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- Publisher Website: 10.1089/cell.2010.0051
- Scopus: eid_2-s2.0-78649507841
- PMID: 20858051
- WOS: WOS:000284619400002
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Article: ROCK inhibition facilitates the generation of human-induced pluripotent stem cells in a defined, feeder-, and serum-free system
Title | ROCK inhibition facilitates the generation of human-induced pluripotent stem cells in a defined, feeder-, and serum-free system | ||||
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Authors | |||||
Keywords | Species Index: Animalia Mus | ||||
Issue Date | 2010 | ||||
Publisher | Mary Ann Liebert, Inc. Publishers. The Journal's web site is located at http://www.liebertpub.com/clo | ||||
Citation | Cellular Reprogramming, 2010, v. 12 n. 6, p. 641-653 How to Cite? | ||||
Abstract | Human-induced pluripotent stem cells (iPSCs) generated from human adult somatic cells through reprogramming hold great promises for future regenerative medicine. However, exposure of human iPSCs to animal feeder and serum in the process of their generation and maintenance imposes risk of transmitting animal pathogens to human subjects, thus hindering the potential therapeutic applications. Here, we report the successful generation of human iPSCs in a feeder-independent culture system with defined factors. Two stable human iPSC lines were established from primary human dermal fibroblasts of two healthy volunteers. These human iPSCs expressed a panel of pluripotency markers including stage-specific embryonic antigen (SSEA)-4, tumor-rejection antigen (TRA)-1-60, TRA-1-81, and alkaline phosphatase, while maintaining normal karyotypes and the exogenous reprogramming factors being silenced. In addition, these human iPSCs can differentiate along lineages representative of the three embryonic germ layers upon formation of embryoid bodies, indicating their pluripotency. Furthermore, subcutaneous transplantation of these cells into immunodeficient mice resulted in teratoma formation in 6 to 8 weeks. Our findings are an important step toward generating patient-specific iPSCs in a more clinically compliant manner by eliminating the need of animal feeder cells and animal serum. © 2010 Mary Ann Liebert, Inc. | ||||
Persistent Identifier | http://hdl.handle.net/10722/134669 | ||||
ISSN | 2023 Impact Factor: 1.2 2023 SCImago Journal Rankings: 0.316 | ||||
PubMed Central ID | |||||
ISI Accession Number ID |
Funding Information: This work was supported by the Hong Kong Research Grant Council (HKU8CRF09 to Prof. Tse and Dr. Siu, and HKU 780110M to Prof. Tse). | ||||
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DC Field | Value | Language |
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dc.contributor.author | Lai, WH | en_HK |
dc.contributor.author | Ho, JCY | en_HK |
dc.contributor.author | Lee, YK | en_HK |
dc.contributor.author | Ng, KM | en_HK |
dc.contributor.author | Au, KW | en_HK |
dc.contributor.author | Chan, YC | en_HK |
dc.contributor.author | Lau, CP | en_HK |
dc.contributor.author | Tse, HF | en_HK |
dc.contributor.author | Siu, CW | en_HK |
dc.date.accessioned | 2011-07-05T08:23:58Z | - |
dc.date.available | 2011-07-05T08:23:58Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Cellular Reprogramming, 2010, v. 12 n. 6, p. 641-653 | en_HK |
dc.identifier.issn | 2152-4971 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/134669 | - |
dc.description.abstract | Human-induced pluripotent stem cells (iPSCs) generated from human adult somatic cells through reprogramming hold great promises for future regenerative medicine. However, exposure of human iPSCs to animal feeder and serum in the process of their generation and maintenance imposes risk of transmitting animal pathogens to human subjects, thus hindering the potential therapeutic applications. Here, we report the successful generation of human iPSCs in a feeder-independent culture system with defined factors. Two stable human iPSC lines were established from primary human dermal fibroblasts of two healthy volunteers. These human iPSCs expressed a panel of pluripotency markers including stage-specific embryonic antigen (SSEA)-4, tumor-rejection antigen (TRA)-1-60, TRA-1-81, and alkaline phosphatase, while maintaining normal karyotypes and the exogenous reprogramming factors being silenced. In addition, these human iPSCs can differentiate along lineages representative of the three embryonic germ layers upon formation of embryoid bodies, indicating their pluripotency. Furthermore, subcutaneous transplantation of these cells into immunodeficient mice resulted in teratoma formation in 6 to 8 weeks. Our findings are an important step toward generating patient-specific iPSCs in a more clinically compliant manner by eliminating the need of animal feeder cells and animal serum. © 2010 Mary Ann Liebert, Inc. | en_HK |
dc.language | eng | en_US |
dc.publisher | Mary Ann Liebert, Inc. Publishers. The Journal's web site is located at http://www.liebertpub.com/clo | en_HK |
dc.relation.ispartof | Cellular Reprogramming | en_HK |
dc.subject | Species Index: Animalia | en_US |
dc.subject | Mus | en_US |
dc.title | ROCK inhibition facilitates the generation of human-induced pluripotent stem cells in a defined, feeder-, and serum-free system | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Ng, KM: skykmng@hkucc.hku.hk | en_HK |
dc.identifier.email | Chan, YC: ycchan09@hku.hk | en_HK |
dc.identifier.email | Tse, HF: hftse@hkucc.hku.hk | en_HK |
dc.identifier.email | Siu, CW: cwdsiu@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ng, KM=rp01670 | en_HK |
dc.identifier.authority | Chan, YC=rp01502 | en_HK |
dc.identifier.authority | Tse, HF=rp00428 | en_HK |
dc.identifier.authority | Siu, CW=rp00534 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1089/cell.2010.0051 | en_HK |
dc.identifier.pmid | 20858051 | - |
dc.identifier.pmcid | PMC2993021 | - |
dc.identifier.scopus | eid_2-s2.0-78649507841 | en_HK |
dc.identifier.hkuros | 169709 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-78649507841&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 12 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 641 | en_HK |
dc.identifier.epage | 653 | en_HK |
dc.identifier.eissn | 2152-4998 | - |
dc.identifier.isi | WOS:000284619400002 | - |
dc.publisher.place | United States | en_HK |
dc.relation.project | Autologous Induced Pluripotent Stem Cells Derived Cardiomyocytes for Cardiac Repair in Porcine Ischemic Cardiomyopathy | - |
dc.identifier.scopusauthorid | Lai, WH=18434390500 | en_HK |
dc.identifier.scopusauthorid | Ho, JCY=7402650173 | en_HK |
dc.identifier.scopusauthorid | Lee, YK=25958641200 | en_HK |
dc.identifier.scopusauthorid | Ng, KM=25122990200 | en_HK |
dc.identifier.scopusauthorid | Au, KW=9738204200 | en_HK |
dc.identifier.scopusauthorid | Chan, YC=7403676116 | en_HK |
dc.identifier.scopusauthorid | Lau, CP=7401968501 | en_HK |
dc.identifier.scopusauthorid | Tse, HF=7006070805 | en_HK |
dc.identifier.scopusauthorid | Siu, CW=7006550690 | en_HK |
dc.identifier.issnl | 2152-4971 | - |