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Jordan, P. M.

Publications and source records attributed to Jordan, P. M..

2 recordsLinked to original sources

Tessellation Of Artificial Touch Via Microstimulation Of Human Somatosensory Cortex

When we interact with objects, we rely on signals from the hand that convey information about the object and our interaction with it. A basic feature of these interactions, the locations of contacts between the hand and object, is often only available via the sense of touch. Information about locations of contact between a brain-controlled bionic hand and an object can be signaled via intracortical microstimulation (ICMS) of somatosensory cortex (S1), which evokes touch sensations that are localized to a specific patch of skin. To provide intuitive location information, tactile sensors on the robotic hand drive ICMS through electrodes that evoke sensations at skin locations matching sensor locations. This approach requires that ICMS-evoked sensations be focal, stable, and distributed over the hand. To systematically investigate the localization of ICMS-evoked sensations, we analyzed the projected fields (PFs) of ICMS-evoked sensations - their location and spatial extent - from reports obtained over multiple years from three participants implanted with microelectrode arrays in S1. First, we found that PFs vary widely in their size across electrodes, are highly stable within electrode, are distributed over large swaths of each participants hand, and increase in size as the amplitude or frequency of ICMS increases. Second, while PF locations match the locations of the receptive fields (RFs) of the neurons near the stimulating electrode, PFs tend to be subsumed by the corresponding RFs. Third, multi-channel stimulation gives rise to a PF that reflects the conjunction of the PFs of the component channels. By stimulating through electrodes with largely overlapping PFs, then, we can evoke a sensation that is experienced primarily at the intersection of the component PFs. To assess the functional consequence of this phenomenon, we implemented multi-channel ICMS-based feedback in a bionic hand and demonstrated that the resulting sensations are more localizable than are those evoked via single-channel ICMS.

neuroscience↗

Lipid droplets are required for lipid mediator production and cancer cell proliferation

Polyunsaturated fatty acids (PUFAs) are components of membrane phospholipids and precursors of bioactive lipid mediators. Here, we investigated the crosstalk of three pathways providing PUFAs for lipid mediator production: (i) secreted group X phospholipase A2 (GX sPLA2) and (ii) cytosolic group IVA PLA2 (cPLA2), which both mobilize PUFAs from phospholipids, and (iii) adipose triglyceride lipase (ATGL), which breaks down triacylglycerols (TAGs) stored in lipid droplets (LDs). Combining lipidomic and functional analyses, we demonstrate that lipid mediator production depends on TAG turnover. GX sPLA2 directs PUFAs into TAGs and ATGL is required for their entry into lipid mediator biosynthetic pathways. ATGL also promotes the incorporation of LD-derived PUFAs into phospholipids representing substrates for cPLA2. Additionally, inhibition of TAG synthesis mediated by acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) reduces the levels of mitogenic lipid signals and compromises tumour growth. This study expands the paradigm of PLA2-driven lipid mediator signalling and identifies LDs as central lipid mediator production hubs.

cell biology↗