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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Main Authors: J. Bertrand, A. Di Polo, L. McKerracher
Format: Article
Language:English
Published: Elsevier 2007-01-01
Series:Neurobiology of Disease
Subjects:
C3
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996106002117
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spelling 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
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