CpG Preconditioning Regulates Mirna Expression That Modulates Genomic Reprogramming Associated with Neuroprotection against Ischemic Injury
Cytosine-phosphate-guanine (CpG) preconditioning reprograms the genomic response to stroke to protect the brain against ischemic injury. The mechanisms underlying genomic reprogramming are incompletely understood. MicroRNAs (miRNAs) regulate gene expression; however, their role in modulating gene re...
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Veröffentlicht in: | Journal of Cerebral Blood Flow and Metabolism 2015-02, Vol.35 (2), p.257-266 |
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creator | Vartanian, Keri B Mitchell, Hugh D Stevens, Susan L Conrad, Valerie K McDermott, Jason E Stenzel-Poore, Mary P |
description | Cytosine-phosphate-guanine (CpG) preconditioning reprograms the genomic response to stroke to protect the brain against ischemic injury. The mechanisms underlying genomic reprogramming are incompletely understood. MicroRNAs (miRNAs) regulate gene expression; however, their role in modulating gene responses produced by CpG preconditioning is unknown. We evaluated brain miRNA expression in response to CpG preconditioning before and after stroke using microarray. Importantly, we have data from previous gene microarrays under the same conditions, which allowed integration of miRNA and gene expression data to specifically identify regulated miRNA gene targets. CpG preconditioning did not significantly alter miRNA expression before stroke, indicating that miRNA regulation is not critical for the initiation of preconditioning-induced neuroprotection. However, after stroke, differentially regulated miRNAs between CpG- and saline-treated animals associated with the upregulation of several neuroprotective genes, implicating these miRNAs in genomic reprogramming that increases neuroprotection. Statistical analysis revealed that the miRNA targets were enriched in the gene population regulated in the setting of stroke, implying that miRNAs likely orchestrate this gene expression. These data suggest that miRNAs regulate endogenous responses to stroke and that manipulation of these miRNAs may have the potential to acutely activate novel neuroprotective processes that reduce damage. |
doi_str_mv | 10.1038/jcbfm.2014.193 |
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(PNNL), Richland, WA (United States)</creatorcontrib><description>Cytosine-phosphate-guanine (CpG) preconditioning reprograms the genomic response to stroke to protect the brain against ischemic injury. The mechanisms underlying genomic reprogramming are incompletely understood. MicroRNAs (miRNAs) regulate gene expression; however, their role in modulating gene responses produced by CpG preconditioning is unknown. We evaluated brain miRNA expression in response to CpG preconditioning before and after stroke using microarray. Importantly, we have data from previous gene microarrays under the same conditions, which allowed integration of miRNA and gene expression data to specifically identify regulated miRNA gene targets. CpG preconditioning did not significantly alter miRNA expression before stroke, indicating that miRNA regulation is not critical for the initiation of preconditioning-induced neuroprotection. However, after stroke, differentially regulated miRNAs between CpG- and saline-treated animals associated with the upregulation of several neuroprotective genes, implicating these miRNAs in genomic reprogramming that increases neuroprotection. Statistical analysis revealed that the miRNA targets were enriched in the gene population regulated in the setting of stroke, implying that miRNAs likely orchestrate this gene expression. These data suggest that miRNAs regulate endogenous responses to stroke and that manipulation of these miRNAs may have the potential to acutely activate novel neuroprotective processes that reduce damage.</description><identifier>ISSN: 0271-678X</identifier><identifier>EISSN: 1559-7016</identifier><identifier>DOI: 10.1038/jcbfm.2014.193</identifier><identifier>PMID: 25388675</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Adjuvants, Immunologic - pharmacology ; Animals ; Brain Ischemia - drug therapy ; Brain Ischemia - metabolism ; Gene Expression Regulation - drug effects ; Male ; Mice ; MicroRNAs - biosynthesis ; Neuroprotective Agents - pharmacology ; Oligodeoxyribonucleotides - pharmacology ; Oligonucleotide Array Sequence Analysis ; Original ; Stroke - drug therapy ; Stroke - metabolism ; Stroke - pathology ; systems biology, microRNA, bioinformatics, stroke, computational biology</subject><ispartof>Journal