Altered expression of synapse and glutamate related genes in post-mortem hippocampus of depressed subjects
Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in regulation of emotions and mood. The exact cellular and molecular mechanisms underlying hippocampal plasticity in response to stress are yet to be ful...
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Published in | The international journal of neuropsychopharmacology Vol. 16; no. 1; pp. 69 - 82 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge, UK
Cambridge University Press
01.02.2013
Oxford University Press |
Subjects | |
Online Access | Get full text |
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Abstract | Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in regulation of emotions and mood. The exact cellular and molecular mechanisms underlying hippocampal plasticity in response to stress are yet to be fully characterized. In this study, we examined the genetic profile of micro-dissected subfields of post-mortem hippocampus from subjects diagnosed with MDD and comparison subjects matched for sex, race and age. Gene expression profiles of the dentate gyrus and CA1 were assessed by 48K human HEEBO whole genome microarrays and a subgroup of identified genes was confirmed by real-time polymerase chain reaction (qPCR). Pathway analysis revealed altered expression of several gene families, including cytoskeletal proteins involved in rearrangement of neuronal processes. Based on this and evidence of hippocampal neuronal atrophy in MDD, we focused on the expression of cytoskeletal, synaptic and glutamate receptor genes. Our findings demonstrate significant dysregulation of synaptic function/structure related genes SNAP25, DLG2 (SAP93), and MAP1A, and 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl)propanoic acid receptor subunit genes GLUR1 and GLUR3. Several of these human target genes were similarly dysregulated in a rat model of chronic unpredictable stress and the effects reversed by antidepressant treatment. Together, these studies provide new evidence that disruption of synaptic and glutamatergic signalling pathways contribute to the pathophysiology underlying MDD and provide interesting targets for novel therapeutic interventions. |
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AbstractList | Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in regulation of emotions and mood. The exact cellular and molecular mechanisms underlying hippocampal plasticity in response to stress are yet to be fully characterized. In this study, we examined the genetic profile of micro-dissected subfields of post-mortem hippocampus from subjects diagnosed with MDD and comparison subjects matched for sex, race and age. Gene expression profiles of the dentate gyrus and CA1 were assessed by 48K human HEEBO whole genome microarrays and a subgroup of identified genes was confirmed by real-time polymerase chain reaction (qPCR). Pathway analysis revealed altered expression of several gene families, including cytoskeletal proteins involved in rearrangement of neuronal processes. Based on this and evidence of hippocampal neuronal atrophy in MDD, we focused on the expression of cytoskeletal, synaptic and glutamate receptor genes. Our findings demonstrate significant dysregulation of synaptic function/structure related genes SNAP25, DLG2 (SAP93), and MAP1A, and 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl)propanoic acid receptor subunit genes GLUR1 and GLUR3. Several of these human target genes were similarly dysregulated in a rat model of chronic unpredictable stress and the effects reversed by antidepressant treatment. Together, these studies provide new evidence that disruption of synaptic and glutamatergic signalling pathways contribute to the pathophysiology underlying MDD and provide interesting targets for novel therapeutic interventions. Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in regulation of emotions and mood. The exact cellular and molecular mechanisms underlying hippocampal plasticity in response to stress are yet to be fully characterized. In this study, we examined the genetic profile of micro-dissected subfields of post-mortem hippocampus from subjects diagnosed with MDD and comparison subjects matched for sex, race and age. Gene expression profiles of the dentate gyrus and CA1 were assessed by 48K human HEEBO whole genome microarrays and a subgroup of identified genes was confirmed by real-time polymerase chain reaction (qPCR). Pathway analysis revealed altered expression of several gene families, including cytoskeletal proteins involved in rearrangement of neuronal processes. Based on