Spatially controlling cardiac fibroblast-to-myofibroblast transition using Young’s modulus patterned GelMA hydrogels
Source abstract
Abstract
The spatial organisation of mechanical cues is increasingly recognised as a key regulator of tissue development and disease, yet in vitro systems capable of replicating such environments remain limited. Fibroblast migration and the fibroblast-to-myofibroblast transition, which affect scar formation, are examples of mechanisms affected by mechanical cues. We report a photolithographic platform that enables precise, spatial patterning of the Young’s modulus of gelatin methacryol (GelMA) hydrogels, using a ruthenium/sodium persulfate (SPS) photoinitiation system. By altering light intensity, we achieved Young’s modulus tunability between 4 kPa and 46 kPa in non-patterned gels. By displaying a binary light intensity pattern over the gel, the Young’s modulus could be switched from 10 kPa to 45 kPa, representing healthy and fibrotic Young’s moduli, over a distance of ∼20 μm (2.3 MPa·mm⁻¹). This system could also generate relatively linear Young’s modulus gradients that are more physiologically relevant, ∼10 kPa⋅mm −1 . Non-patterned and binary-patterned gels confirmed that increasing the Young’s modulus drives the fibroblast-to-myofibroblast transition, observed by significantly greater cell volumes and α-smooth muscle actin (α-SMA) stress fibre formation, from encapsulated cardiac fibroblasts after 7 days. In gradient-patterned gels, fibroblasts exhibited a progressive, modulus-dependent increase in both cell volume and α-SMA stress fibre formation, alongside expressing a durotactic response, moving from healthy to fibrotic environments, and also aligning themselves between ±45 degrees to the Young’s modulus gradient. Beyond cardiac fibrosis, this versatile platform enables rapid generation of biologically relevant mechanical landscapes for diverse mechanobiological applications, bridging the gap between simplified, mechanically uniform models and the heterogeneous microenvironments of native tissues. This study developed a platform for spatially controlling the Young’s modulus of GelMA using a digital light projection system. Using this system, a change in Young’s modulus from 10 kPa to 45 kPa can be achieved with a resolution of 20 µm. Natural Young’s modulus gradients observed in tissues (∼10 kPa/mm) can also be achieved. The fibroblast-to-myofibroblast transition was controlled spatially in the patterned gels, evidenced by changes in cell volume and α-SMA fibrillation. Fibroblasts demonstrated alignment and migration to the Young’s modulus gradient. Our photopatterning system demonstrates ease of pattern/gradient definition with adaptability to a diverse range of systems, highlighting the impact of mechanical properties on cardiac scar formation and offering avenues for studying these effects.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Tissue Engineering and Regenerative Medicine · Cardiac Fibrosis and Remodeling · Cellular Mechanics and Interactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (67)
Show source-provided references
1. Matrix stiffness regulates profibrotic fibroblast differentiation and fibrotic niche activation in systemic sclerosis10.1016/j.ard.2025.05.016 ↗
2. Causes, diagnosis, treatment, and prognosis of cardiac fibrosis: a systematic review
3. Myofibroblasts in the infarct area: concepts and challenges10.1017/S143192761101227X ↗
4. Cardiac fibrosis – A short review of causes and therapeutic strategies10.1016/j.addr.2019.05.011 ↗
5. Properties and functions of fibroblasts and myofibroblasts in myocardial infarction10.3390/cells11091386 ↗
6. A guide for assessment of myocardial stiffness in health and disease10.1038/s44161-021-00007-3 ↗
7. Advancements in hydrogels: a comprehensive review of natural and synthetic innovations for biomedical applications10.3390/polym17152026 ↗
8. Gelatin methacrylate hydrogel for tissue engineering applications—a review on material modifications10.3390/ph15020171 ↗
9. Dynamic composite hydrogels of gelatin methacryloyl (GelMA) with supramolecular fibers for tissue engineering applications10.1016/j.bioadv.2024.213957 ↗
