Modulated expression of human peripheral blood microRNAs from infancy to adulthood and its role in aging

Summary Accumulating evidence suggests a role for microRNAs (miRNAs) in regulating various processes of mammalian postnatal development and aging. To investigate the changes in blood‐based miRNA expression from preterm infants to adulthood, we compared 365 miRNA expression profiles in a screening se...

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Veröffentlicht in:Aging cell 2014-08, Vol.13 (4), p.679-689
Hauptverfasser: Lai, Chi‐Yu, Wu, Yen‐Tzu, Yu, Sung‐Liang, Yu, Ya‐Hui, Lee, Su‐Yin, Liu, Chih‐Min, Hsieh, Wu‐Shiun, Hwu, Hai‐Gwo, Chen, Pau‐Chung, Jeng, Suh‐Fang, Chen, Wei J.
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container_end_page 689
container_issue 4
container_start_page 679
container_title Aging cell
container_volume 13
creator Lai, Chi‐Yu
Wu, Yen‐Tzu
Yu, Sung‐Liang
Yu, Ya‐Hui
Lee, Su‐Yin
Liu, Chih‐Min
Hsieh, Wu‐Shiun
Hwu, Hai‐Gwo
Chen, Pau‐Chung
Jeng, Suh‐Fang
Chen, Wei J.
description Summary Accumulating evidence suggests a role for microRNAs (miRNAs) in regulating various processes of mammalian postnatal development and aging. To investigate the changes in blood‐based miRNA expression from preterm infants to adulthood, we compared 365 miRNA expression profiles in a screening set of preterm infants and adults. Approximately one‐third of the miRNAs were constantly expressed from postnatal development to adulthood, another one‐third were differentially expressed between preterm infants and adults, and the remaining one‐third were not detectable in these two groups. Based on their expression in infants and adults, the miRNAs were categorized into five classes, and six of the seven miRNAs chosen from each class except one with age‐constant expression were confirmed in a validation set containing infants, children, and adults. Comparing the chromosomal locations of the different miRNA classes revealed two hot spots: the miRNA cluster on 14q32.31 exhibited age‐constant expression, and the one on 9q22.21 exhibited up‐regulation in adults. Furthermore, six miRNAs detectable in adults were down‐regulated in older adults, and four chosen for individual quantification were verified in the validation set. Analysis of the network functions revealed that differentially regulated miRNAs between infants and adults and miRNAs that decreased during aging shared two network functions: inflammatory disease and inflammatory response. Four expression patterns existed in the 11 miRNAs from infancy to adulthood, with a significant transition in ages 9–20 years. Our results provide an overview on the regulation pattern of blood miRNAs throughout life and the possible biological functions performed by different classes of miRNAs.
doi_str_mv 10.1111/acel.12225
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To investigate the changes in blood‐based miRNA expression from preterm infants to adulthood, we compared 365 miRNA expression profiles in a screening set of preterm infants and adults. Approximately one‐third of the miRNAs were constantly expressed from postnatal development to adulthood, another one‐third were differentially expressed between preterm infants and adults, and the remaining one‐third were not detectable in these two groups. Based on their expression in infants and adults, the miRNAs were categorized into five classes, and six of the seven miRNAs chosen from each class except one with age‐constant expression were confirmed in a validation set containing infants, children, and adults. Comparing the chromosomal locations of the different miRNA classes revealed two hot spots: the miRNA cluster on 14q32.31 exhibited age‐constant expression, and the one on 9q22.21 exhibited up‐regulation in adults. Furthermore, six miRNAs detectable in adults were down‐regulated in older adults, and four chosen for individual quantification were verified in the validation set. Analysis of the network functions revealed that differentially regulated miRNAs between infants and adults and miRNAs that decreased during aging shared two network functions: inflammatory disease and inflammatory response. Four expression patterns existed in the 11 miRNAs from infancy to adulthood, with a significant transition in ages 9–20 years. 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Aging Cell published by the Anatomical Society and John Wiley &amp; Sons Ltd.