this and evidence of hippocampal neuronal atrophy in MDD, we focused on the expression of cytoskeletal, synaptic and glutamate receptor genes. Our findings demonstrate significant dysregulation of synaptic function/structure related genes SNAP25 , DLG2 ( SAP93 ), and MAP1A , and 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl)propanoic acid receptor subunit genes GLUR1 and GLUR3 . Several of these human target genes were similarly dysregulated in a rat model of chronic unpredictable stress and the effects reversed by antidepressant treatment. Together, these studies provide new evidence that disruption of synaptic and glutamatergic signalling pathways contribute to the pathophysiology underlying MDD and provide interesting targets for novel therapeutic interventions. Abstract Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in regulation of emotions and mood. The exact cellular and molecular mechanisms underlying hippocampal plasticity in response to stress are yet to be fully characterized. In this study, we examined the genetic profile of micro-dissected subfields of post-mortem hippocampus from subjects diagnosed with MDD and comparison subjects matched for sex, race and age. Gene expression profiles of the dentate gyrus and CA1 were assessed by 48K human HEEBO whole genome microarrays and a subgroup of identified genes was confirmed by real-time polymerase chain reaction (qPCR). Pathway analysis revealed altered expression of several gene families, including cytoskeletal proteins involved in rearrangement of neuronal processes. Based on this and evidence of hippocampal neuronal atrophy in MDD, we focused on the expression of cytoskeletal, synaptic and glutamate receptor genes. Our findings demonstrate significant dysregulation of synaptic function/structure related genes SNAP25, DLG2 (SAP93), and MAP1A, and 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl)propanoic acid receptor subunit genes GLUR1 and GLUR3. Several of these human target genes were similarly dysregulated in a rat model of chronic unpredictable stress and the effects reversed by antidepressant treatment. Together, these studies provide new evidence that disruption of synaptic and glutamatergic signalling pathways contribute to the pathophysiology underlying MDD and provide interesting targets for novel therapeutic interventions. [PUBLICATION ABSTRACT] Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in regulation of emotions and mood. The exact cellular and molecular mechanisms underlying hippocampal plasticity in response to stress are yet to be fully characterized. In this study, we examined the genetic profile of micro-dissected subfields of post-mortem hippocampus from subjects diagnosed with MDD and comparison subjects matched for sex, race and age. Gene expression profiles of the dentate gyrus and CA1 were assessed by 48K human HEEBO whole genome microarrays and a subgroup of identified genes was confirmed by real-time polymerase chain reaction (qPCR). Pathway analysis revealed altered expression of several gene families, including cytoskeletal proteins involved in rearrangement of neuronal processes. Based on this and evidence of hippocampal neuronal atrophy in MDD, we focused on the expression of cytoskeletal, synaptic and glutamate receptor genes. Our findings demonstrate significant dysregulation of synaptic function/structure related genes SNAP25, DLG2 (SAP93), and MAP1A, and 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl)propanoic acid receptor subunit genes GLUR1 and GLUR3. Several of these human target genes were similarly dysregulated in a rat model of chronic unpredictable stress and the effects reversed by antidepressant treatment. Together, these studies provide new evidence that disruption of synaptic and glutamatergic signalling pathways contribute to the pathophysiology underlying MDD and provide interesting targets for novel therapeutic interventions.Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in regulation of emotions and mood. The exact cellular and molecular mechanisms underlying hippocampal plasticity in response to stress are yet to be fully characterized. In this study, we examined the genetic profile of micro-dissected subfields of post-mortem hippocampus from subjects diagnosed with MDD and comparison subjects matched for sex, race and age. Gene expression profiles of the dentate gyrus and CA1 were assessed by 48K human HEEBO whole genome microarrays and a subgroup of identified genes was confirmed by real-time polymerase chain reaction (qPCR). Pathway analysis revealed altered expression of several gene families, including cytoskeletal proteins involved in