Microglia in juvenile neuronal ceroid lipofuscinosis are primed toward a pro‐inflammatory phenotype

Juvenile neuronal ceroid lipofuscinosis ( JNCL ) is a lysosomal storage disease caused by an autosomal recessive mutation in CLN 3 . Regions of microglial activation precede and predict areas of neuronal loss in JNCL ; however, the functional role of activated microglia remains to be defined. The inflammasome is a key molecular pathway for activating pro‐ IL ‐1β in microglia, and IL ‐1β is elevated in the brains of JNCL patients and can induce neuronal cell death. Here, we utilized primary microglia isolated from CLN 3 Δex7/8 mutant and wild‐type ( WT ) mice to examine the impact of CLN 3 mutation on microglial activation and inflammasome function. Treatment with neuronal lysates and ceramide, a lipid intermediate elevated in the JNCL brain, led to inflammasome activation and IL ‐1β release in CLN 3 Δex7/8 microglia but not WT cells, as well as increased expression of additional pro‐inflammatory mediators. Similar effects were observed following either TNF ‐α or IL ‐1β treatment, suggesting that CLN 3 Δex7/8 microglia exist in primed state and hyper‐respond to several inflammatory stimuli compared to WT cells. CLN 3 Δex7/8 microglia displayed constitutive caspase‐1 activity that when blocked led to increased glutamate release that coincided with hemichannel opening. Conditioned medium from activated CLN 3 Δex7/8 or WT microglia induced significant cell death in CLN 3 Δex7/8 but not WT neurons, demonstrating that intrinsically diseased CLN 3 Δex7/8 neurons are less equipped to withstand cytotoxic insults generated by activated microglia. Collectively, aberrant microglial activation may contribute to the pathological chain of events leading to neurodegeneration during later stages of JNCL .Juvenile neuronal ceroid lipofuscinosis (JNCL) is a lysosomal storage disease caused by an autosomal recessive mutation in CLN3 . Regions of microglial activation precede and predict areas of neuronal loss in JNCL; however, the functional role of activated microglia remains to be defined. In this report, primary microglia from CLN3 Δex7/8 mutant mice over‐produced numerous inflammatory cytokines in response to stimuli that are present in the JNCL brain, whereas wild‐type microglia were relatively non‐responsive. In addition, activated microglia induced significant cell death in CLN3 Δex7/8 but not wild‐type neurons, demonstrating that intrinsically diseased CLN3 Δex7/8 neurons are less equipped to withstand cytotoxic insults. Collectively, aberrant microglial activation may contribute to the pathological chain of events leading to neurodegeneration during later stages of JNCL.