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Proteome-wide characterization of signalling interactions in the hippocampal CA4/DG subfield of patients with Alzheimer’s disease
Alzheimer’s disease (AD) is the most common form of dementia; however, mechanisms and biomarkers remain unclear. Here, we examined hippocampal CA4 and dentate gyrus subfields, which are less studied in the context of AD pathology, in post-mortem AD and control tissue to identify possible biomarkers....
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Published in: | Scientific reports 2015-06, Vol.5 (1), p.11138-11138, Article 11138 |
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creator | Ho Kim, Jae Franck, Julien Kang, Taewook Heinsen, Helmut Ravid, Rivka Ferrer, Isidro Hee Cheon, Mi Lee, Joo-Yong Shin Yoo, Jong Steinbusch, Harry W Salzet, Michel Fournier, Isabelle Mok Park, Young |
description | Alzheimer’s disease (AD) is the most common form of dementia; however, mechanisms and biomarkers remain unclear. Here, we examined hippocampal CA4 and dentate gyrus subfields, which are less studied in the context of AD pathology, in post-mortem AD and control tissue to identify possible biomarkers. We performed mass spectrometry-based proteomic analysis combined with label-free quantification for identification of differentially expressed proteins. We identified 4,328 proteins, of which 113 showed more than 2-fold higher or lower expression in AD hippocampi than in control tissues. Five proteins were identified as putative AD biomarkers (MDH2, PCLO, TRRAP, YWHAZ and MUC19 isoform 5) and were cross-validated by immunoblotting, selected reaction monitoring and MALDI imaging. We also used a bioinformatics approach to examine upstream signalling interactions of the 113 regulated proteins. Five upstream signalling (IGF1, BDNF, ZAP70, MYC and cyclosporin A) factors showed novel interactions in AD hippocampi. Taken together, these results demonstrate a novel platform that may provide new strategies for the early detection of AD and thus its diagnosis. |
doi_str_mv | 10.1038/srep11138 |
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Taken together, these results demonstrate a novel platform that may provide new strategies for the early detection of AD and thus its diagnosis.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep11138</identifier><identifier>PMID: 26059363</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/154/53/2421 ; 631/1647/2067 ; 631/337/475/2290 ; 631/378/340 ; 82/47 ; 82/58 ; 82/80 ; Alzheimer Disease - metabolism ; Alzheimer's disease ; Bioinformatics ; Biomarkers ; Biomarkers - metabolism ; Brain-derived neurotrophic factor ; Cyclosporin A ; Dementia disorders ; Dentate gyrus ; Dentate Gyrus - metabolism ; Hippocampus ; Humanities and Social Sciences ; Humans ; Immunoblotting ; Insulin-like growth factor I ; Life Sciences ; Mass spectrometry ; Mass spectroscopy ; multidisciplinary ; Myc protein ; Neurodegenerative diseases ; Proteins ; Proteome ; Science ; Signal Transduction ; Upstream ; ZAP-70 protein</subject><ispartof>Scientific reports, 2015-06, Vol.5 (1), p.11138-11138, Article 11138</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Jun 2015</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-35b3f33b374b2214ad752b61ca90e5f2a11664cc27bb0fbcda5d6813287723ab3</citedby><cites>FETCH-LOGICAL-c475t-35b3f33b374b2214ad752b61ca90e5f2a11664cc27bb0fbcda5d6813287723ab3</cites><orcidid>0000-0003-1096-5044 ; 0000-0001-9888-8754</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1899565117/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1899565117?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26059363$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://inserm.hal.science/inserm-02940247$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Ho Kim, Jae</creatorcontrib><creatorcontrib>Franck, Julien</creatorcontrib><creatorcontrib>Kang, Taewook</creatorcontrib><creatorcontrib>Heinsen, Helmut</creatorcontrib><creatorcontrib>Ravid, Rivka</creatorcontrib><creatorcontrib>Ferrer, Isidro</creatorcontrib><creatorcontrib>Hee Cheon, Mi</creatorcontrib><creatorcontrib>Lee, Joo-Yong</creatorcontrib><creatorcontrib>Shin Yoo, Jong</creatorcontrib><creatorcontrib>Steinbusch, Harry W</creatorcontrib><creatorcontrib>Salzet, Michel</creatorcontrib><creatorcontrib>Fournier, Isabelle</creatorcontrib><creatorcontrib>Mok Park, Young</creatorcontrib><title>Proteome-wide characterization of signalling interactions in the hippocampal CA4/DG subfield of patients with Alzheimer’s disease</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Alzheimer’s disease (AD) is the most common form of dementia; however, mechanisms and biomarkers remain unclear. Here, we examined hippocampal CA4 and dentate gyrus subfields, which are less studied in the context of AD pathology, in post-mortem AD and control tissue to identify possible biomarkers. We performed mass spectrometry-based proteomic analysis combined with label-free quantification for identification of differentially expressed proteins. We identified 4,328 proteins, of which 113 showed more than 2-fold higher or lower expression in AD hippocampi than in control tissues. Five proteins were identified as putative AD biomarkers (MDH2, PCLO, TRRAP, YWHAZ and MUC19 isoform 5) and were cross-validated by immunoblotting, selected reaction monitoring and MALDI imaging. We also used a bioinformatics approach to examine upstream signalling interactions of the 113 regulated proteins. Five upstream signalling (IGF1, BDNF, ZAP70, MYC and cyclosporin A) factors showed novel interactions in AD hippocampi. 