of Cerebral Blood Flow and Metabolism, 2015-02, Vol.35 (2), p.257-266</ispartof><rights>2015 ISCBFM</rights><rights>Copyright Nature Publishing Group Feb 2015</rights><rights>Copyright © 2015 International Society for Cerebral Blood Flow & Metabolism, Inc. 2015 International Society for Cerebral Blood Flow & Metabolism, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c584t-d30f165978dfb14ac802ac080b4c8d50bef84ac538b4f73cc0ac0b755bf083373</citedby><cites>FETCH-LOGICAL-c584t-d30f165978dfb14ac802ac080b4c8d50bef84ac538b4f73cc0ac0b755bf083373</cites><orcidid>0000000329612572</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426742/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426742/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,21819,27924,27925,43621,43622,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25388675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1710221$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Vartanian, Keri B</creatorcontrib><creatorcontrib>Mitchell, Hugh D</creatorcontrib><creatorcontrib>Stevens, Susan L</creatorcontrib><creatorcontrib>Conrad, Valerie K</creatorcontrib><creatorcontrib>McDermott, Jason E</creatorcontrib><creatorcontrib>Stenzel-Poore, Mary P</creatorcontrib><creatorcontrib>Pacific Northwest National Lab. (PNNL), Richland, WA (United States)</creatorcontrib><title>CpG Preconditioning Regulates Mirna Expression That Modulates Genomic Reprogramming Associated with Neuroprotection against Ischemic Injury</title><title>Journal of Cerebral Blood Flow and Metabolism</title><addtitle>J Cereb Blood Flow Metab</addtitle><description>Cytosine-phosphate-guanine (CpG) preconditioning reprograms the genomic response to stroke to protect the brain against ischemic injury. The mechanisms underlying genomic reprogramming are incompletely understood. MicroRNAs (miRNAs) regulate gene expression; however, their role in modulating gene responses produced by CpG preconditioning is unknown. We evaluated brain miRNA expression in response to CpG preconditioning before and after stroke using microarray. Importantly, we have data from previous gene microarrays under the same conditions, which allowed integration of miRNA and gene expression data to specifically identify regulated miRNA gene targets. CpG preconditioning did not significantly alter miRNA expression before stroke, indicating that miRNA regulation is not critical for the initiation of preconditioning-induced neuroprotection. However, after stroke, differentially regulated miRNAs between CpG- and saline-treated animals associated with the upregulation of several neuroprotective genes, implicating these miRNAs in genomic reprogramming that increases neuroprotection. Statistical analysis revealed that the miRNA targets were enriched in the gene population regulated in the setting of stroke, implying that miRNAs likely orchestrate this gene expression. These data suggest that miRNAs regulate endogenous responses to stroke and that manipulation of these miRNAs may have the potential to acutely activate novel neuroprotective processes that reduce damage.</description><subject>Adjuvants, Immunologic - pharmacology</subject><subject>Animals</subject><subject>Brain Ischemia - drug therapy</subject><subject>Brain Ischemia - metabolism</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Male</subject><subject>Mice</subject><subject>MicroRNAs - biosynthesis</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Oligodeoxyribonucleotides - pharmacology</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Original</subject><subject>Stroke - drug therapy</subject><subject>Stroke - metabolism</subject><subject>Stroke - pathology</subject><subject>systems biology, microRNA, bioinformatics, stroke, computational biology</subject><issn>0271-678X</issn><issn>1559-7016</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNksGL1DAUxoMo7rh69ShFL4J0TNKkSS_CMqzjwK6KrOAtpGnaZmiTbpKq-zf4T5s647KKB0-BvN_3Xr6XD4CnCK4RLPjrvarbcY0hImtUFffAClFa5Qyi8j5YQcxQXjL-5QQ8CmEPIeQFpQ_BCaYF5yWjK_BjM22zj14rZxsTjbPGdtkn3c2DjDpkl8ZbmZ1_n7wOIVWzq17G7NI1x_pWWzcalRSTd52X47joz0JwyiSgyb6Z2Gfv9exdAqJWy4hMdtLYELNdUL1e5Du7n_3NY_CglUPQT47nKfj89vxq8y6_-LDdbc4uckU5iXlTwBaVtGK8aWtEpOIQSwU5rIniDYW1bnm6TRZr0rJCKZiqNaO0bpP_ghWn4M2h7zTXo26UttHLQUzejNLfCCeN-LNiTS8691UQgktGcGrw_NDAhWhEUCYZ69MGbfInEEMQY5Sgl8cp3l3POkQxmqD0MEir3RwEKkuCESQV_g-UYkJIWS1vf_EXundz-qNhoUgFqwKVMFHrA6W8C8Hr9tYcgmLJjfiVG7HkRqTcJMGzuyu5xX8HJQGvDkCQnb4z89_tfgJBa9AK</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Vartanian, Keri B</creator><creator>Mitchell, Hugh D</creator><creator>Stevens, Susan L</creator><creator>Conrad, Valerie