Transcriptional profile of hippocampal dentate granule cells in four rat epilepsy models
Global expression profiling of neurologic or psychiatric disorders has been confounded by variability among laboratories, animal models, tissues sampled, and experimental platforms, with the result being that few genes demonstrate consistent expression changes. We attempted to minimize these confoun...
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Published in: | Scientific data Vol. 4; no. 1; p. 170061 |
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Abstract | Global expression profiling of neurologic or psychiatric disorders has been confounded by variability among laboratories, animal models, tissues sampled, and experimental platforms, with the result being that few genes demonstrate consistent expression changes. We attempted to minimize these confounds by pooling dentate granule cell transcriptional profiles from 164 rats in seven laboratories, using three status epilepticus (SE) epilepsy models (pilocarpine, kainate, self-sustained SE), plus amygdala kindling. In each epilepsy model, RNA was harvested from laser-captured dentate granule cells from six rats at four time points early in the process of developing epilepsy, and data were collected from two independent laboratories in each rodent model except SSSE. Hierarchical clustering of differentially-expressed transcripts in the three SE models revealed complete separation between controls and SE rats isolated 1 day after SE. However, concordance of gene expression changes in the SE models was only 26–38% between laboratories, and 4.5% among models, validating the consortium approach. Transcripts with unusually highly variable control expression across laboratories provide a ‘red herring’ list for low-powered studies.
Design Type(s)
transcription profiling by array design • intervention design • disease state design • parallel group design
Measurement Type(s)
transcription profiling assay
Technology Type(s)
microarray platform
Factor Type(s)
treatment portion of study execution • sampling time measurement datum
Sample Characteristic(s)
Rattus norvegicus • dentate granule cell
Machine-accessible metadata file describing the reported data
(ISA-Tab format) |
---|---|
AbstractList | Global expression profiling of neurologic or psychiatric disorders has been confounded by variability among laboratories, animal models, tissues sampled, and experimental platforms, with the result being that few genes demonstrate consistent expression changes. We attempted to minimize these confounds by pooling dentate granule cell transcriptional profiles from 164 rats in seven laboratories, using three status epilepticus (SE) epilepsy models (pilocarpine, kainate, self-sustained SE), plus amygdala kindling. In each epilepsy model, RNA was harvested from laser-captured dentate granule cells from six rats at four time points early in the process of developing epilepsy, and data were collected from two independent laboratories in each rodent model except SSSE. Hierarchical clustering of differentially-expressed transcripts in the three SE models revealed complete separation between controls and SE rats isolated 1 day after SE. However, concordance of gene expression changes in the SE models was only 26–38% between laboratories, and 4.5% among models, validating the consortium approach. Transcripts with unusually highly variable control expression across laboratories provide a ‘red herring’ list for low-powered studies. Global expression profiling of neurologic or psychiatric disorders has been confounded by variability among laboratories, animal models, tissues sampled, and experimental platforms, with the result being that few genes demonstrate consistent expression changes. We attempted to minimize these confounds by pooling dentate granule cell transcriptional profiles from 164 rats in seven laboratories, using three status epilepticus (SE) epilepsy models (pilocarpine, kainate, self-sustained SE), plus amygdala kindling. In each epilepsy model, RNA was harvested from laser-captured dentate granule cells from six rats at four time points early in the process of developing epilepsy, and data were collected from two independent laboratories in each rodent model except SSSE. Hierarchical clustering of differentially-expressed transcripts in the three SE models revealed complete separation between controls and SE rats isolated 1 day after SE. However, concordance of gene expression changes in the SE models was only 26–38% between laboratories, and 4.5% among models, validating the consortium approach. Transcripts with unusually highly variable control expression across laboratories provide a ‘red herring’ list for low-powered studies. Design Type(s) transcription profiling by array design • intervention design • disease state design • parallel group design Measurement Type(s) transcription profiling assay Technology Type(s) microarray platform Factor Type(s) treatment portion of study execution • sampling time measurement datum Sample Characteristic(s) Rattus norvegicus • dentate granule cell Machine-accessible metadata file describing the reported data (ISA-Tab format) |
