2026-05-16T21:59:47Zhttps://repisalud.isciii.es/rest/oai/requestoai:repisalud.isciii.es:20.500.12105/251902025-12-18T13:00:41Zcom_20.500.12105_2052com_20.500.12105_2051col_20.500.12105_25179
Repisalud
author
Saraswati, Sarita
author
Martínez, Paula
author
Serrano, Rosa
author
Mejías, Diego
author
Graña-Castro, Osvaldo
author
Álvarez Díaz, Ruth
author
Blasco, Maria A
funder
Agencia Estatal de Investigación (España)
funder
Ministerio de Ciencia e Innovación (España)
funder
Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
funder
Comunidad de Madrid (España)
funder
Unión Europea. Comisión Europea. European Research Council (ERC)
funder
Botín Foundation
funder
World Cancer Research Fund International
2024-10-22T06:37:42Z
2024-10-22T06:37:42Z
2024-10-01
Saraswati S, Martínez P, Serrano R, Mejías D, Graña-Castro O, Álvarez Díaz R, Blasco MA. Renal fibroblasts are involved in fibrogenic changes in kidney fibrosis associated with dysfunctional telomeres. Exp Mol Med. 2024 Oct;56(10):2216-2230.
10.1038/s12276-024-01318-8
2092-6413
1226-3613
Experimental & molecular medicine
39349834
https://hdl.handle.net/20.500.12105/25190
Tubulointerstitial fibrosis associated with chronic kidney disease (CKD) represents a global health care problem. We previously reported that short and dysfunctional telomeres lead to interstitial renal fibrosis; however, the cell-of-origin of kidney fibrosis associated with telomere dysfunction is currently unknown. We induced telomere dysfunction by deleting the Trf1 gene encoding a telomere-binding factor specifically in renal fibroblasts in both short-term and long-term life-long experiments in mice to identify the role of fibroblasts in renal fibrosis. Short-term Trf1 deletion in renal fibroblasts was not sufficient to trigger kidney fibrosis but was sufficient to induce inflammatory responses, ECM deposition, cell cycle arrest, fibrogenesis, and vascular rarefaction. However, long-term persistent deletion of Trf1 in fibroblasts resulted in kidney fibrosis accompanied by an elevated urinary albumin-to-creatinine ratio (uACR) and a decrease in mouse survival. These cellular responses lead to the macrophage-to-myofibroblast transition (MMT), endothelial-to-mesenchymal transition (EndMT), and partial epithelial-to-mesenchymal transition (EMT), ultimately causing kidney fibrosis at the humane endpoint (HEP) when the deletion of Trf1 in fibroblasts is maintained throughout the lifespan of mice. Our findings contribute to a better understanding of the role of dysfunctional telomeres in the onset of the profibrotic alterations that lead to kidney fibrosis.
eng
Renal fibroblasts are involved in fibrogenic changes in kidney fibrosis associated with dysfunctional telomeres
research article
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RenalFibroblastsInvolvedFibrogenic_2024.pdf
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Supplementary_RenalFibroblastsInvolvedFibrogenic_2024.pdf
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Correction_RenalFibroblastsInvolvedFibrogenic_2024.pdf
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RenalFibroblastsInvolvedFibrogenic_2024.pdf.txt
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Supplementary_RenalFibroblastsInvolvedFibrogenic_2024.pdf.txt