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Figure 3 | Respiratory Research

Figure 3

From: Lung epithelium as a sentinel and effector system in pneumonia – molecular mechanisms of pathogen recognition and signal transduction

Figure 3

TLRs mediate activation of NF-κB- and IRF-related gene transcription. (A) Examples of recruited adaptor molecules critical for TLR4 function. With the possible exception of TLR3, all TLRs share a MyD88-dependent pathway for the activation of NF-κB. A protein complex composed of TIRAP, MyD88, IRAK4, IRAK1 and TRAF6 mediates NF-κB stimulation. In addition, TRAM, TRIF as well as TRAF6 and TBK1 stimulate IRF3 activation. (B) Located in the endosomal membrane, TLR3 recognizes dsRNA. Whereas TRIF recruitment connects TLR3 via TBK1 to IRF3 activation, further recruitment of RIP1 and TRAF6 stimulates NF-κB.

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