Abstract
In addition to immediate brain damage, traumatic brain injury (TBI) initiates a cascade of pathophysiological events producing secondary injury. The biochemical and cellular mechanisms that comprise secondary injury are not entirely understood. Herein, we report a substantial deregulation of cerebral sphingolipid metabolism in a mouse model of TBI. Sphingolipid profile analysis demonstrated increases in sphingomyelin species and sphingosine concurrently with up-regulation of intermediates of de novo sphingolipid biosynthesis in the brain. Investigation of intracellular sites of sphingosine accumulation revealed an elevation of sphingosine in mitochondria due to the activation of neutral ceramidase (NCDase) and the reduced activity of sphingosine kinase 2 (SphK2). The lack of change in gene expression suggested that post-translational mechanisms are responsible for the shift in the activities of both enzymes. Immunoprecipitation studies revealed that SphK2 is complexed with NCDase and cytochrome oxidase (COX) subunit 1 in mitochondria and that brain injury hindered SphK2 association with the complex. Functional studies showed that sphingosine accumulation resulted in a decreased activity of COX, a rate-limiting enzyme of the mitochondrial electron transport chain. Knocking down NCDase reduced sphingosine accumulation in mitochondria and preserved COX activity after the brain injury. Also, NCDase knockdown improved brain function recovery and lessened brain contusion volume after trauma. These studies highlight a novel mechanism of secondary TBI involving a disturbance of sphingolipid-metabolizing enzymes in mitochondria and suggest a critical role for mitochondrial sphingosine in promoting brain injury after trauma.
Highlights
A cardinal feature of many neurological disorders is mitochondrial dysfunction
Brain Sphingolipid Metabolism Is Disturbed after traumatic brain injury (TBI)—A sphingolipid profile was determined in brains of mice at 4 h, 1 day, 2 days, and 7 days post-Cortical Impact (CCI)
We have shown that TBI stimulates the utilization of ceramide by neutral ceramidase (NCDase), which results in the accumulation of mitochondrial sphingosine and mitochondrial dysfunction promoting secondary brain injury
Summary
A cardinal feature of many neurological disorders is mitochondrial dysfunction. Results: Knocking down neutral ceramidase reduces mitochondrial sphingosine, preserves mitochondrial function, and improves brain function recovery after trauma. Knocking down NCDase reduced sphingosine accumulation in mitochondria and preserved COX activity after the brain injury. NCDase knockdown improved brain function recovery and lessened brain contusion volume after trauma These studies highlight a novel mechanism of secondary TBI involving a disturbance of sphingolipid-metabolizing enzymes in mitochondria and suggest a critical role for mitochondrial sphingosine in promoting brain injury after trauma. An impairment of the mitochondrial respiratory chain enzyme COX has been implicated in secondary brain damage following TBI, but the mechanisms remain unresolved [8]. NCDase-deficient mice demonstrated greatly improved recovery of behavioral deficits after brain trauma These studies emphasize sphingolipid-metabolizing enzymes as novel regulators of mitochondrial respiratory chain function and identify the sphingolipid responsible for mitochondrial dysfunction after brain trauma
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