Functional genome-wide short hairpin RNA library screening identifies key molecules for extracellular vesicle secretion from microglia

Activated microglia release extracellular vesicles (EVs) as modulators of brain homeostasis and innate immunity. However, the molecules critical for regulating EV production from microglia are poorly understood. Here we establish a murine microglial cell model to monitor EV secretion by measuring the fluorescence signal of tdTomato, which is linked to tetraspanin CD63. Stimulation of tdTomato(+) cells with ATP induces rapid secretion of EVs and a reduction in cellular tdTo-mato intensity, reflecting EV secretion. We generate a GFP(+) tdTo-mato(+) cell library expressing TurboGFP and barcoded short hairpin RNAs for genome-wide screening using next-generation sequencing. We identify Mcfd2, Sepp1, and Sdc1 as critical regulators of ATP-induced EV secretion from murine microglia. Small interfering RNA (siRNA-based) silencing of each of these genes suppresses lipopolysaccharide- and ATP-induced inflammasome activation, as determined by interleukin-1 beta release from primary cultured murine microglia. These molecules are critical for microglial EV secretion and are potential therapeutic targets for neuroinflammatory disorders.

Automated summary

Activated microglia release extracellular vesicles (EVs) to modulate brain homeostasis and innate immunity. This study identifies Mcfd2, Sepp1, and Sdc1 as critical regulators of ATP-induced EV secretion from murine microglia and potential therapeutic targets for neuroinflammatory disorders.