Olfactory ensheathing cells (OECs) are glial cells that are an attractive candidate for neural repair after spinal cord injury and for remyelination of axons in diseases such as multiple sclerosis. OECs appear to migrate within the adult mammalian central nervous system (CNS) in animal models of spinal cord injury, but until recently there has been no systematic examination of the factors inducing or guiding this migration. Previous work in our lab (V.Skihar) implicated microglial reactivity in the generation of a migratory signal(s) inducing OECs to migrate towards an ethidium bromide-induced focal demyelination in the adult rat spinal cord. The long-term objective of this research project was to test the hypothesis that reactive microglial provide a migratory signal(s) driving the migration of OECs within the spinal cord of adult rats.<p>The first set of experiments determined the time-frame in which Wallerian degeneration (WD) induced microglial reactivity occurs in the right dorsal corticospinal tract (dCST) of adult rats at the level of T11 following aspiration of the contralateral sensorimotor cortex. This timing data from this study demonstrated a prominent microglial activation in the right dCST of T11 eight weeks after sensorimotor cortex injury indicating the microglial response to WD of dCST axons was very slow to appear. The second set of experiments determined whether OECs were induced to migrate in response to WD-induced microglial reactivity in the dCST, which based on the first set of experiments was known to occur within 8 weeks of lesioning the left sensorimotor cortex. This second set of experiments also examined the migratory path taken by OECs with respect to the location of reactive microglia (i.e. inside vs outside the right dCST). For these experiments, the left sensorimotor cortex was damaged 8 weeks prior to grafting the OECs at T12. <p>The next group of experiments examined the contribution of TNF-á induced microglial reactivity to generation of a migratory signal. First we identified concentrations of TNF-á that when injected into the DF of the T11 spinal cord segment of an adult rat induced microglial reactivity either along at least a 5 mm distance from the injection site or confined to the immediate vicinity of the injection site. The result of this experiment identified a concentration of 1 ng/µl and 0.01 ng/µl TNF-á as appropriate concentrations to induce the appropriate amount of microglial reactivity, respectively. The final set of experiments used these two concentrations to determine whether TNF-á induced microglial reactivity that is initiated 5 mm rostral to a DiI+ve OEC graft generates a migratory signal(s) inducing OECs to migrate towards the rostral part of T11 and whether the migratory signal(s) was present only if the microglial reactivity extended the full 5 mm distance between the TNF-á injection and the OEC graft. <p>The major findings were: i) there was a significantly higher density of DiI+ve OECs within the right dCST of rats in which there was WD-induced microglial reactivity as compared to the right dCST of rats in which there was no microglial reactivity; ii) the migratory path taken by DiI+ve OECs was preferentially within areas containing reactive microglia (i.e. dCST) and towards the site of TNF-á induced microglial reactivity (i.e. rostral to cell graft as opposed to caudal); iii) significantly more DiI+ve OECs migrated towards the site of a TNF-á injection when the microglia were reactive along the entire length of the migratory path between the cytokine injection and cell graft; and iv) minocycline treatment both dampened microglial reactivity and significantly reduced the number of migrating DiI+ve OECs. The major conclusions are that the migration of OECs within the adult rat spinal cord occurs in response to migratory signal(s) arising as a result of microglial activation and that this migration occurs preferentially along the path of microglial reactivity.

