Generation of Induced Pluripotent Stem Cells from Human Nasal Epithelial Cells Using a Sendai Virus Vector
The generation of induced pluripotent stem cells (iPSCs) by introducing reprogramming factors into somatic cells is a promising method for stem cell therapy in regenerative medicine. Therefore, it is desirable to develop a minimally invasive simple method to create iPSCs. In this study, we generated...
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| Vydané v: | PloS one Ročník 7; číslo 8; s. e42855 |
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| Hlavní autori: | , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
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United States
Public Library of Science
13.08.2012
Public Library of Science (PLoS) |
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| ISSN: | 1932-6203, 1932-6203 |
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| Abstract | The generation of induced pluripotent stem cells (iPSCs) by introducing reprogramming factors into somatic cells is a promising method for stem cell therapy in regenerative medicine. Therefore, it is desirable to develop a minimally invasive simple method to create iPSCs. In this study, we generated human nasal epithelial cells (HNECs)-derived iPSCs by gene transduction with Sendai virus (SeV) vectors. HNECs can be obtained from subjects in a noninvasive manner, without anesthesia or biopsy. In addition, SeV carries no risk of altering the host genome, which provides an additional level of safety during generation of human iPSCs. The multiplicity of SeV infection ranged from 3 to 4, and the reprogramming efficiency of HNECs was 0.08-0.10%. iPSCs derived from HNECs had global gene expression profiles and epigenetic states consistent with those of human embryonic stem cells. The ease with which HNECs can be obtained, together with their robust reprogramming characteristics, will provide opportunities to investigate disease pathogenesis and molecular mechanisms in vitro, using cells with particular genotypes. |
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| AbstractList | The generation of induced pluripotent stem cells (iPSCs) by introducing reprogramming factors into somatic cells is a promising method for stem cell therapy in regenerative medicine. Therefore, it is desirable to develop a minimally invasive simple method to create iPSCs. In this study, we generated human nasal epithelial cells (HNECs)-derived iPSCs by gene transduction with Sendai virus (SeV) vectors. HNECs can be obtained from subjects in a noninvasive manner, without anesthesia or biopsy. In addition, SeV carries no risk of altering the host genome, which provides an additional level of safety during generation of human iPSCs. The multiplicity of SeV infection ranged from 3 to 4, and the reprogramming efficiency of HNECs was 0.08-0.10%. iPSCs derived from HNECs had global gene expression profiles and epigenetic states consistent with those of human embryonic stem cells. The ease with which HNECs can be obtained, together with their robust reprogramming characteristics, will provide opportunities to investigate disease pathogenesis and molecular mechanisms in vitro, using cells with particular genotypes.The generation of induced pluripotent stem cells (iPSCs) by introducing reprogramming factors into somatic cells is a promising method for stem cell therapy in regenerative medicine. Therefore, it is desirable to develop a minimally invasive simple method to create iPSCs. In this study, we generated human nasal epithelial cells (HNECs)-derived iPSCs by gene transduction with Sendai virus (SeV) vectors. HNECs can be obtained from subjects in a noninvasive manner, without anesthesia or biopsy. In addition, SeV carries no risk of altering the host genome, which provides an additional level of safety during generation of human iPSCs. The multiplicity of SeV infection ranged from 3 to 4, and the reprogramming efficiency of HNECs was 0.08-0.10%. iPSCs derived from HNECs had global gene expression profiles and epigenetic states consistent with those of human embryonic stem cells. The ease with which HNECs can be obtained, together with their robust reprogramming characteristics, will provide opportunities to investigate disease pathogenesis and molecular mechanisms in vitro, using cells with particular genotypes. The generation of induced pluripotent stem cells (iPSCs) by introducing reprogramming factors into somatic cells is a promising method for stem cell therapy in regenerative medicine. Therefore, it is desirable to develop a minimally invasive simple method to create iPSCs. In this study, we generated human nasal epithelial cells (HNECs)-derived iPSCs by gene transduction with Sendai virus (SeV) vectors. HNECs can be obtained from subjects in a noninvasive manner, without anesthesia or biopsy. In addition, SeV carries no risk of altering the host genome, which provides an additional level of safety during generation of human iPSCs. The multiplicity of SeV infection ranged from 3 to 4, and the reprogramming efficiency of HNECs was 0.08–0.10%. iPSCs derived from HNECs had global gene expression profiles and epigenetic states consistent with those of human embryonic stem cells. The ease with which HNECs can be obtained, together with their robust reprogramming characteristics, will provide opportunities to investigate disease pathogenesis and molecular mechanisms in vitro, using cells with particular genotypes. |
