Neither here nor there: localizing conflicting visual attributes

NoNatural visual scenes are a rich source of information. Objects often carry luminance, colour, motion, depth and textural cues, each of which can serve to aid detection and localization of the object within a scene. Contemporary neuroscience presumes a modular approach to visual analysis in which each of these attributes are processed within ostensibly independent visual streams and are transmitted to geographically distinct and functionally dedicated centres in visual cortex (van Essen & Maunsell, 1983; Zihl, von Cramon & Mai, 1983; Maunsell & Newsome, 1987; Tootell, Hadjikhani, Mendola, Marrett & Dale, 1998). In the present study we ask how the visual system localizes objects within this framework. Specifically, we investigate how the visual system assigns a unitary location to objects defined by multiple stimulus attributes, where such attributes provide conflicting positional cues. The results show that conflicting sources of visual information can be effortlessly combined to form a global estimate of spatial position, yet, this conflation of visual attributes is achieved at a cost to localization accuracy. Furthermore, our results suggest that the visual system assigns more perceptual weight (Landy, 1993; Landy & Kojima, 2001) to visual attributes which are reliably related to object contours

Export from Pericentriolar Endocytic Recycling Compartment to Cell Surface Depends on Stable, Detyrosinated (Glu) Microtubules and Kinesin

A significant fraction of internalized transferrin (Tf) concentrates in the endocytic recycling compartment (ERC), which is near the microtubule-organizing center in many cell types. Tf then recycles back to the cell surface. The mechanisms controlling the localization, morphology, and function of the ERC are not fully understood. We examined the relationship of Tf trafficking with microtubules (MTs), specifically the subset of stable, detyrosinated Glu MTs. We found some correlation between the level of stable Glu MTs and the distribution of the ERC; in cells with low levels of Glu MTs concentrated near to the centriole, the ERC was often tightly clustered, whereas in cells with higher levels of Glu MTs throughout the cell, the ERC was more dispersed. The clustered ERC in Chinese hamster ovary cells became dispersed when the level of Glu MTs was increased with taxol treatment. Furthermore, in a temperature-sensitive Chinese hamster ovary cell line (B104-5), the cells had more Glu MTs when the ERC became dispersed at elevated temperature. Microinjecting purified anti-Glu tubulin antibody into B104-5 cells at elevated temperature induced the redistribution of the ERC to a tight cluster. Microinjection of anti-Glu tubulin antibody slowed recycling of Tf to the cell surface without affecting Tf internalization or delivery to the ERC. Similar inhibition of Tf recycling was caused by microinjecting anti-kinesin antibody. These results suggest that stable Glu MTs and kinesin play a role in the organization of the ERC and in facilitating movement of vesicles from the ERC to the cell surface