Senescence Induced by UVB in Keratinocytes ...
Document type :
Compte-rendu et recension critique d'ouvrage
Permalink :
Title :
Senescence Induced by UVB in Keratinocytes Impairs Amino Acids Balance
Author(s) :
Bauwens, Emilie [Auteur]
Parée, Tom [Auteur]
Meurant, Sébastien [Auteur]
Bouriez, Inès [Auteur]
Hannart, Clotilde [Auteur]
Wéra, Anne-Catherine [Auteur]
Khelfi, Alexis [Auteur]
Fattaccioli, Antoine [Auteur]
Burteau, Sophie [Auteur]
Demazy, Catherine [Auteur]
Fransolet, Maude [Auteur]
De Schutter, Clémentine [Auteur]
Hétérogénéité, Plasticité et Résistance aux Thérapies des Cancers = Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 [CANTHER]
Martin, Nathalie [Auteur]
Hétérogénéité, Plasticité et Résistance aux Thérapies des Cancers = Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 [CANTHER]
Théry, Julien [Auteur]
Decanter, Gauthier [Auteur]
Penel, Nicolas [Auteur]
Bury, Marina [Auteur]
Pluquet, Olivier [Auteur]
Hétérogénéité, Plasticité et Résistance aux Thérapies des Cancers = Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 [CANTHER]
Garmyn, Marjan [Auteur]
Debacq-Chainiaux, Florence [Auteur]
Parée, Tom [Auteur]
Meurant, Sébastien [Auteur]
Bouriez, Inès [Auteur]
Hannart, Clotilde [Auteur]
Wéra, Anne-Catherine [Auteur]
Khelfi, Alexis [Auteur]
Fattaccioli, Antoine [Auteur]
Burteau, Sophie [Auteur]
Demazy, Catherine [Auteur]
Fransolet, Maude [Auteur]
De Schutter, Clémentine [Auteur]
Hétérogénéité, Plasticité et Résistance aux Thérapies des Cancers = Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 [CANTHER]
Martin, Nathalie [Auteur]
Hétérogénéité, Plasticité et Résistance aux Thérapies des Cancers = Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 [CANTHER]
Théry, Julien [Auteur]
Decanter, Gauthier [Auteur]
Penel, Nicolas [Auteur]
Bury, Marina [Auteur]
Pluquet, Olivier [Auteur]
Hétérogénéité, Plasticité et Résistance aux Thérapies des Cancers = Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 [CANTHER]
Garmyn, Marjan [Auteur]
Debacq-Chainiaux, Florence [Auteur]
Journal title :
Journal of Investigative Dermatology
Pages :
554-565.e9
Publisher :
Nature Publishing Group
Publication date :
2023-04
ISSN :
0022-202X
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
Skin is one of the most exposed organs to external stress. Namely, UV rays are the most harmful stress that could induce important damage leading to skin aging and cancers. At the cellular level, senescence is observed in ...
Show more >Skin is one of the most exposed organs to external stress. Namely, UV rays are the most harmful stress that could induce important damage leading to skin aging and cancers. At the cellular level, senescence is observed in several skin cell types and contributes to skin aging. However, the origin of skin senescent cells is still unclear but is probably related to exposure to stresses. In this work, we developed an in vitro model of UVBinduced premature senescence in normal human epidermal keratinocytes. UVB-induced senescent keratinocytes display a common senescent phenotype resulting in an irreversible cell cycle arrest, an increase in the proportion of senescence-associated b-galactosidase-positive cells, unrepaired DNA damage, and a long-term DNA damage response activation. Moreover, UVB-induced senescent keratinocytes secrete senescenceassociated secretory phenotype factors that influence cutaneous squamous cell carcinoma cell migration. Finally, a global transcriptomic study highlighted that senescent keratinocytes present a decrease in the expression of several amino acid transporters, which is associated with reduced intracellular levels of glycine, alanine, and leucine. Interestingly, the chemical inhibition of the glycine transporter SLC6A9/Glyt1 triggers senescence features.Show less >
Show more >Skin is one of the most exposed organs to external stress. Namely, UV rays are the most harmful stress that could induce important damage leading to skin aging and cancers. At the cellular level, senescence is observed in several skin cell types and contributes to skin aging. However, the origin of skin senescent cells is still unclear but is probably related to exposure to stresses. In this work, we developed an in vitro model of UVBinduced premature senescence in normal human epidermal keratinocytes. UVB-induced senescent keratinocytes display a common senescent phenotype resulting in an irreversible cell cycle arrest, an increase in the proportion of senescence-associated b-galactosidase-positive cells, unrepaired DNA damage, and a long-term DNA damage response activation. Moreover, UVB-induced senescent keratinocytes secrete senescenceassociated secretory phenotype factors that influence cutaneous squamous cell carcinoma cell migration. Finally, a global transcriptomic study highlighted that senescent keratinocytes present a decrease in the expression of several amino acid transporters, which is associated with reduced intracellular levels of glycine, alanine, and leucine. Interestingly, the chemical inhibition of the glycine transporter SLC6A9/Glyt1 triggers senescence features.Show less >
Language :
Anglais
Popular science :
Non
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Submission date :
2024-03-20T03:20:13Z