Olfactory ensheathing cells (OECs) are glial cells that are an attractive candidate for neural repair after spinal cord injury and for remyelination of axons in diseases such as multiple sclerosis. OECs appear to migrate within the adult mammalian central nervous system (CNS) in animal models of spinal cord injury, but until recently there has been no systematic examination of the factors inducing or guiding this migration. Previous work in our lab (V.Skihar) implicated microglial reactivity in the generation of a migratory signal(s) inducing OECs to migrate towards an ethidium bromide-induced focal demyelination in the adult rat spinal cord. The long-term objective of this research project was to test the hypothesis that reactive microglial provide a migratory signal(s) driving the migration of OECs within the spinal cord of adult rats.<p>The first set of experiments determined the time-frame in which Wallerian degeneration (WD) induced microglial reactivity occurs in the right dorsal corticospinal tract (dCST) of adult rats at the level of T11 following aspiration of the contralateral sensorimotor cortex. This timing data from this study demonstrated a prominent microglial activation in the right dCST of T11 eight weeks after sensorimotor cortex injury indicating the microglial response to WD of dCST axons was very slow to appear. The second set of experiments determined whether OECs were induced to migrate in response to WD-induced microglial reactivity in the dCST, which based on the first set of experiments was known to occur within 8 weeks of lesioning the left sensorimotor cortex. This second set of experiments also examined the migratory path taken by OECs with respect to the location of reactive microglia (i.e. inside vs outside the right dCST). For these experiments, the left sensorimotor cortex was damaged 8 weeks prior to grafting the OECs at T12. <p>The next group of experiments examined the contribution of TNF-á induced microglial reactivity to generation of a migratory signal. First we identified concentrations of TNF-á that when injected into the DF of the T11 spinal cord segment of an adult rat induced microglial reactivity either along at least a 5 mm distance from the injection site or confined to the immediate vicinity of the injection site. The result of this experiment identified a concentration of 1 ng/µl and 0.01 ng/µl TNF-á as appropriate concentrations to induce the appropriate amount of microglial reactivity, respectively. The final set of experiments used these two concentrations to determine whether TNF-á induced microglial reactivity that is initiated 5 mm rostral to a DiI+ve OEC graft generates a migratory signal(s) inducing OECs to migrate towards the rostral part of T11 and whether the migratory signal(s) was present only if the microglial reactivity extended the full 5 mm distance between the TNF-á injection and the OEC graft. <p>The major findings were: i) there was a significantly higher density of DiI+ve OECs within the right dCST of rats in which there was WD-induced microglial reactivity as compared to the right dCST of rats in which there was no microglial reactivity; ii) the migratory path taken by DiI+ve OECs was preferentially within areas containing reactive microglia (i.e. dCST) and towards the site of TNF-á induced microglial reactivity (i.e. rostral to cell graft as opposed to caudal); iii) significantly more DiI+ve OECs migrated towards the site of a TNF-á injection when the microglia were reactive along the entire length of the migratory path between the cytokine injection and cell graft; and iv) minocycline treatment both dampened microglial reactivity and significantly reduced the number of migrating DiI+ve OECs. The major conclusions are that the migration of OECs within the adult rat spinal cord occurs in response to migratory signal(s) arising as a result of microglial activation and that this migration occurs preferentially along the path of microglial reactivity.

O objetivo desta Tese foi analisar os efeitos do treino de marcha isolado e em combinação com transplante de glia embainhante olfatória (GEO) na recuperação funcional e na plasticidade neuromuscular dependente da atividade em um modelo experimental de paraplegia. Para tanto, foram realizados 2 experimentos. No 1º experimento foi realizada completa transecção da medula espinal (TME) em ratos Wistar adultos e após 5 dias iniciou-se um protocolo de 9 semanas de treino de marcha em esteira com suporte de peso corporal. No 2º experimento, os animais receberam, imediatamente após a TME, transplante de células gliais embainhantes olfatórias (GEO) e, como no primeiro experimento, iniciaram o treino de marcha 5 dias após a lesão/transplante. Durante o período dos experimentos, estudos comportamentais para acompanhamento da recuperação da função sensório-motora dos animais foram periodicamente realizados. Além disso, ao término da fase de treinamento (10 semanas após a lesão/transplante), análises histológicas e bioquímicas foram realizadas em amostras de