4.8 Article

Vitamin D3 and carbamazepine protect against Clostridioides difficile infection in mice by restoring macrophage lysosome acidification

Journal

AUTOPHAGY
Volume 18, Issue 9, Pages 2050-2067

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15548627.2021.2016004

Keywords

Autophagic flux; Clostridium difficile; macrophages; MITF; toxin B

Categories

Funding

  1. National Natural Science Foundation of China [82070576]
  2. Hong Kong Food and Health Bureau (FHB) Commissioned Health and Medical Research Fund [CID-CUHK-C]

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Clostridioides difficile infection (CDI) is a common cause of nosocomial diarrhea. TcdB impairs lysosomal function in macrophages, leading to inflammation. Vitamin D-3 and carbamazepine protect against CDI by restoring lysosomal function and the expression of the transcription factor MITF in macrophages.
Clostridioides difficile infection (CDI) is a common cause of nosocomial diarrhea. TcdB is a major C. difficile exotoxin that activates macrophages to promote inflammation and epithelial damage. Lysosome impairment is a known trigger for inflammation. Herein, we hypothesize that TcdB could impair macrophage lysosomal function to mediate inflammation during CDI. Effects of TcdB on lysosomal function and the downstream pro-inflammatory SQSTM1/p62-NFKB (nuclear factor kappa B) signaling were assessed in cultured macrophages and in a murine CDI model. Protective effects of two lysosome activators (i.e., vitamin D-3 and carbamazepine) were assessed. Results showed that TcdB inhibited CTNNB1/beta-catenin activity to downregulate MITF (melanocyte inducing transcription factor) and its direct target genes encoding components of lysosomal membrane vacuolar-type ATPase, thereby suppressing lysosome acidification in macrophages. The resulting lysosomal dysfunction then impaired autophagic flux and activated SQSTM1-NFKB signaling to drive the expression of IL1B/IL-1 beta (interleukin 1 beta), IL8 and CXCL2 (chemokine (C-X-C motif) ligand 2). Restoring MITF function by enforced MITF expression or restoring lysosome acidification with 1 alpha,25-dihydroxyvitamin D-3 or carbamazepine suppressed pro-inflammatory cytokine expression in vitro. In mice, gavage with TcdB-hyperproducing C. difficile or injection of TcdB into ligated colon segments caused prominent MITF downregulation in macrophages. Vitamin D-3 and carbamazepine lessened TcdB-induced lysosomal dysfunction, inflammation and histological damage. In conclusion, TcdB inhibits the CTNNB1-MITF axis to suppress lysosome acidification and activates the downstream SQSTM1-NFKB signaling in macrophages during CDI. Vitamin D-3 and carbamazepine protect against CDI by restoring MITF expression and lysosomal function in mice.

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