Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis

The olfactory epithelium (OE) has the remarkable capability to constantly replace olfactory receptor neurons (ORNs) due to the presence of neural stem cells (NSCs). For this reason, the OE provides an excellent model to study neurogenesis and neuronal differentiation. In the present work, we induced...

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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19328451_v77_n11_p1308_Cervino
http://hdl.handle.net/20.500.12110/paper_19328451_v77_n11_p1308_Cervino
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spelling paper:paper_19328451_v77_n11_p1308_Cervino2023-06-08T16:31:44Z Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis neural stem cells neurodifferentiation neurogenesis olfaction olfactory receptor neurons neuromodulin neurotrophic factor neurotrophin brain derived neurotrophic factor caspase 3 cytokeratin 2 nerve cell adhesion molecule neuromodulin olfactory marker protein animal experiment animal tissue apoptosis Article axotomy basal cell cell proliferation controlled study embryo nerve cell degeneration nerve cell differentiation nerve cell necrosis nerve regeneration nervous system development nonhuman olfactory bulb olfactory epithelium olfactory nerve olfactory receptor neuron priority journal smelling Xenopus laevis animal cell differentiation convalescence gene expression regulation metabolism nerve degeneration odor olfactory mucosa olfactory nerve injury pathology physiology regeneration time factor Xenopus laevis Animals Axotomy Brain-Derived Neurotrophic Factor Caspase 3 Cell Differentiation Cell Proliferation GAP-43 Protein Gene Expression Regulation Keratin-2 Nerve Degeneration Neural Cell Adhesion Molecules Olfactory Marker Protein Olfactory Mucosa Olfactory Nerve Injuries Recovery of Function Regeneration Smell Time Factors Xenopus laevis The olfactory epithelium (OE) has the remarkable capability to constantly replace olfactory receptor neurons (ORNs) due to the presence of neural stem cells (NSCs). For this reason, the OE provides an excellent model to study neurogenesis and neuronal differentiation. In the present work, we induced neuronal degeneration in the OE of Xenopus laevis larvae by bilateral axotomy of the olfactory nerves. We found that axotomy induces specific- neuronal death through apoptosis between 24 and 48h post-injury. In concordance, there was a progressive decrease of the mature-ORN marker OMP until it was completely absent 72h post-injury. On the other hand, neurogenesis was evident 48h post-injury by an increase in the number of proliferating basal cells as well as NCAM-180– GAP-43+ immature neurons. Mature ORNs were replenished 21 days post-injury and the olfactory function was partially recovered, indicating that new ORNs were integrated into the olfactory bulb glomeruli. Throughout the regenerative process no changes in the expression pattern of the neurotrophin Brain Derivate Neurotrophic Factor were observed. Taken together, this work provides a sequential analysis of the neurodegenerative and subsequent regenerative processes that take place in the OE following axotomy. © 2017 Wiley Periodicals, Inc. Develop Neurobiol 77: 1308–1320, 2017. © 2017 Wiley Periodicals, Inc. 2017 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19328451_v77_n11_p1308_Cervino http://hdl.handle.net/20.500.12110/paper_19328451_v77_n11_p1308_Cervino
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic neural stem cells
neurodifferentiation
neurogenesis
olfaction
olfactory receptor neurons
neuromodulin
neurotrophic factor
neurotrophin
brain derived neurotrophic factor
caspase 3
cytokeratin 2
nerve cell adhesion molecule
neuromodulin
olfactory marker protein
animal experiment
animal tissue
apoptosis
Article
axotomy
basal cell
cell proliferation
controlled study
embryo
nerve cell degeneration
nerve cell differentiation
nerve cell necrosis
nerve regeneration
nervous system development
nonhuman
olfactory bulb
olfactory epithelium
olfactory nerve
olfactory receptor neuron
priority journal
smelling
Xenopus laevis
animal
cell differentiation
convalescence
gene expression regulation
metabolism
nerve degeneration
odor
olfactory mucosa
olfactory nerve injury
pathology
physiology
regeneration
time factor
Xenopus laevis
Animals
Axotomy
Brain-Derived Neurotrophic Factor
Caspase 3
Cell Differentiation
Cell Proliferation
GAP-43 Protein
Gene Expression Regulation
Keratin-2
Nerve Degeneration
Neural Cell Adhesion Molecules
