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Article: MicroRNA profiling predicts a variance in the proliferative potential of cardiac progenitor cells derived from neonatal and adult murine hearts
Title | MicroRNA profiling predicts a variance in the proliferative potential of cardiac progenitor cells derived from neonatal and adult murine hearts |
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Authors | |
Keywords | C-kit Cardiac progenitor cells MicroRNA profiling MiR-17 cluster Proliferation |
Issue Date | 2012 |
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/yjmcc |
Citation | Journal Of Molecular And Cellular Cardiology, 2012, v. 52 n. 1, p. 264-272 How to Cite? |
Abstract | Cardiac progenitor cells (CPCs) are multipotent cells that may offer tremendous potentials for the regeneration of injured myocardium. To expand the limited number of CPCs for effective clinical regeneration of myocardium, it is important to understand their proliferative potentials. Single-cell based assays were utilized to purify c-kit pos CPCs from human and mouse hearts. MicroRNA profiling identified eight differentially expressed microRNAs in CPCs from neonatal and adult hearts. Notably, the predicted protein targets were predominantly involved in cellular proliferation-related pathways. To directly test this phenotypic prediction, the developmental variance in the proliferation of CPCs was tested. Ki67 protein expression and DNA kinetics were tested in human and mouse in vivo CPCs, and doubling times were tested in primary culture of mouse CPCs. The human embryonic and mouse neonatal CPCs showed a six-fold increase in Ki67 expressing cells, a two-fold increase in the number of cells in S/G2-M phases of cell cycle, and a seven-fold increase in the doubling time in culture when compared to the corresponding adult CPCs. The over-expression of miR-17-92 increased the proliferation in adult CPCs in vivo by two-fold. In addition, the level of retinoblastoma-like 2 (Rbl2/p130) protein was two-fold higher in adult compared to neonatal-mouse CPCs. In conclusion, we demonstrate a differentially regulated cohort of microRNAs that predicts differences in cellular proliferation in CPCs during postnatal development and target microRNAs that are involved in this transition. Our study provides new insights that may enhance the utilization of adult CPCs for regenerative therapy of the injured myocardium. © 2011 Elsevier Ltd. |
Persistent Identifier | http://hdl.handle.net/10722/163441 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.639 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sirish, P | en_US |
dc.contributor.author | López, JE | en_US |
dc.contributor.author | Li, N | en_US |
dc.contributor.author | Wong, A | en_US |
dc.contributor.author | Timofeyev, V | en_US |
dc.contributor.author | Young, JN | en_US |
dc.contributor.author | Majdi, M | en_US |
dc.contributor.author | Li, RA | en_US |
dc.contributor.author | Chen, HSV | en_US |
dc.contributor.author | Chiamvimonvat, N | en_US |
dc.date.accessioned | 2012-09-05T05:31:24Z | - |
dc.date.available | 2012-09-05T05:31:24Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Journal Of Molecular And Cellular Cardiology, 2012, v. 52 n. 1, p. 264-272 | en_US |
dc.identifier.issn | 0022-2828 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/163441 | - |
dc.description.abstract | Cardiac progenitor cells (CPCs) are multipotent cells that may offer tremendous potentials for the regeneration of injured myocardium. To expand the limited number of CPCs for effective clinical regeneration of myocardium, it is important to understand their proliferative potentials. Single-cell based assays were utilized to purify c-kit pos CPCs from human and mouse hearts. MicroRNA profiling identified eight differentially expressed microRNAs in CPCs from neonatal and adult hearts. Notably, the predicted protein targets were predominantly involved in cellular proliferation-related pathways. To directly test this phenotypic