Author/Authors :
Nicolas Chevrier، نويسنده , , Philipp Mertins، نويسنده , , Maxim N. Artyomov، نويسنده , , Alex K. Shalek، نويسنده , , Matteo Iannacone، نويسنده , , Mark F. Ciaccio، نويسنده , , Irit Gat-Viks، نويسنده , , Elena Tonti، نويسنده , , Marciela M. DeGrace، نويسنده , , Karl R. Clauser، نويسنده , , Manuel Garber، نويسنده , , Thomas M. Eisenhaure، نويسنده , , Nir Yosef، نويسنده , , Jacob Robinson، نويسنده , , Amy Sutton، نويسنده , , Mette S. Andersen، نويسنده , , David E. Root، نويسنده , , Ulrich von Andrian، نويسنده , , Richard B. Jones، نويسنده , , Hongkun Park، نويسنده , , et al.، نويسنده ,
Abstract :
Deciphering the signaling networks that underlie normal and disease processes remains a major challenge. Here, we report the discovery of signaling components involved in the Toll-like receptor (TLR) response of immune dendritic cells (DCs), including a previously unkown pathway shared across mammalian antiviral responses. By combining transcriptional profiling, genetic and small-molecule perturbations, and phosphoproteomics, we uncover 35 signaling regulators, including 16 known regulators, involved in TLR signaling. In particular, we find that Polo-like kinases (Plk) 2 and 4 are essential components of antiviral pathways in vitro and in vivo and activate a signaling branch involving a dozen proteins, among which is Tnfaip2, a gene associated with autoimmune diseases but whose role was unknown. Our study illustrates the power of combining systematic measurements and perturbations to elucidate complex signaling circuits and discover potential therapeutic targets.
