Lipoxins Attenuate Renal Fibrosis by Inducing let-7c and Suppressing TGFβR1
Autor: | Karen A. Nolan, Patrick J. Guiry, Alexander P. Maxwell, David A. Savage, Catherine Godson, Eoin P. Brennan, Finian Martin, Denise M. Sadlier, Madeline Murphy, Emma Börgeson, Syed Tasadaque Ali-Shah, Neil G. Docherty, Oisín S. Gough, Caitriona McEvoy, Debra F. Higgins |
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Rok vydání: | 2013 |
Předmět: |
medicine.medical_specialty
Inflammation Biology Kidney Kidney Tubules Proximal Transforming Growth Factor beta1 Downregulation and upregulation Fibrosis Internal medicine medicine Renal fibrosis Humans Receptor Notch1 Receptor Cells Cultured Kidney metabolism General Medicine Cadherins medicine.disease Fibronectins Lipoxins MicroRNAs Basic Research medicine.anatomical_structure Endocrinology Nephrology Cancer research medicine.symptom Signal transduction Thrombospondins Signal Transduction |
Zdroj: | Journal of the American Society of Nephrology. 24:627-637 |
ISSN: | 1046-6673 |
DOI: | 10.1681/asn.2012060550 |
Popis: | Lipoxins, which are endogenously produced lipid mediators, promote the resolution of inflammation, and may inhibit fibrosis, suggesting a possible role in modulating renal disease. Here, lipoxin A4 (LXA4) attenuated TGF-β1-induced expression of fibronectin, N-cadherin, thrombospondin, and the notch ligand jagged-1 in cultured human proximal tubular epithelial (HK-2) cells through a mechanism involving upregulation of the microRNA let-7c. Conversely, TGF-β1 suppressed expression of let-7c. In cells pretreated with LXA4, upregulation of let-7c persisted despite subsequent stimulation with TGF-β1. In the unilateral ureteral obstruction model of renal fibrosis, let-7c upregulation was induced by administering an LXA4 analog. Bioinformatic analysis suggested that targets of let-7c include several members of the TGF-β1 signaling pathway, including the TGF-β receptor type 1. Consistent with this, LXA4-induced upregulation of let-7c inhibited both the expression of TGF-β receptor type 1 and the response to TGF-β1. Overexpression of let-7c mimicked the antifibrotic effects of LXA4 in renal epithelia; conversely, anti-miR directed against let-7c attenuated the effects of LXA4. Finally, we observed that several let-7c target genes were upregulated in fibrotic human renal biopsies compared with controls. In conclusion, these results suggest that LXA4-mediated upregulation of let-7c suppresses TGF-β1-induced fibrosis and that expression of let-7c targets is dysregulated in human renal fibrosis. |
Databáze: | OpenAIRE |
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