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The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms

All cerebellar neurons derive from progenitors that proliferate in two germinal neuroepithelia: the ventricular zone (VZ) generates GABAergic neurons, whereas the rhombic lip is the origin of glutamatergic types. Among VZ-derivatives, GABAergic projection neurons, and interneurons are generated acco...

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Autores principales: Leto, Ketty, Rolando, Chiara, Rossi, Ferdinando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282257/
https://www.ncbi.nlm.nih.gov/pubmed/22363268
http://dx.doi.org/10.3389/fnana.2012.00006
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author Leto, Ketty
Rolando, Chiara
Rossi, Ferdinando
author_facet Leto, Ketty
Rolando, Chiara
Rossi, Ferdinando
author_sort Leto, Ketty
collection PubMed
description All cerebellar neurons derive from progenitors that proliferate in two germinal neuroepithelia: the ventricular zone (VZ) generates GABAergic neurons, whereas the rhombic lip is the origin of glutamatergic types. Among VZ-derivatives, GABAergic projection neurons, and interneurons are generated according to distinct strategies. Projection neurons (Purkinje cells and nucleo-olivary neurons) are produced at the onset of cerebellar neurogenesis by discrete progenitor pools located in distinct VZ microdomains. These cells are specified within the VZ and acquire mature phenotypes according to cell-autonomous developmental programs. On the other hand, the different categories of inhibitory interneurons derive from a single population of Pax-2-positive precursors that delaminate into the prospective white matter (PWM), where they continue to divide up to postnatal development. Heterotopic/heterochronic transplantation experiments indicate that interneuron progenitors maintain full developmental potentialities up to the end of cerebellar development and acquire mature phenotypes under the influence of environmental cues present in the PWM. Furthermore, the final fate choice occurs in postmitotic cells, rather than dividing progenitors. Extracerebellar cells grafted to the prospective cerebellar white matter are not responsive to local neurogenic cues and fail to adopt clear cerebellar identities. Conversely, cerebellar cells grafted to extracerebellar regions retain typical phenotypes of cerebellar GABAergic interneurons, but acquire type-specific traits under the influence of local cues. These findings indicate that interneuron progenitors are multipotent and sensitive to spatio-temporally patterned environmental signals that regulate the genesis of different categories of interneurons, in precise quantities and at defined times and places.
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spelling pubmed-32822572012-02-23 The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms Leto, Ketty Rolando, Chiara Rossi, Ferdinando Front Neuroanat Neuroanatomy All cerebellar neurons derive from progenitors that proliferate in two germinal neuroepithelia: the ventricular zone (VZ) generates GABAergic neurons, whereas the rhombic lip is the origin of glutamatergic types. Among VZ-derivatives, GABAergic projection neurons, and interneurons are generated according to distinct strategies. Projection neurons (Purkinje cells and nucleo-olivary neurons) are produced at the onset of cerebellar neurogenesis by discrete progenitor pools located in distinct VZ microdomains. These cells are specified within the VZ and acquire mature phenotypes according to cell-autonomous developmental programs. On the other hand, the different categories of inhibitory interneurons derive from a single population of Pax-2-positive precursors that delaminate into the prospective white matter (PWM), where they continue to divide up to postnatal development. Heterotopic/heterochronic transplantation experiments indicate that interneuron progenitors maintain full developmental potentialities up to the end of cerebellar development and acquire mature phenotypes under the influence of environmental cues present in the PWM. Furthermore, the final fate choice occurs in postmitotic cells, rather than dividing progenitors. Extracerebellar cells grafted to the prospective cerebellar white matter are not responsive to local neurogenic cues and fail to adopt clear cerebellar identities. Conversely, cerebellar cells grafted to extracerebellar regions retain typical phenotypes of cerebellar GABAergic interneurons, but acquire type-specific traits under the influence of local cues. These findings indicate that interneuron progenitors are multipotent and sensitive to spatio-temporally patterned environmental signals that regulate the genesis of different categories of interneurons, in precise quantities and at defined times and places. Frontiers Research Foundation 2012-02-20 /pmc/articles/PMC3282257/ /pubmed/22363268 http://dx.doi.org/10.3389/fnana.2012.00006 Text en Copyright © 2012 Leto, Rolando and Rossi. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroanatomy
Leto, Ketty
Rolando, Chiara
Rossi, Ferdinando
The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms
title The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms
title_full The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms
title_fullStr The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms
title_full_unstemmed The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms
title_short The Genesis of Cerebellar GABAergic Neurons: Fate Potential and Specification Mechanisms
title_sort genesis of cerebellar gabaergic neurons: fate potential and specification mechanisms
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282257/
https://www.ncbi.nlm.nih.gov/pubmed/22363268
http://dx.doi.org/10.3389/fnana.2012.00006
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