Future Microbiology · 2018 · 42 citations · 33 references
Life SciencesImmunologyPharmacologyApoptosisChemotherapyInnate ImmunityCellular Responses To HypoxiaHypoxia AdaptationMacrophage BiologyPulmonary TuberculosisRedox Metabolism In DiseaseTuberculosis PharmacotherapyDigital Pathology AnalysisHif-1 Alpha RegulationHif-1 SignalingHypoxia-induced Apoptosis ResistanceHypoxia-inducible Factor SignalingHypoxia-inducible SignalingMacrophage ApoptosisMycobacterium Tuberculosis Pathogenesis
AIM: Investigate the role of hypoxia-inducible factor-1α (HIF-1α) in pulmonary tuberculosis (TB). METHODS & RESULTS: A model of progressive pulmonary TB in BALB/c mice, immunohistochemistry and digital pathology were used. High HIF-1α expression was observed during early TB in activated macrophages. During late TB, even higher HIF-1α expression was observed in foamy macrophages, which are resistant to apoptosis. Blocking HIF-1α during early infection with 2-methoxyestradiol worsened the disease, while during late TB, it induced macrophage apoptosis and decreased bacillary loads. CONCLUSION: HIF-1α has a dual role in experimental TB. This finding could have therapeutic implications because combined treatment with 2-methoxyestradiol and antibiotics appeared to eliminate mycobacteria more efficiently than conventional chemotherapy during advanced disease.
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