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Cossentino, I.

Publications and source records attributed to Cossentino, I..

2 recordsLinked to original sources

Cell signaling pathways discovery from multi-modal data

Deciphering cell signaling pathways is key to understanding biology, disease mechanisms, and developing new therapies. Although advances in multi-omics technologies provide richer insight into signaling, the data remain high-dimensional, heterogeneous, and difficult to interpret, and current computational tools for inferring signaling pathways are limited. To address this, we developed Incytr, a method for efficient discovery of cell signaling pathways through integration of diverse data modalities, including transcriptomics, ATAC-seq, proteomics, phosphoproteomics, and kinomics. We demonstrate its application in COVID-19, Alzheimers disease, and cancer, where it successfully recovers known pathways and generates novel, cell-type-specific hypotheses supported by multiple data types. We further show how integrating Incytr-derived pathways with biomarker and drug databases can support target and drug discovery. Finally, we show that using Incytr-derived signaling pathways as training data for simple natural language processing models can deepen our understanding of cell-cell communication and immune cell dynamics, while helping identify new therapeutic targets.

bioinformatics↗

A heteromeric nicotinic acetylcholine receptor promotes sleep by relaying GABAergic signals within a locus of motor and sensory integration

Locomotor inactivity and reduced sensory responsiveness are defining attributes of sleep, yet the underlying mechanisms are not well understood. In particular, the molecular and circuit mechanisms by which sleep-regulatory signals from the brain restrict movement and sensation remain largely ill-defined. Here we identify a nicotinic acetylcholine receptor (nAChR) that promotes sleep in Drosophila through its expression in GABAergic neurons of the ventral nerve cord (VNC), a center for motor and sensory systems. Biochemical, genetic, and pharmacological manipulations indicate that a heteromeric nAChR containing the 1 and {beta}1 subunits promotes sleep by coupling cholinergic input to GABA release in the VNC and the likely inhibition of motor neurons, sensory afferents, or both. The functional parallels of the VNC and the mammalian spinal cord suggest that disruptions of analogous inhibitory circuits in humans may impair suppression of behavioral activity and sensory inputs during sleep and contribute to sleep disorders.

neuroscience↗