tecido retiradas da medula espinal e músculo sóleo. Os resultados mostram que o treino de marcha em esteira promove melhora da função sensório-motora nos membros posteriores (MPs) de ratos com completa transecção da medula espinal (TME). Os animais treinados apresentaram escores mais altos na escala BBB e normalização do reflexo flexor de retirada. Além disso, os animais com TME apresentaram atrofia do soma celular nos motoneurônios alfa, redução na expressão de sinaptofisina e na atividade da Na+,K+-ATPase na região lombar. Os animais treinados mostraram soma motoneuronal, expressão de sinaptofisina e atividade da bomba de Na+,K+-ATPase similares aos controles. No músculo sóleo, a TME causou severa atrofia muscular, que foi acompanhada pela redução na expressão do fator neurotrófico derivado do encéfalo (BDNF) neste músculo. Por outro lado, o treino de marcha foi capaz de parcialmente impedir/reverter a atrofia provocada pela paralisia muscular e promover um significante aumento na expressão do BDNF, o qual teve positiva correlação com o trofismo muscular dependente da atividade motora no músculo sóleo. O transplante de glia embainhante olfatória (GEO) promoveu significativo aumento nos escores da escala BBB nos animais com completa TME. Entretanto, o treino de marcha foi capaz de acelerar este ganho funcional. Apesar de não ser observada significativa regeneração axonal através do local da lesão, sugerindo que as melhoras funcionais ocorreram independentemente da existência de regeneração axonal. Estes resultados sugerem que o treino de marcha após a TME promove plasticidade morfológica e bioquímica dependente da atividade nos tecidos neuromusculares. A melhora funcional ocorreu concomitantemente a estas alterações plásticas. Além disso, a terapia de transplante de GEO mostrou resultados positivos na recuperação da função motora dos MPs que foi acelerada pelo treino de marcha, mesmo na ausência de regeneração axonal através da lesão. Estes dados mostram importantes informações neurobiológicas que fornecem base neurocientífica para o uso seguro e eficaz destas terapias na reabilitação após LME. / The aim of this thesis was to study the effects of treadmill step training alone and in combination with olfactory ensheathing cells (OEC) on functional recovery and activity-dependent neuromuscular plasticity in a traumatic paraplegia model. For this, we made two experiments. In the 1st experiment, complete spinal cord transection (SCT) was made in adult Wistar rats and after 5 days the spinal animals were underwent a 9 week body-weight-supported treadmill training (BWSTT) program. In the 2nd experiment, the spinal animals received acute olfactory ensheathing cell (OEC) transplantation and, similar to the 1st experiment, started a BWSTT 5 days after the injury/transplantation. Behavioral tests were periodically performed in order to study the hindlimb sensorimotor functions in both experiments. Furthermore, after 9 weeks of the training (10 weeks after SCI/transplantation), histological and biochemical analysis were performed in spinal cord and soleus muscle tissues. The results show that treadmill step training improves hindlimb sensorimotor function in rats with complete spinal cord transection (SCT). The trained animals showed higher BBB scores and normalization of the withdrawal reflex. Furthermore, spinal animals showed alpha motoneuron soma size atrophy, decrease in synaptophysin expression and Na+,K+-ATPase activity in lumbar spinal cord. Trained SCT animals showed motoneuron soma size, synaptophysin expression and Na+,K+-ATPase activity values similar to controls. In soleus muscle, SCT led to severe muscular atrophy, which was accompanied by a decrease in brain-derived neurotrophic factor (BDNF) expression in this muscle. On the other hand, treadmill step training was able to revert/prevent this paralysis-induced muscular atrophy and promote significant improvement in soleus BDNF expression, which was positively correlated to activity-dependent muscular trophism. Olfactory ensheathing cell (OEC) transplantation promotes significant improvements in the BBB scores of animals with SCT. However, treadmill step training was able to accelerate this functional gain. There was no significant axonal regeneration that traversed the injury site, which suggests that functional gains occurred in a manner independent of axonal regeneration. Taken as a whole, these results suggest that treadmill step training after SCT promotes activity-dependent morphological and biochemical plasticity in neuromuscular tissues. The functional improvements occurred concomitantly to these plastic changes. Moreover, OEC therapy showed positive results on hindlimb motor function recovery which was accelerated with treadmill step training even in the absence of axonal regeneration across the lesion site. These results represent important neurobiological information for the neuroscientific basis that supports these therapies as an efficient and safe approach in spinal cord injury rehabilitation.

