The age and genomic integrity of neurons after cortical stroke in humans
In this study, the authors use measures of carbon-14 in neuronal DNA from human stroke patient cortical tissue samples to show that, unlike previous studies done in rodents, they do not find any evidence of increased neurogenesis after an ischemic injury. In addition, DNA damage assays suggest that...
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| Vydáno v: | Nature neuroscience Ročník 17; číslo 6; s. 801 - 803 |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
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Nature Publishing Group US
01.06.2014
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| ISSN: | 1097-6256, 1546-1726, 1546-1726 |
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| Abstract | In this study, the authors use measures of carbon-14 in neuronal DNA from human stroke patient cortical tissue samples to show that, unlike previous studies done in rodents, they do not find any evidence of increased neurogenesis after an ischemic injury. In addition, DNA damage assays suggest that there is no increase in DNA rearrangement after this insult.
It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test–derived
14
C concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival. |
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| AbstractList | It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test-derived (14)C concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival. It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test-derived [sup.14]C concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival. It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test-derived C-14 concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival. In this study, the authors use measures of carbon-14 in neuronal DNA from human stroke patient cortical tissue samples to show that, unlike previous studies done in rodents, they do not find any evidence of increased neurogenesis after an ischemic injury. In addition, DNA damage assays suggest that there is no increase in DNA rearrangement after this insult. It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test–derived 14 C concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival. It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test-derived super(14)C concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival. It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test-derived (14)C concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival.It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry; transcriptome, genome and ploidy analyses; and determination of nuclear bomb test-derived (14)C concentration in neuronal DNA, we found neither to be the case. A large proportion of cortical neurons displayed DNA fragmentation and DNA repair a short time after stroke, whereas neurons at chronic stages after stroke showed DNA integrity, demonstrating the relevance of an intact genome for survival. |
| Audience | Academic |
| Author | Ström, Lena Huttner, Hagen B Lindvall, Olle Salehpour, Mehran Sigurgeirsson, Benjamin Bergmann, Olaf Rácz, Attila Solnestam, Beata Werne Schwab, Stefan Hortobágyi, Tibor Ståhl, Patrik Tatarishvili, Jemal Possnert, Göran Dahl, Andreas Csonka, Tamás Méhes, Gábor Scharenberg, Christian Lindgren, Emma Frisén, Jonas Kokaia, Zaal Englund, Elisabet Csiba, László Bernard, Samuel Zdunek, Sofia Lundeberg, Joakim |
| Author_xml | – sequence: 1 givenname: Hagen B surname: Huttner fullname: Huttner, Hagen B organization: Department of Cell and Molecular Biology, Karolinska Institute, Department of Neurology, University of Erlangen-Nuremberg – sequence: 2 givenname: Olaf surname: Bergmann fullname: Bergmann, Olaf organization: Department of Cell and Molecular Biology, Karolinska Institute – sequence: 3 givenname: Mehran surname: Salehpour fullname: Salehpour, Mehran organization: Department of Physics and Astronomy, Ion Physics, Uppsala University – sequence: 4 givenname: Attila surname: Rácz fullname: Rácz, Attila organization: Department of Neurology, University of Erlangen-Nuremberg – sequence: 5 givenname: Jemal surname: Tatarishvili fullname: Tatarishvili, Jemal organization: Lund Stem Cell Center, University Hospital – sequence: 6 givenname: Emma surname: Lindgren fullname: Lindgren, Emma organization: Department of Cell and Molecular Biology, Karolinska Institute – sequence: 7 givenname: Tamás surname: Csonka