Macrophage inflammatory protein-3alpha plays a key role in the inflammatory cascade in rat focal cerebral ischemia.

Abstract Although hypothermia is one of the most robust neuroprotectants clinically available, its underlying mechanisms remain unclear. Through microarray gene expression analysis, we previously identified several key molecules potentially involved in the efficacy of hypothermia in a 2 h middle cerebral artery occlusion (MCAO) rat model, including cytokine and chemokine genes. The present study demonstrated that the expressions of 2 genes, macrophage inflammatory protein - 3alpha ( MIP - 3α ) and its receptor, CC - chemokine receptor 6 ( CCR6 ), were upregulated in the model and were suppressed by hypothermia. To investigate the role of cerebral MIP-3α, it was administered into the rat striatum; dose- and time-dependent induction of CCR6 gene expression was observed. Interleukin (IL)-1β and tumor necrosis factor (TNF)-α injection also induced sequential expressions of MIP - 3 α and CCR6 . MIP-3α was found to be produced by proinflammatory cytokines in rat astrocytes, while it was suppressed by hypothermia. In turn, MIP-3α stimulated IL-1β and inducible nitric oxide synthase expressions in rat microglia and rat brains. Furthermore, intracerebroventricular administration of an anti-rat MIP-3α-neutralizing antibody significantly reduced the infarct in MCAO rat brains. These findings suggest that MIP-3α plays a pivotal role in inflammatory cascades in ischemic brains, and may be a novel therapeutic target for cerebral ischemia.