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Biomedical subjects

Daniel Choquet

Publications and source records attributed to Daniel Choquet.

21 records · Page 2Linked to original sources

Receptor activation and homer differentially control the lateral mobility of metabotropic glutamate receptor 5 in the neuronal membrane.

Glutamate receptors are clustered at the membrane through interactions with intracellular scaffolding proteins and cytoskeletal elements but can also be found in intracellular compartments or dispersed in the membrane. This distribution results from an equilibrium between the different pools of receptors whose dynamic is poorly known. The group I metabotropic glutamate receptor 5 (mGluR5) is concentrated in an annulus around the postsynaptic density but also found in large amounts in the extrasynaptic membrane. To analyze the dynamic of stabilization of mGluR5, we used single-particle tracking, force measurements, and fluorescence recovery to measure the mobility of mGluR5. We found that receptor activation increases receptor diffusion, whereas the scaffolding protein Homer favors confinement of receptor movements within clusters of Homer-mGluR5. However, this stabilization is reversible, because even in the presence of Homer, receptors still enter and exit from clusters at fast rates. Furthermore, clusters themselves are highly dynamic both in their movements and in their composition, which can vary within tens of seconds. Thus, exchange of receptors between dispersed and clustered states is fast and regulated during physiological processes. These properties may explain certain fast changes in receptor composition observed at postsynaptic densities.

Animals↗

Effects of chemical modification, tropomyosin, and myosin subfragment 1 on the yield strength and critical concentration of F-actin.

The effects of coupling with tetramethylrhodamine-5-iodoacetamide and of the decoration with tropomyosin and with myosin subfragment 1 on the elastic properties of F-actin filament are investigated. At 22 degrees C, in 15 mM orthophosphate and 3 mM MgCl2, tetramethylrhodamine F-actin displays a yield strength of 3.69 +/- 0.213 pN and an elastic modulus by stretching of 0.91 MPa. Decoration with tropomyosin increases the yield strength of tetramethylrhodamine F-actin to 10.51 +/- 0.24 pN and the elastic modulus by stretching to 23-75 MPa. Mixtures of myosin subfragment 1 and tetramethylrhodamine F-actin at the 0.2:1, 0.4:1, 0.6:1, 0.8:1, and 1:1 molar ratios are also studied. Both yield strength and the elastic modulus by stretching are found to increase progressively with the ratio. At the 1:1 molar ratio, the yield strength is 15.81 +/- 0.26 pN and the elastic modulus by stretching is 13.45 to 40 MPa. Decoration of tetramethylrhodamine F-actin with both tropomyosin and myosin subfragment 1, at the 1:1 molar ratio with the actin monomer, produces filaments with an yield strength of 22.3 +/- 0.48 pN.

Actins↗

Dynamics of ligand-induced, Rac1-dependent anchoring of cadherins to the actin cytoskeleton.

Cadherin receptors are key morphoregulatory molecules during development. To dissect their mode of action, we developed an approach based on the use of myogenic C2 cells and beads coated with an Ncad-Fc ligand, allowing us to mimic cadherin-mediated adhesion. We used optical tweezers and video microscopy to investigate the dynamics of N-cadherin anchoring within the very first seconds of bead-cell contact. The analysis of the bead movement by single-particle tracking indicated that N-cadherin molecules were freely diffusive in the first few seconds after bead binding. The beads rapidly became diffusion-restricted and underwent an oriented rearward movement as a result of N-cadherin anchoring to the actin cytoskeleton. The kinetics of anchoring were dependent on ligand density, suggesting that it was an inducible process triggered by active cadherin recruitment. This anchoring was inhibited by the dominant negative form of Rac1, but not that of Cdc42. The Rac1 mutant had no effect on cell contact formation or cadherin-catenin complex recruitment, but did inhibit actin recruitment. Our results suggest that cadherin anchoring to the actin cytoskeleton is an adhesion-triggered, Rac1-regulated process enabling the transduction of mechanical forces across the cell membrane; they uncover novel aspects of the action of cadherins in cell sorting, cell migration, and growth cone navigation.

Actins↗