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Delayed Retraction of Filopodia in Gelsolin Null Mice
Growth cones extend dynamic protrusions called filopodia and lamellipodia as exploratory probes that signal the direction of neurite growth. Gelsolin, as an actin filament-severing protein, may serve an important role in the rapid shape changes associated with growth cone structures. In wild-type (w...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132546/ https://www.ncbi.nlm.nih.gov/pubmed/9298983 |
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author | Lu, Mei Witke, Walter Kwiatkowski, David J. Kosik, Kenneth S. |
author_facet | Lu, Mei Witke, Walter Kwiatkowski, David J. Kosik, Kenneth S. |
author_sort | Lu, Mei |
collection | PubMed |
description | Growth cones extend dynamic protrusions called filopodia and lamellipodia as exploratory probes that signal the direction of neurite growth. Gelsolin, as an actin filament-severing protein, may serve an important role in the rapid shape changes associated with growth cone structures. In wild-type (wt) hippocampal neurons, antibodies against gelsolin labeled the neurite shaft and growth cone. The behavior of filopodia in cultured hippocampal neurons from embryonic day 17 wt and gelsolin null (Gsn(−)) mice (Witke, W., A.H. Sharpe, J.H. Hartwig, T. Azuma, T.P. Stossel, and D.J. Kwiatkowski. 1995. Cell. 81:41–51.) was recorded with time-lapse video microscopy. The number of filopodia along the neurites was significantly greater in Gsn(−) mice and gave the neurites a studded appearance. Dynamic studies suggested that most of these filopodia were formed from the region of the growth cone and remained as protrusions from the newly consolidated shaft after the growth cone advanced. Histories of individual filopodia in Gsn(−) mice revealed elongation rates that did not differ from controls but an impaired retraction phase that probably accounted for the increased number of filopodia long the neutrite shaft. Gelsolin appears to function in the initiation of filopodial retraction and in its smooth progression. |
format | Text |
id | pubmed-2132546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21325462008-05-01 Delayed Retraction of Filopodia in Gelsolin Null Mice Lu, Mei Witke, Walter Kwiatkowski, David J. Kosik, Kenneth S. J Cell Biol Article Growth cones extend dynamic protrusions called filopodia and lamellipodia as exploratory probes that signal the direction of neurite growth. Gelsolin, as an actin filament-severing protein, may serve an important role in the rapid shape changes associated with growth cone structures. In wild-type (wt) hippocampal neurons, antibodies against gelsolin labeled the neurite shaft and growth cone. The behavior of filopodia in cultured hippocampal neurons from embryonic day 17 wt and gelsolin null (Gsn(−)) mice (Witke, W., A.H. Sharpe, J.H. Hartwig, T. Azuma, T.P. Stossel, and D.J. Kwiatkowski. 1995. Cell. 81:41–51.) was recorded with time-lapse video microscopy. The number of filopodia along the neurites was significantly greater in Gsn(−) mice and gave the neurites a studded appearance. Dynamic studies suggested that most of these filopodia were formed from the region of the growth cone and remained as protrusions from the newly consolidated shaft after the growth cone advanced. Histories of individual filopodia in Gsn(−) mice revealed elongation rates that did not differ from controls but an impaired retraction phase that probably accounted for the increased number of filopodia long the neutrite shaft. Gelsolin appears to function in the initiation of filopodial retraction and in its smooth progression. The Rockefeller University Press 1997-09-22 /pmc/articles/PMC2132546/ /pubmed/9298983 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 | Article Lu, Mei Witke, Walter Kwiatkowski, David J. Kosik, Kenneth S. Delayed Retraction of Filopodia in Gelsolin Null Mice |
title | Delayed Retraction of Filopodia in Gelsolin Null Mice |
title_full | Delayed Retraction of Filopodia in Gelsolin Null Mice |
title_fullStr | Delayed Retraction of Filopodia in Gelsolin Null Mice |
title_full_unstemmed | Delayed Retraction of Filopodia in Gelsolin Null Mice |
title_short | Delayed Retraction of Filopodia in Gelsolin Null Mice |
title_sort | delayed retraction of filopodia in gelsolin null mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132546/ https://www.ncbi.nlm.nih.gov/pubmed/9298983 |
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