A cardinal role for cathepsin d in co-ordinating the host-mediated apoptosis of macrophages and killing of pneumococci.
The bactericidal function of macrophages against pneumococci is enhanced by their apoptotic demise, which is controlled by the anti-apoptotic protein Mcl-1. Here, we show that lysosomal membrane permeabilization (LMP) and cytosolic translocation of activated cathepsin D occur prior to activation of a mitochondrial pathway of macrophage apoptosis. Pharmacological inhibition or ... knockout of cathepsin D during pneumococcal infection blocked macrophage apoptosis. As a result of cathepsin D activation, Mcl-1 interacted with its ubiquitin ligase Mule and expression declined. Inhibition of cathepsin D had no effect on early bacterial killing but inhibited the late phase of apoptosis-associated killing of pneumococci in vitro. Mice bearing a cathepsin D(-/-) hematopoietic system demonstrated reduced macrophage apoptosis in vivo, with decreased clearance of pneumococci and enhanced recruitment of neutrophils to control pulmonary infection. These findings establish an unexpected role for a cathepsin D-mediated lysosomal pathway of apoptosis in pulmonary host defense and underscore the importance of apoptosis-associated microbial killing to macrophage function.
Mesh Terms:
Animals, Apoptosis, Bone Marrow Cells, Bone Marrow Transplantation, Cathepsin D, Cell Line, Tumor, Cytosol, Female, Host-Pathogen Interactions, Humans, Intracellular Membranes, Macrophages, Mice, Mice, Inbred C57BL, Mice, Knockout, Phagosomes, Streptococcus pneumoniae
Animals, Apoptosis, Bone Marrow Cells, Bone Marrow Transplantation, Cathepsin D, Cell Line, Tumor, Cytosol, Female, Host-Pathogen Interactions, Humans, Intracellular Membranes, Macrophages, Mice, Mice, Inbred C57BL, Mice, Knockout, Phagosomes, Streptococcus pneumoniae
PLoS Pathog.
Date: Feb. 08, 2011
PubMed ID: 21298030
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