Lithium Inhibits Growth of Intracellular Mycobacterium kansasii through Enhancement of Macrophage Apoptosis
2014
Sohn, H., Chungnam National University, Daejeon, Republic of Korea | Kim, K., Chungnam National University, Daejeon, Republic of Korea | Lee, K.S., National Institute of Health, Korea Centers for Disease Control and Prevention, Seoul, Republic of Korea | Choi, H.G., Chungnam National University, Daejeon, Republic of Korea | Lee, K.I., Chungnam National University, Daejeon, Republic of Korea | Shin, A.R., Chungnam National University, Daejeon, Republic of Korea | Kim, J.S., Yonsei University College of Medicine, Seoul, Republic of Korea | Shin, S.J., Yonsei University College of Medicine, Seoul, Republic of Korea | Song, C.H., Chungnam National University, Daejeon, Republic of Korea | Park, J.K., Chungnam National University, Daejeon, Republic of Korea | Kim, H.J., Chungnam National University, Daejeon, Republic of Korea
Mycobacterium kansasii (Mk) is an emerging pathogen that causes a pulmonary disease similar to tuberculosis. Macrophage apoptosis contributes to innate host defense against mycobacterial infection. Recent studies have suggested that lithium significantly enhances the cytotoxic activity of death stimuli in many cell types. We examined the effect of lithium on the viability of host cells and intracellular Mk in infected macrophages. Lithium treatment resulted in a substantial reduction in the viability of intracellular Mk in macrophages. Macrophage cell death was significantly enhanced after adding lithium to Mk-infected cells but not after adding to uninfected macrophages. Lithium-enhanced cell death was due to an apoptotic response, as evidenced by augmented DNA fragmentation and caspase activation. Reactive oxygen species were essential for lithium-induced apoptosis. Intracellular scavenging by N-acetylcysteine abrogated the lithium-mediated decrease in intracellular Mk growth as well as apoptosis. These data suggest that lithium is associated with control of intracellular Mk growth through modulation of the apoptotic response in infected macrophages.
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