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. 2009 Apr 3;3:47–52. doi: 10.2174/1874285800903010047

Table 1.

Cytokine, Chemokine and Nitrite in the Culture Supernatant Fluids of Murine MTB-Infected Bone-Marrow-Derived Macrophages Stimulated with the MALP-2 Derivative or LPS

Stimuli Days MOI TNF-α IL-6 IL-10 MIP-1β NO2
pg/ml pg/ml pg/ml pg/ml µMol/L
Untreated 2 1:1 0 188±62 92±2 1068±38 4.34±0.9
8 1:0.1 0 207±52 304±69 8078±148 n.d.
MALP-2 2 1:1 25±10 824±23* 129±10 970±40 13.05±0.75*
5 ng/ml 8 1:0.1 0 211±53 260±15 7000±75* n.d.
MALP-2 2 1:1 20±5 1243±7* 102±6 1112±25 19.25±0.35**
50 ng/ml 8 1:0.1 0 301±44 418±90 6587±70* n.d.
MALP-2 2 1:1 70±6* 1470±64* 126±6 1537+19* 50.65±0.95**
500 ng/ml 8 1:0.1 10±5 538±151* 361±89 5821±115* n.d
LPS 2 1:1 1879±39**,## 2138±88**,# 109±12 6846±225**,## 142.4±1.8**,##
500 ng/ml 8 1:0.1 336±52**,## 1284±69**,# 504±91 6709±217* n.d.

a)Murine macrophages were infected with MTB at MOI 1:1 for 2 days or at MOI 1:0.1 for 8 days and cultured in the presence of LPS or the MALP-2 derivative at the indicated concentration. Culture supernatants harvested at the indicated time points were used for IL-6, IL-10, TNF-α , MIP-1β detection by specific quantitative sandwich ELISA Kits. The results are presented as mean.

± SEM in pg/ml. Pooled data of 3 independent experiments are shown. Nitrite was detected at 2 days with a specific colorimetric kit. The results are presented as mean ± SEM in µ Mol/L. Pooled data of 3 independent experiments are shown.

*

p<0.05 and

**

p<0.01, level of statistical significance between cytokine or nitrite release in stimulated versus untreated macrophages.

#

p<0.05 and

##

p<0.01, level of statistical significance between cytokine or nitrite release in LPS-treated versus MALP-2 derivative-stimulated macrophages.