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Polarization of M1 and M2 Human Monocyte-Derived Cells and Analysis with Flow Cytometry upon Mycobacterium tuberculosis Infection
Published on: September 18, 2020
Dopamine alters macrophage metabolism promoting intracellular Mycobacterium tuberculosis survival
Radheshyam Modanwal1, Sharmila Talukdar1, Gaurav Kumar Chaubey1
1Institute of Microbial Technology, CSIR, Sector 39A, Chandigarh, 160036, India.
Background:
Dopamine (DA) is thought to aggravate progress of bacterial infections and enhance risk of intracellular bacterial infection like tuberculosis (TB). Though TB patients are known to present with high dopamine levels the causal link between them has remained unexplored. Mycobacterium tuberculosis (M. tb), the causative agent of TB, requires a copious supply of iron and carbon for survival and proliferation within host cells.
Methods:
In vitro and in vivo administration of dopamine induced an increase of non-transferrin bound iron delivery into macrophages along with and lipid accumulation and foamy macrophage formation. The resultant intracellular milieu provided an abundant source of carbon and iron for invading M. tb pathogen. Binding of dopamine to iron was characterized by NMR spectroscopy implicating its role in intracellular trafficking. Using iron sensor M. tb strain, we observed elevated iron levels in intraphagosomal bacteria residing in dopamine treated cells while CFU analysis indicated enhanced M. tb survival and proliferation.
Results:
We found that DA modulates macrophage metabolism resulting in creation of iron and lipid nutrient rich intracellular micro-environment favorable for survival of M. tb.
Conclusions:
Survival of M. tb bacilli in dopamine treated macrophages was significantly enhanced demonstrating that dopamine leads to creation of an intracellular milieu that provides a conducive and nurturing environment for invading pathogenic bacilli.
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