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Mizuno, D.

Publications and source records attributed to Mizuno, D..

2 recordsLinked to original sources

Self-Supervised Discovery of Discrete Local States in Noisy Image Sequences

Scientific image sequences often feature recurring structures with unknown appearance and dynamics. While traditional methods using predefined templates, noise models, or motion classes work well when targets are known, such assumptions can hinder exploratory analysis where discovering that knowledge is the primary goal. This work presents a self-supervised framework that maps noisy video into a discrete vocabulary of local states and their spatiotemporal relationships. The method operates without clean targets, pretrained representations, semantic labels, feature templates, or prescribed trajectories, assuming only that informative structures recur for a finite duration within a bounded spatial neighborhood. A temporally masked vector-quantized network predicts the missing central frame from its neighbors, while a masked Transformer refines token assignments by weighing encoder evidence against contextual compatibility. Project-specific token sets define the feature family, while a support model quantifies the temporal evidence for individual occurrences, facilitating optional conservative suppression. The framework is first demonstrated on synthetic videos of moving particles. Without access to clean frames or particle coordinates during learning and selection, the learned states recover compact, point-spread-function-like structures. Tests on low-signal particle-tracking benchmarks yield frame-wise component precision between 87.0% and 94.5%, with recall decreasing as particle density rises. An experimental example using E. coli further shows that discrete states can separate biological structures from illumination and acquisition artifacts. In all cases, the primary outputs are interpretable state, activity, support, and component maps; rendered images serve as diagnostics rather than optimization targets.

biophysics↗

Activity-dependent glassy cell mechanics : Mechanical properties measured with active microrheology

Active microrheology was conducted in living cells by applying an optical-trapping force to vigorously-fluctuating tracer beads with feedback-tracking technology. The complex shear viscoelastic modulus G({omega}) = G'({omega}) - iG''({omega}) was measured in HeLa cells in an epithelial-like confluent monolayer. We found that G({omega}) {propto} (-i{omega})1/2 over a wide range of frequencies (1 Hz <{omega} /2{pi}<10 kHz). Actin disruption and cell-cycle progression from G1 to S and G2 phases only had a limited effect on G({omega}) in living cells. On the other hand, G ({omega}) was found to be dependent on cell metabolism; ATP-depleted cells showed an increased elastic modulus G'({omega}) at low frequencies, giving rise to a constant plateau such that G({omega}) = G0 + A(-i{omega})1/2. Both the plateau and the additional frequency dependency {propto} (-i{omega})1/2 of ATP-depleted cells are consistent with a rheological response typical of colloidal jamming. On the other hand, the plateau G0 disappeared in ordinary metabolically active cells, implying that living cells fluidize their internal states such that they approach the critical jamming point. Statement of SignificanceIntracellular mechanical properties were measured using optical-trap-based microrheology. Despite expectations to the contrary, shear viscoelasticity was hardly affected by reorganization of cytoskeletal structures during cell-cycle progression (G1 to S and G2 phases), nor by artificial disruption of the actin cytoskeleton induced by chemical inhibitors. Rather, the mechanics of cell interiors is governed by the glassy cytoplasm. Cells depleted of ATP solidified, whereas living cells that maintained metabolic activities were more fluid-like. Instead of a completely fluid response, however, we observed a characteristic power-law viscoelasticity G({omega}) {propto} (-i{omega})1/2 over the whole range of frequencies measured. Based on our current understanding of jamming rheology, we discuss how cells fluidize their internal state in a way that pushes the system towards the critical jamming transition.

biophysics↗