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Regulation of the GABA Cell Phenotype in Hippocampus of Schizophrenics and Bipolars
by
Matzilevich, David
, Subburaju, Sivan
, Walsh, John P.
, Minns, Martin
, Benes, Francine M.
, Lim, Benjamin
in
Biological Sciences
/ Bipolar disorder
/ Bipolar Disorder - diagnosis
/ Bipolar Disorder - metabolism
/ Bipolar Disorder - pathology
/ Case-Control Studies
/ Cell cycle
/ Cell differentiation
/ Cell growth
/ cyclins
/ death
/ Down-Regulation
/ epigenetics
/ Female
/ gamma-aminobutyric acid
/ gamma-Aminobutyric Acid - metabolism
/ Gene expression
/ Gene Expression Profiling
/ Gene Expression Regulation
/ Genes
/ Genotype & phenotype
/ glutamate decarboxylase
/ Glutamate Decarboxylase - metabolism
/ Hippocampus
/ Hippocampus - metabolism
/ Hippocampus - pathology
/ histone deacetylase
/ Humans
/ interleukin-1beta
/ Isoenzymes - metabolism
/ Male
/ Mental disorders
/ Models, Biological
/ Neuroglia
/ Neurons
/ Neurosciences
/ Phenotype
/ Phenotypes
/ Pyramidal cells
/ receptors
/ RNA
/ RNA, Messenger - metabolism
/ Schizophrenia
/ Schizophrenia - diagnosis
/ Schizophrenia - metabolism
/ Schizophrenia - pathology
/ transcription factors
/ transforming growth factor beta 2
2007
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Regulation of the GABA Cell Phenotype in Hippocampus of Schizophrenics and Bipolars
by
Matzilevich, David
, Subburaju, Sivan
, Walsh, John P.
, Minns, Martin
, Benes, Francine M.
, Lim, Benjamin
in
Biological Sciences
/ Bipolar disorder
/ Bipolar Disorder - diagnosis
/ Bipolar Disorder - metabolism
/ Bipolar Disorder - pathology
/ Case-Control Studies
/ Cell cycle
/ Cell differentiation
/ Cell growth
/ cyclins
/ death
/ Down-Regulation
/ epigenetics
/ Female
/ gamma-aminobutyric acid
/ gamma-Aminobutyric Acid - metabolism
/ Gene expression
/ Gene Expression Profiling
/ Gene Expression Regulation
/ Genes
/ Genotype & phenotype
/ glutamate decarboxylase
/ Glutamate Decarboxylase - metabolism
/ Hippocampus
/ Hippocampus - metabolism
/ Hippocampus - pathology
/ histone deacetylase
/ Humans
/ interleukin-1beta
/ Isoenzymes - metabolism
/ Male
/ Mental disorders
/ Models, Biological
/ Neuroglia
/ Neurons
/ Neurosciences
/ Phenotype
/ Phenotypes
/ Pyramidal cells
/ receptors
/ RNA
/ RNA, Messenger - metabolism
/ Schizophrenia
/ Schizophrenia - diagnosis
/ Schizophrenia - metabolism
/ Schizophrenia - pathology
/ transcription factors
/ transforming growth factor beta 2
2007
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Regulation of the GABA Cell Phenotype in Hippocampus of Schizophrenics and Bipolars
by
Matzilevich, David
, Subburaju, Sivan
, Walsh, John P.
, Minns, Martin
, Benes, Francine M.
, Lim, Benjamin
in
Biological Sciences
/ Bipolar disorder
/ Bipolar Disorder - diagnosis
/ Bipolar Disorder - metabolism
/ Bipolar Disorder - pathology
/ Case-Control Studies
/ Cell cycle
/ Cell differentiation
/ Cell growth
/ cyclins
/ death
/ Down-Regulation
/ epigenetics
/ Female
/ gamma-aminobutyric acid
/ gamma-Aminobutyric Acid - metabolism
/ Gene expression
/ Gene Expression Profiling
/ Gene Expression Regulation
/ Genes
/ Genotype & phenotype
/ glutamate decarboxylase
/ Glutamate Decarboxylase - metabolism
/ Hippocampus
/ Hippocampus - metabolism
/ Hippocampus - pathology
/ histone deacetylase
/ Humans
/ interleukin-1beta
/ Isoenzymes - metabolism
/ Male
/ Mental disorders
/ Models, Biological
/ Neuroglia
/ Neurons
/ Neurosciences
/ Phenotype
/ Phenotypes
/ Pyramidal cells
/ receptors
/ RNA
/ RNA, Messenger - metabolism
/ Schizophrenia
/ Schizophrenia - diagnosis
/ Schizophrenia - metabolism
/ Schizophrenia - pathology
/ transcription factors
/ transforming growth factor beta 2
2007
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Regulation of the GABA Cell Phenotype in Hippocampus of Schizophrenics and Bipolars
Journal Article
Regulation of the GABA Cell Phenotype in Hippocampus of Schizophrenics and Bipolars
2007
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Overview
GABAergic dysfunction is present in the hippocampus in schizophrenia (SZ) and bipolar disorder (BD). The trisynaptic pathway was \"deconstructed\" into various layers of sectors CA3/2 and CA1 and gene expression profiling performed. Network association analysis was used to uncover genes that may be related to regulation of glutamate decarboxylase 67 (GAD₆₇), a marker for this system that has been found by many studies to show decreased expression in SZs and BDs. The most striking change was a down-regulation of GAD₆₇ in the stratum oriens (SO) of CA2/3 in both groups; CA1 only showed changes in the SO of schizophrenics. The network generated for GAD₆₇ contained 25 genes involved in the regulation of kainate receptors, TGF-β and Wnt signaling, as well as transcription factors involved in cell growth and differentiation. In SZs, IL-1β, (GRIK2/3), TGF-β2, TGF-βR1, histone deacetylase 1 (HDAC1), death associated protein (DAXX), and cyclin D2 (CCND2) were all significantly up-regulated, whereas in BDs, PAX5, Runx2, LEF1, TLE1, and CCND2 were significantly down-regulated. In the SO of CA1 of BDs, where GAD67 showed no expression change, TGF-β and Wnt signaling genes were all up-regulated, but other transcription factors showed no change in expression. In other layers/sectors, BDs showed no expression changes in these GAD₆₇ network genes. Overall, these results are consistent with the hypothesis that decreased expression of GAD₆₇ may be associated with an epigenetic mechanism in SZ. In BD, however, a suppression of transcription factors involved in cell differentiation may contribute to GABA dysfunction.
Publisher
National Academy of Sciences,National Acad Sciences
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