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Resolution: standard / high Figure 9.
Inhibitory effect of 17-AAG on L. pneumophila-induced IL-8 expression.(A) A549 cells were incubated with 1 μM 17-AAG for 16 h prior to infection with varying
concentrations of AA100jm strain for 6 h. RT-PCR was performed to check the changes
of IL-8 mRNA expression after 17-AAG treatment in L. pneumophila-infected A549 cells. (B) Attenuation of L. pneumophila-induced NF-κB DNA binding by 17-AAG treatment. A549 cells were treated with (+) or
without (-) 17-AAG for 16 h prior to infection with varying concentrations of L. pneumophila for 3 h. The nuclear extracts were isolated from A549 cells infected with L. pneumophila and incubated with 32P-labeled oligonucleotides corresponding to NF-κB. (C) hsp90 protects IKKα and IKKβ
from proteasomal degradation. A549 cells either were pretreated with LLnL (20 μM)
for 1 h, followed or not followed by addition of 17-AAG (1 μM) and incubation for
16 h, or were treated with 17-AAG for 16 h or left untreated as indicated. Whole cell
extracts were immunoblotted with specific antibodies against each protein. Representative
results of three similar experiments in each panel are shown.
Teruya et al. BMC Microbiology 2007 7:102 doi:10.1186/1471-2180-7-102 |