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Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies

Immunohistochemical staining with monoclonal antibodies showed that microtubule-associated protein 1 (MAP1) has a restricted cellular distribution in the rat cerebellum. Anti-MAP1 staining was found only in neurons, where it was much stronger in dendrites than in axons. There were striking variation...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1984
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113089/
https://www.ncbi.nlm.nih.gov/pubmed/6363428
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collection PubMed
description Immunohistochemical staining with monoclonal antibodies showed that microtubule-associated protein 1 (MAP1) has a restricted cellular distribution in the rat cerebellum. Anti-MAP1 staining was found only in neurons, where it was much stronger in dendrites than in axons. There were striking variations in the apparent concentration of MAP1 in different classes of neurons. Purkinje cells were the most strongly labeled, while granule cell neurons gave a faint, threshold-level reaction with the antibody. The reaction of Golgi neurons was intermediate between these two extremes. Equivalent results were obtained using two different methods of tissue preparation. Thus MAP1 appears to be a neuron-specific protein that is highly concentrated in dendrites and occurs at markedly different levels in different types of neurons. These observations provide further indications of heterogeneity among brain microtubules.
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spelling pubmed-21130892008-05-01 Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies J Cell Biol Articles Immunohistochemical staining with monoclonal antibodies showed that microtubule-associated protein 1 (MAP1) has a restricted cellular distribution in the rat cerebellum. Anti-MAP1 staining was found only in neurons, where it was much stronger in dendrites than in axons. There were striking variations in the apparent concentration of MAP1 in different classes of neurons. Purkinje cells were the most strongly labeled, while granule cell neurons gave a faint, threshold-level reaction with the antibody. The reaction of Golgi neurons was intermediate between these two extremes. Equivalent results were obtained using two different methods of tissue preparation. Thus MAP1 appears to be a neuron-specific protein that is highly concentrated in dendrites and occurs at markedly different levels in different types of neurons. These observations provide further indications of heterogeneity among brain microtubules. The Rockefeller University Press 1984-02-01 /pmc/articles/PMC2113089/ /pubmed/6363428 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies
title Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies
title_full Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies
title_fullStr Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies
title_full_unstemmed Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies
title_short Immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies
title_sort immunocytochemical localization of microtubule-associated protein 1 in rat cerebellum using monoclonal antibodies
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113089/
https://www.ncbi.nlm.nih.gov/pubmed/6363428