Regional Differences in Neuroinflammation-Associated Gene Expression in the Brain of Sporadic Creutzfeldt-Jakob Disease Patients
Neuroinflammation is an essential part of neurodegeneration. Yet, the current understanding of neuroinflammation-associated molecular events in distinct brain regions of prion disease patients is insufficient to lay the ground for effective treatment strategies targeting this complex neuropathologic...
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Veröffentlicht in: | International journal of molecular sciences 2020-12, Vol.22 (1), p.140 |
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description | Neuroinflammation is an essential part of neurodegeneration. Yet, the current understanding of neuroinflammation-associated molecular events in distinct brain regions of prion disease patients is insufficient to lay the ground for effective treatment strategies targeting this complex neuropathological process. To address this problem, we analyzed the expression of 800 neuroinflammation-associated genes to create a profile of biological processes taking place in the frontal cortex and cerebellum of patients who suffered from sporadic Creutzfeldt-Jakob disease. The analysis was performed using NanoString nCounter technology with human neuroinflammation panel+. The observed gene expression patterns were regionally and sub-regionally distinct, suggesting a variable neuroinflammatory response. Interestingly, the observed differences could not be explained by the molecular subtypes of sporadic Creutzfeldt-Jakob disease. Furthermore, analyses of canonical pathways and upstream regulators based on differentially expressed genes indicated an overlap between biological processes taking place in different brain regions. This suggests that even smaller-scale spatial data reflecting subtle changes in brain cells' functional heterogeneity and their immediate pathologic microenvironments are needed to explain the observed differential gene expression in a greater detail. |
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Yet, the current understanding of neuroinflammation-associated molecular events in distinct brain regions of prion disease patients is insufficient to lay the ground for effective treatment strategies targeting this complex neuropathological process. To address this problem, we analyzed the expression of 800 neuroinflammation-associated genes to create a profile of biological processes taking place in the frontal cortex and cerebellum of patients who suffered from sporadic Creutzfeldt-Jakob disease. The analysis was performed using NanoString nCounter technology with human neuroinflammation panel+. The observed gene expression patterns were regionally and sub-regionally distinct, suggesting a variable neuroinflammatory response. Interestingly, the observed differences could not be explained by the molecular subtypes of sporadic Creutzfeldt-Jakob disease. Furthermore, analyses of canonical pathways and upstream regulators based on differentially expressed genes indicated an overlap between biological processes taking place in different brain regions. This suggests that even smaller-scale spatial data reflecting subtle changes in brain cells' functional heterogeneity and their immediate pathologic microenvironments are needed to explain the observed differential gene expression in a greater detail.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms22010140</identifier><identifier>PMID: 33375642</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aged ; Biological activity ; Biomarkers ; Brain ; Brain - metabolism ; Brain - pathology ; Cellular Microenvironment - genetics ; Cellular Microenvironment - immunology ; Cerebellum ; Computational Biology - methods ; Creutzfeldt-Jakob Syndrome - etiology ; Creutzfeldt-Jakob Syndrome - metabolism ; Creutzfeldt-Jakob Syndrome - pathology ; Disease ; Disease Susceptibility ; Female ; Gene Expression ; Gene Expression Profiling ; Genes ; Heterogeneity ; Humans ; Inflammation ; Male ; Metabolism ; Microenvironments ; Middle Aged ; Neurodegeneration ; Neurosciences ; Pathogenesis ; Proteins ; Regional differences ; Spatial data ; Transcriptome</subject><ispartof>International journal of molecular sciences, 2020-12, Vol.22 (1), p.140</ispartof><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-6fbe39348be98db0667278f1c6d9f7c74a23949f136866f29d8900c0137cbb8c3</citedby><cites>FETCH-LOGICAL-c412t-6fbe39348be98db0667278f1c6d9f7c74a23949f136866f29d8900c0137cbb8c3</cites><orcidid>0000-0003-0202-9942 ; 0000-0002-6068-901X</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/PMC7795938/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795938/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33375642$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Areškevičiūtė, Aušrinė</creatorcontrib><creatorcontrib>Litman, Thomas</creatorcontrib><creatorcontrib>Broholm, Helle</creatorcontrib><creatorcontrib>Melchior, Linea C</creatorcontrib><creatorcontrib>Nielsen, Pia R</creatorcontrib><creatorcontrib>Green, Alison</creatorcontrib><creatorcontrib>Eriksen, Jens O</creatorcontrib><creatorcontrib>Smith, Colin</creatorcontrib><creatorcontrib>Lund, Eva L</creatorcontrib><title>Regional Differences in Neuroinflammation-Associated Gene Expression in the Brain of Sporadic Creutzfeldt-Jakob Disease Patients</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Neuroinflammation is an essential part of neurodegeneration. Yet, the current understanding of neuroinflammation-associated molecular events in distinct brain regions of prion disease patients is insufficient to lay the ground for effective treatment strategies targeting this complex neuropathological process. To address this problem, we analyzed the expression of 800 neuroinflammation-associated genes to create a profile of biological processes taking place in the frontal cortex and cerebellum of patients who suffered from sporadic Creutzfeldt-Jakob disease. The analysis was performed using NanoString nCounter technology with human neuroinflammation panel+. The observed gene expression patterns were regionally and sub-regionally distinct, suggesting a variable neuroinflammatory response. Interestingly, the observed differences could not be explained by the molecular subtypes of sporadic Creutzfeldt-Jakob disease. Furthermore, analyses of canonical pathways and upstream regulators based on differentially expressed genes indicated an overlap between biological processes taking place in different brain regions. 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Yet, the current understanding of neuroinflammation-associated molecular events in distinct brain regions of prion disease patients is insufficient to lay the ground for effective treatment strategies targeting this complex neuropathological process. To address this problem, we analyzed the expression of 800 neuroinflammation-associated genes to create a profile of biological processes taking place in the frontal cortex and cerebellum of patients who suffered from sporadic Creutzfeldt-Jakob disease. The analysis was performed using NanoString nCounter technology with human neuroinflammation panel+. The observed gene expression patterns were regionally and sub-regionally distinct, suggesting a variable neuroinflammatory response. Interestingly, the observed differences could not be explained by the molecular subtypes of sporadic Creutzfeldt-Jakob disease. Furthermore, analyses of canonical pathways and upstream regulators based on differentially expressed genes indicated an overlap between biological processes taking place in different brain regions. This suggests that even smaller-scale spatial data reflecting subtle changes in brain cells' functional heterogeneity and their immediate pathologic microenvironments are needed to explain the observed differential gene expression in a greater detail.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>33375642</pmid><doi>10.3390/ijms22010140</doi><orcidid>https://orcid.org/0000-0003-0202-9942</orcidid><orcidid>https://orcid.org/0000-0002-6068-901X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Biological activity Biomarkers Brain Brain - metabolism Brain - pathology Cellular Microenvironment - genetics Cellular Microenvironment - immunology Cerebellum Computational Biology - methods Creutzfeldt-Jakob Syndrome - etiology Creutzfeldt-Jakob Syndrome - metabolism Creutzfeldt-Jakob Syndrome - pathology Disease Disease Susceptibility Female Gene Expression Gene Expression Profiling Genes Heterogeneity Humans Inflammation Male Metabolism Microenvironments Middle Aged Neurodegeneration Neurosciences Pathogenesis Proteins Regional differences Spatial data Transcriptome |
title | Regional Differences in Neuroinflammation-Associated Gene Expression in the Brain of Sporadic Creutzfeldt-Jakob Disease Patients |
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