The DOI matches its Crossref record; 209 of the 211 references it cites were found in a registry or an index.
Mechanical regulation of myofibroblast phenoconversion and collagen contraction
Abstract
Activated fibroblasts promote physiological wound repair following tissue injury. However, dysregulation of fibroblast activation contributes to the development of fibrosis by enhanced production and contraction of collagen-rich extracellular matrix. At the peak of their activities, fibroblasts undergo phenotypic conversion into highly contractile myofibroblasts by developing muscle-like features, including formation of contractile actin-myosin bundles. The phenotype and function of fibroblasts and myofibroblasts are mechanically regulated by matrix stiffness using a feedback control system that is integrated with the progress of tissue remodelling. The actomyosin contraction machinery and cell-matrix adhesion receptors are critical elements that are needed for mechanosensing by fibroblasts and the translation of mechanical signals into biological responses. Here, we focus on mechanical and chemical regulation of collagen contraction by fibroblasts and the involvement of these factors in their phenotypic conversion to myofibroblasts.
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“During fibroblast-to-myofibroblast transition, a complex mechanochemical signaling is activated involving profibrotic secreted factors such as TGFβ and Wnt and ECM-degrading enzymes and intracellular effectors required for stress fiber contractility [127,131].”
From Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes (2019) · cites this paper as [131]
Citations
Cites
Myofibroblasts and mechano-regulation of connective tissue remodelling
Tomasek, J. J., Gabbiani, G., Hinz, B., Chaponnier, C., & Brown, R. A. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm809 · Cited by 4,290
Self-citationTGF-β: the master regulator of fibrosis
Meng, X.-M., Nikolic-Paterson, D. J., & Lan, H. Y. (2016) · Nature Reviews Nephrology · doi:10.1038/nrneph.2016.48 · Cited by 3,528
Mechanotransduction Across the Cell Surface and Through the Cytoskeleton
Wang, N., Butler, J. P., & Ingber, D. E. (1993) · Science · doi:10.1126/science.7684161 · Cited by 3,007
Non-muscle myosin II takes centre stage in cell adhesion and migration
Vicente‐Manzanares, M., Ma, X., Adelstein, R. S., & Horwitz, A. R. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2786 · Cited by 2,137
Mechanotransduction and extracellular matrix homeostasis
Humphrey, J. D., Dufresne, E. R., & Schwartz, M. A. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3896 · Cited by 2,124
Cell adhesion: integrating cytoskeletal dynamics and cellular tension
Parsons, J. T., Horwitz, A. R., & Schwartz, M. A. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2957 · Cited by 2,081
Hinz, B., Phan, S. H., Thannickal, V. J., Galli, A., Bochaton-Piallat, M.-L., & Gabbiani, G. (2007) · The American Journal of Pathology · doi:10.2353/ajpath.2007.070112 · Cited by 2,068
Self-citationROCKs: multifunctional kinases in cell behaviour
Riento, K., & Ridley, A. J. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1128 · Cited by 1,941
Cardiac Fibrosis: The Fibroblast Awakens