fullname: Csonka, Tamás organization: Department of Neuropathology, Institute of Pathology, University of Debrecen, Medical and Health Science Centre – sequence: 8 givenname: László surname: Csiba fullname: Csiba, László organization: Department of Neurology, University of Debrecen, Medical and Health Science Centre – sequence: 9 givenname: Tibor surname: Hortobágyi fullname: Hortobágyi, Tibor organization: Department of Neuropathology, Institute of Pathology, University of Debrecen, Medical and Health Science Centre – sequence: 10 givenname: Gábor surname: Méhes fullname: Méhes, Gábor organization: Department of Neuropathology, Institute of Pathology, University of Debrecen, Medical and Health Science Centre – sequence: 11 givenname: Elisabet surname: Englund fullname: Englund, Elisabet organization: Department of Pathology, University Hospital – sequence: 12 givenname: Beata Werne surname: Solnestam fullname: Solnestam, Beata Werne organization: Department of Gene Technology, Royal Institute of Technology, SciLifeLab – sequence: 13 givenname: Sofia surname: Zdunek fullname: Zdunek, Sofia organization: Department of Cell and Molecular Biology, Karolinska Institute – sequence: 14 givenname: Christian surname: Scharenberg fullname: Scharenberg, Christian organization: Center for Hematology and Regenerative Medicine, Karolinska University Hospital, Huddinge, Department of Medicine, Skaraborgs Sjukhus Skövde – sequence: 15 givenname: Lena surname: Ström fullname: Ström, Lena organization: Department of Cell and Molecular Biology, Karolinska Institute – sequence: 16 givenname: Patrik surname: Ståhl fullname: Ståhl, Patrik organization: Department of Cell and Molecular Biology, Karolinska Institute – sequence: 17 givenname: Benjamin surname: Sigurgeirsson fullname: Sigurgeirsson, Benjamin organization: Department of Gene Technology, Royal Institute of Technology, SciLifeLab – sequence: 18 givenname: Andreas surname: Dahl fullname: Dahl, Andreas organization: Deep Sequencing Group, SFB655, Biotechnology Center, TU-Dresden – sequence: 19 givenname: Stefan surname: Schwab fullname: Schwab, Stefan organization: Department of Neurology, University of Erlangen-Nuremberg – sequence: 20 givenname: Göran surname: Possnert fullname: Possnert, Göran organization: Department of Physics and Astronomy, Ion Physics, Uppsala University – sequence: 21 givenname: Samuel surname: Bernard fullname: Bernard, Samuel organization: Department of Mathematics, Institut Camille Jordan, Université de Lyon – sequence: 22 givenname: Zaal surname: Kokaia fullname: Kokaia, Zaal organization: Lund Stem Cell Center, University Hospital – sequence: 23 givenname: Olle surname: Lindvall fullname: Lindvall, Olle organization: Lund Stem Cell Center, University Hospital – sequence: 24 givenname: Joakim surname: Lundeberg fullname: Lundeberg, Joakim organization: Department of Gene Technology, Royal Institute of Technology, SciLifeLab – sequence: 25 givenname: Jonas surname: Frisén fullname: Frisén, Jonas email: jonas.frisen@ki.se organization: Department of Cell and Molecular Biology, Karolinska Institute |
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| Snippet | In this study, the authors use measures of carbon-14 in neuronal DNA from human stroke patient cortical tissue samples to show that, unlike previous studies... It has been unclear whether ischemic stroke induces neurogenesis or neuronal DNA rearrangements in the human neocortex. Using immunohistochemistry;... |
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| SubjectTerms | 13/31 13/51 45/23 45/91 631/378/368/2431 Aged Aged, 80 and over Analysis Animal Genetics and Genomics Basic Medicine Behavioral Sciences Biological Techniques Biomedicine bomb peak brief-communication cell regeneration Cellular Senescence - physiology Chromosomes cortical stroke DNA DNA Fragmentation DNA repair DNA Repair - physiology Dynamical Systems Female Genetic aspects Genomes Hospitals Humans Ischemia Male Mathematics Medical and Health Sciences Medicin och hälsovetenskap Medicinska och farmaceutiska grundvetenskaper Middle Aged Neocortex - pathology Neocortex - physiology Neurobiology Neurogenesis Neurons Neurons - pathology Neurons - physiology Neurosciences Neurovetenskaper Physiological aspects Stroke Stroke (Disease) Stroke - genetics Stroke - pathology |
| Title | The age and genomic integrity of neurons after cortical stroke in humans |
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