O objetivo desta Tese foi analisar os efeitos do treino de marcha isolado e em combinação com transplante de glia embainhante olfatória (GEO) na recuperação funcional e na plasticidade neuromuscular dependente da atividade em um modelo experimental de paraplegia. Para tanto, foram realizados 2 experimentos. No 1º experimento foi realizada completa transecção da medula espinal (TME) em ratos Wistar adultos e após 5 dias iniciou-se um protocolo de 9 semanas de treino de marcha em esteira com suporte de peso corporal. No 2º experimento, os animais receberam, imediatamente após a TME, transplante de células gliais embainhantes olfatórias (GEO) e, como no primeiro experimento, iniciaram o treino de marcha 5 dias após a lesão/transplante. Durante o período dos experimentos, estudos comportamentais para acompanhamento da recuperação da função sensório-motora dos animais foram periodicamente realizados. Além disso, ao término da fase de treinamento (10 semanas após a lesão/transplante), análises histológicas e bioquímicas foram realizadas em amostras de tecido retiradas da medula espinal e músculo sóleo. Os resultados mostram que o treino de marcha em esteira promove melhora da função sensório-motora nos membros posteriores (MPs) de ratos com completa transecção da medula espinal (TME). Os animais treinados apresentaram escores mais altos na escala BBB e normalização do reflexo flexor de retirada. Além disso, os animais com TME apresentaram atrofia do soma celular nos motoneurônios alfa, redução na expressão de sinaptofisina e na atividade da Na+,K+-ATPase na região lombar. Os animais treinados mostraram soma motoneuronal, expressão de sinaptofisina e atividade da bomba de Na+,K+-ATPase similares aos controles. No músculo sóleo, a TME causou severa atrofia muscular, que foi acompanhada pela redução na expressão do fator neurotrófico derivado do encéfalo (BDNF) neste músculo. Por outro lado, o treino de marcha foi capaz de parcialmente impedir/reverter a atrofia provocada pela paralisia muscular e promover um significante aumento na expressão do BDNF, o qual teve positiva correlação com o trofismo muscular dependente da atividade motora no músculo sóleo. O transplante de glia embainhante olfatória (GEO) promoveu significativo aumento nos escores da escala BBB nos animais com completa TME. Entretanto, o treino de marcha foi capaz de acelerar este ganho funcional. Apesar de não ser observada significativa regeneração axonal através do local da lesão, sugerindo que as melhoras funcionais ocorreram independentemente da existência de regeneração axonal. Estes resultados sugerem que o treino de marcha após a TME promove plasticidade morfológica e bioquímica dependente da atividade nos tecidos neuromusculares. A melhora funcional ocorreu concomitantemente a estas alterações plásticas. Além disso, a terapia de transplante de GEO mostrou resultados positivos na recuperação da função motora dos MPs que foi acelerada pelo treino de marcha, mesmo na ausência de regeneração axonal através da lesão. Estes dados mostram importantes informações neurobiológicas que fornecem base neurocientífica para o uso seguro e eficaz destas terapias na reabilitação após LME. / The aim of this thesis was to study the effects of treadmill step training alone and in combination with olfactory ensheathing cells (OEC) on functional recovery and activity-dependent neuromuscular plasticity in a traumatic paraplegia model. For this, we made two experiments. In the 1st experiment, complete spinal cord transection (SCT) was made in adult Wistar rats and after 5 days the spinal animals were underwent a 9 week body-weight-supported treadmill training (BWSTT) program. In the 2nd experiment, the spinal animals received acute olfactory ensheathing cell (OEC) transplantation and, similar to the 1st experiment, started a BWSTT 5 days after the injury/transplantation. Behavioral tests were periodically performed in order to study the hindlimb sensorimotor functions in both experiments. Furthermore, after 9 weeks of the training (10 weeks after SCI/transplantation), histological and biochemical analysis were performed in spinal cord and soleus muscle tissues. The results show that treadmill step training improves hindlimb sensorimotor function in rats with complete spinal cord transection (SCT). The trained animals showed higher BBB scores and normalization of the withdrawal reflex. Furthermore, spinal animals showed alpha motoneuron soma size atrophy, decrease in synaptophysin expression and Na+,K+-ATPase activity in lumbar spinal cord. Trained SCT animals showed motoneuron soma size, synaptophysin expression and Na+,K+-ATPase activity values similar to controls. In soleus muscle, SCT led to severe muscular atrophy, which was accompanied by a decrease in brain-derived neurotrophic factor (BDNF) expression in this muscle. On the other hand, treadmill step training was able to revert/prevent this paralysis-induced muscular atrophy and promote significant improvement in soleus BDNF expression, which was positively correlated to activity-dependent muscular trophism. Olfactory ensheathing cell (OEC) transplantation promotes significant improvements in the BBB scores of animals with SCT. However, treadmill step training was able to accelerate this functional gain. There was no significant axonal regeneration that traversed the injury site, which suggests that functional gains occurred in a manner independent of axonal regeneration. Taken as a whole, these results suggest that treadmill step training after SCT promotes activity-dependent morphological and biochemical plasticity in neuromuscular tissues. The functional improvements occurred concomitantly to these plastic changes. Moreover, OEC therapy showed positive results on hindlimb motor function recovery which was accelerated with treadmill step training even in the absence of axonal regeneration across the lesion site. These results represent important neurobiological information for the neuroscientific basis that supports these therapies as an efficient and safe approach in spinal cord injury rehabilitation.

