The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
A crucial role of β1 integrins for keratinocyte migration in vitro and during cutaneous wound repair
Abstract
Integrins are ubiquitous transmembrane receptors that play crucial roles in cell-cell and cell-matrix interactions. In this study, we have determined the effects of the loss of β1 integrins in keratinocytes in vitro and during cutaneous wound repair. Flow cytometry of cultured β1-deficient keratinocytes confirmed the absence of β1 integrins and showed downregulation of α6β4 but not of αv integrins. β1-null keratinocytes were characterised by poor adhesion to various substrates, by a reduced proliferation rate and by a strongly impaired migratory capacity. In vivo, the loss of β1 integrins in keratinocytes caused a severe defect in wound healing. β1-null keratinocytes showed impaired migration and were more densely packed in the hyperproliferative epithelium. Surprisingly, their proliferation rate was not reduced in early wounds and even increased in late wounds. The failure in re-epithelialisation resulted in a prolonged inflammatory response, leading to dramatic alterations in the expression of important wound-regulated genes. Ultimately, β1-deficient epidermis did cover the wound bed, but the epithelial architecture was abnormal. These findings demonstrate a crucial role of β1 integrins in keratinocyte migration and wound re-epithelialisation. Movies available on-line
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Cites
Fibronectin matrix deposition and fibronectin receptor expression in healing and normal skin
Clark, R. A. F. (1990) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12876104 · Cited by 312
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Alonso, L., & Fuchs, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1734203100 · Cited by 521
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Friedl, P., Hegerfeldt, Y., & Tusch, M. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.041821pf · Cited by 444
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Baum, C. L., & Arpey, C. J. (2005) · Dermatologic Surgery · doi:10.1097/00042728-200506000-00011 · Cited by 404
Cell-Extracellular Matrix Interactions in Normal and Diseased Skin
Watt, F. M., & Fujiwara, H. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005124 · Cited by 384
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Grose, R., & Werner, S. (2004) · Molecular Biotechnology · doi:10.1385/mb:28:2:147 · Cited by 197
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Agren, M. S., & Werthen, M. (2007) · The International Journal of Lower Extremity Wounds · doi:10.1177/1534734607301394 · Cited by 136
Rezvani, H. R., Ali, N., Serrano-Sanchez, M., Dubus, P., Varon, C., Ged, C., Pain, C., Cario-André, M., Seneschal, J., Taïeb, A., et al. (2011) · Journal of Cell Science · doi:10.1242/jcs.082370 · Cited by 90
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Hosokawa, R., Urata, M. M., Ito, Y., Bringas, P., & Chai, Y. (2005) · Journal of Investigative Dermatology · doi:10.1111/j.0022-202x.2005.23963.x · Cited by 63
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Piwko-Czuchra, A., Koegel, H., Meyer, H., Bauer, M., Werner, S., Brakebusch, C., & Fässler, R. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005488 · Cited by 52
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Kang, Y.-A., Choi, H.-R., Na, J.-I., Huh, C.-H., Kim, M.-J., Youn, S.-W., Kim, K.-H., & Park, K.-C. (2009) · Archives of Dermatological Research · doi:10.1007/s00403-009-0942-x · Cited by 51
Stem cell recovering effect of copper‐free GHK in skin
Choi, H., Kang, Y., Ryoo, S., Shin, J., Na, J., Huh, C., & Park, K. (2012) · Journal of Peptide Science · doi:10.1002/psc.2455 · Cited by 35
Redox Status Is Critical for Stemness in Skin Equivalents
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Metadata
- Authors
- Grose, R., Hutter, C., Bloch, W., Thorey, I., Watt, F. M., Fässler, R., Brakebusch, C., & Werner, S.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2002-05-01
- Volume
- 129
- Issue
- 9
- Pages
- 2303-2315
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2133120721
- Cited by
- 277
- References
- 1
- FWCI
- 7.22
- Type
- journal article
- Language
- en
- Open access
- closed
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