In the intricate world of cellular migration, a groundbreaking discovery has unveiled that cells do not merely respond instinctively to their environments but instead harbor a sophisticated form of mechanical memory. This revolutionary insight, emerging from collaborative research led by Professor David Brückner at the University of Basel and Professor Sylvain Gabriele from the University of Mons, throws new light on how cells manage to traverse complex physiological landscapes. Published in the prestigious journal Nature Physics, the study reveals that migrating cells possess the remarkable ability to “remember” the shapes they adapted when navigating through constricted spaces, fundamentally altering the speed and efficiency of their subsequent movement.
Cells within the human body are often envisioned as static entities; however, select populations such as immune cells, embryonic cells, and cancer cells demonstrate extraordinary mobility. These motile cells face the daunting challenge of squeezing through sometimes minuscule gaps in tissues—spaces frequently narrower than the cells themselves. This confinement necessitates intricate morphological transformations, involving significant energy expenditure to alter cytoskeletal architecture and cell shape. Until now, the mechanisms by which cells adapt dynamically and streamline their movement through these narrow passages remained poorly understood.
Employing microfabricated dumbbell-shaped patterns on chips, the research team carefully mimicked these physiological constraints by creating two square-shaped wells connected by a narrow “bridge” space. This configuration simulated the tight interstitial spaces cells encounter in actual tissue matrices. The team observed how individual cells deployed microscopic arm-like protrusions, or lamellipodia, to explore and propel through these confined channels. Notably, cancer cells stood out for their relentless oscillatory movement across the microbridge, highlighting their inherent migratory capacity.
Detailed observation revealed that cells adopt two distinct morphologies during confined migration: an elongated form characterized by bilateral protrusions exploring their surroundings, and a compacted form, where a singular, dominant protrusion guides the cellular body forward. Initially, cells stretch as they probe the environment, with opposing protrusions pulling in different directions. However, increased duration within the narrow domain triggers a transition to the compact morphology, optimizing energy use by focusing propulsion in a single direction. This switch signifies a critical behavioral shift that enhances the cell’s migratory efficacy through constrained spaces.
What captured the researchers’ attention was the persistence of this compact morphology even after cells exited the confined zones. Retaining the compact shape in open space suggests that cells “anticipate” and prepare for future constrictions, effectively priming themselves for upcoming migratory challenges. This adaptive strategy underscores an element of cellular foresight, whereby the history of mechanical stresses experienced by the cell influences its future shape and movement dynamics. However, not all cells maintained this compact form indefinitely; some reverted to the more exploratory elongated shape, indicative of a flexible response rather than a fixed behavior, which could help navigate complex and branching tissue landscapes.
At the heart of this morphological memory lies the remodeling of the actin cortex, a dense meshwork of actin filaments situated just beneath the plasma membrane. This cytoskeletal layer governs both the mechanical resilience and shape integrity of the cell. Under sustained confinement, the actin cortex thickens and reinforces, embedding a mechanical signature of the cell’s previous deformations. This structural metamorphosis provides the physical basis for the memory effect, enabling the cell to maintain a compact shape beyond the immediate constriction. Yet, the process of remodeling is temporally regulated, requiring prolonged confinement to induce sufficient changes, providing a delay mechanism that encodes the duration and extent of mechanical stress encountered.
The innovative mathematical model devised by Professor Brückner further elucidates these phenomena by quantitatively describing the biophysical variables governing cellular migration and memory. By integrating cytoskeletal dynamics with mechanical feedback, the model recapitulates the observed morphological transitions and explains how energy partitioning between exploratory protrusions and directionally focused motion is balanced. This synthesis of theory and experiment advances our grasp of cell motility and mechanical adaptation, offering predictive insights into migratory behavior across diverse contexts.
Understanding this mechanical memory has profound implications for biology and medicine. In physiological scenarios such as wound healing and immune surveillance, efficient navigation through variable tissue architectures is paramount. Migrating cells that retain their compact shape after passing through narrow spaces may accelerate tissue repair and immune responses by avoiding the energetic costs of constant reshaping. Conversely, in pathological contexts, such as cancer metastasis, this mechanical memory could inadvertently facilitate the rapid dissemination of tumor cells, enhancing their invasiveness and complicating treatment strategies.
Cells’ ability to adapt dynamically to physical constraints also prompts a reevaluation of the extracellular matrix’s role. Instead of serving merely as a passive scaffold, the tissue environment interacts continuously with cellular biomechanics, imposing spatial cues that elicit lasting cytoskeletal rearrangements. The interplay between these mechanical stimuli and cellular memory mechanisms suggests a feedback loop that could influence tissue morphogenesis and disease progression at the multicellular level.
Intriguingly, this discovery opens new avenues for therapeutic intervention aimed at modulating cytoskeletal remodeling and mechanical memory. Targeting actin cortex dynamics could impair the invasive capabilities of metastatic cells or enhance the responsiveness of immune cells within dense tissue matrices. Such strategies would require a nuanced understanding of the molecular pathways governing cortical actin turnover and its integration with cellular energy metabolism, underscoring the interdisciplinary nature of future research.
Moreover, this study revitalizes the concept of cell shape not merely as a consequence but as an active player in cellular function. Mechanical memory embedded in morphology blurs the lines between structural biology and information storage, extending the paradigm of cellular memory beyond genetic and biochemical signals. The emergent properties of cytoskeletal materials reveal an intriguing form of biomechanical information encoding, which might be harnessed in synthetic biology and tissue engineering efforts to design cells with predefined migratory or functional patterns.
Looking forward, further investigation is needed to dissect how mechanical memory interfaces with other sensory and signaling pathways within migrating cells. For instance, elucidating how biochemical signals modulate cytoskeletal remodeling or how extracellular stiffness gradients influence memory persistence will provide a more comprehensive picture. Additionally, exploring variations across cell types and physiological conditions will illuminate the universality and adaptability of this mechanism within multicellular organisms.
Ultimately, the revelation that cells harbor a mechanical memory encoded by their actin cortex not only challenges our understanding of cellular migration but also inspires a conceptual shift in how life adapts to the physical constraints of the environment. This pioneering work exemplifies the power of combining sophisticated experimental setups with theoretical physics to unravel the subtle principles guiding living systems. As research builds upon these findings, we edge closer to decoding the fundamental language through which cells navigate the labyrinthine architecture of life.
Subject of Research: Cell migration mechanics; mechanical memory in confined migrating cells
Article Title: The actin cortex acts as a mechanical memory of morphology in confined migrating cells.
News Publication Date: 25-Aug-2025
Web References: 10.1038/s41567-025-02980-z
References: Article published in Nature Physics
Keywords: Cell migration, mechanical memory, actin cortex, cytoskeleton remodeling, confined migration, cancer metastasis, wound healing, immune cell migration, cell morphology, biophysical modeling
Tags: cancer cell mobilitycellular adaptation mechanismscellular migration strategiescytoskeletal architecture changesembryonic cell migrationenergy expenditure in cell movementmechanical memory in cellsmotility of immune cellsNature Physics publicationnavigating tight spaces in tissuesProfessor David Brückner research findingsresearch on cell behavior
