BioPhenics

Publications

Année de publication : 2012

Alejandra Garcia-Cattaneo, François-Xavier Gobert, Mélanie Müller, Florent Toscano, Marcella Flores, Aurianne Lescure, Elaine Del Nery, Philippe Benaroch (2012 May 18)

Cleavage of Toll-like receptor 3 by cathepsins B and H is essential for signaling.

Proceedings of the National Academy of Sciences of the United States of America : 9053-8 : DOI : 10.1073/pnas.1115091109 En savoir plus
Résumé

Toll-like receptor (TLR) 3 is an endosomal TLR that mediates immune responses against viral infections upon activation by its ligand double-stranded RNA, a replication intermediate of most viruses. TLR3 is expressed widely in the body and activates both the innate and adaptive immune systems. However, little is known about how TLR3 intracellular trafficking and maturation are regulated. Here we show that newly synthesized endogenous TLR3 is transported through the ER and Golgi apparatus to endosomes, where it is rapidly cleaved. TLR3 protein expression is up-regulated by its own ligand, leading to the accumulation of its cleaved form. In agreement with its proposed role as a transporter, UNC93B1 expression is required for TLR3 cleavage and signaling. Furthermore, TLR3 signaling and cleavage are sensitive to cathepsin inhibition. Cleavage occurs between aa 252 and 346, and results in a functional receptor that signals upon activation. A truncated form of TLR3 lacking the N-terminal 345 aa also signals from acidic compartments in response to ligand activation. Screening of the human cathepsin family by RNA interference identified cathepsins B and H as key mediators of TLR3 processing. Taken together, our data indicate that TLR3 proteolytic processing is essential for its function, and suggest a mechanism of tight control of TLR3 signaling and thus immunity.

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Année de publication : 2008

Ilaria Cascone, Rasim Selimoglu, Cafer Ozdemir, Elaine Del Nery, Charles Yeaman, Michael White, Jacques Camonis (2008 Feb 3)

Distinct roles of RalA and RalB in the progression of cytokinesis are supported by distinct RalGEFs.

The EMBO journal : 2375-87 : DOI : 10.1038/emboj.2008.166 En savoir plus
Résumé

The Ras family G-proteins RalA and RalB make critical non-overlapping contributions to the generation of a tumorigenic regulatory network, supporting bypass of the normal restraints on both cell proliferation and survival. The Sec6/8 complex, or exocyst, has emerged as a principal direct effector complex for Ral GTPases. Here, we show that RalA and RalB support mitotic progression through mobilization of the exocyst for two spatially and kinetically distinct steps of cytokinesis. RalA is required to tether the exocyst to the cytokinetic furrow in early cytokinesis. RalB is then required for recruitment of the exocyst to the midbody of this bridge to drive abscission and completion of cytokinesis. The collaborative action of RalA and RalB is specified by discrete subcellular compartmentalization and unique pairs of RalGEF proteins that provide inputs from both Ras-family protein-dependent and protein-independent regulatory cues. This suggests that Ral GTPases integrate diverse upstream signals to choreograph multiple roles for the exocyst in mitotic progression.

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