A TRP Channel Senses Lysosome Neutralization by Pathogens to Trigger Their Expulsion.
Vertebrate cells have evolved elaborate cell-autonomous defense programs to monitor subcellular compartments for infection and to evoke counter-responses. These programs are activated by pathogen-associated pattern molecules and by various strategies intracellular pathogens employ to alter cellular microenvironments. Here, we show that, when uropathogenic E. coli (UPEC) infect bladder epithelial cells (BECs), they are targeted by autophagy but avoid degradation because of their capacity to neutralize lysosomal pH. This change is detected by mucolipin TRP channel 3 (TRPML3), a transient receptor potential cation channel localized to lysosomes. TRPML3 activation then spontaneously initiates lysosome exocytosis, resulting in expulsion of exosome-encased bacteria. These studies reveal a cellular default system for lysosome homeostasis that has been co-opted by the autonomous defense program to clear recalcitrant pathogens.
Duke Scholars
Altmetric Attention Stats
Dimensions Citation Stats
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Uropathogenic Escherichia coli
- Urinary Tract Infections
- Urinary Bladder
- Transient Receptor Potential Channels
- TRPC Cation Channels
- Mice
- Lysosomes
- Exocytosis
- Escherichia coli Infections
- Developmental Biology
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Uropathogenic Escherichia coli
- Urinary Tract Infections
- Urinary Bladder
- Transient Receptor Potential Channels
- TRPC Cation Channels
- Mice
- Lysosomes
- Exocytosis
- Escherichia coli Infections
- Developmental Biology