| Summary: | Previous studies have shown that NACHT, leucine rich repeat and PYD domain containing 5 (Nlrp5) deficient embryos fail to develop beyond the two-cell stage. Despite this strong phenotype, little is known of the function of NALP5 and the pathways affected by its deficiency. We showed that Nlrp5 deficient oocytes and embryos exhibit a decrease in caspase activity. In addition, the kinetics of NF-κB-p65 nuclear translocation is altered, which leads to negative downstream effects. Autophagy is known to be regulated downstream of NF-κB and is a key event during the oocyte-to-embryo transition. We observed defective execution of autophagy in
Nlrp5 deficient two-cells evidenced by absence of autophagosome formation and abnormal lysosomal maturation. We found that inactivating autophagy leads to an accumulation of lipid droplets and embryos lacking Nlrp5 exhibit this accumulation. Thus, NALP5 may be an integral component responsible for autophagy mediated lipid metabolism, which when compromised causes developmental arrest.
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