Travers, J. G., Kamal, F. A., Robbins, J., Yutzey, K. E., & Blaxall, B. C. (2016) · Circulation Research · doi:10.1161/circresaha.115.306565 · Cited by 1,596
Stretching Single Talin Rod Molecules Activates Vinculin Binding
Hernández, A. E. D. R., Pérez‐Jiménez, R., Liu, R., Roca‐Cusachs, P., Fernández, J. M., & Sheetz, M. P. (2009) · Science · doi:10.1126/science.1162912 · Cited by 1,492
Research works printed but not linked: 7
- Martinez, 2017, Idiopathic pulmonary fibrosis, Nature reviews, Dis. Prim., 3, 17074
- Ampe, 2017, vol. 235, 1
- Coelho, 2016, Contribution of collagen adhesion receptors to tissue fibrosis, Cell Tissue Res., 365, 521, 10.1007/s00441-016-2440-8 · DOI
- Coelho, 2018, Mechanical signaling through the discoidin domain receptor 1 plays a central role in tissue fibrosis, Cell Adhes. Migrat., 12, 348
- Leitinger, 2014, 310, 39
- Froese, 2016, Stretch induced activation of TGF-beta1 in pulmonary fibrosis, Am. J. Respir. Crit. Care Med., 194, 84, 10.1164/rccm.201508-1638OC · DOI · Paper page
- Piersma, 2015, YAP1 is a driver of myofibroblast differentiation in normal and diseased fibroblasts, Am. J. Pathol., 185, 3326, 10.1016/j.ajpath.2015.08.011 · DOI · Paper page
Cited by
Sorted by citations
Items 101–182 of 182
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Nie, Y., Hu, C., Huang, X., Zeng, H., Wang, Z., Liang, J., & Wang, J. (2025) · ACS Applied Bio Materials · doi:10.1021/acsabm.5c00523 · Cited by 8
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Abignano, G., Hermes, H. M., Piera-Velázquez, S., Addya, S., Galdo, F. D., & Jiménez, S. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-99292-y · Cited by 8
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BackgroundCellular Transdifferentiation: A Crucial Mechanism of Fibrosis in Systemic Sclerosis
Jiménez, S. A., & Piera-Velázquez, S. (2023) · Current Rheumatology Reviews · doi:10.2174/0115733971261932231025045400 · Cited by 7
Leask, A., Fadl, A., & Naik, A. (2024) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2024.2323528 · Cited by 7
de Hilster, R. H. J., Reinders-Luinge, M., Schuil, A., Borghuis, T., Harmsen, M. C., Burgess, J. K., & Hylkema, M. N. (2024) · Bioengineering · doi:10.3390/bioengineering11090946 · Cited by 9
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BackgroundSchoberleitner, I., Faserl, K., Lackner, M., Coraça-Huber, D. C., Augustin, A., Imsirovic, A., Sigl, S., & Wolfram, D. (2024) · Biomolecules · doi:10.3390/biom14111433 · Cited by 7
Quillen, S. E., Kimball, E., Ritter-Gordy, K. A., Du, L., Yuan, Z., Pease, M. E., Madhoun, S., Nguyen, T. D., Johnson, T. V., Quigley, H. A., et al. (2024) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.65.13.43 · Cited by 7
Burke, O. M., Bilik, S. M., Dodson, C., Johnson, J. A. K., Ferrari, L. M., Imisheva, K., Pachalis, H., Frerichs, V. R., Jeffrey, A., Sawaya, A. P., et al. (2026) · American Journal of Clinical Dermatology · doi:10.1007/s40257-026-01007-4 · Cited by 7
“These cells also exert contractile forces that contribute to tissue rigidity [60, 61].”
Vaughan, M. B., Xu, G., Morris, T. L., Kshetri, P., & Herwig, J. X. (2019) · Cell Adhesion & Migration · doi:10.1080/19336918.2019.1644855 · Cited by 7
“myofibroblasts, identifiable by the presence of the alpha-smooth muscle actin isoform assembled into cytoskeletal stress fibers [19,20].”
