Importance of extra- and intracellular domains of TLR1 and TLR2 in NFκB signaling

Citations of this article
Mendeley users who have this article in their library.


Recognition of ligands by toll-like receptor (TLR) 2 requires interactions with other TLRs. TLRs form a combinatorial repertoire to discriminate between the diverse microbial ligands. Diversity results from extracellular and intracellular interactions of different TLRs. This paper demonstrates that TLR1 and TLR2 are required for ara-lipoarabinomannan- and tripalmitoyl cysteinyl lipopeptide-stimulated cytokine secretion from mononuclear cells. Confocal microscopy revealed that TLR1 and TLR2 cotranslationally form heterodimeric complexes on the cell surface and in the cytosol. Simultaneous cross-linking of both receptors resulted in ligand-independent signal transduction. Using chimeric TLRs, we found that expression of the extracellular domains along with simultaneous expression of the intracellular domains of both TLRs was necessary to achieve functional signaling. The domains from each receptor did not need to be contained within a single contiguous protein. Chimeric TLR analysis further defined the toll/IL-lR domains as the area of crucial intracellular TLR1-TLR2 interaction.




Sandor, F., Latz, E., Re, F., Mandell, L., Repik, G., Golenbock, D. T., … Finberg, R. W. (2003). Importance of extra- and intracellular domains of TLR1 and TLR2 in NFκB signaling. Journal of Cell Biology, 162(6), 1099–1110.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free