Alkyl hydroperoxide reductase subunit C (AhpC) protects bacterial and human cells against reactive nitrogen intermediates
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作者:
Chen, L
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Cornell Univ, Coll Med, Dept Med, Div Hematol Oncol,Seaver Lab, New York, NY 10021 USACornell Univ, Coll Med, Dept Med, Div Hematol Oncol,Seaver Lab, New York, NY 10021 USA
Chen, L
[1
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Xie, QW
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Cornell Univ, Coll Med, Dept Med, Div Hematol Oncol,Seaver Lab, New York, NY 10021 USACornell Univ, Coll Med, Dept Med, Div Hematol Oncol,Seaver Lab, New York, NY 10021 USA
Xie, QW
[1
]
Nathan, C
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Cornell Univ, Coll Med, Dept Med, Div Hematol Oncol,Seaver Lab, New York, NY 10021 USACornell Univ, Coll Med, Dept Med, Div Hematol Oncol,Seaver Lab, New York, NY 10021 USA
Nathan, C
[1
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[1] Cornell Univ, Coll Med, Dept Med, Div Hematol Oncol,Seaver Lab, New York, NY 10021 USA
In Salmonella typhimurium, ahpC encodes subunit C of alkyl hydroperoxide reductase, an enzyme that reduces organic peroxides. Here, we asked if ahpC could protect cells from reactive nitrogen intermediates (RNI). Salmonella disrupted in ahpC became hypersusceptible to RNI, ahpC from either Mycobacterium tuberculosis or S. typhimurium fully complemented the defect. Unlike protection against cumene hydroperoxide, protection afforded by ahpC against RNI was independent of the reducing flavoprotein, AhpF. Mycobacterial ahpC protected human cells from necrosis and apoptosis caused by RNI delivered exogenously or produced endogenously by transfected nitric oxide synthase. Resistance to RNI appears to be a physiologic function of ahpC. ahpC is the most widely distributed gene known that protects cells directly from RNI, and provides an enzymatic defense against an element of antitubercular immunity.