemical Research
Vol/bind	16
Udgave nummer	3
Sider (fra-til)	341-6
Antal sider	6
ISSN	0364-3190
Status	Udgivet - 1991

Bibliografisk note

Keywords: Animals; Animals, Newborn; Astrocytes; Cells, Cultured; Cerebellum; Immunoenzyme Techniques; Microscopy, Immunoelectron; Rats; Rats, Inbred Strains; Receptors, GABA-A

Citationsformater

@article{68ed0dc0e31411ddb5fc000ea68e967b,

title = "Light and electron microscopic localization of GABAA-receptors on cultured cerebellar granule cells and astrocytes using immunohistochemical techniques",

abstract = "GABAA-receptors were localized in explant cultures of rat cerebellum and in dissociated primary cultures of rat cerebellar granule cells and rat cerebellar astrocytes using the monoclonal antibody bd-17 directed against the beta-subunit of the GABAA/benzodiazepine/chloride channel complex. At the light microscope level specific staining of GABAA-receptors was localized in various types of neurones in explant cultures of rat cerebellum using the indirect peroxidase-antiperoxidase (PAP) technique, whereas no specific staining was found in astrocytes. At the electron microscope level labeling of GABAA-receptors was observed in the plasma membrane of both the cell bodies and processes in dissociated primary cultures of cerebellar granule cells using an indirect preembedding immunogold staining technique which in contrast to the classical PAP technique allows quantitative estimations to be performed. Quantification of the labeling intensity revealed a higher concentration of GABAA-receptors per microns plasma membrane in the cell bodies than in the processes. In discrete areas an extremely high density of the GABAA-receptors was observed. No specific labeling of GABAA-receptors was observed in dissociated primary cultures of cerebellar astrocytes.",

author = "Hansen, {Gert Helge} and E H{\"o}sli and B Belhage and A Schousboe and L H{\"o}sli",

note = "Keywords: Animals; Animals, Newborn; Astrocytes; Cells, Cultured; Cerebellum; Immunoenzyme Techniques; Microscopy, Immunoelectron; Rats; Rats, Inbred Strains; Receptors, GABA-A",

year = "1991",

language = "English",

volume = "16",

pages = "341--6",

journal = "Neurochemical Research",

issn = "0364-3190",

publisher = "Springer",

number = "3",

}

TY - JOUR

T1 - Light and electron microscopic localization of GABAA-receptors on cultured cerebellar granule cells and astrocytes using immunohistochemical techniques

AU - Hansen, Gert Helge

AU - Hösli, E

AU - Belhage, B

AU - Schousboe, A

AU - Hösli, L

N1 - Keywords: Animals; Animals, Newborn; Astrocytes; Cells, Cultured; Cerebellum; Immunoenzyme Techniques; Microscopy, Immunoelectron; Rats; Rats, Inbred Strains; Receptors, GABA-A

PY - 1991

Y1 - 1991

N2 - GABAA-receptors were localized in explant cultures of rat cerebellum and in dissociated primary cultures of rat cerebellar granule cells and rat cerebellar astrocytes using the monoclonal antibody bd-17 directed against the beta-subunit of the GABAA/benzodiazepine/chloride channel complex. At the light microscope level specific staining of GABAA-receptors was localized in various types of neurones in explant cultures of rat cerebellum using the indirect peroxidase-antiperoxidase (PAP) technique, whereas no specific staining was found in astrocytes. At the electron microscope level labeling of GABAA-receptors was observed in the plasma membrane of both the cell bodies and processes in dissociated primary cultures of cerebellar granule cells using an indirect preembedding immunogold staining technique which in contrast to the classical PAP technique allows quantitative estimations to be performed. Quantification of the labeling intensity revealed a higher concentration of GABAA-receptors per microns plasma membrane in the cell bodies than in the processes. In discrete areas an extremely high density of the GABAA-receptors was observed. No specific labeling of GABAA-receptors was observed in dissociated primary cultures of cerebellar astrocytes.

AB - GABAA-receptors were localized in explant cultures of rat cerebellum and in dissociated primary cultures of rat cerebellar granule cells and rat cerebellar astrocytes using the monoclonal antibody bd-17 directed against the beta-subunit of the GABAA/benzodiazepine/chloride channel complex. At the light microscope level specific staining of GABAA-receptors was localized in various types of neurones in explant cultures of rat cerebellum using the indirect peroxidase-antiperoxidase (PAP) technique, whereas no specific staining was found in astrocytes. At the electron microscope level labeling of GABAA-receptors was observed in the plasma membrane of both the cell bodies and processes in dissociated primary cultures of cerebellar granule cells using an indirect preembedding immunogold staining technique which in contrast to the classical PAP technique allows quantitative estimations to be performed. Quantification of the labeling intensity revealed a higher concentration of GABAA-receptors per microns plasma membrane in the cell bodies than in the processes. In discrete areas an extremely high density of the GABAA-receptors was observed. No specific labeling of GABAA-receptors was observed in dissociated primary cultures of cerebellar astrocytes.

M3 - Journal article

C2 - 1664060

SN - 0364-3190

VL - 16

SP - 341

EP - 346

JO - Neurochemical Research

JF - Neurochemical Research

IS - 3

ER -