O objetivo desta Tese foi analisar os efeitos do treino de marcha isolado e em combinação com transplante de glia embainhante olfatória (GEO) na recuperação funcional e na plasticidade neuromuscular dependente da atividade em um modelo experimental de paraplegia. Para tanto, foram realizados 2 experimentos. No 1º experimento foi realizada completa transecção da medula espinal (TME) em ratos Wistar adultos e após 5 dias iniciou-se um protocolo de 9 semanas de treino de marcha em esteira com suporte de peso corporal. No 2º experimento, os animais receberam, imediatamente após a TME, transplante de células gliais embainhantes olfatórias (GEO) e, como no primeiro experimento, iniciaram o treino de marcha 5 dias após a lesão/transplante. Durante o período dos experimentos, estudos comportamentais para acompanhamento da recuperação da função sensório-motora dos animais foram periodicamente realizados. Além disso, ao término da fase de treinamento (10 semanas após a lesão/transplante), análises histológicas e bioquímicas foram realizadas em amostras de tecido retiradas da medula espinal e músculo sóleo. Os resultados mostram que o treino de marcha em esteira promove melhora da função sensório-motora nos membros posteriores (MPs) de ratos com completa transecção da medula espinal (TME). Os animais treinados apresentaram escores mais altos na escala BBB e normalização do reflexo flexor de retirada. Além disso, os animais com TME apresentaram atrofia do soma celular nos motoneurônios alfa, redução na expressão de sinaptofisina e na atividade da Na+,K+-ATPase na região lombar. Os animais treinados mostraram soma motoneuronal, expressão de sinaptofisina e atividade da bomba de Na+,K+-ATPase similares aos controles. No músculo sóleo, a TME causou severa atrofia muscular, que foi acompanhada pela redução na expressão do fator neurotrófico derivado do encéfalo (BDNF) neste músculo. Por outro lado, o treino de marcha foi capaz de parcialmente impedir/reverter a atrofia provocada pela paralisia muscular e promover um significante aumento na expressão do BDNF, o qual teve positiva correlação com o trofismo muscular dependente da atividade motora no músculo sóleo. O transplante de glia embainhante olfatória (GEO) promoveu significativo aumento nos escores da escala BBB nos animais com completa TME. Entretanto, o treino de marcha foi capaz de acelerar este ganho funcional. Apesar de não ser observada significativa regeneração axonal através do local da lesão, sugerindo que as melhoras funcionais ocorreram independentemente da existência de regeneração axonal. Estes resultados sugerem que o treino de marcha após a TME promove plasticidade morfológica e bioquímica dependente da atividade nos tecidos neuromusculares. A melhora funcional ocorreu concomitantemente a estas alterações plásticas. Além disso, a terapia de transplante de GEO mostrou resultados positivos na recuperação da função motora dos MPs que foi acelerada pelo treino de marcha, mesmo na ausência de regeneração axonal através da lesão. Estes dados mostram importantes informações neurobiológicas que fornecem base neurocientífica para o uso seguro e eficaz destas terapias na reabilitação após LME. / The aim of this thesis was to study the effects of treadmill step training alone and in combination with olfactory ensheathing cells (OEC) on functional recovery and activity-dependent neuromuscular plasticity in a traumatic paraplegia model. For this, we made two experiments. In the 1st experiment, complete spinal cord transection (SCT) was made in adult Wistar rats and after 5 days the spinal animals were underwent a 9 week body-weight-supported treadmill training (BWSTT) program. In the 2nd experiment, the spinal animals received acute olfactory ensheathing cell (OEC) transplantation and, similar to the 1st experiment, started a BWSTT 5 days after the injury/transplantation. Behavioral tests were periodically performed in order to study the hindlimb sensorimotor functions in both experiments. Furthermore, after 9 weeks of the training (10 weeks after SCI/transplantation), histological and biochemical analysis were performed in spinal cord and soleus muscle tissues. The results show that treadmill step training improves hindlimb sensorimotor function in rats with complete spinal cord transection (SCT). The trained animals showed higher BBB scores and normalization of the withdrawal reflex. Furthermore, spinal animals showed alpha motoneuron soma size atrophy, decrease in synaptophysin expression and Na+,K+-ATPase activity in lumbar spinal cord. Trained SCT animals showed motoneuron soma size, synaptophysin expression and Na+,K+-ATPase activity values similar to