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dc.contributor.author
de la Cruz Thea, Benjamín Isaías  
dc.contributor.author
Natali, Lautaro  
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Ho Xuan, Hung  
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Bruckmann, Astrid  
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Coll Bonfill, Núria  
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Strieder, Nicholas  
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Peinado, Víctor I.  
dc.contributor.author
Meister, Gunter  
dc.contributor.author
Musri, Melina Mara  
dc.date.available
2025-05-22T13:39:49Z  
dc.date.issued
2024-08  
dc.identifier.citation
de la Cruz Thea, Benjamín Isaías; Natali, Lautaro; Ho Xuan, Hung; Bruckmann, Astrid; Coll Bonfill, Núria; et al.; Differentiation and Growth-Arrest-Related lncRNA (DAGAR): Initial Characterization in Human Smooth Muscle and Fibroblast Cells; Molecular Diversity Preservation International; International Journal of Molecular Sciences; 25; 17; 8-2024; 1-23  
dc.identifier.issn
1422-0067  
dc.identifier.uri
http://hdl.handle.net/11336/262339  
dc.description.abstract
Vascular smooth muscle cells (SMCs) can transition between a quiescent contractile or "differentiated" phenotype and a "proliferative-dedifferentiated" phenotype in response to environmental cues, similar to what in occurs in the wound healing process observed in fibroblasts. When dysregulated, these processes contribute to the development of various lung and cardiovascular diseases such as Chronic Obstructive Pulmonary Disease (COPD). Long non-coding RNAs (lncRNAs) have emerged as key modulators of SMC differentiation and phenotypic changes. In this study, we examined the expression of lncRNAs in primary human pulmonary artery SMCs (hPASMCs) during cell-to-cell contact-induced SMC differentiation. We discovered a novel lncRNA, which we named Differentiation And Growth Arrest-Related lncRNA (DAGAR) that was significantly upregulated in the quiescent phenotype with respect to proliferative SMCs and in cell-cycle-arrested MRC5 lung fibroblasts. We demonstrated that DAGAR expression is essential for SMC quiescence and its knockdown hinders SMC differentiation. The treatment of quiescent SMCs with the pro-inflammatory cytokine Tumor Necrosis Factor (TNF), a known inducer of SMC dedifferentiation and proliferation, elicited DAGAR downregulation. Consistent with this, we observed diminished DAGAR expression in pulmonary arteries from COPD patients compared to non-smoker controls. Through pulldown experiments followed by mass spectrometry analysis, we identified several proteins that interact with DAGAR that are related to cell differentiation, the cell cycle, cytoskeleton organization, iron metabolism, and the N-6-Methyladenosine (m6A) machinery. In conclusion, our findings highlight DAGAR as a novel lncRNA that plays a crucial role in the regulation of cell proliferation and SMC differentiation. This paper underscores the potential significance of DAGAR in SMC and fibroblast physiology in health and disease.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Molecular Diversity Preservation International  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
SMOOTH MUSCLE CELLS  
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LONG NONCODING RNA  
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DAGAR  
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N-6-METHYLADENOSINE  
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Bioquímica y Biología Molecular  
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Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Differentiation and Growth-Arrest-Related lncRNA (DAGAR): Initial Characterization in Human Smooth Muscle and Fibroblast Cells  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2025-05-22T09:30:44Z  
dc.journal.volume
25  
dc.journal.number
17  
dc.journal.pagination
1-23  
dc.journal.pais
Suiza  
dc.description.fil
Fil: de la Cruz Thea, Benjamín Isaías. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Universidad Nacional de Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra; Argentina  
dc.description.fil
Fil: Natali, Lautaro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Universidad Nacional de Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra; Argentina  
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Fil: Ho Xuan, Hung. Universitat Regensburg; Alemania  
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Fil: Bruckmann, Astrid. Universitat Regensburg; Alemania  
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Fil: Coll Bonfill, Núria. Saint Louis University School Of Medicine; Estados Unidos  
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Fil: Strieder, Nicholas. Universitat Regensburg; Alemania  
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Fil: Peinado, Víctor I.. Universidad de Barcelona; España  
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Fil: Meister, Gunter. Universitat Regensburg; Alemania  
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Fil: Musri, Melina Mara. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Universidad Nacional de Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra; Argentina  
dc.journal.title
International Journal of Molecular Sciences  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/1422-0067/25/17/9497  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.3390/ijms25179497