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spelling paper:paper_16011848_v11_n8_p966_Campolongo2023-06-08T16:25:01Z Hippocampal SPARC regulates depression-related behavior Benedetti, Lorena Gabriela Podhajcer, Osvaldo Luis Depino, Amaicha Mara Anxiety-related behavior c-Fos Knockout mouse Neurogenesis Neuronal activity SPARC adenovirus vector osteonectin osteonectin SPARC protein, mouse animal experiment anxiety disorder article behavior disorder cell proliferation dentate gyrus depression forced swimming test hippocampus maze test mouse nervous system development nonhuman oncogene c fos phenotype priority journal protein expression regulatory mechanism stereotactic procedure age animal anxiety depression female genetics hippocampus knockout mouse male pathophysiology Mus Age Factors Animals Anxiety Cell Proliferation Dentate Gyrus Depression Female Hippocampus Male Mice Mice, Knockout Neurogenesis Osteonectin Phenotype SPARC (secreted protein acidic and rich in cysteine) is a matricellular protein highly expressed during development, reorganization and tissue repair. In the central nervous system, glial cells express SPARC during development and in neurogenic regions of the adult brain. Astrocytes control the glutamate receptor levels in the developing hippocampus through SPARC secretion. To further characterize the role of SPARC in the brain, we analyzed the hippocampal-dependent adult behavior of SPARC KO mice. We found that SPARC KOmice show increased levels of anxiety-related behaviors and reduced levels of depression-related behaviors. The antidepressant-like phenotype could be rescued by adenoviral vector-mediated expression of SPARC in the adult hippocampus, but anxiety-related behavior persisted in these mice. To identify the cellular mechanisms underlying these behavioral alterations, we analyzed neuronal activity and neurogenesis in the dentate gyrus (DG). SPARC KO mice have increased levels of neuronal activity, evidenced as more neurons that express c-Fos after a footshock. SPARC also affects cell proliferation in the subgranular zone of the DG, although it does not affect maturation and survival of new neurons. SPARC expression in the adult DGdoes not revert the proliferation phenotype in KO mice, but our results suggest a role of SPARC in limiting the survival of new neurons in the DG. This work suggests that SPARC could affect anxiety-related behavior by modulating neuronal activity, and that depression-related behavior is dependent upon the adult expression of SPARC, which affects adult brain function by mechanisms that need to be elucidated. © 2012 The Authors Genes, Brain and Behavior © 2012 Blackwell Publishing Ltd and International Behavioural and Neural Genetics Society. Fil:Benedetti, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Podhajcer, O.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Depino, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2012 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_16011848_v11_n8_p966_Campolongo http://hdl.handle.net/20.500.12110/paper_16011848_v11_n8_p966_Campolongo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Anxiety-related behavior
c-Fos
Knockout mouse
Neurogenesis
Neuronal activity
SPARC
adenovirus vector
osteonectin
osteonectin
SPARC protein, mouse
animal experiment
anxiety disorder
article
behavior disorder
cell proliferation
dentate gyrus
depression
forced swimming test
hippocampus
maze test
mouse
nervous system development
nonhuman
oncogene c fos
phenotype
priority journal
protein expression
regulatory mechanism
stereotactic procedure
age
animal
anxiety
depression
female
genetics
hippocampus
knockout mouse
male
pathophysiology
Mus
Age Factors
Animals
Anxiety
Cell Proliferation
Dentate Gyrus
Depression
Female
Hippocampus
Male
Mice
Mice, Knockout
Neurogenesis
Osteonectin
Phenotype
spellingShingle Anxiety-related behavior
c-Fos
Knockout mouse
Neurogenesis
Neuronal activity
SPARC
adenovirus vector
osteonectin
osteonectin
SPARC protein, mouse
animal experiment
anxiety disorder
article
behavior disorder
cell proliferation
dentate gyrus
depression
forced swimming test
hippocampus
