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Biology subjects

Bosse, F.

Publications and source records attributed to Bosse, F..

2 recordsLinked to original sources

Low-Dimensional Representations of Visuomotor Coordination for Natural Behavior

Understanding how the eyes, head, and hands coordinate in natural contexts is a critical challenge in visuomotor coordination research, often constrained by sedentary tasks, cued actions, or restricted settings. To address this gap, we conducted an experiment where participants could self-generate pick-and-place actions on a life-size shelf in a virtual environment, recording concurrent gaze and body movements. Subjects exhibited intricate translation and rotation movements of the eyes, head, and hands during the task. We employed a time-dependent principal component analysis to study the relationship between the movements of the eyes, head, and hands relative to the onset of the action. We reduced the overall dimensionality into 2D representations, capturing up to 65% of the movement variance just in time with the actions. Our analysis revealed a synergistic coupling of the eye-head and eye-hand systems, as well as a strong coupling within the head-hand system. The eyes synchronized with the head and hands close to the action onset, with variations in coupling observed in horizontal and vertical planes, indicating distinct mechanisms for coordination in the brain. Crucially, the head and hands remained tightly coupled throughout the observation period, suggesting a shared neural code driving these effectors. Notably, the low-dimensional representations of the eye-head-hand movement vectors showed maximum predictive accuracy of the actions location ~200ms before the action onset, highlighting just-in-time coordination among the three effectors. Furthermore, the predictive accuracy was significantly influenced by the location of the upcoming action. Our study emphasizes the differential visuomotor control subject to the task structure, providing insights into the dynamic interplay of eye, head, and hand movements during natural behavior. NEW & NOTEWORTHYStudying natural, self-initiated, complex visuomotor coordination, we observe low-dimensional dynamics with distinct patterns along horizontal and vertical axes. The eyes horizontal movement showed notable independence, aligning with head and hand movements just in time for action. Notably, around critical events, the dimensionality of the complex movements is further reduced, indicating dynamic correspondence of eye-head-hand coordination.

neuroscience↗

Unexpected Kif4a functions in adult regeneration encompass a dual role in neurons and in proliferative repair Schwann cells.

Contrary to the adult central nervous system (CNS), the peripheral nervous system (PNS) has an intrinsic ability to regenerate that, among others, passes by expressing regeneration-associated genes such as kinesin family members. We here show that Kinesin family motor protein 4a (KIF4A), associated to neurodevelopmental disorders and thought for long to be only embryonically expressed, is highly abundant in axons and Schwann cells of adult rat CNS and rat and human PNS. Moreover, Kif4a is up-regulated in injured PNS neurons, being detected in their nuclei and regrowing axons, consistent with its functions as a chromokinesin and in the axonal transport of e.g. {beta}1-integrin and L1CAM. Interestingly, Kif4a is also highly up-regulated in Schwann cells transdifferentiating into a proliferative repair phenotype at the injured distal nerve stumps. A role for Kif4a in cultured Schwann cells proliferation was confirmed, with Kif4a mRNA expression being [~]6-fold higher in proliferating versus growth-arrested Schwann cells, and Kif4a knockdown impairing Schwann cells proliferation. To our knowledge, this is the first description of KIF4A expression in adult nervous systems, up-regulation in neuroregeneration and pro-neuroregenerative roles, including promoting Schwann cells proliferation. KIF4A dual role in axonal regeneration, through neurons and glia, places as an attractive target for future neuroregeneration therapies.

neuroscience↗