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Fig. 11 | Journal of Neuroinflammation

Fig. 11

From: Microglia-derived IL-1β contributes to axon development disorders and synaptic deficit through p38-MAPK signal pathway in septic neonatal rats

Fig. 11

TOCI. An illustration demonstrates the cellular and molecular events associated with PWMD in the septic developing brain. Microglia are activated after LPS intraperitoneal injection and release proinflammatory cytokine IL-1β, which inhibits the generation of NFL, NFM, and NFH in the axon through its IL-1R1 via p38-MAPK signaling pathway. This suppresses axon development and contributes to axonal hypomyelination in septic neonatal brain. Moreover, the synaptogenesis of neurons involved in this process is ultimately affected

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