Olfactory Marker Protein
Olfactory Mucosa
Olfactory Nerve Injuries
Recovery of Function
Regeneration
Smell
Time Factors
Xenopus laevis
spellingShingle neural stem cells
neurodifferentiation
neurogenesis
olfaction
olfactory receptor neurons
neuromodulin
neurotrophic factor
neurotrophin
brain derived neurotrophic factor
caspase 3
cytokeratin 2
nerve cell adhesion molecule
neuromodulin
olfactory marker protein
animal experiment
animal tissue
apoptosis
Article
axotomy
basal cell
cell proliferation
controlled study
embryo
nerve cell degeneration
nerve cell differentiation
nerve cell necrosis
nerve regeneration
nervous system development
nonhuman
olfactory bulb
olfactory epithelium
olfactory nerve
olfactory receptor neuron
priority journal
smelling
Xenopus laevis
animal
cell differentiation
convalescence
gene expression regulation
metabolism
nerve degeneration
odor
olfactory mucosa
olfactory nerve injury
pathology
physiology
regeneration
time factor
Xenopus laevis
Animals
Axotomy
Brain-Derived Neurotrophic Factor
Caspase 3
Cell Differentiation
Cell Proliferation
GAP-43 Protein
Gene Expression Regulation
Keratin-2
Nerve Degeneration
Neural Cell Adhesion Molecules
Olfactory Marker Protein
Olfactory Mucosa
Olfactory Nerve Injuries
Recovery of Function
Regeneration
Smell
Time Factors
Xenopus laevis
Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis
topic_facet neural stem cells
neurodifferentiation
neurogenesis
olfaction
olfactory receptor neurons
neuromodulin
neurotrophic factor
neurotrophin
brain derived neurotrophic factor
caspase 3
cytokeratin 2
nerve cell adhesion molecule
neuromodulin
olfactory marker protein
animal experiment
animal tissue
apoptosis
Article
axotomy
basal cell
cell proliferation
controlled study
embryo
nerve cell degeneration
nerve cell differentiation
nerve cell necrosis
nerve regeneration
nervous system development
nonhuman
olfactory bulb
olfactory epithelium
olfactory nerve
olfactory receptor neuron
priority journal
smelling
Xenopus laevis
animal
cell differentiation
convalescence
gene expression regulation
metabolism
nerve degeneration
odor
olfactory mucosa
olfactory nerve injury
pathology
physiology
regeneration
time factor
Xenopus laevis
Animals
Axotomy
Brain-Derived Neurotrophic Factor
Caspase 3
Cell Differentiation
Cell Proliferation
GAP-43 Protein
Gene Expression Regulation
Keratin-2
Nerve Degeneration
Neural Cell Adhesion Molecules
Olfactory Marker Protein
Olfactory Mucosa
Olfactory Nerve Injuries
Recovery of Function
Regeneration
Smell
Time Factors
Xenopus laevis
description The olfactory epithelium (OE) has the remarkable capability to constantly replace olfactory receptor neurons (ORNs) due to the presence of neural stem cells (NSCs). For this reason, the OE provides an excellent model to study neurogenesis and neuronal differentiation. In the present work, we induced neuronal degeneration in the OE of Xenopus laevis larvae by bilateral axotomy of the olfactory nerves. We found that axotomy induces specific- neuronal death through apoptosis between 24 and 48h post-injury. In concordance, there was a progressive decrease of the mature-ORN marker OMP until it was completely absent 72h post-injury. On the other hand, neurogenesis was evident 48h post-injury by an increase in the number of proliferating basal cells as well as NCAM-180– GAP-43+ immature neurons. Mature ORNs were replenished 21 days post-injury and the olfactory function was partially recovered, indicating that new ORNs were integrated into the olfactory bulb glomeruli. Throughout the regenerative process no changes in the expression pattern of the neurotrophin Brain Derivate Neurotrophic Factor were observed. Taken together, this work provides a sequential analysis of the neurodegenerative and subsequent regenerative processes that take place in the OE following axotomy. © 2017 Wiley Periodicals, Inc. Develop Neurobiol 77: 1308–1320, 2017. © 2017 Wiley Periodicals, Inc.
title Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis
title_short Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis
title_full Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis
title_fullStr Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis
title_full_unstemmed Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis
title_sort neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of xenopus laevis
publishDate 2017
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19328451_v77_n11_p1308_Cervino
http://hdl.handle.net/20.500.12110/paper_19328451_v77_n11_p1308_Cervino
_version_ 1768546650230358016