Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers

The hypothesis of a common origin for the high-order memory centers in bilateral animals is based on the evidence that several key features, including gene expression and neuronal network patterns, are shared across several phyla. Central to this hypothesis is the assumption that the arthropods'...

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Autores principales: Maza, Francisco Javier, Sztarker, Julieta, Locatelli, Fernando Federico, Delorenzi, Alejandro
Publicado: 2016
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00278424_v113_n49_pE7957_Maza
http://hdl.handle.net/20.500.12110/paper_00278424_v113_n49_pE7957_Maza
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spelling paper:paper_00278424_v113_n49_pE7957_Maza2023-06-08T14:54:32Z Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers Maza, Francisco Javier Sztarker, Julieta Locatelli, Fernando Federico Delorenzi, Alejandro Arthropoda Evolution Homology In vivo Ca2+ imaging Memory centers allatostatin calcium synapsin Article controlled study crab escape behavior hippocampus histology immunohistochemistry immunoreactivity long term memory mechanical stimulation memory mushroom body nerve cell nerve cell plasticity nervous system development neuropil nonhuman priority journal protein expression short term memory stimulus synapse vesicle visual stimulation animal Decapoda (Crustacea) male memory mushroom body physiology Animals Decapoda (Crustacea) Male Memory Mushroom Bodies Neuronal Plasticity The hypothesis of a common origin for the high-order memory centers in bilateral animals is based on the evidence that several key features, including gene expression and neuronal network patterns, are shared across several phyla. Central to this hypothesis is the assumption that the arthropods' higher order neuropils of the forebrain [the mushroom bodies (MBs) of insects and the hemiellipsoid bodies (HBs) of crustaceans] are homologous structures. However, even though involvement in memory processes has been repeatedly demonstrated for the MBs, direct proof of such a role in HBs is lacking. Here, through neuroanatomical and immunohistochemical analysis, we identified, in the crab Neohelice granulata, HBs that resemble the calyxless MBs found in several insects. Using in vivo calcium imaging, we revealed training-dependent changes in neuronal responses of vertical and medial lobes of the HBs. These changes were stimulus-specific, and, like in the hippocampus and MBs, the changes reflected the context attribute of the memory trace, which has been envisioned as an essential feature for the HBs. The present study constitutes functional evidence in favor of a role for the HBs in memory processes, and provides key physiological evidence supporting a common origin of the arthropods' high-order memory centers. Fil:Maza, F.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Sztarker, J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Locatelli, F.F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Delorenzi, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2016 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00278424_v113_n49_pE7957_Maza http://hdl.handle.net/20.500.12110/paper_00278424_v113_n49_pE7957_Maza
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Arthropoda
Evolution
Homology
In vivo Ca2+ imaging
Memory centers
allatostatin
calcium
synapsin
Article
controlled study
crab
escape behavior
hippocampus
histology
immunohistochemistry
immunoreactivity
long term memory
mechanical stimulation
memory
mushroom body
nerve cell
nerve cell plasticity
nervous system development
neuropil
nonhuman
priority journal
protein expression
short term memory
stimulus
synapse vesicle
visual stimulation
animal
Decapoda (Crustacea)
male
memory
mushroom body
physiology
Animals
Decapoda (Crustacea)
Male
Memory
Mushroom Bodies
Neuronal Plasticity
spellingShingle Arthropoda
Evolution
Homology
In vivo Ca2+ imaging
Memory centers
allatostatin
calcium
synapsin
Article
controlled study
crab
escape behavior
hippocampus
histology
immunohistochemistry
immunoreactivity
long term memory
mechanical stimulation
memory
mushroom body
nerve cell
nerve cell plasticity
nervous system development
neuropil
nonhuman
priority journal
protein expression
short term memory
stimulus
synapse vesicle
visual stimulation
animal
Decapoda (Crustacea)
male
memory
mushroom body
physiology
Animals
Decapoda (Crustacea)
Male
Memory
Mushroom Bodies
Neuronal Plasticity
Maza, Francisco Javier
Sztarker, Julieta
Locatelli, Fernando Federico
Delorenzi, Alejandro
Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers
topic_facet Arthropoda
Evolution
Homology
In vivo Ca2+ imaging
Memory centers
allatostatin
calcium
synapsin
Article
controlled study
crab
escape behavior
hippocampus
histology
immunohistochemistry
immunoreactivity
long term memory
mechanical stimulation
memory
mushroom body
nerve cell
nerve cell plasticity
nervous system development
neuropil
nonhuman
priority journal
protein expression
short term memory
stimulus
synapse vesicle
visual stimulation
animal
Decapoda (Crustacea)
male
memory
mushroom body
physiology
Animals
Decapoda (Crustacea)
Male
Memory
Mushroom Bodies
Neuronal Plasticity
description The hypothesis of a common origin for the high-order memory centers in bilateral animals is based on the evidence that several key features, including gene expression and neuronal network patterns, are shared across several phyla. Central to this hypothesis is the assumption that the arthropods' higher order neuropils of the forebrain [the mushroom bodies (MBs) of insects and the hemiellipsoid bodies (HBs) of crustaceans] are homologous structures. However, even though involvement in memory processes has been repeatedly demonstrated for the MBs, direct proof of such a role in HBs is lacking. Here, through neuroanatomical and immunohistochemical analysis, we identified, in the crab Neohelice granulata, HBs that resemble the calyxless MBs found in several insects. Using in vivo calcium imaging, we revealed training-dependent changes in neuronal responses of vertical and medial lobes of the HBs. These changes were stimulus-specific, and, like in the hippocampus and MBs, the changes reflected the context attribute of the memory trace, which has been envisioned as an essential feature for the HBs. The present study constitutes functional evidence in favor of a role for the HBs in memory processes, and provides key physiological evidence supporting a common origin of the arthropods' high-order memory centers.
author Maza, Francisco Javier
Sztarker, Julieta
Locatelli, Fernando Federico
Delorenzi, Alejandro
author_facet Maza, Francisco Javier
Sztarker, Julieta
Locatelli, Fernando Federico
Delorenzi, Alejandro
author_sort Maza, Francisco Javier
title Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers
title_short Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers
title_full Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers
title_fullStr Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers
title_full_unstemmed Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers
title_sort context-dependent memory traces in the crab's mushroom bodies: functional support for a common origin of high-order memory centers
publishDate 2016
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00278424_v113_n49_pE7957_Maza
http://hdl.handle.net/20.500.12110/paper_00278424_v113_n49_pE7957_Maza
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AT sztarkerjulieta contextdependentmemorytracesinthecrabsmushroombodiesfunctionalsupportforacommonoriginofhighordermemorycenters
AT locatellifernandofederico contextdependentmemorytracesinthecrabsmushroombodiesfunctionalsupportforacommonoriginofhighordermemorycenters
AT delorenzialejandro contextdependentmemorytracesinthecrabsmushroombodiesfunctionalsupportforacommonoriginofhighordermemorycenters
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