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Chrzanowski, W.

Publications and source records attributed to Chrzanowski, W..

2 recordsLinked to original sources

Modeling 3D Mesoscaled Neuronal Complexity through Learning-based Dynamic Morphometric Convolution

Accurate reconstruction of neuronal morphology from three-dimensional (3D) light microscopy is fundamental to neuroscience. Nevertheless, neuronal arbors intrinsically exhibit slender, tortuous geometries with high orientation variability, posing significant challenges for standard 3D convolutions whose static, axis-aligned receptive fields lack adaptability to such complex morphology. To address this, we propose the Dynamic Morph-Aware Convolution (DMAC) framework, which incorporates inherent geometric priors into convolution by jointly adapting both the shape and orientation of the kernel. This enables morphology-aware feature extraction tailored to arborized and variably oriented neuronal trajectories. Specifically, we first apply dynamic tubular convolutions to bridge the structural mismatch between isotropic convolution kernels and the slender morphology of neurons. To sufficiently accommodate the 3D orientation variability of neuronal branches, we further introduce a rotation mechanism that dynamically reorients the tubular kernel via two learnable angles (elevation and azimuth), enabling precise alignment with local neuronal directions. We validate our method through extensive experiments on four mesoscaled neuronal imaging datasets, including two from the BigNeuron project (Drosophila and Mouse) and two additional benchmarks (NeuroFly and CWMBS). Our approach consistently outperforms state-of-the-art methods, achieving average improvements of 5.4% in Entire Structure Average (ESA), 6.9% in Different Structure Average (DSA), and 7.5% in Percentage of Different Structure (PDS). These results demonstrate the effectiveness of our proposed DMAC in capturing complex morphological variations and enhancing structural fidelity across diverse mesoscaled neuronal morphologies.

neuroscience↗

Nanocharacterisation of extracellular vesicles uncovers the correlation between isolation methods, physicochemical composition and their biological function

Extracellular vesicles (EVs) have been lauded as next generation medicines, but very few EV-based therapeutics have progressed to clinical use. Limited clinical translation is largely due to technical barriers that hamper our ability to mass-produce EVs, i.e. to isolate, purify and characterise them effectively. Technical limitations in comprehensive characterisation of EVs leads to unpredicted biological effects of EVs. Here, using a range of optical and non-optical techniques, we showed that the differences in molecular composition of EVs isolated using two isolation methods correlated with the differences in their biological function. Our results demonstrated that the isolation method determines the composition of isolated EVs at single and sub-population levels. Besides the composition, we measured for the first time the dry mass and predicted sedimentation of EVs. These parameters were shown to correlate well with the biological and functional effects of EVs on single cell and cell cultures. We anticipate that our new multiscale characterisation approach, which goes beyond traditional experimental methodology, will support fundamental understanding of EVs as well as elucidate the functional effects of EVs in in vitro and in vivo studies. Our findings and methodology will be pivotal for developing optimal isolation methods and establishing EVs as mainstream therapeutics and diagnostics. This innovative approach is applicable to a wide range of sectors including biopharma and biotechnology as well as to regulatory agencies.

cell biology↗