BackgroundSantos, G. L., DeGrave, A. N., Rehman, A., Disi, S. A., Xhaxho, K., Schröder, H., Bao, G., Meyer, T., Tiburcy, M., Dworatzek, E., et al. (2022) · Biomaterials Advances · doi:10.1016/j.bioadv.2022.213041 · Cited by 8
Cavanzo, N. P., Riesmeijer, S. A., Holt-Kedde, I. L., Werker, P., Piersma, B., Olinga, P., & Bank, R. (2022) · Scientific Reports · doi:10.1038/s41598-022-18116-9 · Cited by 5
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Johns, K. L., Faralli, J. A., Filla, M. S., Shah, N., Sun, Y. Y., Keller, K. E., & Peters, D. M. P. (2025) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.66.6.31 · Cited by 6
“42 Given that EndoMT is believed to contribute to the increased rigidity of the TM/SC tissue and alter the pressure-dependent contractile properties of the TM/SC outflow pathway that controls IOP, 3 this suggests that a switch in activity from α 5 β 1 to α v β 3 integrin likely contributes to the…”
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Yustisia, Y., & Kato, K. (2025) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-025-01109-z · Cited by 6
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BackgroundShiraishi, M., Suzuki, K., & Yamaguchi, A. (2023) · The FASEB Journal · doi:10.1096/fj.202201899r · Cited by 7
RetractedWound repair and scarring of genital skin
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BackgroundWikan, N., Potikanond, S., & Nimlamool, W. (2022) · Cells · doi:10.3390/cells11172731 · Cited by 6
“One of the distinct molecular hallmarks contributing to mesenchymal features is the upregulation of vimentin intermediate filaments [10,38].”
BackgroundEndocytic recycling is central to circadian collagen fibrillogenesis and disrupted in fibrosisPreprint
Chang, J., Pickard, A., Herrera, J., O’Keefe, S. M., Garva, R., Knox, J., Jowitt, T. A., Hartshorn, M., Hoyle, A., Dingle, L., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.25.436925 · Cited by 7
Doan, K. T., Kshetri, P., Attamakulsri, N., Newsome, D. R., Zhou, F., Murray, C. K., Chen, W. R., Xu, G., & Vaughan, M. B. (2019) · Molecules · doi:10.3390/molecules24152713 · Cited by 5
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BackgroundResearch progress on scar-free healing
Yang, W., Liu, L., & Cheng, X. (2025) · Annals of Medicine · doi:10.1080/07853890.2025.2575109 · Cited by 6
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Qin, Y., Yang, G., Zhang, T., Yang, Y., Wan, L., Zhang, T., Wang, L., Hu, Z., Dai, Z., Zhou, H., et al. (2026) · Bone Research · doi:10.1038/s41413-025-00501-5 · Cited by 5
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BackgroundHan, X., Xu, L., Dou, T., Du, R. H., Deng, L., & Wang, X. (2023) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.2c01502 · Cited by 4
Bernardo, A., Díaz‐Valdivia, N., Fernández‐Nogueira, P., & Alcaraz, J. (2025) · FEBS Open Bio · doi:10.1002/2211-5463.70102 · Cited by 5
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Nishida, K., Sugioka, K., Murakami, J., Kodama-Takahashi, A., Nanri, I., Mishima, H., Nishida, T., & Kusaka, S. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.107933 · Cited by 3
Wickström, S. A., & Roca‐Cusachs, P. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.05.033 · Cited by 3
Eremichev, R. Y., & Макаревич, П. И. (2024) · Tsitologiya · doi:10.31857/s0041377124030011 · Cited by 2
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Wenkai, Y. E., Xinan, M. E. N. G., & Suhong, X. U. (2025) · Journal of Zhejiang University (Medical Sciences) · doi:10.3724/zdxbyxb-2024-0535 · Cited by 2
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“Myofibroblasts are central effectors, secreting ECM proteins, especially collagens I and III [11,78,79].”
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Zhang, H., Luo, D., Cai, G., Hu, M., Fan, Z., & Li, M. (2026) · Journal of Controlled Release · doi:10.1016/j.jconrel.2026.114700 · Cited by 2
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“[ 15, 16] However, it aligns with the notion of collagen hyperplasia resulting from repeated pressure stimuli that damage the skin [32, 33].”
Lee, H. J., Lau, L. N., Sidhu, S. K., Park, J., & Yeo, I.-S. L. (2025) · Prosthesis · doi:10.3390/prosthesis7030052 · Cited by 1
“Collagen gel is the main ECM component and has excellent cell adhesion, but has the disadvantages of being temperature-sensitive and contractile, so its structure easily collapses [47].”
