Fig 1.
Nickel and cobalt trigger NF-κB activation, which is not inhibited by lipid IVa.
(A, B) Dose-dependent activation of human TLR4/MD-2 by nickel and cobalt. HEK293/hTLR4 cells were transfected with plasmid encoding hMD-2 and luciferase reporter plasmids. Cells were stimulated with LPS (0, 1, 5, 10, 100 ng/ml) and nickel (A) or cobalt (B) (0.10, 0.25, 0.50, 0.75, 1.0, 2.0, 4.0 mM) for 6 hours, lysed and tested for luciferase activity. (C) Copper and cadmium do not activate human TLR4/MD-2 receptor complex at low, non-toxic concentrations. (D) Tetraacylated lipid IVa (compound 406) does not inhibit human TLR4 activation by nickel or cobalt ions. #p≥0,01 (not significant); *p<0,01; ***p<0,0001 (t-test, compared to the unstimulated control unless indicated otherwise by brackets).
Fig 2.
Nickel and cobalt trigger cytokine production and phosphorylation of intracellular signaling proteins.
(A) Nickel and cobalt stimulation elicits hIL-8 production. HUVEC cells were stimulated with LPS, nickel or cobalt for either 6 or 16 hours. hIL-8 concentration was measured in cell culture supernatants by ELISA. (B) THP-1 cells were stimulated with LPS or metal ions for 16 hours. Cytokine concentration was measured in cell culture supernatants by ELISA. (C) THP-1 cells were stimulated and the phosphorylation of the inhibitor of kappaB-alpha was detected with western blot. #p≥0,01 (not significant); *p<0,01; **p<0,001; ***p<0,0001 (t-test, compared to the unstimulated control). (D) THP-1 cells were stimulated with LPS alone or simultaneously with nickel for 6h. hTNF-α concentration was measured in cell culture supernatants by ELISA. #p≥0,01 (not significant); *p<0,01; **p<0,001; ***p<0,0001 (t-test, compared to the unstimulated control (as indicated by brackets) or compared to the cells not treated with nickel).
Fig 3.
Nickel and cobalt activate HEK293 cells via human TLR4 and require MD-2 for activation.
(A) HEK293/hTLR4 cells were transfected with the luciferase reporter plasmids with or without the plasmid encoding hMD-2. After stimulation, the luciferase activity was measured. (B) Mouse TLR4 with either mouse or human MD-2 does not support activation by nickel or cobalt. HEK293/mTLR4 cells were transfected with the luciferase reporter plasmids with or without plasmid encoding MD-2. (C) Mutation of histidines at positions 456 and 458 in hTLR4 nearly abolishes responsiveness to nickel and cobalt ions. HEK293 cells were transfected with luciferase reporter plasmids, plasmid encoding hMD-2 and plasmid encoding either wild type or mutant hTLR4. Luciferase activity was measured as indicated in Methods. #p≥0,01 (not significant); *p<0,01; **p<0,001; ***p<0,0001 (t-test, compared to the unstimulated control). The chart legend applies to all three panels.
Fig 4.
Activation of human TLR4 by metal ions requires different TLR4 and MD-2 residues than activation by endotoxin.
(A) hTLR4 amino acid residues that are essential for activation by LPS are not needed for activation by nickel or cobalt. HEK293 cells were transfected with luciferase reporter plasmids, plasmid encoding hMD-2 and plasmid encoding either wild type hTLR4 or the hTLR4 mutant hF440A. (B) hMD-2 amino acid residues that are essential for activation by LPS are not needed for activation by nickel or cobalt. HEK293/hTLR4 cells were transfected with luciferase reporter plasmids and with plasmid encoding either wild type or mutant hMD-2. #p≥0,01 (not significant); *p<0,01; **p<0,001; (t-test, compared to the unstimulated control (as indicated by brackets) or compared to the wt hTLR4 with the corresponding treatment).
Fig 5.
Nickel and cobalt activate MyD88-dependent and -independent pathways.
HEK293/hTLR4 cells were transfected with luciferase reporter plasmids (constitutive Renilla-luciferase reporter and inducible) (A) IFNβ-responsive or (B) IP-10-responsive firefly-luciferase reporter) and with plasmid encoding wild type hMD-2. *p<0,01; **p<0,001; (t-test, compared to the unstimulated control). The chart legend applies to both panels.
Fig 6.
MD-2 provides crucial stabilization that supports the formation of TLR4/MD-2 heterodimer with nickel or cobalt ions.
(A) A ribbon representation of a TLR4/MD-2 heterodimer (pdb id 3fxi). Amino acid residues of both TLR4 and MD-2 that form hydrophobic interactions with each other are shown as spheres and indicated with arrows. (B) A ribbon representation of the intrinsic dimerization interface between both TLR4 ectodomains. Amino acid residues that engage in direct interactions with one another are shown as spheres. Histidines H431, H456 and H458 are represented as sticks and colored orange. Green spheres represent metal ions that are coordinated between the indicated histidines. (C) A ribbon representation of TLR4 dimer without MD-2 shown from a top view. Without MD-2 both TLR4 ectodomains lack proper stabilization and can wobble around one another, causing disruption of a proper conformation that would enable cytoplasmic TIR domain dimerization and consecutive triggering of the TLR4 receptor signaling pathway. Figures were prepared with the UCSF Chimera package [31].