The role of TNF-a in the control of mycobacterial growth in murine macropha
ges was studied in vitro. Infection of macrophages from TNF-a gene disrupte
d (TNF-knockout (KO)) mice with recombinant Mycobacterium bovis bacillus Ca
lmette Guerin (BCG) expressing the vector only (BCG-vector) resulted in log
arithmic growth of the intracellular bacilli. Infection with BCG-secreting
murine TNF-a (BCG-TNF) led to bacillary killing. Killing of BCG-TNF was ass
ociated with rapid accumulation of inducible NO synthase (iNOS) protein and
the production of nitrite. The uncontrolled growth of BCG-vector was assoc
iated with low iNOS expression but no nitrite production. Thus, iNOS expres
sion appears to be TNF-a independent but iNOS generation of NO requires TNF
-a. In cultures of TNF-KO macrophages infected with BCG-TNF, inhibition of
iNOS by aminoguanidine (AMG) abolished the killing of the bacilli. However,
the growth of the organisms was still inhibited, suggesting an iNOS-indepe
ndent TNF-alpha -mediated growth inhibition. To confirm this, macrophages f
rom iNOS-KO mice were infected with either BCG-vector or BCG-TNF. As expect
ed, no nitrite was detected in the culture medium. TNF-a was detected only
when the cells were infected with BCG-TNF. In the iNOS-KO macrophages, the
growth of BCG was inhibited only in the BCG-TNF infection. These results su
ggest that in the absence of iNOS activity, TNF-a stimulates macrophages to
control the growth of intracellular BCG. Thus, there appears to be both a
TNF-alpha -dependent-iNOS-dependent killing pathway as well as a TNF-alpha-
dependent-iNOS-independent growth inhibitory pathway for the control of in
tracellular mycobacteria in murine macrophages. The Journal of immunology 2
001,166:6728-6734.