Podocyte Regeneration Driven by Renal Progenitors Determines Glomerular Disease Remission and Can Be Pharmacologically Enhanced

• Published in: Stem cell reports Vol. 5; no. 2; pp. 248 - 263
• Main Authors: Lasagni, Laura, Angelotti, Maria Lucia, Ronconi, Elisa, Lombardi, Duccio, Nardi, Sara, Peired, Anna, Becherucci, Francesca, Mazzinghi, Benedetta, Sisti, Alessandro, Romoli, Simone, Burger, Alexa, Schaefer, Beat, Buccoliero, Annamaria, Lazzeri, Elena, Romagnani, Paola
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 11.08.2015; Elsevier
• Subjects: Animals; Cell Differentiation; Cells, Cultured; Glycogen Synthase Kinase 3 - antagonists & inhibitors; Indoles - pharmacology; Indoles - therapeutic use; Mice; Mice, Inbred C57BL; Oximes - pharmacology; Oximes - therapeutic use; Podocytes - cytology; Podocytes - drug effects; Podocytes - metabolism; Regeneration; Renal Insufficiency, Chronic - drug therapy; Renal Insufficiency, Chronic - pathology; Stem Cells - cytology; Stem Cells - drug effects; Stem Cells - metabolism
• ISSN: 2213-6711; 2213-6711
• DOI: 10.1016/j.stemcr.2015.07.003

Podocyte loss is a general mechanism of glomerular dysfunction that initiates and drives the progression of chronic kidney disease, which affects 10% of the world population. Here, we evaluate whether the regenerative response to podocyte injury influences chronic kidney disease outcome. In models of focal segmental glomerulosclerosis performed in inducible transgenic mice where podocytes are tagged, remission or progression of disease was determined by the amount of regenerated podocytes. When the same model was established in inducible transgenic mice where renal progenitors are tagged, the disease remitted if renal progenitors successfully differentiated into podocytes, while it persisted if differentiation was ineffective, resulting in glomerulosclerosis. Treatment with BIO, a GSK3s inhibitor, significantly increased disease remission by enhancing renal progenitor sensitivity to the differentiation effect of endogenous retinoic acid. These results establish renal progenitors as critical determinants of glomerular disease outcome and a pharmacological enhancement of their differentiation as a possible therapeutic strategy. [Display omitted] •Renal progenitors can generate differentiated podocytes after glomerular injury•Renal progenitor response critically determines glomerular disease remission•Inefficient renal progenitor to podocyte differentiation dictates disease chronicization•Renal progenitor differentiation into podocytes can be enhanced with drugs In this article, Romagnani, Lasagni, and colleagues show that podocyte regeneration is a critical determinant of the outcome of glomerular disorders and that enhancement of renal progenitor differentiation into podocyte through pharmacological treatment shifts the disease from progression to remission.