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.
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22 September 1997
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September 22 1997
Delayed Retraction of Filopodia in Gelsolin Null Mice
Mei Lu,
Mei Lu
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
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Walter Witke,
Walter Witke
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
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David J. Kwiatkowski,
David J. Kwiatkowski
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
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Kenneth S. Kosik
Kenneth S. Kosik
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
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Mei Lu
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
Walter Witke
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
David J. Kwiatkowski
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
Kenneth S. Kosik
*Center for Neurologic Diseases, and ‡Division of Experimental Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115; and §Mouse Biology Programme, European Molecular Biology Laboratory, 00015 Monterotondo/Rome, Italy
Please address all correspondence to Dr. Kenneth S. Kosik, Center for Neurological Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115; Tel.: (617) 525-5230; Fax: (617) 525-5252.
M. Lu was supported by National Institutes of Health training grant (NS07009-21) through Dr. G. Strichartz. This work was supported by National Institutes of Health grants NS29031 (K.S. Kosik) and HL54188 and HL48743 (D.J. Kwiatkowski).
Received:
March 12 1997
Revision Received:
July 08 1997
Online ISSN: 1540-8140
Print ISSN: 0021-9525
1997
J Cell Biol (1997) 138 (6): 1279–1287.
Article history
Received:
March 12 1997
Revision Received:
July 08 1997
Citation
Mei Lu, Walter Witke, David J. Kwiatkowski, Kenneth S. Kosik; Delayed Retraction of Filopodia in Gelsolin Null Mice . J Cell Biol 22 September 1997; 138 (6): 1279–1287. doi: https://doi.org/10.1083/jcb.138.6.1279
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