ZIP8 impacts protease activity in macrophages in response to Streptococcus pneumoniae

Abstract Zinc (Zn) is essential for immune function and Zn deficiency increases the incidence of community acquired pneumonia. The Zn transporter ZIP8 is required by myeloid cells to defend against pathogens. Previously, we reported that S. pneumoniae infected ZIP8 knockout mice (Zip8KO) have increased bacterial burden and mortality and that Zip8KO bone marrow derived macrophages (BMDMs) have reduced phagocytic activity. Others have shown that Zn induces cathepsin expression via the TFEB pathway. However, it is unknown whether ZIP8 impacts TFEB-dependent phagolysosomal processing in macrophages. Based on this, we hypothesized that ZIP8 facilitates phagolysosomal processing and eradication of bacteria via TFEB. BMDMs were derived from wild type and Zip8KO mice and then exposed to S. pneumoniae(MOI=10) for 1 hour. At 6–18 hours post challenge we assessed cathepsin B and L mRNA and protein levels as well as total protease, cathepsin B and L activity. In conjunction, we measured p-TFEB and total TFEB proteins levels. Active TFEB and cathepsin B protein levels were significantly lower in Zip8KO BMDMs with no difference in cathepsin L. Strikingly, Zip8KO BMDMs had significantly reduced total protease, cathepsin B and cathepsin L activity which also corresponded with decreased mRNA levels. Based on these findings we predict that ZIP8 loss in macrophages impairs phagolysosomal processing and bacterial eradication in a TFEB-dependent manner. Overall, this warrants future studies given the high incidence of Zn deficiency and the rs13107325 defective ZIP8 allele in humans. National Heart, Lung and Blood Institute #1R01HL156952-01-A1 (DLK)