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Biology subjects

Alghamdi, A. A.

Publications and source records attributed to Alghamdi, A. A..

2 recordsLinked to original sources

Differential impact of ageing on reward driven changes in motor control

Abstract Background: Reward can influence both the selection and execution of goal-directed actions. Healthy ageing is associated with changes in reward processing, raising the possibility that reward effects on motor control may be reduced in older adults. Objective: This study examined how monetary reward affects action execution and action selection during reaching movements and whether these effects differ between younger and older adults. Methods: 28 younger adults and 28 older adults performed a reward-based reaching task. Behaviourally non-distracted trials were used to assess action execution, whereas distractor-containing trials were used to assess action selection. Outcomes included maximum velocity, movement time, endpoint error, reaction time, and selection accuracy. Results: Reward increased maximum velocity and reduced movement time in both age groups without increasing error. These reward-related changes in movement vigour were larger in younger adults. During action selection, reward shortened reaction time but reduced selection accuracy in both groups, indicating faster but less accurate responses. The reward-related changes in reaction time and selection accuracy did not differ significantly between age groups. Conclusion: Ageing did not produce a uniform reduction in reward responsiveness. Instead, ageing attenuated reward-driven movement invigoration, while reward-related changes in action-selection behaviour were similar across age groups. These findings may inform the design of reward-based interventions that promote movement vigour without encouraging speed at the expense of accurate action selection.

neuroscience↗

NRP2 as an emerging angiogenic player; promoting endothelial cell adhesion and migration by regulating recycling of α5 integrin.

Angiogenesis relies on the ability of endothelial cells (ECs) to migrate over the extracellular matrix via integrin receptors to respond to an angiogenic stimulus. Of the two neuropilin (NRP) orthologs to be identified, both have been reported to be expressed on normal blood and lymphatic ECs, and to play roles in the formation of blood and lymphatic vascular networks during angiogenesis. Whilst the role of NRP1 and its interactions with integrins during angiogenesis has been widely studied, the role of NRP2 in ECs is poorly understood. Here we demonstrate that NRP2 promotes Rac-1 mediated EC adhesion and migration over fibronectin (FN) matrices in a mechanistically distinct fashion to NRP1, showing no dependence on {beta}3 integrin (ITGB3) expression, or VEGF stimulation. Furthermore, we highlight evidence of a regulatory crosstalk between NRP2 and 5 integrin (ITGA5) in ECs, with NRP2 depletion eliciting an upregulation of ITGA5 expression and disruptions in ITGA5 cellular organisation. Finally, we propose a mechanism whereby NRP2 promotes ITGA5 recycling in ECs; NRP2 depleted ECs were found to exhibit reduced levels of total ITGA5 subunit recycling compared to wild-type (WT) ECs. Our findings expose NRP2 as a novel angiogenic player by promoting ITGA5-mediated EC adhesion and migration on FN.

cell biology↗