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
Hlavní autoři: Huttner, Hagen B, Bergmann, Olaf, Salehpour, Mehran, Rácz, Attila, Tatarishvili, Jemal, Lindgren, Emma, Csonka, Tamás, Csiba, László, Hortobágyi, Tibor, Méhes, Gábor, Englund, Elisabet, Solnestam, Beata Werne, Zdunek, Sofia, Scharenberg, Christian, Ström, Lena, Ståhl, Patrik, Sigurgeirsson, Benjamin, Dahl, Andreas, Schwab, Stefan, Possnert, Göran, Bernard, Samuel, Kokaia, Zaal, Lindvall, Olle, Lundeberg, Joakim, Frisén, Jonas
Médium: Journal Article
Jazyk:angličtina
Vydáno: New York Nature Publishing Group US 01.06.2014
Nature Publishing Group
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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.
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
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ContentType Journal Article
Copyright Springer Nature America, Inc. 2014
COPYRIGHT 2014 Nature Publishing Group
Copyright Nature Publishing Group Jun 2014
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Institutionen för kliniska vetenskaper, Lund
Lunds universitet
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SSID ssj0007589
Score 2.4683409
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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StartPage 801
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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Volume 17
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