Podocytes are new cellular targets of haemoglobin-mediated renal damage

J Pathol. 2018 Mar;244(3):296-310. doi: 10.1002/path.5011. Epub 2018 Jan 10.

Abstract

Recurrent and massive intravascular haemolysis induces proteinuria, glomerulosclerosis, and progressive impairment of renal function, suggesting podocyte injury. However, the effects of haemoglobin (Hb) on podocytes remain unexplored. Our results show that cultured human podocytes or podocytes isolated from murine glomeruli bound and endocytosed Hb through the megalin-cubilin receptor system, thus resulting in increased intracellular Hb catabolism, oxidative stress, activation of the intrinsic apoptosis pathway, and altered podocyte morphology, with decreased expression of the slit diaphragm proteins nephrin and synaptopodin. Hb uptake activated nuclear factor erythroid-2-related factor 2 (Nrf2) and induced expression of the Nrf2-related antioxidant proteins haem oxygenase-1 (HO-1) and ferritin. Nrf2 activation and Hb staining was observed in podocytes of mice with intravascular haemolysis. These mice developed proteinuria and showed podocyte injury, characterized by foot process effacement, decreased synaptopodin and nephrin expression, and podocyte apoptosis. These pathological effects were enhanced in Nrf2-deficient mice, whereas Nrf2 activation with sulphoraphane protected podocytes against Hb toxicity both in vivo and in vitro. Supporting the translational significance of our findings, we observed podocyte damage and podocytes stained for Hb, HO-1, ferritin and phosphorylated Nrf2 in renal sections and urinary sediments of patients with massive intravascular haemolysis, such as atypical haemolytic uraemic syndrome and paroxysmal nocturnal haemoglobinuria. In conclusion, podocytes take up Hb both in vitro and during intravascular haemolysis, promoting oxidative stress, podocyte dysfunction, and apoptosis. Nrf2 may be a potential therapeutic target to prevent loss of renal function in patients with intravascular haemolysis. Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Keywords: Nrf2; apoptosis; haemoglobin; intravascular haemolysis; oxidative stress; podocyte.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / genetics
  • Acute Kidney Injury / metabolism*
  • Acute Kidney Injury / pathology
  • Adult
  • Anemia, Hemolytic / genetics
  • Anemia, Hemolytic / metabolism*
  • Anemia, Hemolytic / pathology
  • Animals
  • Apoptosis*
  • Cell Line
  • Disease Models, Animal
  • Endocytosis
  • Female
  • Ferritins / metabolism
  • Heme Oxygenase-1 / metabolism
  • Hemoglobins / metabolism*
  • Hemolysis
  • Humans
  • Low Density Lipoprotein Receptor-Related Protein-2 / metabolism
  • Male
  • Membrane Proteins / metabolism
  • Mice, Inbred C57BL
  • Mice, Knockout
  • NF-E2-Related Factor 1 / genetics
  • NF-E2-Related Factor 1 / metabolism
  • NF-E2-Related Factor 2 / genetics
  • NF-E2-Related Factor 2 / metabolism
  • Oxidative Stress
  • Phosphorylation
  • Podocytes / metabolism*
  • Podocytes / ultrastructure
  • Receptors, Cell Surface / metabolism
  • Young Adult

Substances

  • Hemoglobins
  • LRP2 protein, human
  • Low Density Lipoprotein Receptor-Related Protein-2
  • Lrp2 protein, mouse
  • Membrane Proteins
  • NF-E2-Related Factor 1
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Nfe2L1 protein, mouse
  • Receptors, Cell Surface
  • intrinsic factor-cobalamin receptor
  • Ferritins
  • HMOX1 protein, human
  • Heme Oxygenase-1
  • Hmox1 protein, mouse