Role of Xanthine Oxidase in Heme-induced Vascular Dysfunction

NIH RePORTER · NIH · R01 · $534,408 · view on reporter.nih.gov ↗

Abstract

PROJECT SUMMARY/ABSTRACT Vascular injury resulting from hemolysis or ruptured red blood cells is an important clinical issue associated with numerous hemolytic pathologies including sickle cell disease (SCD), sepsis and iatrogenic issues in cardiopulmonary bypass surgery, ventricular assist devices and valve replacement. During hemolysis, red cells release hemoglobin that subsequently discharges heme leading to an oxidative milieu in the intravascular space. Interestingly, substantial elevation in circulating levels of xanthine oxidase (XO) is also reported to be associated with numerous hemolytic diseases. While elevated levels of heme are well characterized in hemolysis pathobiology, the relationship between heme and increased XO activity is unclear. Here, we provide new data connecting a murine model of intravascular heme injury to excessive amplification in circulating XO levels (>20-fold). This is important as decades-long bias in the literature would suggest this level of XO amplification in the circulation to be considered deleterious. Contrary to this long-standing dogma, our new data suggest XO instead assumes a protective role during heme overload. Pilot studies demonstrate inhibition of XO with febuxostat during heme overload decreases survival, accelerates organ damage, and elevates inflammatory responses compared to controls. Consistent with this, plasma from both SCD patients and a murine model of SCD demonstrate elevation in circulating XO. Importantly, biochemical studies have identified a novel function for XO: the “splitting” of heme via H2O2 production and subsequent chelation of heme-derived free iron via uric acid in order to protect the endothelium from overt heme damage. As such, we hypothesize that following hemopexin saturation, hepatic XO is released to the circulation, binds to endothelium, and assumes a vaso- protective role during heme overload and SCD-associated heme crisis due to its ability to degrade heme and subsequently chelate free iron by producing uric acid. We will test this hypothesis using three specific aims: Aim 1: Define if XO mediates protection during intravascular heme overload. Aim 2: Determine if XO facilitates “heme splitting” and subsequent iron chelation via XO-derived uric acid. Aim 3: Investigate whether elevated XO in SCD protects against heme-induced vaso-occlusive crisis. Filling this knowledge gap may uncover new strategies to address the vascular dysfunction allied to intravascular hemolysis, in general, and SCD, in specific.

Key facts

NIH application ID
10400232
Project number
5R01HL153532-02
Recipient
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
Principal Investigator
Eric Eugene Kelley
Activity code
R01
Funding institute
NIH
Fiscal year
2022
Award amount
$534,408
Award type
5
Project period
2021-05-01 → 2025-02-28