International Journal of Molecular Sciences (Oct 2022)

Cell-Free Hemoglobin in Acute Kidney Injury after Lung Transplantation and Experimental Renal Ischemia/Reperfusion

  • Robert Greite,
  • Li Wang,
  • Lukas Gohlke,
  • Sebastian Schott,
  • Kirill Kreimann,
  • Julian Doricic,
  • Andreas Leffler,
  • Igor Tudorache,
  • Jawad Salman,
  • Ruslan Natanov,
  • Fabio Ius,
  • Christine Fegbeutel,
  • Axel Haverich,
  • Ralf Lichtinghagen,
  • Rongjun Chen,
  • Song Rong,
  • Hermann Haller,
  • Vijith Vijayan,
  • Magnus Gram,
  • Irina Scheffner,
  • Faikah Gueler,
  • Wilfried Gwinner,
  • Stephan Immenschuh

DOI
https://doi.org/10.3390/ijms232113272
Journal volume & issue
Vol. 23, no. 21
p. 13272

Abstract

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Cell-free hemoglobin (CFH), a pro-oxidant and cytotoxic compound that is released in hemolysis, has been associated with nephrotoxicity. Lung transplantation (LuTx) is a clinical condition with a high incidence of acute kidney injury (AKI). In this study, we investigated the plasma levels of CFH and haptoglobin, a CFH-binding serum protein, in prospectively enrolled LuTx patients (n = 20) with and without AKI. LuTx patients with postoperative AKI had higher CFH plasma levels at the end of surgery compared with no-AKI patients, and CFH correlated with serum creatinine at 48 h. Moreover, CFH levels inversely correlated with haptoglobin levels, which were significantly reduced at the end of surgery in LuTx patients with AKI. Because multiple other factors can contribute to AKI development in the complex clinical setting of LuTx, we next investigated the role of exogenous CFH administration in a mouse model of mild bilateral renal ischemia reperfusion injury (IRI). Exogenous administration of CFH after reperfusion caused overt AKI with creatinine increase, tubular injury, and enhanced markers of renal inflammation compared with vehicle-treated animals. In conclusion, CFH is a possible factor contributing to postoperative AKI after LuTx and promotes AKI in an experimental model of mild transient renal ischemia. Targeting CFH might be a therapeutic option to prevent AKI after LuTx.

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