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  • 1
    Publication Date: 2014-07-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Obokata, Haruko -- Sasai, Yoshiki -- Niwa, Hitoshi -- Kadota, Mitsutaka -- Andrabi, Munazah -- Takata, Nozomu -- Tokoro, Mikiko -- Terashita, Yukari -- Yonemura, Shigenobu -- Vacanti, Charles A -- Wakayama, Teruhiko -- England -- Nature. 2014 Jul 3;511(7507):112. doi: 10.1038/nature13599.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24990752" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2014-01-31
    Description: We recently discovered an unexpected phenomenon of somatic cell reprogramming into pluripotent cells by exposure to sublethal stimuli, which we call stimulus-triggered acquisition of pluripotency (STAP). This reprogramming does not require nuclear transfer or genetic manipulation. Here we report that reprogrammed STAP cells, unlike embryonic stem (ES) cells, can contribute to both embryonic and placental tissues, as seen in a blastocyst injection assay. Mouse STAP cells lose the ability to contribute to the placenta as well as trophoblast marker expression on converting into ES-like stem cells by treatment with adrenocorticotropic hormone (ACTH) and leukaemia inhibitory factor (LIF). In contrast, when cultured with Fgf4, STAP cells give rise to proliferative stem cells with enhanced trophoblastic characteristics. Notably, unlike conventional trophoblast stem cells, the Fgf4-induced stem cells from STAP cells contribute to both embryonic and placental tissues in vivo and transform into ES-like cells when cultured with LIF-containing medium. Taken together, the developmental potential of STAP cells, shown by chimaera formation and in vitro cell conversion, indicates that they represent a unique state of pluripotency.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Obokata, Haruko -- Sasai, Yoshiki -- Niwa, Hitoshi -- Kadota, Mitsutaka -- Andrabi, Munazah -- Takata, Nozomu -- Tokoro, Mikiko -- Terashita, Yukari -- Yonemura, Shigenobu -- Vacanti, Charles A -- Wakayama, Teruhiko -- England -- Nature. 2014 Jan 30;505(7485):676-80. doi: 10.1038/nature12969.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Laboratory for Cellular Reprogramming, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan [2] Laboratory for Genomic Reprogramming, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan [3] Laboratory for Tissue Engineering and Regenerative Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA. ; Laboratory for Organogenesis and Neurogenesis, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan. ; Laboratory for Pluripotent Stem Cell Studies, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan. ; Genome Resource and Analysis Unit, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan. ; Laboratory for Genomic Reprogramming, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan. ; 1] Laboratory for Cellular Reprogramming, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan [2] Laboratory for Genomic Reprogramming, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan. ; Electron Microscopy Laboratory, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan. ; Laboratory for Tissue Engineering and Regenerative Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA. ; 1] Laboratory for Genomic Reprogramming, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan [2] Faculty of Life and Environmental Sciences, University of Yamanashi, Yamanashi 400-8510, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24476891" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenocorticotropic Hormone/pharmacology ; Animals ; *Cell Differentiation/drug effects/genetics ; Cell Lineage/drug effects ; *Cellular Reprogramming/drug effects ; Embryonic Stem Cells/*cytology/drug effects/metabolism ; Epigenesis, Genetic/drug effects/genetics ; Female ; Fibroblast Growth Factor 4/pharmacology ; Induced Pluripotent Stem Cells/*cytology/drug effects ; Leukemia Inhibitory Factor/pharmacology ; Mice ; Mice, Inbred ICR ; Placenta/*cytology/drug effects ; Pregnancy ; Trophoblasts/*cytology/drug effects
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2014-07-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Obokata, Haruko -- Wakayama, Teruhiko -- Sasai, Yoshiki -- Kojima, Koji -- Vacanti, Martin P -- Niwa, Hitoshi -- Yamato, Masayuki -- Vacanti, Charles A -- England -- Nature. 2014 Jul 3;511(7507):112. doi: 10.1038/nature13598.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24990753" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2014-01-31
    Description: Here we report a unique cellular reprogramming phenomenon, called stimulus-triggered acquisition of pluripotency (STAP), which requires neither nuclear transfer nor the introduction of transcription factors. In STAP, strong external stimuli such as a transient low-pH stressor reprogrammed mammalian somatic cells, resulting in the generation of pluripotent cells. Through real-time imaging of STAP cells derived from purified lymphocytes, as well as gene rearrangement analysis, we found that committed somatic cells give rise to STAP cells by reprogramming rather than selection. STAP cells showed a substantial decrease in DNA methylation in the regulatory regions of pluripotency marker genes. Blastocyst injection showed that STAP cells efficiently contribute to chimaeric embryos and to offspring via germline transmission. We also demonstrate the derivation of robustly expandable pluripotent cell lines from STAP cells. Thus, our findings indicate that epigenetic fate determination of mammalian cells can be markedly converted in a context-dependent manner by strong environmental cues.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Obokata, Haruko -- Wakayama, Teruhiko -- Sasai, Yoshiki -- Kojima, Koji -- Vacanti, Martin P -- Niwa, Hitoshi -- Yamato, Masayuki -- Vacanti, Charles A -- England -- Nature. 2014 Jan 30;505(7485):641-7. doi: 10.1038/nature12968.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Laboratory for Tissue Engineering and Regenerative Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA [2] Laboratory for Cellular Reprogramming, RIKEN Center for Developmental biology, Kobe 650-0047, Japan [3] Laboratory for Genomic Reprogramming, RIKEN Center for Developmental biology, Kobe 650-0047, Japan. ; 1] Laboratory for Genomic Reprogramming, RIKEN Center for Developmental biology, Kobe 650-0047, Japan [2] Faculty of Life and Environmental Sciences, University of Yamanashi, Yamanashi 400-8510, Japan. ; Laboratory for Organogenesis and Neurogenesis, RIKEN Center for Developmental biology, Kobe 650-0047, Japan. ; Laboratory for Tissue Engineering and Regenerative Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA. ; 1] Laboratory for Tissue Engineering and Regenerative Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA [2] Department of Pathology, Irwin Army Community Hospital, Fort Riley, Kansas 66442, USA. ; Laboratory for Pluripotent Stem Cell Studies, RIKEN Center for Developmental biology, Kobe 650-0047, Japan. ; Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Tokyo 162-8666, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24476887" target="_blank"〉PubMed〈/a〉
    Keywords: Acids/*pharmacology ; Animals ; Antigens, CD45/metabolism ; Cell Dedifferentiation/drug effects ; Cell Proliferation ; Cellular Reprogramming/*drug effects ; Chimera/metabolism ; DNA Methylation/drug effects ; Embryonic Stem Cells/cytology/metabolism ; Female ; Green Fluorescent Proteins/genetics/metabolism ; Hydrogen-Ion Concentration ; Induced Pluripotent Stem Cells/*cytology/*drug effects/metabolism ; Lymphocytes/cytology/drug effects/metabolism ; Male ; Mice ; Mice, Inbred ICR ; Octamer Transcription Factor-3/metabolism ; Organ Specificity
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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