rearrangement of neuronal processes. Based on this and evidence of hippocampal neuronal atrophy in MDD, we focused on the expression of cytoskeletal, synaptic and glutamate receptor genes. Our findings demonstrate significant dysregulation of synaptic function/structure related genes SNAP25, DLG2 (SAP93), and MAP1A, and 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl)propanoic acid receptor subunit genes GLUR1 and GLUR3. Several of these human target genes were similarly dysregulated in a rat model of chronic unpredictable stress and the effects reversed by antidepressant treatment. Together, these studies provide new evidence that disruption of synaptic and glutamatergic signalling pathways contribute to the pathophysiology underlying MDD and provide interesting targets for novel therapeutic interventions. |
Author | Jurjus, George J. Banasr, Mounira Simen, Arthur A. Stockmeier, Craig A. Overholser, James C. Duman, Ronald S. Newton, Samuel S. Duric, Vanja Dieter, Lesa |
AuthorAffiliation | 1 Department of Psychiatry, Yale University, New Haven, CT, USA 2 Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, USA 3 Department of Psychiatry, Louis Stokes Cleveland VA Medical Center, Cleveland, OH, USA 4 Department of Psychology, Case Western Reserve University, Cleveland, OH, USA |
AuthorAffiliation_xml | – name: 1 Department of Psychiatry, Yale University, New Haven, CT, USA – name: 3 Department of Psychiatry, Louis Stokes Cleveland VA Medical Center, Cleveland, OH, USA – name: 2 Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, USA – name: 4 Department of Psychology, Case Western Reserve University, Cleveland, OH, USA |
Author_xml | – sequence: 1 givenname: Vanja surname: Duric fullname: Duric, Vanja organization: 1Department of Psychiatry, Yale University, New Haven, CT, USA – sequence: 2 givenname: Mounira surname: Banasr fullname: Banasr, Mounira organization: 1Department of Psychiatry, Yale University, New Haven, CT, USA – sequence: 3 givenname: Craig A. surname: Stockmeier fullname: Stockmeier, Craig A. organization: 2Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, USA – sequence: 4 givenname: Arthur A. surname: Simen fullname: Simen, Arthur A. organization: 1Department of Psychiatry, Yale University, New Haven, CT, USA – sequence: 5 givenname: Samuel S. surname: Newton fullname: Newton, Samuel S. organization: 1Department of Psychiatry, Yale University, New Haven, CT, USA – sequence: 6 givenname: James C. surname: Overholser fullname: Overholser, James C. organization: 4Department of Psychology, Case Western Reserve University, Cleveland, OH, USA – sequence: 7 givenname: George J. surname: Jurjus fullname: Jurjus, George J. organization: 3Department of Psychiatry, Louis Stokes Cleveland VA Medical Center, Cleveland, OH, USA – sequence: 8 givenname: Lesa surname: Dieter fullname: Dieter, Lesa organization: 4Department of Psychology, Case Western Reserve University, Cleveland, OH, USA – sequence: 9 givenname: Ronald S. surname: Duman fullname: Duman, Ronald S. email: ronald.duman@yale.edu organization: 1Department of Psychiatry, Yale University, New Haven, CT, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22339950$$D View this record in MEDLINE/PubMed |
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Snippet | Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in... Abstract Major depressive disorder (MDD) has been linked to changes in function and activity of the hippocampus, one of the central limbic regions involved in... |
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SubjectTerms | Adult Aged Aged, 80 and over Animals Depressive Disorder, Major - genetics Depressive Disorder, Major - metabolism Depressive Disorder, Major - pathology Female Gene Expression Regulation Genes Guanylate Kinases - biosynthesis Guanylate Kinases - genetics Hippocampus - metabolism Hippocampus - pathology Humans Male Microtubule-Associated Proteins - biosynthesis Microtubule-Associated Proteins - genetics Middle Aged Nerve Tissue Proteins - biosynthesis Nerve Tissue Proteins - genetics Rats Rats, Sprague-Dawley Receptors, AMPA - biosynthesis Receptors, AMPA - genetics Receptors, Glutamate - biosynthesis Receptors, Glutamate - genetics Synapses - genetics Synapses - metabolism Synaptosomal-Associated Protein 25 - biosynthesis Synaptosomal-Associated Protein 25 - genetics Tumor Suppressor Proteins - biosynthesis Tumor Suppressor Proteins - genetics |
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Title | Altered expression of synapse and glutamate related genes in post-mortem hippocampus of depressed subjects |
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