ArticlebioRxiv : the preprint server for biology2025
Learning Epithelial Elasticity via Local Tension Remodeling.
Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Biological materials, like epithelial tissues, exhibit remarkable adaptability to mechanical stresses, dynamically remodeling their structure in response to external and internal forces. A key challenge is understanding how these tissues store a memory of past mechanical stimuli. Here, we investigate this memory using an active Vertex Model of epithelial sheets incorporating a local, mechanosensitive tension-remodeling rule where junctional tension updates depend on strain, acting as a slow, history-dependent variable. We demonstrate three hallmark mechanical consequences of this memory mechanism. First, a localized, short contractile cue permanently reprograms the global shear modulus, with the direction of change (stiffening or softening) controlled by the tension remodeling rate. Second, the tissue stores a long-range mechanical memory: a prior stimulus at one site modulates the tissue's response to a subsequent, distant stimulus, mediated by coupling across the entire junctional network. Finally, we show that simple cyclic bulk deformation acts as a training protocol that autonomously tunes the tissue's constitutive properties, including programming the Poisson ratio to auxetic (negative) values. These findings position epithelial mechanics within the framework of unsupervised physical learning, identifying the mechanosensitive remodeling rates as powerful control parameters for designing programmable tissue-scale rheology.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.