K</creator><creator>McDermott, Jason E</creator><creator>Stenzel-Poore, Mary P</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>OTOTI</scope><scope>5PM</scope><orcidid>https://orcid.org/0000000329612572</orcidid></search><sort><creationdate>20150201</creationdate><title>CpG Preconditioning Regulates Mirna Expression That Modulates Genomic Reprogramming Associated with Neuroprotection against Ischemic Injury</title><author>Vartanian, Keri B ; Mitchell, Hugh D ; Stevens, Susan L ; Conrad, Valerie K ; McDermott, Jason E ; Stenzel-Poore, Mary P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c584t-d30f165978dfb14ac802ac080b4c8d50bef84ac538b4f73cc0ac0b755bf083373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adjuvants, Immunologic - pharmacology</topic><topic>Animals</topic><topic>Brain Ischemia - drug therapy</topic><topic>Brain Ischemia - metabolism</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Male</topic><topic>Mice</topic><topic>MicroRNAs - biosynthesis</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Oligodeoxyribonucleotides - pharmacology</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Original</topic><topic>Stroke - drug therapy</topic><topic>Stroke - metabolism</topic><topic>Stroke - pathology</topic><topic>systems biology, microRNA, bioinformatics, stroke, computational biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vartanian, Keri B</creatorcontrib><creatorcontrib>Mitchell, Hugh D</creatorcontrib><creatorcontrib>Stevens, Susan L</creatorcontrib><creatorcontrib>Conrad, Valerie K</creatorcontrib><creatorcontrib>McDermott, Jason E</creatorcontrib><creatorcontrib>Stenzel-Poore, Mary P</creatorcontrib><creatorcontrib>Pacific Northwest National Lab. 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(PNNL), Richland, WA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CpG Preconditioning Regulates Mirna Expression That Modulates Genomic Reprogramming Associated with Neuroprotection against Ischemic Injury</atitle><jtitle>Journal of Cerebral Blood Flow and Metabolism</jtitle><addtitle>J Cereb Blood Flow Metab</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>35</volume><issue>2</issue><spage>257</spage><epage>266</epage><pages>257-266</pages><issn>0271-678X</issn><eissn>1559-7016</eissn><abstract>Cytosine-phosphate-guanine (CpG) preconditioning reprograms the genomic response to stroke to protect the brain against ischemic injury. The mechanisms underlying genomic reprogramming are incompletely understood. MicroRNAs (miRNAs) regulate gene expression; however, their role in modulating gene responses produced by CpG preconditioning is unknown. We evaluated brain miRNA expression in response to CpG preconditioning before and after stroke using microarray. Importantly, we have data from previous gene microarrays under the same conditions, which allowed integration of miRNA and gene expression data to specifically identify regulated miRNA gene targets. CpG preconditioning did not significantly alter miRNA expression before stroke, indicating that miRNA regulation is not critical for the initiation of preconditioning-induced neuroprotection. However, after stroke, differentially regulated miRNAs between CpG- and saline-treated animals associated with the upregulation of several neuroprotective genes, implicating these miRNAs in genomic reprogramming that increases neuroprotection. Statistical analysis revealed that the miRNA targets were enriched in the gene population regulated in the setting of stroke, implying that miRNAs likely orchestrate this gene expression. These data suggest that miRNAs regulate endogenous responses to stroke and that manipulation of these miRNAs may have the potential to acutely activate novel neuroprotective processes that reduce damage.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>25388675</pmid><doi>10.1038/jcbfm.2014.193</doi><tpages>10</tpages><orcidid>https://orcid.org/0000000329612572</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvants, Immunologic - pharmacology Animals Brain Ischemia - drug therapy Brain Ischemia - metabolism Gene Expression Regulation - drug effects Male Mice MicroRNAs - biosynthesis Neuroprotective Agents - pharmacology Oligodeoxyribonucleotides - pharmacology Oligonucleotide Array Sequence Analysis Original Stroke - drug therapy Stroke - metabolism Stroke - pathology systems biology, microRNA, bioinformatics, stroke, computational biology |
title | CpG Preconditioning Regulates Mirna Expression That Modulates Genomic Reprogramming Associated with Neuroprotection against Ischemic Injury |
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