Nobili, R., Barbagallo, C., Ragusa, M., Genovese, J., D'Agostino, V., Diociaiuti, A., Castiglia, D., Odorisio, T., Zambruno, G., Hachem, M. E., et al. (2025) · Non-coding RNA Research · doi:10.1016/j.ncrna.2025.08.005 · Cited by 1
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Hsieh, P.-L., Chang, F.-Y., Tang, P.-H., Liao, Y.-W., Yu, C.-C., & Liu, C.-M. (2025) · Journal of Dental Sciences · doi:10.1016/j.jds.2025.07.001 · Cited by 1
“28,29 In Fig.”
Johns, K. L., Faralli, J. A., Filla, M. S., Shah, N., Keller, K. E., & Peters, D. M. P. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1730542 · Cited by 1
“The transition into a myofibroblast phenotype is often preceded by the activation of α v β 3 integrin (Hinz and Gabbiani, 2010; Hinz et al., 2019; Faralli et al., 2023; Goffin et al., 2006; Hinz, 2010).”
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Yannas, I. V. (2024) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2024.112174 · Cited by 1
Wei, Y., Deng, J., Yin, M., Xu, G., He, J., Wang, X., Zhang, L., Li, Z., Huang, G., & Wu, J. (2023) · International Wound Journal · doi:10.1111/iwj.14095 · Cited by 1
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Pasvanis, Z., Boynes, A., Kong, R. C. K., Chan, E. C., Wong, R. C. B., & Gaskin, J. C. F. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.09.583791 · Cited by 1
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Backgroundvan Amstel, R. N., Weide, G., Wesselink, E. O., Noten, K., Jacobs, K., Pool‐Goudzwaard, A., & Jaspers, R. T. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4905444 · Cited by 1
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Leask, A. (2021) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-021-00626-2
“These data collectively emphasize a critical role of TGFbeta and mechanosignaling in fibrogenesis (Hinz et al. 2019; Leask 2021), and suggest a potential basis for examining the fundamental mechanisms underlying how the microenvironment activates MSC in SSc fibrosis.”
BackgroundMyofibroblasts: 50 years and aging well
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Ocon, A. J., Lokineni, S., & Korman, B. D. (2022) · Current Treatment Options in Rheumatology · doi:10.1007/s40674-021-00189-8
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Chang, J., Pickard, A., Herrera, J., O’Keefe, S. M., Garva, R., Hoyle, A., Dingle, L., Wong, J. K. F., Reid, A. J., Zeltz, C., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4132722
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Shiraishi, M., Suzuki, K., & Yamaguchi, A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.05.515315
Peidl, A., Nguyen, J., Chitturi, P., Riser, B. L., & Leask, A. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2744-0_21 · Cited by 1
Zhou, X., Yin, X., Yin, Q., Liu, W., & Zhou, D. X. (2024) · Research Square · doi:10.21203/rs.3.rs-3913941/v1
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Niya, C., Liming, H., Jiang, Z., Zeng, Y., Ge, W., & Xie, X. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4818804
Su, D., Chen, L., Yang, K., Huangfu, Q., & Wang, N. (2024) · Journal of the Pakistan Medical Association · doi:10.47391/jpma.10211
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van Amstel, R. N., Schipholt, I. J. L., Weide, G., Pool‐Goudzwaard, A., & Jaspers, R. T. (2026) · Musculoskeletal Science and Practice · doi:10.1016/j.msksp.2026.103507
Zhong, L., Zhang, H., Huang, Y., Zhang, L., Zhang, L., Liu, Q., Liao, Y., Zhang, Q., Fu, W., Wang, C., et al. (2026) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2026.107504
Jiang, Y., Han, X., Deng, L., & Wang, X. (2026) · ACS Omega · doi:10.1021/acsomega.6c00173
Gao, L., Wang, S., Zhang, J., Gao, L., Kang, N., Zhou, J., & Zhou, J. (2026) · Molecular Human Reproduction · doi:10.1093/molehr/gaag028
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(2026) · Elsevier eBooks · doi:10.1016/b978-3-437-55038-6.00004-x
Zhan, L., Xiang, H., Kong, Y., Lei, Y., Xiao, S., Chen, S., Li, J., Li, Z., Ni, R., Peng, D., et al. (2026) · Animal Models and Experimental Medicine · doi:10.1002/ame2.70249
Du, L., Suarez, A., Jha, V., Volety, P., Lockard, C. A., Sutton, B. P., Smith, A. B., Ziv‐Gal, A., Damon, B. M., Bagchi, I. C., et al. (2026) · Biology of Reproduction · doi:10.1093/biolre/ioag156
Rahayu, I., Arfian, N., Timotius, K. H., & Wahyuningsih, M. S. H. (2026) · Journal of Applied Pharmaceutical Science · doi:10.1177/22313354261464247
“60 Upon stimulation by TGF-β, these contrac - tile fibers are characterized by the presence of α-SMA, which serves as a widely recognized marker for identifying mature myofibroblasts in tissues.”