prediction, the developmental variance in the proliferation of CPCs was tested. Ki67 protein expression and DNA kinetics were tested in human and mouse in vivo CPCs, and doubling times were tested in primary culture of mouse CPCs. The human embryonic and mouse neonatal CPCs showed a six-fold increase in Ki67 expressing cells, a two-fold increase in the number of cells in S/G2-M phases of cell cycle, and a seven-fold increase in the doubling time in culture when compared to the corresponding adult CPCs. The over-expression of miR-17-92 increased the proliferation in adult CPCs in vivo by two-fold. In addition, the level of retinoblastoma-like 2 (Rbl2/p130) protein was two-fold higher in adult compared to neonatal-mouse CPCs. In conclusion, we demonstrate a differentially regulated cohort of microRNAs that predicts differences in cellular proliferation in CPCs during postnatal development and target microRNAs that are involved in this transition. Our study provides new insights that may enhance the utilization of adult CPCs for regenerative therapy of the injured myocardium. © 2011 Elsevier Ltd. | en_US |
dc.language | eng | en_US |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/yjmcc | en_US |
dc.relation.ispartof | Journal of Molecular and Cellular Cardiology | en_US |
dc.rights | NOTICE: this is the author’s version of a work that was accepted for publication in Journal of Molecular and Cellular Cardiology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Journal of Molecular and Cellular Cardiology, [VOL 52, ISSUE 1, 2012] DOI 10.1016/j.yjmcc.2011.10.012 | - |
dc.subject | C-kit | - |
dc.subject | Cardiac progenitor cells | - |
dc.subject | MicroRNA profiling | - |
dc.subject | MiR-17 cluster | - |
dc.subject | Proliferation | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Cell Cycle - Physiology | en_US |
dc.subject.mesh | Cell Proliferation | en_US |
dc.subject.mesh | Cell Separation | en_US |
dc.subject.mesh | Cells, Cultured | en_US |
dc.subject.mesh | Cluster Analysis | en_US |
dc.subject.mesh | Gene Expression Profiling | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Kinetics | en_US |
dc.subject.mesh | Mice | en_US |
dc.subject.mesh | Micrornas - Genetics - Metabolism | en_US |
dc.subject.mesh | Myoblasts, Cardiac - Metabolism | en_US |
dc.subject.mesh | Phenotype | en_US |
dc.subject.mesh | Proto-Oncogene Proteins C-Kit - Metabolism | en_US |
dc.subject.mesh | Retinoblastoma-Like Protein P130 - Metabolism | en_US |
dc.title | MicroRNA profiling predicts a variance in the proliferative potential of cardiac progenitor cells derived from neonatal and adult murine hearts | en_US |
dc.type | Article | en_US |
dc.identifier.email | Li, RA:ronaldli@hkucc.hku.hk | en_US |
dc.identifier.authority | Li, RA=rp01352 | en_US |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1016/j.yjmcc.2011.10.012 | en_US |
dc.identifier.pmid | 22062954 | - |
dc.identifier.pmcid | PMC3362795 | - |
dc.identifier.scopus | eid_2-s2.0-84155188929 | en_US |
dc.identifier.hkuros | 212205 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84155188929&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 52 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 264 | en_US |
dc.identifier.epage | 272 | en_US |
dc.identifier.isi | WOS:000303275000030 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Sirish, P=36873197300 | en_US |
dc.identifier.scopusauthorid | López, JE=36986226000 | en_US |
dc.identifier.scopusauthorid | Li, N=36014373300 | en_US |
dc.identifier.scopusauthorid | Wong, A=54790379900 | en_US |
dc.identifier.scopusauthorid | Timofeyev, V=8966886700 | en_US |
dc.identifier.scopusauthorid | Young, JN=8277142200 | en_US |
dc.identifier.scopusauthorid | Majdi, M=36981350100 | en_US |
dc.identifier.scopusauthorid | Li, RA=7404724466 | en_US |
dc.identifier.scopusauthorid | Chen, HSV=52663310300 | en_US |
dc.identifier.scopusauthorid | Chiamvimonvat, N=7004461965 | en_US |
dc.identifier.citeulike | 9949531 | - |
dc.identifier.issnl | 0022-2828 | - |