pdx1 knockout leads to a diabetic nephropathy-like phenotype in zebrafish and identifies phosphatidylethanolamine as metabolite promoting early diabetic kidney damage

The pdx1−/− zebrafish mutant was recently established as a novel animal model of diabetic retinopathy. In this study, we investigate whether knockout of pdx1 also leads to diabetic kidney disease (DKD). pdx1−/− larvae exhibit several signs of early DKD, such as glomerular hypertrophy, impairments in...

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Hauptverfasser: Wiggenhauser, Lucas (VerfasserIn) , Metzger, Lena (VerfasserIn) , Bennewitz, Katrin (VerfasserIn) , Soleymani Zaraj Abadi, Silas (VerfasserIn) , Boger, Mike (VerfasserIn) , Tabler, Christoph Tobias (VerfasserIn) , Haußer-Siller, Ingrid (VerfasserIn) , Sticht, Carsten (VerfasserIn) , Wohlfart, Paulus (VerfasserIn) , Volk, Nadine (VerfasserIn) , Heidenreich, Elena (VerfasserIn) , Büttner, Michael (VerfasserIn) , Hammes, Hans-Peter (VerfasserIn) , Kroll, Jens (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: January 21, 2022
In: Diabetes
Year: 2022, Jahrgang: 71, Heft: 5, Pages: 1073-1080
ISSN:1939-327X
DOI:10.2337/db21-0645
Online-Zugang:Resolving-System, Volltext: https://doi.org/10.2337/db21-0645
Verlag, lizenzpflichtig, Volltext: https://diabetesjournals.org/diabetes/article/71/5/1073/141050/pdx1-Knockout-Leads-to-a-Diabetic-Nephropathy-Like
Volltext
Verfasserangaben:Lucas M. Wiggenhauser, Lena Metzger, Katrin Bennewitz, Silas Soleymani, Mike Boger, Christoph T. Tabler, Ingrid Hausser, Carsten Sticht, Paulus Wohlfart, Nadine Volk, Elena Heidenreich, Michael Buettner, Hans-Peter Hammes, and Jens Kroll

MARC

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520 |a The pdx1−/− zebrafish mutant was recently established as a novel animal model of diabetic retinopathy. In this study, we investigate whether knockout of pdx1 also leads to diabetic kidney disease (DKD). pdx1−/− larvae exhibit several signs of early DKD, such as glomerular hypertrophy, impairments in the filtration barrier corresponding to microalbuminuria, and glomerular basement membrane (GBM) thickening. Adult pdx1−/− mutants show progressive GBM thickening in comparison with the larval state. Heterozygous pdx1 knockout also leads to glomerular hypertrophy as initial establishment of DKD similar to the pdx1−/− larvae. RNA sequencing of adult pdx1+/− kidneys uncovered regulations in multiple expected diabetic pathways related to podocyte disruption and hinting at early vascular dysregulation without obvious morphological alterations. Metabolome analysis and pharmacological intervention experiments revealed the contribution of phosphatidylethanolamine in the early establishment of kidney damage. In conclusion, this study identified the pdx1 mutant as a novel model for the study of DKD, showing signs of the early disease progression already in the larval stage and several selective features of later DKD in adult mutants. 
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