Dissociations between performance and visual fixations after subordinate- and basic-level training with novel objects.

Previous work suggests that subordinate-level object training improves exemplar-level perceptual discrimination over basic-level training. However, the extent to which visual fixation strategies and the use of visual features, such as color and spatial frequency (SF), change with improved discrimination was not previously known. In the current study, adults (n = 24) completed 6 days of training with 2 families of computer-generated novel objects. Participants were trained to identify one object family at the subordinate level and the other object family at the basic level. Before and after training, discrimination accuracy and visual fixations were measured for trained and untrained exemplars. To examine the impact of training on visual feature use, image color and SF were manipulated and tested before and after training. Discrimination accuracy increased for the object family trained at the subordinate-level, but not for the family trained at the basic level. This increase was seen for all image manipulations (color, SF) and generalized to untrained exemplars within the trained family. Both subordinate- and basic-level training increased average fixation duration and saccadic amplitude and decreased the number of total fixations. Collectively, these results suggest a dissociation between discrimination accuracy, indicative of recognition, and the associated pattern of changes present for visual fixations.

Neural and behavioral effects of subordinate-level training of novel objects across manipulations of color and spatial frequency.

Perceptual expertise is marked by subordinate-level recognition of objects in the expert domain. In this study, participants learned one family of full-color, artificial objects at the subordinate (species) level and another family at the basic (family) level. Discrimination of trained and untrained exemplars was tested before and after training across several image manipulations [full-color, grayscale, low spatial frequency (LSF) and high spatial frequency (HSF)] while event-related potentials (ERPs) were recorded. Regardless of image manipulation, discrimination (indexed by d') of trained and of untrained exemplars was enhanced after subordinate-level training, but not after basic-level training. Enhanced discrimination after subordinate-level training generalized to untrained exemplars and to grayscale images and images in which LSF or HSF information was removed. After training, the N170 and N250, recorded over occipital and occipitotemporal brain regions, were both more enhanced after subordinate-level training than after basic-level training. However, the topographic distribution of enhanced responses differed across components. The N170 latency predicted reaction time after both basic-level training and subordinate-level training, highlighting an association between behavioral and neural responses. These findings further elucidate the role of the N170 and N250 as ERP indices of subordinate-level expert object processing and demonstrate how low-level manipulations of color and spatial frequency impact behavior and the N170 and N250 components independent of training or expertise.

A putative role for cell cycle-related proteins in microtubule-based neuroplasticity.

Cyclins and cyclin-dependent kinases (Cdks) are the main components that control the orderly progression through cell cycle. In the mature nervous system, terminally differentiated neurons are permanently withdrawn from cell cycle, as mitotic quiescence is essential for the functional stability of the complexly wired neuronal system. Recently, we characterized the expression and colocalization of cyclins and Cdks in terminally differentiated pyramidal neurons. The functional impact of the expression of cell cycle-related proteins in differentiated neurons, however, has not been elucidated yet. In the present study, we show by immunoelectron microscopy and immunobiochemical methods an association of cyclins and Cdks with the microtubule network. Cyclins D, E, A and B as well as Cdks 1, 2 and 4 were also found to be associated with the microtubule-associated protein tau. Cyclin/Cdk complexes, in addition, exhibit kinase activity towards tau. In vitro, downregulation of cyclins and Cdks by a siRNA approach and by pharmacological inhibition promotes neurite extension. Taken together, these results indicate that the expression of cell cycle-related proteins in terminal differentiated neurons is associated with physiological functions beyond cell cycle control that might be involved in microtubule-based mechanisms of neuroplasticity.