10. Small and ultra small angle neutron scattering on pure and supramolecular composite GelMA hydrogels10.1016/j.jcis.2025.138443 ↗
11. The future of visible light photoinitiators of polymerization for photocrosslinking applications10.1016/j.eurpolymj.2023.111883 ↗
12. Visible light cross-linking of gelatin hydrogels offers an enhanced cell microenvironment with improved light penetration depth10.1002/mabi.201900098 ↗
13. Fibroblast alignment and matrix remodeling induced by a stiffness gradient in a skin-derived extracellular matrix hydrogel10.1016/j.actbio.2024.05.018 ↗
14. Visible-light stiffness patterning of GelMA hydrogels towards In vitro scar tissue models10.3389/fcell.2022.946754 ↗
15. Steering cell orientation through light-based spatiotemporal modulation of the mechanical environment10.1088/1758-5090/ad3aa6 ↗
16. Fabrication of stiffness gradients of GelMA hydrogels using a 3D printed micromixer10.1002/mabi.202000107 ↗
17. Stereolithography apparatus and digital light processing-based 3D bioprinting for tissue fabrication
18. Droplet-based microfluidics for engineering shape-controlled hydrogels with stiffness gradient10.1088/1758-5090/ad6d8e ↗
19. Integrin-mediated mechanotransduction10.1083/jcb.201609037 ↗
20. Mechanical control of cardiac myofibroblasts10.1016/j.yjmcc.2015.11.025 ↗
21. Substrate stiffness modulates cardiac fibroblast activation, senescence and proinflammatory secretory phenotype10.1152/ajpheart.00483.2023 ↗
22. Substrate stiffness controls proinflammatory responses in human gingival fibroblasts10.1038/s41598-023-28541-z ↗
23. Bridging 2D and 3D culture: probing impact of extracellular environment on fibroblast activation in layered hydrogels10.1002/aic.16837 ↗
24. 3D culture of fibroblasts and neuronal cells on microfabricated free-floating carriers10.1016/j.colsurfb.2023.113350 ↗
25. Control of fibroblast shape in sequentially formed 3D hybrid hydrogels regulates cellular responses to microenvironmental cues10.1038/s41427-020-0226-7 ↗
26. 3D matrix stiffness modulation unveils cardiac fibroblast phenotypic switching
27. Study of cell migration trajectory on two-dimensional continuous stiffness gradient surface edited by grayscale photopolymerization10.1016/j.talanta.2024.126899 ↗
28. A photopolymerized hydrogel system with dual stiffness gradients reveals distinct actomyosin-based mechano-responses in fibroblast durotaxis10.1021/acsnano.2c05941 ↗
29. Guiding cell migration in 3D: a collagen matrix with graded directional stiffness10.1002/cm.20331 ↗
30. 3D mesenchymal cell migration is driven by anterior cellular contraction that generates an extracellular matrix prestrain10.1016/j.devcel.2021.02.017 ↗
31. Functionalization, preparation and use of cell-laden gelatin methacryloyl–based hydrogels as modular tissue culture platforms10.1038/nprot.2016.037 ↗
32. Quantification of fractional and absolute functionalization of gelatin hydrogels by optimized ninhydrin assay and 1H NMR10.1007/s00216-020-02792-5 ↗
33. Scikit-image: image processing in Python10.7717/peerj.453 ↗
34. N. Sofroniew, T. Lambert, G. Bokota, J. Nunez-Iglesias, P. Sobolewski, A. Sweet, L. Gaifas, K. Evans, A. Burt, D.D. Pop, K. Yamauchi, M.W. Mendonça, L. Liu, G. Buckley, W.-M. Vierdag, T. Monko, C. Willing, L. Royer, A.C Solak, K.I.S. Harrington, J. Abramo, J. Ahlers, D.A. Moré, O. Amsalem, A. Anderson, A. Annex, C. Aronssohn, F. Balzaretti, P. Boone, J. Bragantini, M. Bussonnier, C. Caporal, I. Coccimiglio, J. Eglinger, A. Eisenbarth, J. Freeman, C. Gohlke, K. Gunalan, Y.O. Halchenko, H. Har-Gil, M. Harfouche, V. Hilsenstein, K. Hutchings, R. Kozar, J. Lauer, G. Lichtner, H. Liu, Z. Liu, A. Lowe, L. Marconato, S. Martin, A. McGovern, L. Migas, N. Miller, S. Miñano, H. Muñoz, J.-H. Müller, C. Nauroth-Kreß, H.A. Obenhaus, D. Palecek, C. Pape, E. Perlman, K. Pevey, G. Peña-Castellanos, A. Pierré, D. Pinto, J. Rodríguez-Guerra, D. Ross, C.T. Russell, J. Ryan, G. Selzer, M. Smith, P. Smith, K. Sofiiuk, J. Soltwedel, D. Stansby, J. Vanaret, P. Wadhwa, M. Weigert, J. Windhager, P. Winston, R. Zhao, napari: a multi-dimensional image viewer for Python, (2025). https://doi.org/10.5281/ZENODO.3555620.
