miR-127 Protects proximal tubule cells against ischemia/reperfusion: identification of kinesin family member 3B as miR-127 target
EntidadUAM. Departamento de Bioquímica
EditorPublic Library of Science
Fecha de edición2012-09-04
10.1371/journal.pone.0044305Plos One 7.9 (2012): e44305
Financiado porThis work was supported by grant FIS PS09/02183 funding by Instituto de Salud Carlos III and Ayuda Intramural Fundación para la Investigación en Biomedicina del Hospital Universitario Ramón y Cajal 122/2009
MateriasBiological Transpor; Sprague-Dawley; MicroRNAs; Kinesin; Reperfusion Injury; Medicina
Derechos© 2012 Aguado-Fraile et al.
Esta obra está bajo una Licencia Creative Commons Atribución 4.0 Internacional.
Ischemia/reperfusion (I/R) is at the basis of renal transplantation and acute kidney injury. Molecular mechanisms underlying proximal tubule response to I/R will allow the identification of new therapeutic targets for both clinical settings. microRNAs have emerged as crucial and tight regulators of the cellular response to insults including hypoxia. Here, we have identified several miRNAs involved in the response of the proximal tubule cell to I/R. Microarrays and RT-PCR analysis of proximal tubule cells submitted to I/R mimicking conditions in vitro demonstrated that miR-127 is induced during ischemia and also during reperfusion. miR-127 is also modulated in a rat model of renal I/R. Interference approaches demonstrated that ischemic induction of miR-127 is mediated by Hypoxia Inducible Factor-1alpha (HIF-1α) stabilization. Moreover, miR-127 is involved in cell-matrix and cell-cell adhesion maintenance, since overexpression of miR-127 maintains focal adhesion complex assembly and the integrity of tight junctions. miR-127 also regulates intracellular trafficking since miR-127 interference promotes dextran-FITC uptake. In fact, we have identified the Kinesin Family Member 3B (KIF3B), involved in cell trafficking, as a target of miR-127 in rat proximal tubule cells. In summary, we have described a novel role of miR-127 in cell adhesion and its regulation by HIF-1α. We also identified for the first time KIF3B as a miR-127 target. Both, miR-127 and KIF3B appear as key mediators of proximal epithelial tubule cell response to I/R with potential al application in renal ischemic damage management
Google Scholar:Aguado-Fraile, Elia - Ramos, Edurne - Sáenz-Morales, David - Conde, Elisa - Blanco-Sánchez, Ignacio - Stamatakis, Konstantinos - del Peso, Luis - Cuppen, Edwin - Brüne, Bernhard - García Bermejo, María Laura
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