Pasvanis, Z., Boynes, A., Kong, R. C. K., Chan, E. C., Wong, R. C. B., & Gaskin, J. C. F. (2026) · Biomedicines · doi:10.3390/biomedicines14081718 · Cited by 2
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Hardened ground: ECM stiffness as a unifying biomechanical driver of reproductive stem cell aging
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“(d) Window of reversibility: Fibrotic crosslinking may be reversible at early stages; advanced fibrosis with pre-existing AGE crosslinks is largely refractory to pharmacological intervention alone (Miroshnikova et al. 2016; Hinz et al. 2019).”
Current therapeutic strategies and available research models for investigating hypertrophic scars
Chu, A., Kumar, S., & Francois Berthiaume, B. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1887685 · Cited by 1
“This is mediated through macrophage-mediated TGF-β signaling, exacerbated by a decreased level of metalloproteinases (MMPs) which degrade the ECM and excess collagen (Hinz et al., 2019; Younesi et al., 2024; Jia et al., 2025).”
Ning, J. Y., Wang, B., Yamamoto, M. I., & Yamada, K. H. (2026) · Cells · doi:10.3390/cells15191772
“Conversely, MLC phosphatase (MLCP) dephosphorylates MLC, reducing actomyosin interactions and contractile activity [222].”
Deb, D., Ray, S., Sharma, P., Sharma, P., & Sikder, K. (2026) · Chronobiology International · doi:10.1080/07420528.2026.2745644
Metadata
- Authors
- Hinz, B., McCulloch, C. A., & Coelho, N. M.
- Affiliations
- University of Toronto (CA)
- Corresponding author
- Coelho, Nuno M.
- Venue
- Experimental Cell Research
- Publisher
- Elsevier BV
- Published
- 2019-06
- Volume
- 379
- Issue
- 1
- Pages
- 119-128
- ISSN
- 0014-4827 (ISSN-L)
- OpenAlex
- W2934133090
- Semantic Scholar
- 6f2d57f6aad8ed5a88713504974535d1eb19f620
- Cited by
- 182
- References
- 211
- Citations by year
- 2026: 23 · 2025: 19 · 2024: 28 · 2023: 27 · 2022: 20 · 2021: 38 · 2020: 14 · 2019: 13
- FWCI
- 2.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Experimental Cell Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research CIHR (#375597)
- Canada Foundation for Innovation and Ontario Research Fund (#36050)
- E-Rare Joint Transnational Program ‘Development of Innovative Therapeutic Approaches for Rare Diseases’ (# ERL-138395)
- CMC is supported by a CIHR Operating grant (MOP416228)
- Canada Research Chair in Matrix Dynamics
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Health Sciences › Medicine › Surgery › Wound Healing and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Keywords
- collagen contraction, fibroblast activation, extracellular matrix stiffness, mechanotransduction, actomyosin contractility, fibrosis, tissue remodeling, wound healing
- MeSH terms
- Animals, Collagen, Extracellular Matrix, Fibrosis, Humans, Phenotype, Wound Healing, Myofibroblasts
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