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10.1177/1753425919875796

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suck abstract from ncbi


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pmid31533549      Innate+Immun 2019 ; 25 (8): 530-538
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  • Transient receptor potential melastatin 2-mediated heme oxygenase-1 has a role for bacterial clearance by regulating autophagy in peritoneal macrophages during polymicrobial sepsis #MMPMID31533549
  • Qian X; Cheng H; Chen X
  • Innate Immun 2019[Nov]; 25 (8): 530-538 PMID31533549show ga
  • Our previous study indicated an important protective role of transient receptor potential melastatin 2 (TRPM2) in controlling bacterial clearance in macrophages during polymicrobial sepsis by regulating heme oxygenase-1. Autophagy is necessary for macrophages to kill invasive bacteria. In the present study, TRPM2 knockout (KO) mice show decreased heme oxygenase-1 and autophagy in peritoneal macrophages after caecal ligation and puncture surgery. Caecal ligation and puncture-induced autophagy in peritoneal macrophages is dependent on heme oxygenase-1. TRPM2 KO mice treated with heme oxygenase-1 inducer before caecal ligation and puncture significantly increase autophagy of peritoneal macrophages, bacterial clearance rate and survival rate. In addition, TRPM2 KO mice treated with heme oxygenase-1 inducer before caecal ligation and puncture significantly attenuate organ injury and systemic inflammation. These improvements are reversed by autophagy inhibitor. Therefore, our findings suggest that TRPM2-mediated heme oxygenase-1 has a role for bacterial clearance possibly by regulating autophagy in peritoneal macrophages during polymicrobial sepsis.
  • |Animals[MESH]
  • |Autophagy[MESH]
  • |Bacterial Load[MESH]
  • |Cecum/surgery[MESH]
  • |Cells, Cultured[MESH]
  • |Clusterin/genetics/*metabolism[MESH]
  • |Disease Models, Animal[MESH]
  • |Heme Oxygenase-1/*metabolism[MESH]
  • |Humans[MESH]
  • |Macrophages, Peritoneal/*physiology[MESH]
  • |Male[MESH]
  • |Mice[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Mice, Knockout[MESH]


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