Neural regeneration dynamics of Xenopus laevis olfactory epithelium after zinc sulfate-induced damage

Neural stem cells (NSCs) of the olfactory epithelium (OE) are responsible for tissue maintenance and the neural regeneration after severe damage of the tissue. In the normal OE, NSCs are located in the basal layer, olfactory receptor neurons (ORNs) mainly in the middle layer, and sustentacular (SUS)...

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Autor principal: Frontera, J.L
Otros Autores: Raices, M., Cervino, A.S, Pozzi, A.G, Paz, D.A
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier B.V. 2016
Acceso en línea:Registro en Scopus
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024 7 |2 scopus  |a 2-s2.0-84962683231 
024 7 |2 cas  |a zinc sulfate, 7733-02-0; Zinc Sulfate 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JCNAE 
100 1 |a Frontera, J.L. 
245 1 0 |a Neural regeneration dynamics of Xenopus laevis olfactory epithelium after zinc sulfate-induced damage 
260 |b Elsevier B.V.  |c 2016 
270 1 0 |m Paz, D.A.; IFIBYNE-CONICET, Pabellón 2, Piso 4, Ciudad Universitaria, Argentina; email: dante@bg.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Neural stem cells (NSCs) of the olfactory epithelium (OE) are responsible for tissue maintenance and the neural regeneration after severe damage of the tissue. In the normal OE, NSCs are located in the basal layer, olfactory receptor neurons (ORNs) mainly in the middle layer, and sustentacular (SUS) cells in the most apical olfactory layer. In this work, we induced severe damage of the OE through treatment with a zinc sulfate (ZnSO4) solution directly in the medium, which resulted in the loss of ORNs and SUS cells, but retention of the basal layer. During recovery following injury, the OE exhibited increased proliferation of NSCs and rapid neural regeneration. After 24 h of recovery, new ORNs and SUS cells were observed. Normal morphology and olfactory function were reached after 168 h (7 days) of recovery after ZnSO4 treatment. Taken together, these data support the hypothesis that NSCs in the basal layer activate after OE injury and that these are sufficient for complete neural regeneration and olfactory function restoration. Our analysis provides histological and functional insights into the dynamics between olfactory neurogenesis and the neuronal integration into the neuronal circuitry of the olfactory bulb that restores the function of the olfactory system. © 2016.  |l eng 
536 |a Detalles de la financiación: Universidad de Buenos Aires, UBACyT 100148BA 
536 |a Detalles de la financiación: PIP 11220120100376 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: This study was supported by grants from Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET PIP 11220120100376 ) and Universidad de Buenos Aires (UBACyT 100148BA ). The monoclonal Cytokeratins II (1h5) and monoclonal β-tubulin (E7) developed by Michael Klymkowsly were obtained from the Developmental Studies Hybridoma Bank, developed under the auspices of the NICHD and maintained by the University of Iowa, Department of Biology, Iowa City, IA, USA. The authors are grateful to Dr. Itzick Vatnick from Widener University, Chester, PA, USA, for the critical reading of this manuscript. 
593 |a Departamento de Fisiología, Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina 
593 |a Departamento de Biodiversidad y Biología Experimental, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina 
593 |a Instituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE-CONICET), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina 
690 1 0 |a NEURAL STEM CELLS 
690 1 0 |a NEUROGENESIS 
690 1 0 |a OLFACTION 
690 1 0 |a OLFACTORY INJURY 
690 1 0 |a OLFACTORY RECEPTOR NEURONS 
690 1 0 |a ZINC SULFATE 
690 1 0 |a ZINC SULFATE 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL MODEL 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a BASAL CELL 
690 1 0 |a BASEMENT MEMBRANE 
690 1 0 |a CELL ACTIVATION 
690 1 0 |a CELL LOSS 
690 1 0 |a CELL MATURATION 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a CELL REGENERATION 
690 1 0 |a CELL STRUCTURE 
690 1 0 |a CELLS 
690 1 0 |a CELLULAR DISTRIBUTION 
690 1 0 |a CONCENTRATION (PARAMETERS) 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CONVALESCENCE 
690 1 0 |a EMBRYO 
690 1 0 |a EPITHELIUM CELL 
690 1 0 |a NERVE CELL DIFFERENTIATION 
690 1 0 |a NERVE REGENERATION 
690 1 0 |a NEURAL STEM CELL 
690 1 0 |a NEUROEPITHELIUM 
690 1 0 |a NONHUMAN 
690 1 0 |a OLFACTORY BULB 
690 1 0 |a OLFACTORY EPITHELIUM 
690 1 0 |a OLFACTORY NERVE INJURY 
690 1 0 |a OLFACTORY RECEPTOR 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a SENSORY STIMULATION 
690 1 0 |a SMELLING 
690 1 0 |a SUSTENTACULAR CELL 
690 1 0 |a TADPOLE 
690 1 0 |a THICKNESS 
690 1 0 |a TISSUE REGENERATION 
690 1 0 |a TISSUE STRUCTURE 
690 1 0 |a XENOPUS LAEVIS 
690 1 0 |a ANIMAL 
690 1 0 |a CHEEK 
690 1 0 |a DRUG EFFECTS 
690 1 0 |a GROWTH, DEVELOPMENT AND AGING 
690 1 0 |a NERVOUS SYSTEM DEVELOPMENT 
690 1 0 |a OLFACTORY MUCOSA 
690 1 0 |a OLFACTORY RECEPTOR NEURON 
690 1 0 |a PHYSIOLOGY 
690 1 0 |a ANIMALS 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a CHEEK 
690 1 0 |a NERVE REGENERATION 
690 1 0 |a NEURAL STEM CELLS 
690 1 0 |a NEUROGENESIS 
690 1 0 |a OLFACTORY BULB 
690 1 0 |a OLFACTORY MUCOSA 
690 1 0 |a OLFACTORY RECEPTOR NEURONS 
690 1 0 |a XENOPUS LAEVIS 
690 1 0 |a ZINC SULFATE 
700 1 |a Raices, M. 
700 1 |a Cervino, A.S. 
700 1 |a Pozzi, A.G. 
700 1 |a Paz, D.A. 
773 0 |d Elsevier B.V., 2016  |g v. 77  |h pp. 1-9  |p J. Chem. Neuroanat.  |x 08910618  |w (AR-BaUEN)CENRE-5470  |t Journal of Chemical Neuroanatomy 
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