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Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death

BACKGROUND: For the establishment of functional neural circuits that support a wide range of animal behaviors, initial circuits formed in early development have to be reorganized. One way to achieve this is local remodeling of the circuitry hardwiring. To genetically investigate the underlying mecha...

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Autores principales: Shimono, Kohei, Fujimoto, Azusa, Tsuyama, Taiichi, Yamamoto-Kochi, Misato, Sato, Motohiko, Hattori, Yukako, Sugimura, Kaoru, Usui, Tadao, Kimura, Ken-ichi, Uemura, Tadashi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762467/
https://www.ncbi.nlm.nih.gov/pubmed/19799768
http://dx.doi.org/10.1186/1749-8104-4-37
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author Shimono, Kohei
Fujimoto, Azusa
Tsuyama, Taiichi
Yamamoto-Kochi, Misato
Sato, Motohiko
Hattori, Yukako
Sugimura, Kaoru
Usui, Tadao
Kimura, Ken-ichi
Uemura, Tadashi
author_facet Shimono, Kohei
Fujimoto, Azusa
Tsuyama, Taiichi
Yamamoto-Kochi, Misato
Sato, Motohiko
Hattori, Yukako
Sugimura, Kaoru
Usui, Tadao
Kimura, Ken-ichi
Uemura, Tadashi
author_sort Shimono, Kohei
collection PubMed
description BACKGROUND: For the establishment of functional neural circuits that support a wide range of animal behaviors, initial circuits formed in early development have to be reorganized. One way to achieve this is local remodeling of the circuitry hardwiring. To genetically investigate the underlying mechanisms of this remodeling, one model system employs a major group of Drosophila multidendritic sensory neurons - the dendritic arborization (da) neurons - which exhibit dramatic dendritic pruning and subsequent growth during metamorphosis. The 15 da neurons are identified in each larval abdominal hemisegment and are classified into four categories - classes I to IV - in order of increasing size of their receptive fields and/or arbor complexity at the mature larval stage. Our knowledge regarding the anatomy and developmental basis of adult da neurons is still fragmentary. RESULTS: We identified multidendritic neurons in the adult Drosophila abdomen, visualized the dendritic arbors of the individual neurons, and traced the origins of those cells back to the larval stage. There were six da neurons in abdominal hemisegment 3 or 4 (A3/4) of the pharate adult and the adult just after eclosion, five of which were persistent larval da neurons. We quantitatively analyzed dendritic arbors of three of the six adult neurons and examined expression in the pharate adult of key transcription factors that result in the larval class-selective dendritic morphologies. The 'baseline design' of A3/4 in the adult was further modified in a segment-dependent and age-dependent manner. One of our notable findings is that a larval class I neuron, ddaE, completed dendritic remodeling in A2 to A4 and then underwent caspase-dependent cell death within 1 week after eclosion, while homologous neurons in A5 and in more posterior segments degenerated at pupal stages. Another finding is that the dendritic arbor of a class IV neuron, v'ada, was immediately reshaped during post-eclosion growth. It exhibited prominent radial-to-lattice transformation in 1-day-old adults, and the resultant lattice-shaped arbor persisted throughout adult life. CONCLUSION: Our study provides the basis on which we can investigate the genetic programs controlling dendritic remodeling and programmed cell death of adult neurons, and the life-long maintenance of dendritic arbors.
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spelling pubmed-27624672009-10-16 Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death Shimono, Kohei Fujimoto, Azusa Tsuyama, Taiichi Yamamoto-Kochi, Misato Sato, Motohiko Hattori, Yukako Sugimura, Kaoru Usui, Tadao Kimura, Ken-ichi Uemura, Tadashi Neural Dev Research Article BACKGROUND: For the establishment of functional neural circuits that support a wide range of animal behaviors, initial circuits formed in early development have to be reorganized. One way to achieve this is local remodeling of the circuitry hardwiring. To genetically investigate the underlying mechanisms of this remodeling, one model system employs a major group of Drosophila multidendritic sensory neurons - the dendritic arborization (da) neurons - which exhibit dramatic dendritic pruning and subsequent growth during metamorphosis. The 15 da neurons are identified in each larval abdominal hemisegment and are classified into four categories - classes I to IV - in order of increasing size of their receptive fields and/or arbor complexity at the mature larval stage. Our knowledge regarding the anatomy and developmental basis of adult da neurons is still fragmentary. RESULTS: We identified multidendritic neurons in the adult Drosophila abdomen, visualized the dendritic arbors of the individual neurons, and traced the origins of those cells back to the larval stage. There were six da neurons in abdominal hemisegment 3 or 4 (A3/4) of the pharate adult and the adult just after eclosion, five of which were persistent larval da neurons. We quantitatively analyzed dendritic arbors of three of the six adult neurons and examined expression in the pharate adult of key transcription factors that result in the larval class-selective dendritic morphologies. The 'baseline design' of A3/4 in the adult was further modified in a segment-dependent and age-dependent manner. One of our notable findings is that a larval class I neuron, ddaE, completed dendritic remodeling in A2 to A4 and then underwent caspase-dependent cell death within 1 week after eclosion, while homologous neurons in A5 and in more posterior segments degenerated at pupal stages. Another finding is that the dendritic arbor of a class IV neuron, v'ada, was immediately reshaped during post-eclosion growth. It exhibited prominent radial-to-lattice transformation in 1-day-old adults, and the resultant lattice-shaped arbor persisted throughout adult life. CONCLUSION: Our study provides the basis on which we can investigate the genetic programs controlling dendritic remodeling and programmed cell death of adult neurons, and the life-long maintenance of dendritic arbors. BioMed Central 2009-10-02 /pmc/articles/PMC2762467/ /pubmed/19799768 http://dx.doi.org/10.1186/1749-8104-4-37 Text en Copyright © 2009 Shimono et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shimono, Kohei
Fujimoto, Azusa
Tsuyama, Taiichi
Yamamoto-Kochi, Misato
Sato, Motohiko
Hattori, Yukako
Sugimura, Kaoru
Usui, Tadao
Kimura, Ken-ichi
Uemura, Tadashi
Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death
title Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death
title_full Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death
title_fullStr Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death
title_full_unstemmed Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death
title_short Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death
title_sort multidendritic sensory neurons in the adult drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762467/
https://www.ncbi.nlm.nih.gov/pubmed/19799768
http://dx.doi.org/10.1186/1749-8104-4-37
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