Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence
BACKGROUND: Cellular senescence is induced either internally, for example by replication exhaustion and cell division, or externally, for example by irradiation. In both cases, cellular damages accumulate which, if not successfully repaired, can result in senescence induction. Recently, we determine...
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Sociedad de Biología de Chile
2016
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oai:scielo:S0716-976020160001000342016-12-01Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescenceMarthandan,ShivaMenzel,UwePriebe,SteffenGroth,MarcoGuthke,ReinhardPlatzer,MatthiasHemmerich,PeterKaether,ChristophDiekmann,Stephan Senescence Fibroblasts γ-irradiation Aging Transcriptome analysis DNA repair BACKGROUND: Cellular senescence is induced either internally, for example by replication exhaustion and cell division, or externally, for example by irradiation. In both cases, cellular damages accumulate which, if not successfully repaired, can result in senescence induction. Recently, we determined the transcriptional changes combined with the transition into replicative senescence in primary human fibroblast strains. Here, by γ-irradiation we induced premature cellular senescence in the fibroblast cell strains (HFF and MRC-5) and determined the corresponding transcriptional changes by high-throughput RNA sequencing. RESULTS: Comparing the transcriptomes, we found a high degree of similarity in differential gene expression in replicative as well as in irradiation induced senescence for both cell strains suggesting, in each cell strain, a common cellular response to error accumulation. On the functional pathway level, "Cell cycle" was the only pathway commonly down-regulated in replicative and irradiation-induced senescence in both fibroblast strains, confirming the tight link between DNA repair and cell cycle regulation. However, "DNA repair" and "replication" pathways were down-regulated more strongly in fibroblasts undergoing replicative exhaustion. We also retrieved genes and pathways in each of the cell strains specific for irradiation induced senescence. CONCLUSION: We found the pathways associated with "DNA repair" and "replication" less stringently regulated in irradiation induced compared to replicative senescence. The strong regulation of these pathways in replicative senescence highlights the importance of replication errors for its induction.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.49 20162016-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602016000100034en10.1186/s40659-016-0095-2 |
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Scielo Chile |
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Scielo Chile |
language |
English |
topic |
Senescence Fibroblasts γ-irradiation Aging Transcriptome analysis DNA repair |
spellingShingle |
Senescence Fibroblasts γ-irradiation Aging Transcriptome analysis DNA repair Marthandan,Shiva Menzel,Uwe Priebe,Steffen Groth,Marco Guthke,Reinhard Platzer,Matthias Hemmerich,Peter Kaether,Christoph Diekmann,Stephan Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence |
description |
BACKGROUND: Cellular senescence is induced either internally, for example by replication exhaustion and cell division, or externally, for example by irradiation. In both cases, cellular damages accumulate which, if not successfully repaired, can result in senescence induction. Recently, we determined the transcriptional changes combined with the transition into replicative senescence in primary human fibroblast strains. Here, by γ-irradiation we induced premature cellular senescence in the fibroblast cell strains (HFF and MRC-5) and determined the corresponding transcriptional changes by high-throughput RNA sequencing. RESULTS: Comparing the transcriptomes, we found a high degree of similarity in differential gene expression in replicative as well as in irradiation induced senescence for both cell strains suggesting, in each cell strain, a common cellular response to error accumulation. On the functional pathway level, "Cell cycle" was the only pathway commonly down-regulated in replicative and irradiation-induced senescence in both fibroblast strains, confirming the tight link between DNA repair and cell cycle regulation. However, "DNA repair" and "replication" pathways were down-regulated more strongly in fibroblasts undergoing replicative exhaustion. We also retrieved genes and pathways in each of the cell strains specific for irradiation induced senescence. CONCLUSION: We found the pathways associated with "DNA repair" and "replication" less stringently regulated in irradiation induced compared to replicative senescence. The strong regulation of these pathways in replicative senescence highlights the importance of replication errors for its induction. |
author |
Marthandan,Shiva Menzel,Uwe Priebe,Steffen Groth,Marco Guthke,Reinhard Platzer,Matthias Hemmerich,Peter Kaether,Christoph Diekmann,Stephan |
author_facet |
Marthandan,Shiva Menzel,Uwe Priebe,Steffen Groth,Marco Guthke,Reinhard Platzer,Matthias Hemmerich,Peter Kaether,Christoph Diekmann,Stephan |
author_sort |
Marthandan,Shiva |
title |
Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence |
title_short |
Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence |
title_full |
Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence |
title_fullStr |
Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence |
title_full_unstemmed |
Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence |
title_sort |
conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence |
publisher |
Sociedad de Biología de Chile |
publishDate |
2016 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602016000100034 |
work_keys_str_mv |
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1718441555199524864 |