Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists
Inactivation of Rho GTPase with a single intraocular injection of Rho antagonists stimulates survival and regeneration of retinal ganglion cells (RGCs) after optic nerve injury. However, this effect is short-lived. Here we tested the impact of multiple injections of C3-like Rho antagonists on RGC vi...
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doaj-b3882d7549464d8190f0a49e0e7295c82021-03-20T04:53:30ZengElsevierNeurobiology of Disease1095-953X2007-01-012516572Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonistsJ. Bertrand0A. Di Polo1L. McKerracher2Université de Montréal, Département de Pathologie et biologie cellulaire, 2900 Edouard Montpetit, Pavillon Roger-Gaudry, S-520, Montréal, Québec, Canada H3T 1J4Corresponding author. Fax: +514 343 5755.; Université de Montréal, Département de Pathologie et biologie cellulaire, 2900 Edouard Montpetit, Pavillon Roger-Gaudry, S-520, Montréal, Québec, Canada H3T 1J4Université de Montréal, Département de Pathologie et biologie cellulaire, 2900 Edouard Montpetit, Pavillon Roger-Gaudry, S-520, Montréal, Québec, Canada H3T 1J4Inactivation of Rho GTPase with a single intraocular injection of Rho antagonists stimulates survival and regeneration of retinal ganglion cells (RGCs) after optic nerve injury. However, this effect is short-lived. Here we tested the impact of multiple injections of C3-like Rho antagonists on RGC viability and axon regeneration after optic nerve lesion. Our data show that both neuronal survival and axon regeneration were enhanced with repeated delivery of cell-permeable C3. We found an ∼1.5-fold increase in RCG survival when additional Rho antagonist injections were performed after the first week from the time of lesion. In contrast, increased regeneration required early inactivation of Rho and injections performed in the second week did not further enhance regenerative outcome. These results reveal differences in the length of the therapeutic windows through which Rho inactivation acts on RGC survival or regeneration after axotomy.http://www.sciencedirect.com/science/article/pii/S0969996106002117Rho GTPaseRetinal ganglion cell (RGC)Optic nerveNeuroprotectionRegenerationC3 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
J. Bertrand A. Di Polo L. McKerracher |
spellingShingle |
J. Bertrand A. Di Polo L. McKerracher Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists Neurobiology of Disease Rho GTPase Retinal ganglion cell (RGC) Optic nerve Neuroprotection Regeneration C3 |
author_facet |
J. Bertrand A. Di Polo L. McKerracher |
author_sort |
J. Bertrand |
title |
Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists |
title_short |
Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists |
title_full |
Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists |
title_fullStr |
Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists |
title_full_unstemmed |
Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists |
title_sort |
enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable c3-like rho antagonists |
publisher |
Elsevier |
series |
Neurobiology of Disease |
issn |
1095-953X |
publishDate |
2007-01-01 |
description |
Inactivation of Rho GTPase with a single intraocular injection of Rho antagonists stimulates survival and regeneration of retinal ganglion cells (RGCs) after optic nerve injury. However, this effect is short-lived. Here we tested the impact of multiple injections of C3-like Rho antagonists on RGC viability and axon regeneration after optic nerve lesion. Our data show that both neuronal survival and axon regeneration were enhanced with repeated delivery of cell-permeable C3. We found an ∼1.5-fold increase in RCG survival when additional Rho antagonist injections were performed after the first week from the time of lesion. In contrast, increased regeneration required early inactivation of Rho and injections performed in the second week did not further enhance regenerative outcome. These results reveal differences in the length of the therapeutic windows through which Rho inactivation acts on RGC survival or regeneration after axotomy. |
topic |
Rho GTPase Retinal ganglion cell (RGC) Optic nerve Neuroprotection Regeneration C3 |
url |
http://www.sciencedirect.com/science/article/pii/S0969996106002117 |
work_keys_str_mv |
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