maze test
mouse
nervous system development
nonhuman
oncogene c fos
phenotype
priority journal
protein expression
regulatory mechanism
stereotactic procedure
age
animal
anxiety
depression
female
genetics
hippocampus
knockout mouse
male
pathophysiology
Mus
Age Factors
Animals
Anxiety
Cell Proliferation
Dentate Gyrus
Depression
Female
Hippocampus
Male
Mice
Mice, Knockout
Neurogenesis
Osteonectin
Phenotype
Benedetti, Lorena Gabriela
Podhajcer, Osvaldo Luis
Depino, Amaicha Mara
Hippocampal SPARC regulates depression-related behavior
topic_facet Anxiety-related behavior
c-Fos
Knockout mouse
Neurogenesis
Neuronal activity
SPARC
adenovirus vector
osteonectin
osteonectin
SPARC protein, mouse
animal experiment
anxiety disorder
article
behavior disorder
cell proliferation
dentate gyrus
depression
forced swimming test
hippocampus
maze test
mouse
nervous system development
nonhuman
oncogene c fos
phenotype
priority journal
protein expression
regulatory mechanism
stereotactic procedure
age
animal
anxiety
depression
female
genetics
hippocampus
knockout mouse
male
pathophysiology
Mus
Age Factors
Animals
Anxiety
Cell Proliferation
Dentate Gyrus
Depression
Female
Hippocampus
Male
Mice
Mice, Knockout
Neurogenesis
Osteonectin
Phenotype
description SPARC (secreted protein acidic and rich in cysteine) is a matricellular protein highly expressed during development, reorganization and tissue repair. In the central nervous system, glial cells express SPARC during development and in neurogenic regions of the adult brain. Astrocytes control the glutamate receptor levels in the developing hippocampus through SPARC secretion. To further characterize the role of SPARC in the brain, we analyzed the hippocampal-dependent adult behavior of SPARC KO mice. We found that SPARC KOmice show increased levels of anxiety-related behaviors and reduced levels of depression-related behaviors. The antidepressant-like phenotype could be rescued by adenoviral vector-mediated expression of SPARC in the adult hippocampus, but anxiety-related behavior persisted in these mice. To identify the cellular mechanisms underlying these behavioral alterations, we analyzed neuronal activity and neurogenesis in the dentate gyrus (DG). SPARC KO mice have increased levels of neuronal activity, evidenced as more neurons that express c-Fos after a footshock. SPARC also affects cell proliferation in the subgranular zone of the DG, although it does not affect maturation and survival of new neurons. SPARC expression in the adult DGdoes not revert the proliferation phenotype in KO mice, but our results suggest a role of SPARC in limiting the survival of new neurons in the DG. This work suggests that SPARC could affect anxiety-related behavior by modulating neuronal activity, and that depression-related behavior is dependent upon the adult expression of SPARC, which affects adult brain function by mechanisms that need to be elucidated. © 2012 The Authors Genes, Brain and Behavior © 2012 Blackwell Publishing Ltd and International Behavioural and Neural Genetics Society.
author Benedetti, Lorena Gabriela
Podhajcer, Osvaldo Luis
Depino, Amaicha Mara
author_facet Benedetti, Lorena Gabriela
Podhajcer, Osvaldo Luis
Depino, Amaicha Mara
author_sort Benedetti, Lorena Gabriela
title Hippocampal SPARC regulates depression-related behavior
title_short Hippocampal SPARC regulates depression-related behavior
title_full Hippocampal SPARC regulates depression-related behavior
title_fullStr Hippocampal SPARC regulates depression-related behavior
title_full_unstemmed Hippocampal SPARC regulates depression-related behavior
title_sort hippocampal sparc regulates depression-related behavior
publishDate 2012
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_16011848_v11_n8_p966_Campolongo
http://hdl.handle.net/20.500.12110/paper_16011848_v11_n8_p966_Campolongo
work_keys_str_mv AT benedettilorenagabriela hippocampalsparcregulatesdepressionrelatedbehavior
AT podhajcerosvaldoluis hippocampalsparcregulatesdepressionrelatedbehavior
AT depinoamaichamara hippocampalsparcregulatesdepressionrelatedbehavior
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