Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
26
pubmed:dateCreated
2011-7-1
pubmed:abstractText
Ontogenesis of T cells in the thymus is a complex process whose molecular control is poorly understood. The present study investigated microRNAs involved in human thymocyte differentiation by comparing the microRNA expression profiles of thymocytes at the double-positive, single-positive CD4(+) and single-positive CD8(+) maturation stages. Microarray analysis showed that each thymocyte population displays a distinct microRNA expression profile that reflects their developmental relationships. Moreover, analysis of small-RNA libraries generated from human unsorted and double-positive thymocytes and from mature peripheral CD4(+) and CD8(+) T lymphocytes, together with the microarray data, indicated a trend toward up-regulation of microRNA expression during T-cell maturation after the double-positive stage and revealed a group of microRNAs regulated during normal T-cell development, including miR-150, which is strongly up-regulated as maturation progresses. We showed that miR-150 targets NOTCH3, a member of the Notch receptor family that plays important roles both in T-cell differentiation and leukemogenesis. Forced expression of miR-150 reduces NOTCH3 levels in T-cell lines and has adverse effects on their proliferation and survival. Overall, these findings suggest that control of the Notch pathway through miR-150 may have an important impact on T-cell development and physiology.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1528-0020
pubmed:author
pubmed:issnType
Electronic
pubmed:day
30
pubmed:volume
117
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7053-62
pubmed:meshHeading
pubmed-meshheading:21551231-3' Untranslated Regions, pubmed-meshheading:21551231-Adult, pubmed-meshheading:21551231-Apoptosis, pubmed-meshheading:21551231-Cell Differentiation, pubmed-meshheading:21551231-Cell Line, pubmed-meshheading:21551231-Cell Line, Tumor, pubmed-meshheading:21551231-Cell Proliferation, pubmed-meshheading:21551231-Cells, Cultured, pubmed-meshheading:21551231-Child, Preschool, pubmed-meshheading:21551231-Gene Expression Profiling, pubmed-meshheading:21551231-Gene Expression Regulation, pubmed-meshheading:21551231-Genes, Reporter, pubmed-meshheading:21551231-Humans, pubmed-meshheading:21551231-Infant, pubmed-meshheading:21551231-Infant, Newborn, pubmed-meshheading:21551231-MicroRNAs, pubmed-meshheading:21551231-Precursor Cell Lymphoblastic Leukemia-Lymphoma, pubmed-meshheading:21551231-RNA, Messenger, pubmed-meshheading:21551231-Receptors, Notch, pubmed-meshheading:21551231-T-Lymphocyte Subsets, pubmed-meshheading:21551231-T-Lymphocytes, pubmed-meshheading:21551231-Thymus Gland
pubmed:year
2011
pubmed:articleTitle
Modulation of microRNA expression in human T-cell development: targeting of NOTCH3 by miR-150.
pubmed:affiliation
Department of Oncology and Surgical Sciences, University of Padova, Padova, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't