behavior/neurological
• mice fail to recovery from carrageenan-induced inflammatory hyperalgesia unlike wild-type mice
• however, mice do resolve carrageenan-induced inflammation
|
• mice fail to recovery from carrageenan-induced inflammatory hyperalgesia unlike wild-type mice
|
mortality/aging
• mice are protected from HSV-1 encephalitis and lethality
|
immune system
• macrophage mitochondria fail to transfer MTDR-labeled mitochondria to sensory neurons unlike wild-type mice
• however, mitochondria exhibit normal respiration and vesicle release
|
• in the brains following HSV-1 infection
|
• from peritoneal or bone-marrow macrophages stimulated with HSV-1
• however, secretion after ATP stimulation is normal
|
• from macrophages stimulated with HSV-1, Pam2CSK4 or LPS
|
• mice are protected from HSV-1 encephalitis and lethality with reduced type I IFN production and lower viral titers mouse due to reduced viral replication and more efficient clearance
• mouse embryonic fibroblasts and peritoneal macrophages infected with HSV-1 exhibit reduced infection ex vivo
• however, IL-6 and chemokine (CCL5 and CCL2) levels in the brain are the same as in injected wild-type mice
|
• mice are protected from HSV-1 encephalitis and lethality
|
hematopoietic system
• macrophage mitochondria fail to transfer MTDR-labeled mitochondria to sensory neurons unlike wild-type mice
• however, mitochondria exhibit normal respiration and vesicle release
|