Spatio-Temporal Regulation of Rac1 Localization and Lamellipodia Dynamics during Epithelial Cell-Cell Adhesion
Developmental Cell, ISSN: 1534-5807, Vol: 3, Issue: 2, Page: 259-270
2002
- 305Citations
- 200Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations305
- Citation Indexes305
- 305
- CrossRef283
- Captures200
- Readers200
- 200
Article Description
Cadherin-dependent epithelial cell-cell adhesion is thought to be regulated by Rho family small GTPases and PI 3-kinase, but the mechanisms involved are poorly understood. Using time-lapse microscopy and quantitative image analysis, we show that cell-cell contact in MDCK epithelial cells coincides with a spatio-temporal reorganization of plasma membrane Rac1 and lamellipodia from noncontacting to contacting surfaces. Within contacts, Rac1 and lamellipodia transiently concentrate at newest sites, but decrease at older, stabilized sites. Significantly, Rac1 mutants alter kinetics of cell-cell adhesion and strengthening, but not the eventual generation of cell-cell contacts. Products of PI 3-kinase activity also accumulate dynamically at contacts, but are not essential for either initiation or development of cell-cell adhesion. These results define a role for Rac1 in regulating the rates of initiation and strengthening of cell-cell adhesion.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1534580702002162; http://dx.doi.org/10.1016/s1534-5807(02)00216-2; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0036696823&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/12194856; https://linkinghub.elsevier.com/retrieve/pii/S1534580702002162; http://linkinghub.elsevier.com/retrieve/pii/S1534580702002162; http://api.elsevier.com/content/article/PII:S1534580702002162?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S1534580702002162?httpAccept=text/plain; http://dx.doi.org/10.1016/s1534-5807%2802%2900216-2; https://dx.doi.org/10.1016/s1534-5807%2802%2900216-2; http://f1000.com/1009554#eval154859; http://f1000.com/1009554#eval129409
Elsevier BV
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