Cargando…

Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation

BACKGROUND: Retina and/or optic nerve injury may cause irreversible blindness, due to degeneration of retinal ganglion cells. We and others have previously shown that the intravitreal injection of mesenchymal stem cells (MSCs) protects injured retinal ganglion cells and stimulates their regeneration...

Descripción completa

Detalles Bibliográficos
Autores principales: Mesentier-Louro, Louise A., Teixeira-Pinheiro, Leandro C., Gubert, Fernanda, Vasques, Juliana F., Silva-Junior, Almir J., Chimeli-Ormonde, Luiza, Nascimento-dos-Santos, Gabriel, Mendez-Otero, Rosalia, Santiago, Marcelo F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472105/
https://www.ncbi.nlm.nih.gov/pubmed/30995945
http://dx.doi.org/10.1186/s13287-019-1226-9
_version_ 1783412179183075328
author Mesentier-Louro, Louise A.
Teixeira-Pinheiro, Leandro C.
Gubert, Fernanda
Vasques, Juliana F.
Silva-Junior, Almir J.
Chimeli-Ormonde, Luiza
Nascimento-dos-Santos, Gabriel
Mendez-Otero, Rosalia
Santiago, Marcelo F.
author_facet Mesentier-Louro, Louise A.
Teixeira-Pinheiro, Leandro C.
Gubert, Fernanda
Vasques, Juliana F.
Silva-Junior, Almir J.
Chimeli-Ormonde, Luiza
Nascimento-dos-Santos, Gabriel
Mendez-Otero, Rosalia
Santiago, Marcelo F.
author_sort Mesentier-Louro, Louise A.
collection PubMed
description BACKGROUND: Retina and/or optic nerve injury may cause irreversible blindness, due to degeneration of retinal ganglion cells. We and others have previously shown that the intravitreal injection of mesenchymal stem cells (MSCs) protects injured retinal ganglion cells and stimulates their regeneration after optic nerve injury, but the long-term effects of this therapy are still unknown. METHODS: We injected rat MSC (rMSC) intravitreally in adult (3–5 months) Lister Hooded rats of either sex after optic nerve crush. Retinal ganglion cell survival, axonal regeneration, and reconnection were analyzed 60 and 240 days after crush by immunohistochemistry for Tuj1, anterograde labeling with cholera-toxin B and by immunohistochemistry for nerve growth factor-induced gene A (NGFI-A, driven by light stimulation) in the superior colliculus after a cycle of light deprivation-stimulation. Visual behaviors (optokinetic reflex, looming response, and preference for dark) were analyzed 70 days after crush. RESULTS: rMSC treatment doubled the number of surviving retinal ganglion cells, preferentially of a larger subtype, and of axons regenerating up to 0.5 mm. Some axons regenerated to the lateral geniculate nucleus and superior colliculus. NGFI-A+ cells were doubled in rMSC-treated animals 60 days after crush, but equivalent to vehicle-injected animals 240 days after crush, suggesting that newly formed synapses degenerated. Animals did not recover visual behaviors. CONCLUSIONS: We conclude that rMSC-induced neuroprotection is sustained at longer time points. Although rMSCs promoted long-term neuroprotection and long-distance axon regeneration, the reconnection of retinal ganglion cells with their targets was transitory, indicating that they need additional stimuli to make stable reconnections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-019-1226-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6472105
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-64721052019-04-24 Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation Mesentier-Louro, Louise A. Teixeira-Pinheiro, Leandro C. Gubert, Fernanda Vasques, Juliana F. Silva-Junior, Almir J. Chimeli-Ormonde, Luiza Nascimento-dos-Santos, Gabriel Mendez-Otero, Rosalia Santiago, Marcelo F. Stem Cell Res Ther Research BACKGROUND: Retina and/or optic nerve injury may cause irreversible blindness, due to degeneration of retinal ganglion cells. We and others have previously shown that the intravitreal injection of mesenchymal stem cells (MSCs) protects injured retinal ganglion cells and stimulates their regeneration after optic nerve injury, but the long-term effects of this therapy are still unknown. METHODS: We injected rat MSC (rMSC) intravitreally in adult (3–5 months) Lister Hooded rats of either sex after optic nerve crush. Retinal ganglion cell survival, axonal regeneration, and reconnection were analyzed 60 and 240 days after crush by immunohistochemistry for Tuj1, anterograde labeling with cholera-toxin B and by immunohistochemistry for nerve growth factor-induced gene A (NGFI-A, driven by light stimulation) in the superior colliculus after a cycle of light deprivation-stimulation. Visual behaviors (optokinetic reflex, looming response, and preference for dark) were analyzed 70 days after crush. RESULTS: rMSC treatment doubled the number of surviving retinal ganglion cells, preferentially of a larger subtype, and of axons regenerating up to 0.5 mm. Some axons regenerated to the lateral geniculate nucleus and superior colliculus. NGFI-A+ cells were doubled in rMSC-treated animals 60 days after crush, but equivalent to vehicle-injected animals 240 days after crush, suggesting that newly formed synapses degenerated. Animals did not recover visual behaviors. CONCLUSIONS: We conclude that rMSC-induced neuroprotection is sustained at longer time points. Although rMSCs promoted long-term neuroprotection and long-distance axon regeneration, the reconnection of retinal ganglion cells with their targets was transitory, indicating that they need additional stimuli to make stable reconnections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-019-1226-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-17 /pmc/articles/PMC6472105/ /pubmed/30995945 http://dx.doi.org/10.1186/s13287-019-1226-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mesentier-Louro, Louise A.
Teixeira-Pinheiro, Leandro C.
Gubert, Fernanda
Vasques, Juliana F.
Silva-Junior, Almir J.
Chimeli-Ormonde, Luiza
Nascimento-dos-Santos, Gabriel
Mendez-Otero, Rosalia
Santiago, Marcelo F.
Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation
title Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation
title_full Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation
title_fullStr Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation
title_full_unstemmed Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation
title_short Long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation
title_sort long-term neuronal survival, regeneration, and transient target reconnection after optic nerve crush and mesenchymal stem cell transplantation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472105/
https://www.ncbi.nlm.nih.gov/pubmed/30995945
http://dx.doi.org/10.1186/s13287-019-1226-9
work_keys_str_mv AT mesentierlourolouisea longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT teixeirapinheiroleandroc longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT gubertfernanda longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT vasquesjulianaf longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT silvajunioralmirj longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT chimeliormondeluiza longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT nascimentodossantosgabriel longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT mendezoterorosalia longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation
AT santiagomarcelof longtermneuronalsurvivalregenerationandtransienttargetreconnectionafteropticnervecrushandmesenchymalstemcelltransplantation