Vitamin D differentially regulates -induced intestine epithelial autophagy and interleukin-1β expression.

AIM

To investigate the effects of active vitamin D3 on autophagy and interleukin (IL)-1β expression in -infected intestinal epithelial cells (IECs).

METHODS

Caco-2 cells, NOD2 siRNA-, Atg16L1 siRNA- or vitamin D receptor (VDR) siRNA-transfected Caco-2 cells were pretreated with 1,25-dihydroxyvitamin D3 (1,25D3), and then infected by wild-type strain SL1344. The conversion of LC3-I to LC3-II was detected by Western blot analysis and LC3 autophagosome was analyzed by immunofluorescence. Caco-2 cells or VDR siRNA-transfected cells were pretreated with 1,25D3, and then infected by SL1344. Membrane protein and total RNA were analyzed by Western blot and RT-PCR for VDR and Atg16L1 protein and mRNA expression, respectively. Atg16L1 siRNA-transfected Caco-2 cells were pretreated by 1,25D3 and then infected with SL1344. Total RNA was analyzed by RT-PCR for IL-1β mRNA expression.

RESULTS

The active form of vitamin D, 1,25D3, showed enhanced VDR-mediated Atg16L1 mRNA expression, membranous Atg16L1 protein expression leading to enhanced autophagic LC3II protein expression and LC3 punctae in -infected Caco-2 cells which was counteracted by Atg16L1 and VDR siRNA, but Atg16L1 mediated suppression of IL-1β expression. Thus, active vitamin D may enhance autophagy but suppress inflammatory IL-1β expression in -infected IECs.

CONCLUSION

Active vitamin D might enhance autophagic clearance of infection, while modulation of inflammatory responses prevents the host from detrimental effects of overwhelming inflammation.