Pathomorphological sequence of nephron loss in diabetic nephropathy

• Published in: American journal of physiology. Renal physiology 2021-11, Vol.321 (5), p.F600-F616
• Main Authors: Löwen, Jana, Gröne, Elisabeth F, Groß-Weißmann, Marie-Luise, Bestvater, Felix, Gröne, Hermann-Josef, Kriz, Wilhelm
• Format: Article
• Language: English
• Subjects: Biopsy; Blood vessels; Bowman Capsule - pathology; Bowman's capsule; Capillaries; Capillaries - pathology; Capillary Permeability; Degeneration; Diabetes; Diabetes mellitus; Diabetic Nephropathies - metabolism; Diabetic Nephropathies - pathology; Disease Progression; Endothelial cells; Endothelial Cells - pathology; Epithelium; Fibrosis; Glomerular Basement Membrane - pathology; Glomerulonephritis - metabolism; Glomerulonephritis - pathology; Humans; Mesangium; Microscopy, Electron, Transmission; Neovascularization, Pathologic; Nephrons - metabolism; Nephrons - pathology; Nephrons - ultrastructure; Nephropathy; Podocytes - pathology; Sclerosis; Tubules
• ISSN: 1931-857X; 1522-1466
• DOI: 10.1152/ajprenal.00669.2020

Following our previous reports on mesangial sclerosis and vascular proliferation in diabetic nephropathy (DN) (Kriz W, Löwen J, Federico G, van den Born J, Gröne E, Gröne HJ. 312: F1101-F1111, 2017; Löwen J, Gröne E, Gröne HJ, Kriz W. 317: F399-F410, 2019), we now describe the advanced stages of DN terminating in glomerular obsolescence and tubulointerstitial fibrosis based on a total of 918 biopsies. The structural aberrations emerged from two defects: ) increased synthesis of glomerular basement membrane (GBM) components by podocytes and endothelial cells leading to an accumulation of GBM material in the mesangium and ) a defect of glomerular vessels consisting of increased leakiness and an increased propensity to proliferate. Both defects may lead to glomerular degeneration. The progressing compaction of accumulated worn-out GBM material together with the retraction of podocytes out of the tuft and the collapse and hyalinosis of capillaries results in a shrunken tuft that fuses with Bowman's capsule (BC) to glomerular sclerosis. The most frequent pathway to glomerular decay starts with local tuft expansions that result in contacts of structurally intact podocytes to the parietal epithelium initiating the formation of tuft adhesions, which include the penetration of glomerular capillaries into BC. Exudation of plasma from such capillaries into the space between the parietal epithelium and its basement membrane causes the formation of insudative fluid accumulations within BC spreading around the glomerular circumference and, via the glomerulotubular junction, onto the tubule. Degeneration of the corresponding tubule develops secondarily to the glomerular damage, either due to cessation of filtration in cases of global sclerosis or due to encroachment of the insudative spaces. The degenerating tubules induce the proliferation of myofibroblasts resulting in interstitial fibrosis. Based on analysis of 918 human biopsies, essential derangement in diabetic nephropathy consists of accumulation of worn-out glomerular basement membrane in the mesangium that may advance to global sclerosis. The most frequent pathway to nephron dropout starts with the penetration of glomerular capillaries into Bowman's capsule (BC), delivering an exudate into BC that spreads around the entire glomerular circumference and via the glomerulotubular junction onto the tubule, resulting in glomerular sclerosis and chronic tubulointerstitial damage.