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metabolism</topic><topic>Alzheimer's disease</topic><topic>Bioinformatics</topic><topic>Biomarkers</topic><topic>Biomarkers - metabolism</topic><topic>Brain-derived neurotrophic factor</topic><topic>Cyclosporin A</topic><topic>Dementia disorders</topic><topic>Dentate gyrus</topic><topic>Dentate Gyrus - metabolism</topic><topic>Hippocampus</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Insulin-like growth factor I</topic><topic>Life Sciences</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>multidisciplinary</topic><topic>Myc protein</topic><topic>Neurodegenerative diseases</topic><topic>Proteins</topic><topic>Proteome</topic><topic>Science</topic><topic>Signal Transduction</topic><topic>Upstream</topic><topic>ZAP-70 protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ho Kim, Jae</creatorcontrib><creatorcontrib>Franck, Julien</creatorcontrib><creatorcontrib>Kang, Taewook</creatorcontrib><creatorcontrib>Heinsen, Helmut</creatorcontrib><creatorcontrib>Ravid, Rivka</creatorcontrib><creatorcontrib>Ferrer, Isidro</creatorcontrib><creatorcontrib>Hee Cheon, Mi</creatorcontrib><creatorcontrib>Lee, Joo-Yong</creatorcontrib><creatorcontrib>Shin Yoo, Jong</creatorcontrib><creatorcontrib>Steinbusch, Harry W</creatorcontrib><creatorcontrib>Salzet, Michel</creatorcontrib><creatorcontrib>Fournier, Isabelle</creatorcontrib><creatorcontrib>Mok Park, Young</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ho Kim, Jae</au><au>Franck, Julien</au><au>Kang, Taewook</au><au>Heinsen, Helmut</au><au>Ravid, Rivka</au><au>Ferrer, Isidro</au><au>Hee Cheon, Mi</au><au>Lee, Joo-Yong</au><au>Shin Yoo, Jong</au><au>Steinbusch, Harry W</au><au>Salzet, Michel</au><au>Fournier, Isabelle</au><au>Mok Park, Young</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proteome-wide characterization of signalling interactions in the hippocampal CA4/DG subfield of patients with Alzheimer’s disease</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2015-06-10</date><risdate>2015</risdate><volume>5</volume><issue>1</issue><spage>11138</spage><epage>11138</epage><pages>11138-11138</pages><artnum>11138</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Alzheimer’s disease (AD) is the most common form of dementia; however, mechanisms and biomarkers remain unclear. Here, we examined hippocampal CA4 and dentate gyrus subfields, which are less studied in the context of AD pathology, in post-mortem AD and control tissue to identify possible biomarkers. We performed mass spectrometry-based proteomic analysis combined with label-free quantification for identification of differentially expressed proteins. We identified 4,328 proteins, of which 113 showed more than 2-fold higher or lower expression in AD hippocampi than in control tissues. Five proteins were identified as putative AD biomarkers (MDH2, PCLO, TRRAP, YWHAZ and MUC19 isoform 5) and were cross-validated by immunoblotting, selected reaction monitoring and MALDI imaging. We also used a bioinformatics approach to examine upstream signalling interactions of the 113 regulated proteins. Five upstream signalling (IGF1, BDNF, ZAP70, MYC and cyclosporin A) factors showed novel interactions in AD hippocampi. Taken together, these results demonstrate a novel platform that may provide new strategies for the early detection of AD and thus its diagnosis.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26059363</pmid><doi>10.1038/srep11138</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1096-5044</orcidid><orcidid>https://orcid.org/0000-0001-9888-8754</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/154/53/2421 631/1647/2067 631/337/475/2290 631/378/340 82/47 82/58 82/80 Alzheimer Disease - metabolism Alzheimer's disease Bioinformatics Biomarkers Biomarkers - metabolism Brain-derived neurotrophic factor Cyclosporin A Dementia disorders Dentate gyrus Dentate Gyrus - metabolism Hippocampus Humanities and Social Sciences Humans Immunoblotting Insulin-like growth factor I Life Sciences Mass spectrometry Mass spectroscopy multidisciplinary Myc protein Neurodegenerative diseases Proteins Proteome Science Signal Transduction Upstream ZAP-70 protein |
title | Proteome-wide characterization of signalling interactions in the hippocampal CA4/DG subfield of patients with Alzheimer’s disease |
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