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Micropatterned Substrates for Studying Astrocytes in Culture

Recent studies of the physiological roles of astrocytes have ignited renewed interest in the functional significance of these glial cells in the central nervous system. Many of the newly discovered astrocytic functions were initially demonstrated and characterized in cell culture systems. We discuss...

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Detalles Bibliográficos
Autores principales: Lee, William, Parpura, Vladimir
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796922/
https://www.ncbi.nlm.nih.gov/pubmed/20198155
http://dx.doi.org/10.3389/neuro.01.033.2009
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author Lee, William
Parpura, Vladimir
author_facet Lee, William
Parpura, Vladimir
author_sort Lee, William
collection PubMed
description Recent studies of the physiological roles of astrocytes have ignited renewed interest in the functional significance of these glial cells in the central nervous system. Many of the newly discovered astrocytic functions were initially demonstrated and characterized in cell culture systems. We discuss the use of microculture techniques and micropatterning of cell-adhesive substrates in studies of astrocytic Ca(2+) excitability and bidirectional neuron-astrocyte signaling. This culturing approach aims to reduce the level of complexity of the system by limiting the interacting partners and by controlling the localization of cells. It provides tight control over experimental conditions allowing detailed characterization of cellular functions and intercellular communication. Although such a reductionist approach yields some difference in observations between astrocytic properties in culture and in situ, general phenomena discovered in cell culture systems, however, have also been found in vivo.
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spelling pubmed-27969222010-03-02 Micropatterned Substrates for Studying Astrocytes in Culture Lee, William Parpura, Vladimir Front Neurosci Neuroscience Recent studies of the physiological roles of astrocytes have ignited renewed interest in the functional significance of these glial cells in the central nervous system. Many of the newly discovered astrocytic functions were initially demonstrated and characterized in cell culture systems. We discuss the use of microculture techniques and micropatterning of cell-adhesive substrates in studies of astrocytic Ca(2+) excitability and bidirectional neuron-astrocyte signaling. This culturing approach aims to reduce the level of complexity of the system by limiting the interacting partners and by controlling the localization of cells. It provides tight control over experimental conditions allowing detailed characterization of cellular functions and intercellular communication. Although such a reductionist approach yields some difference in observations between astrocytic properties in culture and in situ, general phenomena discovered in cell culture systems, however, have also been found in vivo. Frontiers Research Foundation 2009-12-15 /pmc/articles/PMC2796922/ /pubmed/20198155 http://dx.doi.org/10.3389/neuro.01.033.2009 Text en Copyright © 2009 Lee and Parpura. http://www.frontiersin.org/licenseagreement This is an open-access publication subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Lee, William
Parpura, Vladimir
Micropatterned Substrates for Studying Astrocytes in Culture
title Micropatterned Substrates for Studying Astrocytes in Culture
title_full Micropatterned Substrates for Studying Astrocytes in Culture
title_fullStr Micropatterned Substrates for Studying Astrocytes in Culture
title_full_unstemmed Micropatterned Substrates for Studying Astrocytes in Culture
title_short Micropatterned Substrates for Studying Astrocytes in Culture
title_sort micropatterned substrates for studying astrocytes in culture
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796922/
https://www.ncbi.nlm.nih.gov/pubmed/20198155
http://dx.doi.org/10.3389/neuro.01.033.2009
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