ArticleNumber | 170061 |
Author | Roopra, Avtar Wang, Yu Wadman, Wytse J. Coulter, Douglas A. McNamara, James Wasterlain, Claude Rogawski, Michael A. Gorter, Jan A. Pitkänen, Asla Dingledine, Raymond Nadler, J. Victor Skene, Pate Sloviter, Robert S. Fritsch, Brita Lelutiu, Nadia |
Author_xml | – sequence: 1 givenname: Raymond surname: Dingledine fullname: Dingledine, Raymond email: rdingle@emory.edu organization: Department of Pharmacology, Emory University – sequence: 2 givenname: Douglas A. surname: Coulter fullname: Coulter, Douglas A. organization: Department of Neurology, Children’s Hospital of Philadelphia – sequence: 3 givenname: Brita surname: Fritsch fullname: Fritsch, Brita organization: Department of Neurology, University Hospital Freiburg – sequence: 4 givenname: Jan A. surname: Gorter fullname: Gorter, Jan A. organization: Swammerdam Institute for Life Science, Center for Neuroscience, University of Amsterdam – sequence: 5 givenname: Nadia surname: Lelutiu fullname: Lelutiu, Nadia organization: Department of Pharmacology, Emory University – sequence: 6 givenname: James surname: McNamara fullname: McNamara, James organization: Department of Neurobiology, Duke University – sequence: 7 givenname: J. Victor surname: Nadler fullname: Nadler, J. Victor organization: Department of Neurobiology, Duke University – sequence: 8 givenname: Asla surname: Pitkänen fullname: Pitkänen, Asla organization: A.I.Virtanen Institute for Molecular Sciences, University of Eastern Finland – sequence: 9 givenname: Michael A. surname: Rogawski fullname: Rogawski, Michael A. organization: Departments of Neurology and Pharmacology, School of Medicine, University of California, Davis – sequence: 10 givenname: Pate surname: Skene fullname: Skene, Pate organization: Department of Neurobiology, Duke University – sequence: 11 givenname: Robert S. surname: Sloviter fullname: Sloviter, Robert S. organization: Department of Neurobiology, Morehouse School of Medicine – sequence: 12 givenname: Yu surname: Wang fullname: Wang, Yu organization: Department of Neurobiology, Duke University – sequence: 13 givenname: Wytse J. surname: Wadman fullname: Wadman, Wytse J. organization: Swammerdam Institute for Life Science, Center for Neuroscience, University of Amsterdam – sequence: 14 givenname: Claude surname: Wasterlain fullname: Wasterlain, Claude organization: Department of Neurology and Brain Research Institute, and VA Greater Los Angeles Health Care System, Univ. California Los Angeles – sequence: 15 givenname: Avtar surname: Roopra fullname: Roopra, Avtar email: asroopra@wisc.edu organization: Department of Neuroscience, Univ. Wisconsin |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28485718$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 R.D. designed and coordinated the project, contributed tissue, analyzed the data and wrote the manuscript. D.C. contributed tissue and revised the manuscript. B.F. contributed tissue. J.G. contributed tissue and revised the manuscript. N.L. performed LCM and wrote the manuscript. J.M. contributed tissue and revised the manuscript. J.V.N. contributed tissue and revised the manuscript. A.P. contributed tissue and revised the manuscript. M.R. contributed tissue and revised the manuscript. P.S. performed LCM and revised the manuscript. R.S.S. performed histology and revised the manuscript. Y.W. performed LCM. W.W. contributed tissue and revised the manuscript. C.W. contributed tissue and revised the manuscript. A.R. analyzed data and wrote the manuscript. |
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SubjectTerms | 631/337/2019 692/617/375/178 Animals Data Descriptor Disease Models, Animal Epilepsy - genetics Hippocampus Humanities and Social Sciences multidisciplinary Rats Science Species Specificity Status Epilepticus - genetics Transcriptome |
Title | Transcriptional profile of hippocampal dentate granule cells in four rat epilepsy models |
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