35. A threshold selection method from gray-level histograms10.1109/TSMC.1979.4310076 ↗
36. A practical guide to evaluating colocalization in biological microscopy10.1152/ajpcell.00462.2010 ↗
37. Generalized cell morphological parameters based on interferometric phase microscopy and their application to cell life cycle characterization10.1364/BOE.3.001757 ↗
38. J. Cohen, Statistical power analysis for the behavioral sciences, 0 ed., Routledge, 2013. https://doi.org/10.4324/9780203771587.10.4324/9780203771587 ↗
39. The photoinitiator lithium phenyl (2,4,6-Trimethylbenzoyl) phosphinate with exposure to 405 nm light is cytotoxic to mammalian cells but not mutagenic in bacterial reverse mutation assays10.3390/polym12071489 ↗
40. GelMA hydrogel dual photo-crosslinking to dynamically modulate ECM stiffness10.3389/fbioe.2024.1363525 ↗
41. Effect of light intensity on the free-radical photopolymerization kinetics of 2-hydroxyethyl methacrylate: experiments and simulations10.1021/acs.jpcb.0c03140 ↗
42. Experimental and theoretical investigations of free radical photopolymerization: inhibition and termination reactions10.1016/j.polymer.2018.11.057 ↗
43. Stiffness gradients mimicking In vivo tissue variation regulate mesenchymal stem cell fate10.1371/journal.pone.0015978 ↗
44. Time-sequential fibroblast-to-myofibroblast transition in elastin-variable 3D hydrogel environments by collagen networks10.1186/s40824-023-00439-x ↗
45. Effects of encapsulated cells on the physical–Mechanical properties and microstructure of gelatin methacrylate hydrogels10.3390/ijms20205061 ↗
46. Subcellular force imbalance in Actin bundles induces nuclear repositioning and durotaxis10.1021/acsami.3c07546 ↗
47. Zyxin is involved in fibroblast rigidity sensing and durotaxis10.3389/fcell.2021.735298 ↗
48. Substrates with engineered step changes in rigidity induce traction force polarity and durotaxis10.1007/s12195-013-0307-6 ↗
49. An optimized method of culturing neurons based on polyacrylamide gel10.52601/bpr.2023.230033 ↗
50. Effects of substrate stiffness on the tenoinduction of human mesenchymal stem cells10.1016/j.actbio.2017.05.058 ↗
51. Cancer cells sense solid stress to enhance metastasis by CKAP4 phase separation-mediated microtubule branching10.1038/s41421-024-00737-1 ↗
52. Mechanical response of neural cells to physiologically relevant stiffness gradients10.1002/adhm.201901036 ↗
53. Fabrication of tapered fluidic microchannels conducive to angiogenic sprouting within Gelatin methacryloyl hydrogels10.1016/j.joen.2020.08.026 ↗
54. In situ modulation of intestinal organoid epithelial curvature through photoinduced viscoelasticity directs crypt morphogenesis10.1126/sciadv.add5668 ↗
55. Embryonic cardiomyocytes beat best on a matrix with heart-like elasticity: scar-like rigidity inhibits beating10.1242/jcs.029678 ↗
56. Mesenchymal stem cell injection after myocardial infarction improves myocardial compliance10.1152/ajpheart.01017.2005 ↗
57. The effect of matrix characteristics on fibroblast proliferation in 3D gels10.1016/j.biomaterials.2010.07.046 ↗
58. Cardiac fibroblast to myofibroblast differentiation in vivo and in vitro: expression of focal adhesion components in neonatal and adult rat ventricular myofibroblasts10.1002/dvdy.22280 ↗
59. Controlling fibroblast proliferation with dimensionality-specific response by stiffness of injectable gelatin hydrogels10.1163/156856211X598193 ↗
60. Effect of the pore size in a 3D bioprinted gelatin scaffold on fibroblast proliferation10.1016/j.jiec.2018.07.013 ↗
61. Shear properties of passive ventricular myocardium10.1152/ajpheart.00111.2002 ↗
62. Inter-donor variability of extracellular matrix production in long-term cultures of human fibroblasts10.1039/D1BM01933C ↗
63. A. Detwiler, K. Polkoff, L. Gaffney, D. Freytes, J. Piedrahita, Donor age and time in culture affect dermal fibroblast contraction in a hydrogel skin graft model, (2021). https://doi.org/10.1101/2021.11.29.469875.10.1101/2021.11.29.469875 ↗
64. The long-term culture of Human fibroblasts reveals a spectroscopic signature of senescence10.3390/ijms23105830 ↗
65. Cell culture and passaging alters gene expression pattern and proliferation rate in rheumatoid arthritis synovial fibroblasts10.1186/ar3010 ↗
66. Chronic activation of human cardiac fibroblasts in vitro attenuates the reversibility of the myofibroblast phenotype10.1038/s41598-023-39369-y ↗
67. Phenotypic characterization of primary cardiac fibroblasts from patients with HFpEF