Nature Communications · 2017 · 109 citations · 47 references
Life SciencesCell BiologyMolecular BiologyCell SignalingGene ExpressionSignal TransductionInnate Immune ActivationInnate Immune ModulationInnate Immune ResponseInnate Immune Signaling PathwaysProtein Phosphatase SignalingPulmonary TuberculosisEffector Protein BindingEffector Protein SecretionInnate Immunity PathwaysMicrobe-host Interaction GenesMycobacterium Tuberculosis InfectionMycobacterium Tuberculosis PathogenesisPhosphatase Enzyme ActivitySecreted Effector Proteins
Mycobacterium tuberculosis PtpA is a secreted effector protein that dephosphorylates several proteins in the host cell cytoplasm, such as p-JNK, p-p38, and p-VPS33B, leading to suppression of host innate immunity. Here we show that, in addition, PtpA enters the nucleus of host cells and regulates the expression of host genes, some of which are known to be involved in host innate immunity or in cell proliferation and migration (such as GADD45A). PtpA can bind directly to the promoter region of GADD45A in vitro. Both phosphatase activity and DNA-binding ability of PtpA are important in suppressing host innate immune responses. Furthermore, PtpA-expressing Mycobacterium bovis BCG promotes proliferation and migration of human lung adenoma A549 cells in vitro and in a mouse xenograft model. Further research is needed to test whether mycobacteria, via PtpA, might affect cell proliferation or migration in humans. Mycobacterium tuberculosis secretes a protein, PtpA, that dephosphorylates proteins in the host cell cytoplasm, weakening immune responses. Here, the authors show that PtpA also enters the nucleus, affects the expression of several host genes, and promotes proliferation and migration of a cancer cell line.
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