Nrf2 Regulates Granuloma Formation and Macrophage Activation during Mycobacterium avium Infection via Mediating Nramp1 and HO-1 Expressions
Masayuki Nakajima, Masashi Matsuyama, Mio Kawaguchi, Takumi Kiwamoto, Yosuke Matsuno, Yuko Morishima, Kazufumi Yoshida, Mingma Sherpa, et al. (13 authors)
mBio · 2021-02
Abstract
complex (MAC) is the most common cause of pulmonary NTM disease worldwide. It is thought that both environmental exposure and host susceptibility are required for the establishment of pulmonary MAC disease, because pulmonary MAC diseases are most commonly observed in slender, postmenopausal women without a clearly recognized immunodeficiency. However, host factors that regulate MAC susceptibility have not been elucidated until now. This study shows that Nrf2 is a critical regulator of host susceptibility to pulmonary MAC disease by promoting phagolysosome fusion and granuloma formation via activating Nramp1 and HO-1 genes, respectively. The Nrf2 system is activated in alveolar macrophages, the most important cells during MAC infection, as both the main reservoir of infection and bacillus-killing cells. Thus, augmentation of Nrf2 might be a useful therapeutic approach for protection against pulmonary MAC disease.
MeSH terms
- Mycobacterium avium complex
- Nontuberculous mycobacteria
- Macrophage
- Pulmonary disease
- Mycobacterium
- Microbiology
- Immunology
- Granuloma
- Disease
- Granuloma formation
- Medicine
- Chronic granulomatous disease
- Mycobacterium avium-intracellulare infection
- Biology