The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Vinculin in cell–cell and cell–matrix adhesions
Open accessAbstract
Vinculin was identified as a component of focal adhesions and adherens junctions nearly 40 years ago. Since that time, remarkable progress has been made in understanding its activation, regulation and function. Here we discuss the current understanding of the roles of vinculin in cell-cell and cell-matrix adhesions. Emphasis is placed on the how vinculin is recruited, activated and regulated. We also highlight the recent understanding of how vinculin responds to and transmits force at integrin- and cadherin-containing adhesion complexes to the cytoskeleton. Furthermore, we discuss roles of vinculin in binding to and rearranging the actin cytoskeleton.
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Cites
α-Catenin as a tension transducer that induces adherens junction development
Yonemura, S., Wada, Y., Watanabe, T., Nagafuchi, A., & Shibata, M. (2010) · Nature Cell Biology · doi:10.1038/ncb2055 · Cited by 972
Cadherin-based intercellular adhesions organize epithelial cell–matrix traction forces
Mertz, A. F., Che, Y., Banerjee, S., Goldstein, J. M., Rosowski, K. A., Revilla, S. F., Niessen, C. M., Marchetti, M. C., Dufresne, E. R., & Horsley, V. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1217279110 · Cited by 243
α-Catenin cytomechanics – role in cadherin-dependent adhesion and mechanotransduction
Barry, A. K., Tabdili, H., Muhamed, I., Wu, J., Shashikanth, N., Gomez, G. A., Yap, A. S., Gottardi, C. J., de Rooij, J., Wang, N., et al. (2014) · Journal of Cell Science · doi:10.1242/jcs.139014 · Cited by 119
Cited by
Targeting integrin pathways: mechanisms and advances in therapy
Pang, X., He, X., Qiu, Z., Zhang, H., Xie, R., Liu, Z., Gu, Y., Zhao, N., Xiang, Q., & Cui, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01259-6 · Cited by 1,275
The extracellular matrix in tumor progression and metastasis
Eble, J. A., & Niland, S. (2019) · Clinical & Experimental Metastasis · doi:10.1007/s10585-019-09966-1 · Cited by 613
Heterogeneity and Actin Cytoskeleton in Osteoclast and Macrophage Multinucleation
Takito, J., & Nakamura, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186629 · Cited by 50
Chau, T. C. Y., Keyser, M. S., Da Silva, J. A., Morris, E. K., Yordanov, T. E., Duscyz, K. P., Paterson, S., Yap, A. S., Hogan, B. M., & Lagendijk, A. K. (2022) · Development · doi:10.1242/dev.200454 · Cited by 18
The MeshCODE to scale—visualising synaptic binary information
(2022) · doi:10.3389/fncel.2022.1014629 · Cited by 14
Metadata
- Authors
- Bays, J. L., & DeMali, K. A.
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2017-04-11
- Volume
- 74
- Issue
- 16
- Pages
- 2999-3009
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- OpenAlex
- W2606271937
- Cited by
- 459
- References
- 3
- FWCI
- 13.57
- Type
- journal article
- Language
- en
- Open access
- hybrid
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
