02 · Force balance over time
Pulling and pushing alternate through the sequence
Inward contractility is plotted above zero; outward contractility is plotted below. T003 is push-dominant, while T023 carries the strongest inward pull.
Cell–matrix force reconstruction
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Introduction
3D traction reconstruction · 30 timepoints
The cell alternates between front and rear anchoring while exerting intermittent outward pressure near its center. A stabilized inverse model resolves these forces without discarding the large collagen deformations.
↓ Advance one view at a time
01 · T003
The opening view places the cell within the deformation-colored collagen network. The following views isolate the projected force pattern around the same cell.
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02 · Force balance over time
Inward contractility is plotted above zero; outward contractility is plotted below. T003 is push-dominant, while T023 carries the strongest inward pull.
03 · Physical scale
A linear elastic estimate gives the correct scale. Near the cell, a complete 2–3 nN traction field can generate approximately 0.4–0.7 µm of displacement.
For an unbounded linear material, u = F / 4πGr. Using the project’s linearized shear modulus, 2.4 nN produces 0.40 µm at 5 µm from the load and 0.66 µm at 3 µm.
Move across the curves to inspect force, distance, and predicted displacement.
04 · Forward simulation
A balanced SAENOpy force dipole uses the peak inward contractility, 3.22 nN. The simulated peak displacement is 1.08 µm, close to the 1.01 µm maximum measured at T023.
Displacement arrows are enlarged 5× for visibility; all reported values use the unscaled field.
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05 · Reconstruction method
Each regime solves a slightly different objective. The force field is warm-started from the previous solution, but the loss can reset when a penalty changes.
α = 10⁸ · bulk / shell = 1
Fit the measured displacement before preferring forces near the cell surface.
α = 10⁸ · bulk / shell: 10³ → 10⁶
Raise the cost of bulk forces in two warm-started solves.
bulk / shell = 10⁶ · α: 10⁸ → 10⁶
Lower α along the stable branch. Force and torque balance remain active throughout.
Loss falls within each regime. At both boundaries the objective changes, causing a small reset; the previous force field is reused as the next starting point.
minf ‖umodel(f) − umeasured‖² + αΣshell‖fᵢ‖² + rαΣbulk‖fᵢ‖² + wF‖Σfᵢ‖² + wτ‖Σrᵢ × fᵢ‖²
The curve explains the optimization logic; it is not presented as a measured convergence trace.
06 · Production settings
Beyond slide 04
The main presentation ends here. Continue to the reconstruction details, validation plots, additional 3D frames, and current interpretation.
S1 · Parameter stability
Whole-series contractility plateaus from α = 107 to 108.
S2 · Validation
Pulling is enriched at a cell end in 29 frames; central pushing appears in 18 frames.
S3 · T022
Later in the sequence, the leading end becomes the main anchor. Central outward traction remains detectable while the cell advances through the constriction.
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S4 · T023
The strongest force frame combines pulling at both ends with outward traction near the central internal signal. This is consistent with pressure used to widen a pore.
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S5 · Interpretation
Early frames are more often rear-dominant. From T013 onward, front pulling becomes more common before rear dominance returns near the end.
Central pushing is intermittent. The robust conclusion is an alternating end-anchor mechanism with occasional central outward pressure—not a fixed pattern at every timepoint.
T000–T012
intermittent
T013–T026
S6 · Method and limits
The force scale is reproducible across α and predicts held-out displacement blocks. Absolute nN values still depend on the assumed collagen material law and the displacement reference.
Broad-domain fit keeps bulk forces visible during reconstruction.
Penalty continuation transfers support into a 3 µm surface shell.
Force and torque balance removes non-physical branches.
Seven-α validation identifies the decade-wide contractility plateau.
Validated reconstruction · α = 107 · production full series