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Permanent defects in renal medullary structure and function after reversal of urinary obstruction
Thitinee Vanichapol, Alex Gonzalez, Rachel Delgado, Maya Brewer, Kelly A. Clouthier, Anna A. Menshikh, William E. Snyder, Teebro Rahman, Veronika Sander, Haichun Yang, Alan J. Davidson, Mark P. de Caestecker
Thitinee Vanichapol, Alex Gonzalez, Rachel Delgado, Maya Brewer, Kelly A. Clouthier, Anna A. Menshikh, William E. Snyder, Teebro Rahman, Veronika Sander, Haichun Yang, Alan J. Davidson, Mark P. de Caestecker
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Research Article Nephrology

Permanent defects in renal medullary structure and function after reversal of urinary obstruction

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Abstract

Urinary obstruction causes injury to the renal medulla, impairing the ability to concentrate urine and increasing the risk of progressive kidney disease. However, the regenerative capacity of the renal medulla after reversal of obstruction is poorly understood. To investigate this, we developed a mouse model of reversible urinary obstruction. Despite robust regeneration and complete histological recovery of the renal medulla, these mice exhibited a permanent defect in urinary concentrating capacity. However, there were lasting changes in the composition, organization, and transcriptional profiles of epithelial, endothelial, and interstitial cells. Persistent inflammatory responses were also seen in patients with renal stone disease, but there were also adaptive responses to the increasingly hypoxic environment of the renal medulla that occurred only after reversal of obstruction. These findings indicate that while partial repair occurs after reversal of urinary obstruction, there are lasting structural and functional changes across all major cellular compartments of the renal medulla. These changes reflect shared and distinct responses to different renal medullary injuries in humans and mice.

Authors

Thitinee Vanichapol, Alex Gonzalez, Rachel Delgado, Maya Brewer, Kelly A. Clouthier, Anna A. Menshikh, William E. Snyder, Teebro Rahman, Veronika Sander, Haichun Yang, Alan J. Davidson, Mark P. de Caestecker

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Figure 4

Permanent reduction in inner medullary LOH with expansion of injured cells.

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Permanent reduction in inner medullary LOH with expansion of injured cel...
(A and C) Reclustering of LOH cells identified 10 distinct cell populations in the combined dataset (A) and after R-UUO (C); (B) top 5 DEGs for each LOH cluster; (D) fractional representation of LOH clusters after R-UUO; (E) genetics labeling of IM LOH cells using Six2-Cre mice; (F) fluorescence images of Six2 lineage cells in the IM after R-UUO (scale bars = 200 μm); (G) quantification of Six2 lineage cells in the IM 84 days after R-UUO; (H) fluorescence images with overlays showing AQP1 and Six2 lineage staining in the distal IM 28 days after R-UUO (scale bars = 200 μm); (I and J) quantification of AQP1+ and Six2+ cells in the distal IM as the percentage of cells (I); AQP1+Six2+ DTLs (% of Six2+ cells), and AQP1+Six2– DVRs (% of total cells) 28 days after R-UUO (J). Data points, means ± SEM. P values determined by t test. (K) Dot plot of the top 20 DEGs from injured LOH-4 cells in other LOH cell types after R-UUO; (L) UMAPs illustrating expression of injury markers Lcn2 and Ly6e after R-UUO.

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