controls. In soleus muscle, SCT led to severe muscular atrophy, which was accompanied by a decrease in brain-derived neurotrophic factor (BDNF) expression in this muscle. On the other hand, treadmill step training was able to revert/prevent this paralysis-induced muscular atrophy and promote significant improvement in soleus BDNF expression, which was positively correlated to activity-dependent muscular trophism. Olfactory ensheathing cell (OEC) transplantation promotes significant improvements in the BBB scores of animals with SCT. However, treadmill step training was able to accelerate this functional gain. There was no significant axonal regeneration that traversed the injury site, which suggests that functional gains occurred in a manner independent of axonal regeneration. Taken as a whole, these results suggest that treadmill step training after SCT promotes activity-dependent morphological and biochemical plasticity in neuromuscular tissues. The functional improvements occurred concomitantly to these plastic changes. Moreover, OEC therapy showed positive results on hindlimb motor function recovery which was accelerated with treadmill step training even in the absence of axonal regeneration across the lesion site. These results represent important neurobiological information for the neuroscientific basis that supports these therapies as an efficient and safe approach in spinal cord injury rehabilitation.

Les lésions médullaires traumatiques (LMT) conduisent à une atteinte des voies nerveuses sensitives et motrices. Leur taux de mortalité reste très élevé, d'où la nécessité de trouver de nouveaux traitements. Les Cellules Gliales Olfactives (CGOs) représentent un candidat intéressant de par leur fonction au sein du système olfactif primaire. La découverte d'une population de cellule souche neurale bordant le canal central de la moelle spinale (MS) adulte, appelées cellules épendymaires, suscite un nouvel espoir dans le domaine des biothérapies. Ce travail de thèse a permis d'étudier l'effet d'une transplantation de CGOs sue le comportement des cellules résidentes de la moelle spinale et notamment les cellules souches épendymaires qui, en association avec les astrocytes et les péricytes, participent aux mécanismes de guérison des LMT. L'utilisation du modèle murin hFoxJ1-CreERT2::YFP (permettant le suivi spécifique des cellules épendymaires et de leur progénie), a montré que les CGOs augmentaient in vitro le potentiel d'auto-renouvellement des cellules souches de la MS et modifiaient leur voie de différenciation vers un type neural. In vivo, la transplantation de CGOs augmente la prolifération des cellules épendymaires ainsi que leur différenciation en astrocytes hypo-réactifs conduisant à la formation d'un environnement post-lésionnel bénéfique à la survie neuronal et l'établissement d'une neurogenèse. Nos travaux ont montré pour la première fois que la transplantation de CGOs après LMT permettait la génération de nouveaux neurones. Ceci constitue un nouvel espoir dans l'établissement de stratégies thérapeutiques pour le traitement des LMT chez l'Homme. / The spinal cord injuries (SCI) lead to the damages of the spinal cord or nerves and often cause permanent changes in body functions leading to the death. Cell therapies have raised great hope for regenerative medicine. Clinical data showed that the olfactory ensheathing cells (OECs) enhanced functional recovery after SCI and could be a very attractive therapeutic approach. Moreover, the discovery of a new endogenous resident stem cell population, lining the central canal of the spinal cord, named ependymal stem cells, represents a new hope for the therapy. This thesis analyzed the role of OECs transplantation, on the behaviour of ependymal stem cells since these cells, together with astrocytes and pericytes significantly contribute to the recovery of SCI. The use of the mouse model hFoxJ1-CreERT2::YFP (allowing to specifically follow the ependymal stem cells ant their progeny) showed that OECs increased in vitro the self-renewal potential of spinal cord stem cells and modified their differentiation pathway towards a neural type. In vivo, OECs transplantation significantly increases the proliferation of ependymal cells and their differenciation into hypo-reactive astrocytes leading to the formation of a beneficial environment to neuronal survival and the neurogenesis establishment. Our results also showed for the first time that OECs transplantation after SCI allows the generation of new neurons by non-ependymal cell-derived progenitors. These results represent a new hope in the establishment of therapeutic strategies for the treatment of SCI in humans.