| Literature DB >> 27939674 |
Hae Woong Choi1, Samantha E Bowen2, Yuxuan Miao2, Cheryl Y Chan3, Edward A Miao4, Magnus Abrink5, Adam J Moeser6, Soman N Abraham7.
Abstract
Programmed death and shedding of epithelial cells is a powerful defense mechanism to reduce bacterial burden during infection but this activity cannot be indiscriminate because of the critical barrier function of the epithelium. We report that during cystitis, shedding of infected bladder epithelial cells (BECs) was preceded by the recruitment of mast cells (MCs) directly underneath the superficial epithelium where they docked and extruded their granules. MCs were responding to interleukin-1β (IL-1β) secreted by BECs after inflammasome and caspase-1 signaling. Upon uptake of granule-associated chymase (mouse MC protease 4 [mMCPT4]), BECs underwent caspase-1-associated cytolysis and exfoliation. Thus, infected epithelial cells require a specific cue for cytolysis from recruited sentinel inflammatory cells before shedding.Entities:
Keywords: IL-1β; bladder epithelial cells; caspase 1; chymase; cytolysis; cytolytic granules; exfoliation; inflammasome; mast cells; uropathogenic E. coli
Mesh:
Substances:
Year: 2016 PMID: 27939674 PMCID: PMC5177478 DOI: 10.1016/j.immuni.2016.11.003
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745