Neutrophil Enzyme Myeloperoxidase Modulates Neuronal Response in a Model of Subarachnoid Hemorrhage by Venous Injury

• Published in: Stroke (1970) 2021-10, Vol.52 (10), p.3374-3384
• Main Authors: Coulibaly, Aminata P., Pezuk, Pinar, Varghese, Paul, Gartman, William, Triebwasser, Danielle, Kulas, Joshua A., Liu, Lei, Syed, Mariam, Tvrdik, Petr, Ferris, Heather, Provencio, J. Javier
• Format: Article
• Language: English
• Subjects: Animals; Astrocytes - pathology; Calcium Signaling; Cerebral Veins - injuries; Cognition Disorders - etiology; Hydrogen Peroxide - cerebrospinal fluid; Hydrogen Peroxide - pharmacology; Inflammation - pathology; Maze Learning; Memory Disorders - etiology; Memory Disorders - psychology; Mice; Mice, Inbred C57BL; Mice, Knockout; Neuroglia - enzymology; Neurons - pathology; Neutrophils - enzymology; Peroxidase - genetics; Peroxidase - metabolism; Spatial Memory; Subarachnoid Hemorrhage - pathology; Subarachnoid Hemorrhage - psychology
• ISSN: 0039-2499; 1524-4628
• DOI: 10.1161/STROKEAHA.120.033513

Aneurysmal subarachnoid hemorrhage (SAH) is associated with the development of delayed cognitive deficits. Neutrophil infiltration into the central nervous system is linked to the development of these deficits after SAH. It is however unclear how neutrophil activity influences central nervous system function in SAH. The present project aims to elucidate which neutrophil factors mediate central nervous system injury and cognitive deficits after SAH. Using a murine model of SAH and mice deficient in neutrophil effector functions, we determined which neutrophil effector function is critical to the development of deficits after SAH. In vivo and in vitro techniques were used to investigate possible pathways of neutrophils effect after SAH. Our results show that mice lacking functional MPO (myeloperoxidase), a neutrophil enzyme, lack both the meningeal neutrophil infiltration (wild type, sham 872 cells/meninges versus SAH 3047, P=0.023; myeloperoxidase knockout [MPOKO], sham 1677 versus SAH 1636, P=NS) and erase the cognitive deficits on Barnes maze associated with SAH (MPOKO sham versus SAH, P=NS). The reintroduction of biologically active MPO, and its substrate hydrogen peroxide (H2O2), to the cerebrospinal fluid of MPOKO mice at the time of hemorrhage restores the spatial memory deficit observed after SAH (time to goal box MPOKO sham versus MPOKO+MPO/H2O2, P=0.001). We find evidence of changes in neurons, astrocytes, and microglia with MPO/H2O2 suggesting the effect of MPO may have complex interactions with many cell types. Neurons exposed to MPO/H2O2 show decreased calcium activity at baseline and after stimulation with potassium chloride. Although astrocytes and microglia are affected, changes seen in astrocytes are most consistent with inflammatory changes that likely affect neurons. These results implicate MPO as a mediator of neuronal dysfunction in SAH through its effect on both neurons and glia. These results show that, in SAH, the activity of innate immune cells in the meninges modulates the activity and function of the underlying brain tissue.