GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage
Idiopathic pulmonary fibrosis is a lethal lung fibrotic disease, associated with aging with a mean survival of 2-5 years and no curative treatment. The GSE4 peptide is able to rescue cells from senescence, DNA and oxidative damage, inflammation, and induces telomerase activity. Here, we investigated...
| Autores: | , , , , , , , , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de publicación: | 2025 |
| País: | España |
| Recursos: | Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) |
| Repositorio: | Docu-menta. Repositorio Institucional del CIEMAT |
| Idioma: | inglés |
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| Acesso em linha: | https://hdl.handle.net/20.500.14855/4404 |
| Access Level: | acceso abierto |
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GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damagePintado-Berninches, LauraMontes-Worboys, AnaManguan-García, CristinaArias-Salgado, Elena G.Serrano, AdelaFernandez-Varas, BeatrizGuerrero-López, RosaIarriccio, LauraPlanas, LurdesGuenechea, GuillermoCortijo, JulioSastre, LeandroMolina-Molina, MariaPerona, RosarioIdiopathic pulmonary fibrosis is a lethal lung fibrotic disease, associated with aging with a mean survival of 2-5 years and no curative treatment. The GSE4 peptide is able to rescue cells from senescence, DNA and oxidative damage, inflammation, and induces telomerase activity. Here, we investigated the protective effect of GSE4 expression in vitro in rat alveolar epithelial cells (AECs), and in vivo in a bleomycin model of lung fibrosis. Bleomycin-injured rat AECs, expressing GSE4 or treated with GSE4-PLGA/PEI nanoparticles showed an increase of telomerase activity, decreased DNA damage, and decreased expression of IL6 and cleaved-caspase 3. In addition, these cells showed an inhibition in expression of fibrotic markers induced by TGF-βsuch as collagen-I and III among others. Furthermore, treatment with GSE4-PLGA/PEI nanoparticles in a rat model of bleomycin-induced fibrosis, increased telomerase activity and decreased DNA damage in proSP-C cells. Both in preventive and therapeutic protocols GSE4-PLGA/ PEI nanoparticles prevented and attenuated lung damage monitored by SPECT-CT and inhibited collagen deposition. Lungs of rats treated with bleomycin and GSE4-PLGA/PEI nanoparticles showed reduced expression of α-SMA and pro-inflammatory cytokines, increased number of pro-SPC- Multicellular structures and increased DNA synthesis in proSP-C cells, indicating therapeutic efficacy of GSE4-nanoparticles in experimental lung fibrosis and a possible curative treatment for lung fibrotic patients.20252025-01-2820252025-01-2820252025-01-28journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/20.500.14855/4404reponame:Docu-menta. Repositorio Institucional del CIEMATinstname:Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:dnet:documenta___::08b5d3fd5893bc700a5feba4bad42e782026-06-18T12:40:47Z |
| dc.title.none.fl_str_mv |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage |
| title |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage |
| spellingShingle |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage Pintado-Berninches, Laura |
| title_short |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage |
| title_full |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage |
| title_fullStr |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage |
| title_full_unstemmed |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage |
| title_sort |
GSE4-loaded nanoparticles a potential therapy for lung fibrosis that enhances pneumocyte growth, reduces apoptosis and DNA damage |
| dc.creator.none.fl_str_mv |
Pintado-Berninches, Laura Montes-Worboys, Ana Manguan-García, Cristina Arias-Salgado, Elena G. Serrano, Adela Fernandez-Varas, Beatriz Guerrero-López, Rosa Iarriccio, Laura Planas, Lurdes Guenechea, Guillermo Cortijo, Julio Sastre, Leandro Molina-Molina, Maria Perona, Rosario |
| author |
Pintado-Berninches, Laura |
| author_facet |
Pintado-Berninches, Laura Montes-Worboys, Ana Manguan-García, Cristina Arias-Salgado, Elena G. Serrano, Adela Fernandez-Varas, Beatriz Guerrero-López, Rosa Iarriccio, Laura Planas, Lurdes Guenechea, Guillermo Cortijo, Julio Sastre, Leandro Molina-Molina, Maria Perona, Rosario |
| author_role |
author |
| author2 |
Montes-Worboys, Ana Manguan-García, Cristina Arias-Salgado, Elena G. Serrano, Adela Fernandez-Varas, Beatriz Guerrero-López, Rosa Iarriccio, Laura Planas, Lurdes Guenechea, Guillermo Cortijo, Julio Sastre, Leandro Molina-Molina, Maria Perona, Rosario |
| author2_role |
author author author author author author author author author author author author author |
| dc.contributor.none.fl_str_mv |
|
| description |
Idiopathic pulmonary fibrosis is a lethal lung fibrotic disease, associated with aging with a mean survival of 2-5 years and no curative treatment. The GSE4 peptide is able to rescue cells from senescence, DNA and oxidative damage, inflammation, and induces telomerase activity. Here, we investigated the protective effect of GSE4 expression in vitro in rat alveolar epithelial cells (AECs), and in vivo in a bleomycin model of lung fibrosis. Bleomycin-injured rat AECs, expressing GSE4 or treated with GSE4-PLGA/PEI nanoparticles showed an increase of telomerase activity, decreased DNA damage, and decreased expression of IL6 and cleaved-caspase 3. In addition, these cells showed an inhibition in expression of fibrotic markers induced by TGF-βsuch as collagen-I and III among others. Furthermore, treatment with GSE4-PLGA/PEI nanoparticles in a rat model of bleomycin-induced fibrosis, increased telomerase activity and decreased DNA damage in proSP-C cells. Both in preventive and therapeutic protocols GSE4-PLGA/ PEI nanoparticles prevented and attenuated lung damage monitored by SPECT-CT and inhibited collagen deposition. Lungs of rats treated with bleomycin and GSE4-PLGA/PEI nanoparticles showed reduced expression of α-SMA and pro-inflammatory cytokines, increased number of pro-SPC- Multicellular structures and increased DNA synthesis in proSP-C cells, indicating therapeutic efficacy of GSE4-nanoparticles in experimental lung fibrosis and a possible curative treatment for lung fibrotic patients. |
| publishDate |
2025 |
| dc.date.none.fl_str_mv |
2025 2025-01-28 2025 2025-01-28 2025 2025-01-28 |
| dc.type.none.fl_str_mv |
journal article http://purl.org/coar/resource_type/c_6501 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/20.500.14855/4404 |
| url |
https://hdl.handle.net/20.500.14855/4404 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 |
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info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 |
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openAccess |
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application/pdf |
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reponame:Docu-menta. Repositorio Institucional del CIEMAT instname:Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) |
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Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) |
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Docu-menta. Repositorio Institucional del CIEMAT |
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Docu-menta. Repositorio Institucional del CIEMAT |
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