</rights><rights>COPYRIGHT 2014 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2014 The Anatomical Society and John Wiley &amp; Sons Ltd</rights><rights>2014 The Authors. published by the Anatomical Society and John Wiley &amp; Sons Ltd. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326935/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326935/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,1414,11545,27907,27908,45557,45558,46035,46459,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24803090$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lai, Chi‐Yu</creatorcontrib><creatorcontrib>Wu, Yen‐Tzu</creatorcontrib><creatorcontrib>Yu, Sung‐Liang</creatorcontrib><creatorcontrib>Yu, Ya‐Hui</creatorcontrib><creatorcontrib>Lee, Su‐Yin</creatorcontrib><creatorcontrib>Liu, Chih‐Min</creatorcontrib><creatorcontrib>Hsieh, Wu‐Shiun</creatorcontrib><creatorcontrib>Hwu, Hai‐Gwo</creatorcontrib><creatorcontrib>Chen, Pau‐Chung</creatorcontrib><creatorcontrib>Jeng, Suh‐Fang</creatorcontrib><creatorcontrib>Chen, Wei J.</creatorcontrib><title>Modulated expression of human peripheral blood microRNAs from infancy to adulthood and its role in aging</title><title>Aging cell</title><addtitle>Aging Cell</addtitle><description>Summary Accumulating evidence suggests a role for microRNAs (miRNAs) in regulating various processes of mammalian postnatal development and aging. 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Furthermore, six miRNAs detectable in adults were down‐regulated in older adults, and four chosen for individual quantification were verified in the validation set. Analysis of the network functions revealed that differentially regulated miRNAs between infants and adults and miRNAs that decreased during aging shared two network functions: inflammatory disease and inflammatory response. Four expression patterns existed in the 11 miRNAs from infancy to adulthood, with a significant transition in ages 9–20 years. 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To investigate the changes in blood‐based miRNA expression from preterm infants to adulthood, we compared 365 miRNA expression profiles in a screening set of preterm infants and adults. Approximately one‐third of the miRNAs were constantly expressed from postnatal development to adulthood, another one‐third were differentially expressed between preterm infants and adults, and the remaining one‐third were not detectable in these two groups. Based on their expression in infants and adults, the miRNAs were categorized into five classes, and six of the seven miRNAs chosen from each class except one with age‐constant expression were confirmed in a validation set containing infants, children, and adults. Comparing the chromosomal locations of the different miRNA classes revealed two hot spots: the miRNA cluster on 14q32.31 exhibited age‐constant expression, and the one on 9q22.21 exhibited up‐regulation in adults. Furthermore, six miRNAs detectable in adults were down‐regulated in older adults, and four chosen for individual quantification were verified in the validation set. Analysis of the network functions revealed that differentially regulated miRNAs between infants and adults and miRNAs that decreased during aging shared two network functions: inflammatory disease and inflammatory response. Four expression patterns existed in the 11 miRNAs from infancy to adulthood, with a significant transition in ages 9–20 years. Our results provide an overview on the regulation pattern of blood miRNAs throughout life and the possible biological functions performed by different classes of miRNAs.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>24803090</pmid><doi>10.1111/acel.12225</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Online Library Open Access; PubMed Central; Alma/SFX Local Collection
subjects Adult
aging
Aging - blood
Aging - genetics
Child
Child, Preschool
Chromosomes, Human - genetics
Comparative analysis
development
Gene Expression Profiling
Gene Expression Regulation, Developmental
Gene Regulatory Networks - genetics
Humans
Infant
Infant, Newborn
Infants (Premature)
MicroRNA
MicroRNAs - blood
MicroRNAs - classification
MicroRNAs - genetics
network function
Original
peripheral blood
title Modulated expression of human peripheral blood microRNAs from infancy to adulthood and its role in aging
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