TY - JOUR
T1 - Tension anisotropy drives fibroblast phenotypic transition by self-reinforcing cell–extracellular matrix mechanical feedback
AU - Alisafaei, Farid
AU - Shakiba, Delaram
AU - Hong, Yuan
AU - Ramahdita, Ghiska
AU - Huang, Yuxuan
AU - Iannucci, Leanne E.
AU - Davidson, Matthew D.
AU - Jafari, Mohammad
AU - Qian, Jin
AU - Qu, Chengqing
AU - Ju, David
AU - Flory, Dashiell R.
AU - Huang, Yin Yuan
AU - Gupta, Prashant
AU - Jiang, Shumeng
AU - Mujahid, Aliza
AU - Singamaneni, Srikanth
AU - Pryse, Kenneth M.
AU - Chao, Pen hsiu Grace
AU - Burdick, Jason A.
AU - Lake, Spencer P.
AU - Elson, Elliot L.
AU - Huebsch, Nathaniel
AU - Shenoy, Vivek B.
AU - Genin, Guy M.
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2025.
PY - 2025/6
Y1 - 2025/6
N2 - Mechanical factors such as stress in the extracellular environment affect the phenotypic commitment of cells. Stress fields experienced by cells in tissues are multiaxial, but how cells integrate such information is largely unknown. Here we report that the anisotropy of stress fields is a critical factor triggering a phenotypic transition in fibroblast cells, outweighing the role of stress amplitude, a factor previously described to modulate such a transition. Combining experimental and computational approaches, we identified a self-reinforcing mechanism in which cellular protrusions interact with collagen fibres to establish tension anisotropy. This anisotropy, in turn, stabilizes the protrusions and enhances their contractile forces. Disruption of this self-reinforcing process, either by reducing tension anisotropy or by inhibiting contractile protrusions, prevents the phenotypic conversion of fibroblasts to contractile myofibroblasts. Overall, our findings support stress anisotropy as a factor modulating cellular responses, expanding our understanding of the role of mechanical forces in biological processes.
AB - Mechanical factors such as stress in the extracellular environment affect the phenotypic commitment of cells. Stress fields experienced by cells in tissues are multiaxial, but how cells integrate such information is largely unknown. Here we report that the anisotropy of stress fields is a critical factor triggering a phenotypic transition in fibroblast cells, outweighing the role of stress amplitude, a factor previously described to modulate such a transition. Combining experimental and computational approaches, we identified a self-reinforcing mechanism in which cellular protrusions interact with collagen fibres to establish tension anisotropy. This anisotropy, in turn, stabilizes the protrusions and enhances their contractile forces. Disruption of this self-reinforcing process, either by reducing tension anisotropy or by inhibiting contractile protrusions, prevents the phenotypic conversion of fibroblasts to contractile myofibroblasts. Overall, our findings support stress anisotropy as a factor modulating cellular responses, expanding our understanding of the role of mechanical forces in biological processes.
UR - http://www.scopus.com/inward/record.url?scp=105000704174&partnerID=8YFLogxK
U2 - 10.1038/s41563-025-02162-5
DO - 10.1038/s41563-025-02162-5
M3 - Article
C2 - 40128624
AN - SCOPUS:105000704174
SN - 1476-1122
VL - 24
SP - 955
EP - 965
JO - Nature Materials
JF - Nature Materials
IS - 6
ER -