Nicotine promotes Staphylococcus aureus-induced osteomyelitis by activating the Nrf2/Slc7a11 signaling axis

Xuyou Zhou,Sushuang Ma, Yuan Xu, Chongkai Sun, Juncheng Liao,Mingrui Song, Guanzhi Li,Yuchen Liu,Peng Chen,Yanjun Hu,Yutian Wang,Bin Yu

International Immunopharmacology(2024)

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Abstract
Although smoking is a significant risk factor for osteomyelitis, there is limited experimental evidence that nicotine, a key tobacco constituent, is associated with this condition, leaving its mechanistic implications uncharacterized. This study revealed that nicotine promotes Staphylococcus aureus-induced osteomyelitis by increasing Nrf2 and Slc7a11 expression in vivo and in vitro. Inhibition of Slc7a11 using Erastin augmented bacterial phagocytosis/killing capabilities and fortified antimicrobial responses in an osteomyelitis model. Moreover, untargeted metabolomic analysis demonstrated that Erastin mitigated the effects of nicotine on S. aureus-induced osteomyelitis by altering glutamate/glutathione metabolism. These findings suggest that nicotine aggravates S. aureus-induced osteomyelitis by activating the Nrf2/Slc7a11 signaling pathway and that Slc7a11 inhibition can counteract the detrimental health effects of nicotine.
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Key words
Nicotine,Osteomyelitis,Macrophage,Nrf2/Slc7a11 signaling axis,Glutamate/glutathioine metabolism,Erastin
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