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Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain

The neuronal microtubule-associated protein tau is required for the development of cell polarity in cultured neurons. Using PC12 cells that stably express tau and tau amino-terminal fragments, we report that tau interacts with the neural plasma membrane through its amino-terminal projection domain....

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2120645/
https://www.ncbi.nlm.nih.gov/pubmed/8522593
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collection PubMed
description The neuronal microtubule-associated protein tau is required for the development of cell polarity in cultured neurons. Using PC12 cells that stably express tau and tau amino-terminal fragments, we report that tau interacts with the neural plasma membrane through its amino-terminal projection domain. In differentiated PC12 transfectants, tau is found in growth cone-like structures in a nonmicrotubule-dependent manner. In hippocampal neurons, tau is differentially extracted by detergent and enriched in the growth cone and the distal axon when membrane is left intact. In PC12 transfectants, overexpression of tau's amino-terminal fragment, but not of full-length tau, suppresses NGF-induced process formation. Our data suggest that tau's amino-terminal projection domain has an important role in neuritic development and establishes tau as a mediator of microtubule-plasma membrane interactions.
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spelling pubmed-21206452008-05-01 Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain J Cell Biol Articles The neuronal microtubule-associated protein tau is required for the development of cell polarity in cultured neurons. Using PC12 cells that stably express tau and tau amino-terminal fragments, we report that tau interacts with the neural plasma membrane through its amino-terminal projection domain. In differentiated PC12 transfectants, tau is found in growth cone-like structures in a nonmicrotubule-dependent manner. In hippocampal neurons, tau is differentially extracted by detergent and enriched in the growth cone and the distal axon when membrane is left intact. In PC12 transfectants, overexpression of tau's amino-terminal fragment, but not of full-length tau, suppresses NGF-induced process formation. Our data suggest that tau's amino-terminal projection domain has an important role in neuritic development and establishes tau as a mediator of microtubule-plasma membrane interactions. The Rockefeller University Press 1995-12-01 /pmc/articles/PMC2120645/ /pubmed/8522593 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
Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain
title Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain
title_full Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain
title_fullStr Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain
title_full_unstemmed Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain
title_short Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain
title_sort interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2120645/
https://www.ncbi.nlm.nih.gov/pubmed/8522593