| Audience | Academic |
| Author | Satomi, Kaishi Noguchi, Emiko Fujioka, Tsuyoshi Horiuchi, Yasue Hasegawa, Mamoru Hamada, Yuko Imoto, Yoshimasa Nakamura, Yukio Ono, Mizuho Arinami, Tadao Matsuo-Takasaki, Mami |
| AuthorAffiliation | 1 Department of Medical Genetics, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan 6 DNAVEC Research Inc, Tsukuba, Ibaraki, Japan 2 Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America 7 Cell Engineering Division, RIKEN BioResource Center, Tsukuba, Ibaraki, Japan 3 Department of Regenerative Medicine and Stem Cell Biology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan 8 Japan Science and Technology Agency, Core Research for Evolutional Science and Technology (CREST), Chiyoda, Tokyo, Japan University of Milan, Italy 4 Department of Otorhinolaryngology Head and Neck Surgery, Faculty of Medical Sciences, University of Fukui, Fukui City, Fukui, Japan 5 Department of Diagnostic Pathology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan |
| AuthorAffiliation_xml | – name: 6 DNAVEC Research Inc, Tsukuba, Ibaraki, Japan – name: 3 Department of Regenerative Medicine and Stem Cell Biology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan – name: 8 Japan Science and Technology Agency, Core Research for Evolutional Science and Technology (CREST), Chiyoda, Tokyo, Japan – name: 1 Department of Medical Genetics, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan – name: 2 Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America – name: University of Milan, Italy – name: 4 Department of Otorhinolaryngology Head and Neck Surgery, Faculty of Medical Sciences, University of Fukui, Fukui City, Fukui, Japan – name: 7 Cell Engineering Division, RIKEN BioResource Center, Tsukuba, Ibaraki, Japan – name: 5 Department of Diagnostic Pathology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan |
| Author_xml | – sequence: 1 givenname: Mizuho surname: Ono fullname: Ono, Mizuho – sequence: 2 givenname: Yuko surname: Hamada fullname: Hamada, Yuko – sequence: 3 givenname: Yasue surname: Horiuchi fullname: Horiuchi, Yasue – sequence: 4 givenname: Mami surname: Matsuo-Takasaki fullname: Matsuo-Takasaki, Mami – sequence: 5 givenname: Yoshimasa surname: Imoto fullname: Imoto, Yoshimasa – sequence: 6 givenname: Kaishi surname: Satomi fullname: Satomi, Kaishi – sequence: 7 givenname: Tadao surname: Arinami fullname: Arinami, Tadao – sequence: 8 givenname: Mamoru surname: Hasegawa fullname: Hasegawa, Mamoru – sequence: 9 givenname: Tsuyoshi surname: Fujioka fullname: Fujioka, Tsuyoshi – sequence: 10 givenname: Yukio surname: Nakamura fullname: Nakamura, Yukio – sequence: 11 givenname: Emiko surname: Noguchi fullname: Noguchi, Emiko |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22912751$$D View this record in MEDLINE/PubMed |
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| Copyright | COPYRIGHT 2012 Public Library of Science Ono et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2012 Ono et al 2012 Ono et al |
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| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Conceived and designed the experiments: Y. Horiuchi MMT TA EN. Performed the experiments: MO Y. Hamada YI KS TF. Analyzed the data: MO TH EN. Contributed reagents/materials/analysis tools: MMT YN MH. Wrote the paper: MO Y. Hamada MMT EN. Competing Interests: The authors have declared that no competing interests exist. |
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| SubjectTerms | Anesthesia B cells Biology Biopsy Blood Cellular Reprogramming DNA methylation Efficiency Embryo cells Embryonic stem cells Epigenetic inheritance Epigenetics Epithelial cells Female Fibroblasts Gene expression Genes Genetic vectors Genetic Vectors - genetics Genomes Genomics Genotypes Health aspects Humans Induced Pluripotent Stem Cells - cytology Induced Pluripotent Stem Cells - metabolism Infections Lymphocytes Medical research Medicine Molecular modelling Morphology Nasal Mucosa - cytology Otolaryngology Pathogenesis Pluripotency Proteins Regenerative medicine Sendai virus - genetics Somatic cells Stem cell transplantation Stem cells Transduction, Genetic - methods Vectors Viruses |
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| Title | Generation of Induced Pluripotent Stem Cells from Human Nasal Epithelial Cells Using a Sendai Virus Vector |
| URI | https://www.ncbi.nlm.nih.gov/pubmed/22912751 https://www.proquest.com/docview/1326242138 https://www.proquest.com/docview/1034796064 https://pubmed.ncbi.nlm.nih.gov/PMC3418281 https://doaj.org/article/e73a8e3c58e944f2b2b7dfe2839974c9 http://dx.doi.org/10.1371/journal.pone.0042855 |
| Volume | 7 |
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