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Garnero, M.

Publications and source records attributed to Garnero, M..

2 recordsLinked to original sources

Sharp and Fast Dynamic Extraction and Tracking of Emitted Cellular Transients

Genetically encoded fluorescent sensors have expanded our ability to image cellular activity and transmitter release. Yet, sparse and low-salience events remain difficult to resolve against complex and fluctuating fluorescence backgrounds. Here we introduce DETECT, Dynamic Extraction and Tracking of Emitted Cellular Transients, which combines adaptive background suppression, probabilistic classification and multi-object tracking to extract fluorescence events while preserving their identity. Across synthetic datasets, DETECT improved detection and segmentation accuracy and reduced computational cost relative to established event-based methods. We validated DETECT across confocal, two-photon and miniscope imaging, ex vivo and in vivo, using calcium indicators and monoamine sensors. Beyond its technical performance, DETECT extends event-based analysis to low-salience fluorescence signals while resolving events spanning broad ranges of amplitude, morphology and dynamics. By resolving spontaneous dopamine and noradrenaline signals as distinct, trackable release events, DETECT reveals the spatiotemporal organization of neuromodulatory activity and provides a broadly applicable approach to quantitative fluorescence analysis.

neuroscience↗

Astrocytes control oxytocin-based maternal behavior via connexin 30

Prosocial and affiliative behaviors rely on complex neuroendocrine neuronal circuits. Dynamic neuroglial interactions play prominent roles in shaping synaptic networks, whose alterations contribute to psychiatric disorders associated with social deficits. However, a role for astrocytes in regulating maternal behavior remains elusive. Here we show that female mice exhibiting increased oxytocin levels in the hypothalamic supraoptic nucleus upon social interactions with pups display neuroglial structural plasticity and downregulation of astroglial connexin 30, a protein involved in morphological remodeling. We found that impairing astroglial connexin 30 expression alters the structural properties of astrocytes by decreasing their volume and coverage of oxytocinergic synapses in the supraoptic nucleus of female mice. This functionally sets levels of plasma oxytocin and maternal behavior, exacerbating maternal care in virgin pup-naive female mice deficient for astroglial Cx30. Hypothalamic astrocytes, via connexin 30, are thus key determinants of oxytocin-based maternal behavior, whose alteration is known to impair social skills development in offspring.

neuroscience↗