File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.bbrc.2008.12.160
- Scopus: eid_2-s2.0-59249094356
- PMID: 19135029
- WOS: WOS:000263336700019
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Effects of iron oxide nanoparticles on cardiac differentiation of embryonic stem cells
Title | Effects of iron oxide nanoparticles on cardiac differentiation of embryonic stem cells | ||||
---|---|---|---|---|---|
Authors | |||||
Keywords | Cardiac differentiation Embryonic stem cell Superparamagnetic iron oxide | ||||
Issue Date | 2009 | ||||
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/wps/find/journaldescription.cws_home/622790/description | ||||
Citation | Biochemical And Biophysical Research Communications, 2009, v. 379 n. 4, p. 898-903 How to Cite? | ||||
Abstract | The therapeutic potential of transplantation of embryonic stem cells (ESCs) in animal model of myocardial infarction has been consistently demonstrated. The development of superparamagnetic iron oxide (SPIO) nanoparticles labeling and cardiac magnetic resonance imaging (MRI) have been increasingly used to track the migration of transplanted cells in vivo allowing cell fate determination. However, the impact of SPIO- labeling on cell phenotype and cardiac differentiation capacity of ESCs remains unclear. In this study, we demonstrated that ESCs labeled with SPIO compared to their unlabeled counterparts had similar cardiogenic capacity, and SPIO-labeling did not affect calcium-handling property of ESC-derived cardiomyocytes. Moreover, transplantation of SPIO-labeled ESCs via direct intra-myocardial injection to infarct myocardium resulted in significant improvement in heart function. These findings demonstrated the feasibility of in vivo ESC tracking using SPIO-labeling and cardiac MRI without affecting the cardiac differentiation potential and functional properties of ESCs. © 2009 Elsevier Inc. All rights reserved. | ||||
Persistent Identifier | http://hdl.handle.net/10722/91551 | ||||
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.770 | ||||
ISI Accession Number ID |
Funding Information: This Study was supported by Research Grants Council of Hong Kong, General Research Fund (No. HKU 7594/05M), | ||||
References | |||||
Grants |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Au, KW | en_HK |
dc.contributor.author | Liao, SY | en_HK |
dc.contributor.author | Lee, YK | en_HK |
dc.contributor.author | Lai, WH | en_HK |
dc.contributor.author | Ng, KM | en_HK |
dc.contributor.author | Chan, YC | en_HK |
dc.contributor.author | Yip, MC | en_HK |
dc.contributor.author | Ho, CY | en_HK |
dc.contributor.author | Wu, EX | en_HK |
dc.contributor.author | Li, RA | en_HK |
dc.contributor.author | Siu, CW | en_HK |
dc.contributor.author | Tse, HF | en_HK |
dc.date.accessioned | 2010-09-17T10:21:14Z | - |
dc.date.available | 2010-09-17T10:21:14Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Biochemical And Biophysical Research Communications, 2009, v. 379 n. 4, p. 898-903 | en_HK |
dc.identifier.issn | 0006-291X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/91551 | - |
dc.description.abstract | The therapeutic potential of transplantation of embryonic stem cells (ESCs) in animal model of myocardial infarction has been consistently demonstrated. The development of superparamagnetic iron oxide (SPIO) nanoparticles labeling and cardiac magnetic resonance imaging (MRI) have been increasingly used to track the migration of transplanted cells in vivo allowing cell fate determination. However, the impact of SPIO- labeling on cell phenotype and cardiac differentiation capacity of ESCs remains unclear. In this study, we demonstrated that ESCs labeled with SPIO compared to their unlabeled counterparts had similar cardiogenic capacity, and SPIO-labeling did not affect calcium-handling property of ESC-derived cardiomyocytes. Moreover, transplantation of SPIO-labeled ESCs via direct intra-myocardial injection to infarct myocardium resulted in significant improvement in heart function. These findings demonstrated the feasibility of in vivo ESC tracking using SPIO-labeling and cardiac MRI without affecting the cardiac differentiation potential and functional properties of ESCs. © 2009 Elsevier Inc. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/wps/find/journaldescription.cws_home/622790/description | en_HK |
dc.relation.ispartof | Biochemical and Biophysical Research Communications | en_HK |
dc.subject | Cardiac differentiation | en_HK |
dc.subject | Embryonic stem cell | en_HK |
dc.subject | Superparamagnetic iron oxide | en_HK |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Cell Differentiation - drug effects | en_HK |
dc.subject.mesh | Cell Line | en_HK |
dc.subject.mesh | Cell Movement - drug effects | en_HK |
dc.subject.mesh | Embryonic Stem Cells - cytology - drug effects - transplantation | en_HK |
dc.subject.mesh | Ferric Compounds - adverse effects | en_HK |
dc.subject.mesh | Green Fluorescent Proteins - analysis - biosynthesis | en_HK |
dc.subject.mesh | Magnetic Resonance Imaging - methods | en_HK |
dc.subject.mesh | Mice | en_HK |
dc.subject.mesh | Myocytes, Cardiac - cytology - drug effects | en_HK |
dc.subject.mesh | Nanoparticles - adverse effects | en_HK |
dc.subject.mesh | Staining and Labeling - methods | en_HK |
dc.title | Effects of iron oxide nanoparticles on cardiac differentiation of embryonic stem cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chan, YC:yauchi@graduate.hku.hk | en_HK |
dc.identifier.email | Wu, EX:ewu1@hkucc.hku.hk | en_HK |
dc.identifier.email | Li, RA:ronaldli@hkucc.hku.hk | en_HK |
dc.identifier.email | Siu, CW:cwdsiu@hkucc.hku.hk | en_HK |
dc.identifier.email | Tse, HF:hftse@hkucc.hku.hk | en_HK |
dc.identifier.authority | Chan, YC=rp01502 | en_HK |
dc.identifier.authority | Wu, EX=rp00193 | en_HK |
dc.identifier.authority | Li, RA=rp01352 | en_HK |
dc.identifier.authority | Siu, CW=rp00534 | en_HK |
dc.identifier.authority | Tse, HF=rp00428 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.bbrc.2008.12.160 | en_HK |
dc.identifier.pmid | 19135029 | - |
dc.identifier.scopus | eid_2-s2.0-59249094356 | en_HK |
dc.identifier.hkuros | 155630 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-59249094356&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 379 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 898 | en_HK |
dc.identifier.epage | 903 | en_HK |
dc.identifier.eissn | 1090-2104 | - |
dc.identifier.isi | WOS:000263336700019 | - |
dc.publisher.place | United States | en_HK |
dc.relation.project | Embryonic stem cell transplantation as a novel therapy for post-infarct left ventricular remodeling | - |
dc.identifier.scopusauthorid | Au, KW=9738204200 | en_HK |
dc.identifier.scopusauthorid | Liao, SY=22433820700 | en_HK |
dc.identifier.scopusauthorid | Lee, YK=25958641200 | en_HK |
dc.identifier.scopusauthorid | Lai, WH=18434390500 | en_HK |
dc.identifier.scopusauthorid | Ng, KM=7403178872 | en_HK |
dc.identifier.scopusauthorid | Chan, YC=7403676116 | en_HK |
dc.identifier.scopusauthorid | Yip, MC=36741863200 | en_HK |
dc.identifier.scopusauthorid | Ho, CY=25958716700 | en_HK |
dc.identifier.scopusauthorid | Wu, EX=7202128034 | en_HK |
dc.identifier.scopusauthorid | Li, RA=7404724466 | en_HK |
dc.identifier.scopusauthorid | Siu, CW=7006550690 | en_HK |
dc.identifier.scopusauthorid | Tse, HF=7006070805 | en_HK |
dc.identifier.issnl | 0006-291X | - |