Learning Physiology From Inherited Kidney Disorders

• Published in: Physiological reviews Vol. 99; no. 3; pp. 1575 - 1653
• Main Authors: van der Wijst, Jenny, Belge, Hendrica, Bindels, René J M, Devuyst, Olivier
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.07.2019
• Subjects: Calcium; Endocytosis; Fanconi syndrome; Genome-wide association studies; Genomes; Hereditary diseases; Homeostasis; Kidney diseases; Magnesium; Reabsorption; Sodium; Therapeutic applications; Transcription factors; Uric acid
• ISSN: 0031-9333; 1522-1210
• DOI: 10.1152/physrev.00008.2018

The identification of genes causing inherited kidney diseases yielded crucial insights in the molecular basis of disease and improved our understanding of physiological processes that operate in the kidney. Monogenic kidney disorders are caused by mutations in genes coding for a large variety of proteins including receptors, channels and transporters, enzymes, transcription factors, and structural components, operating in specialized cell types that perform highly regulated homeostatic functions. Common variants in some of these genes are also associated with complex traits, as evidenced by genome-wide association studies in the general population. In this review, we discuss how the molecular genetics of inherited disorders affecting different tubular segments of the nephron improved our understanding of various transport processes and of their involvement in homeostasis, while providing novel therapeutic targets. These include inherited disorders causing a dysfunction of the proximal tubule (renal Fanconi syndrome), with emphasis on epithelial differentiation and receptor-mediated endocytosis, or affecting the reabsorption of glucose, the handling of uric acid, and the reabsorption of sodium, calcium, and magnesium along the kidney tubule.