Anaerobic Glycolysis Maintains the Glomerular Filtration Barrier Independent of Mitochondrial Metabolism and Dynamics
Paul T. Brinkkoetter,
Tillmann Bork,
Sarah Salou,
Wei Liang,
Athanasia Mizi,
Cem Özel,
Sybille Koehler,
H. Henning Hagmann,
Christina Ising,
Alexander Kuczkowski,
Svenia Schnyder,
Ahmed Abed,
Bernhard Schermer,
Thomas Benzing,
Oliver Kretz,
Victor G. Puelles,
Simon Lagies,
Manuel Schlimpert,
Bernd Kammerer,
Christoph Handschin,
Christoph Schell,
Tobias B. Huber
Affiliations
Paul T. Brinkkoetter
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Tillmann Bork
Department of Medicine IV, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Sarah Salou
Department of Medicine IV, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Wei Liang
Department of Medicine IV, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Athanasia Mizi
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Cem Özel
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Sybille Koehler
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
H. Henning Hagmann
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Christina Ising
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Alexander Kuczkowski
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Svenia Schnyder
Biozentrum, University of Basel, Basel, Switzerland
Ahmed Abed
Department of Medicine IV, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Bernhard Schermer
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Thomas Benzing
Department II of Internal Medicine and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany; Cologne Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Cologne, Germany
Oliver Kretz
III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Victor G. Puelles
III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Division of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany; Department of Nephrology, Monash Health, Melbourne, VIC, Australia
Simon Lagies
Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg, Freiburg, Germany; Faculty of Biology, University of Freiburg, Freiburg, Germany
Manuel Schlimpert
Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg, Freiburg, Germany; Faculty of Biology, University of Freiburg, Freiburg, Germany
Bernd Kammerer
BIOSS Centre for Biological Signalling Studies, University of Freiburg, Freiburg, Germany
Christoph Handschin
Biozentrum, University of Basel, Basel, Switzerland
Christoph Schell
Institute of Surgical Pathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Tobias B. Huber
III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Corresponding author
Summary: The cellular responses induced by mitochondrial dysfunction remain elusive. Intrigued by the lack of almost any glomerular phenotype in patients with profound renal ischemia, we comprehensively investigated the primary sources of energy of glomerular podocytes. Combining functional measurements of oxygen consumption rates, glomerular metabolite analysis, and determination of mitochondrial density of podocytes in vivo, we demonstrate that anaerobic glycolysis and fermentation of glucose to lactate represent the key energy source of podocytes. Under physiological conditions, we could detect neither a developmental nor late-onset pathological phenotype in podocytes with impaired mitochondrial biogenesis machinery, defective mitochondrial fusion-fission apparatus, or reduced mtDNA stability and transcription caused by podocyte-specific deletion of Pgc-1α, Drp1, or Tfam, respectively. Anaerobic glycolysis represents the predominant metabolic pathway of podocytes. These findings offer a strategy to therapeutically interfere with the enhanced podocyte metabolism in various progressive kidney diseases, such as diabetic nephropathy or focal segmental glomerulosclerosis (FSGS). : Glomerular podocytes form the third and most outer layer of the kidney filtration barrier responsible for restricting the passage of proteins into the urine. Brinkkoetter et al. show that podocyte metabolism primarily relies on anaerobic glycolysis and the fermentation of glucose to lactate. Keywords: glomerular filtration barrier, podocytes, anaerobic glycolysis, metabolomics