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Laumonnerie, C.

Publications and source records attributed to Laumonnerie, C..

2 recordsLinked to original sources

An Interpretable 3D Bag-Of-Visual-Words Pipeline for Volumetric Microscopy Classification

Fluorescence microscopy increasingly produces complex volumetric datasets whose biologically meaningful differences are difficult to capture with hand-crafted measurements, especially when signal is distributed across three-dimensional space. Here, we present an interpretable 3D Bag-of-Visual-Words (BoVW) pipeline for classification and analysis of volumetric microscopy data. The framework detects multiscale local keypoints, computes rotationally robust 3D gradient-based descriptors, and aggregates them into image-level visual-word representations. These features are then used for low-dimensional visualization and logistic regression classification, while model weights are mapped back to the original volumes to generate attention maps that localize discriminative structures. We applied the pipeline to two cerebellar granule neuron datasets spanning both ideal and non-ideal imaging conditions. In a near-isotropic lattice light-sheet dataset of chromatin organization, the method separated control and NIPBL loss-of-function nuclei and supported accurate classification, with strongest performance in the facultative heterochromatin and H3.3 channels. Attention mapping and downstream connected-component and Haralick analyses revealed that loss-of-function nuclei contained more fragmented high-attention regions and smoother, more homogeneous chromatin-associated textures than controls. We then evaluated the same framework on an anisotropic confocal timelapse dataset of receptor clustering in dense neuronal cultures, where single-cell segmentation was impractical. Despite these challenges, the representation captured the expected ligand-driven clustering response and resolved subtler differences associated with a polarity protein overexpression. Together, these results establish a simple, interpretable, and broadly applicable framework for extracting biologically meaningful structure from volumetric microscopy datasets while preserving native 3D context.

cell biology↗

Antagonistic action of Siah2 and Pard3/JamC to promote germinal zone exit of differentiated cerebellar granule neurons by modulating Ntn1 signaling via Dcc

Germinal zone (GZ) exit is at the top of a cascade of events promoting the maturation of neurons and their assembly into neuronal circuits. Developing neurons and their progenitors must interpret varied niche signals like morphogens, guidance molecules, extracellular matrix, or adhesive cues to navigate GZ occupancy. How newborn neurons integrate multiple cell-extrinsic niche cues with their cell-intrinsic machinery in exiting a GZ is unknown. We establish cooperation between cell polarity-regulated adhesion and Netrin-1 signaling comprises a coincidence detection circuit repelling maturing neurons from their GZ. In this circuit, the Partitioning defective 3 (Pard3) polarity protein and Junctional adhesion molecule-C (JAM-C) adhesion protein promote, while the Seven in absentia 2 (Siah2) ubiquitin ligase inhibits, Deleted in colorectal cancer (DCC) receptor surface recruitment to gate differentiation linked repulsion to GZ Netrin-1. These results demonstrate cell polarity as a central integrator of adhesive- and guidance cues cooperating to spur GZ exit. Highlights-Netrin1 expressed in the cerebellar GZ ranges from an attractive to repulsive cue depending on differentiation status or extracellular matrix context. -Modulation of DCC expression levels impacts the nature of the Netrin1 response and GZ occupancy status. -Siah2, Pard3, and JamC function to modulate responsiveness to purified Netrin1 and cooperate with Dcc to regulate GZ exit. -Pard3 and JamC promote both basal and Netrin1 stimulated DCC surface recruitment to control GZ exit and Netrin1 repulsion

neuroscience↗