MicroRNAs in brain aging
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chand Parvez Danka Mohammed | - |
dc.contributor.author | Jun Soo Park | - |
dc.contributor.author | Hong Gil Nam | - |
dc.contributor.author | Keetae Kim | - |
dc.date.available | 2018-01-08T05:17:15Z | - |
dc.date.created | 2017-08-03 | - |
dc.date.issued | 2017-12 | - |
dc.identifier.issn | 0047-6374 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/4182 | - |
dc.description.abstract | Brain aging is one of the most crucial biological processes that affect the physiological balance betweenhealth and disease. Age-associated dysfunction of brain leads to severe health problems in current agingsociety. MicroRNAs (miRNAs) have emerged as important regulators in most physiological processesincluding fine-tuning of the short-term, cellular regulatory functions as well as modulation of long-termorganismal lifespan. In this review, we discuss critical roles of miRNAs in the progression of normal andpathological brain aging. 50% of all known miRNAs are found in brain including cortex and hippocam-pus. A significant number of expressed miRNAs were differentially regulated during aging, implicatingmiRNAs as regulators of brain aging. The ability of miRNAs to regulate multiple targets within a pathwayor even multiple pathways allows for coordinated regulation of brain functions. miRNA-mediated, brainfunctional changes are evident in cognition, inflammation, neuroprotection, lipid metabolism, mitochon-drial function and lifespan. Dysregulation of brain miRNAs contributes to accelerated cognitive declineand increased neurological disorders. Elucidating mechanisms by which miRNAs and their multiple tar-gets are temporally and spatially regulated in normal and pathological brain aging will provide a deeperunderstanding on the process of interrelated pathways of brain aging, and a new insight into therapeuticinterventions. © 2017 Elsevier B.V. All rights reserved. | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | ELSEVIER IRELAND LTD | - |
dc.subject | Aging, microRNA, Brain, Target, Dysregulation | - |
dc.title | MicroRNAs in brain aging | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000423006300002 | - |
dc.identifier.scopusid | 2-s2.0-85010192488 | - |
dc.identifier.rimsid | 59919 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Chand Parvez Danka Mohammed | - |
dc.contributor.affiliatedAuthor | Hong Gil Nam | - |
dc.identifier.doi | 10.1016/j.mad.2017.01.007 | - |
dc.identifier.bibliographicCitation | MECHANISMS OF AGEING AND DEVELOPMENT, v.168, pp.3 - 9 | - |
dc.citation.title | MECHANISMS OF AGEING AND DEVELOPMENT | - |
dc.citation.volume | 168 | - |
dc.citation.startPage | 3 | - |
dc.citation.endPage | 9 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 4 | - |
dc.description.scptc | 5 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | TEMPORAL-LOBE EPILEPSY | - |
dc.subject.keywordPlus | IMMATURE RAT MODEL | - |
dc.subject.keywordPlus | NEURODEGENERATION | - |
dc.subject.keywordPlus | INFLAMMATION | - |
dc.subject.keywordPlus | HIPPOCAMPUS | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | NEURONS | - |
dc.subject.keywordPlus | DISEASE | - |
dc.subject.keywordPlus | MOUSE | - |
dc.subject.keywordPlus | HOMEOSTASIS | - |
dc.subject.keywordAuthor | Aging | - |
dc.subject.keywordAuthor | microRNA | - |
dc.subject.keywordAuthor | Brain | - |
dc.subject.keywordAuthor | Target | - |
dc.subject.keywordAuthor | Dysregulation | - |