The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Cortactin: The Gray Eminence of the Cytoskeleton
Abstract
Cortactin, an actin filament-binding protein and target of multiple kinases, has emerged as a central element connecting signaling pathways with cytoskeleton restructuring. It is involved in a perplexingly diverse array of cellular processes, including cell motility, invasiveness, synaptogenesis, endocytosis, intercellular contact assembly, and host-pathogen interactions, where the common denominator appears to be a role in the coordination of membrane dynamics with cytoskeletal remodeling. Although in recent years our knowledge about cortactin has increased exponentially, the exact mechanisms underlying its fundamental roles remain to be defined.
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Cites
Naisbitt, S., Kim, E., Tu, J. C., Xiao, B., Sala, C., Valtschanoff, J., Weinberg, R. J., Worley, P. F., & Sheng, M. (1999) · Neuron · doi:10.1016/s0896-6273(00)80809-0 · Cited by 1,009
Activation of Arp2/3 complex-mediated actin polymerization by cortactin
Uruno, T., Liu, J., Zhang, P., Fan, Y.-X., Egile, C., Li, R., Mueller, S. C., & Zhan, X. (2001) · Nature Cell Biology · doi:10.1038/35060051 · Cited by 568 · cited 3×
“The breakthrough in our understanding of the basic function of cortactin was the discovery that it associates with and acts as an activator of the Arp2/3 complex (94, 99, 102).”
BackgroundMerrifield, C. J., Perrais, D., & Zenisek, D. (2005) · Cell · doi:10.1016/j.cell.2005.03.015 · Cited by 476 · cited 1×
“(69) studied the dynamics of individual CCPs using evanescent field microscopy and a witty technique, the pH-sensitive labeling of transferrin receptors, with which the closure and scission of CCPs can be resolved in real time.”
BackgroundCortactin-Src kinase signaling pathway is involved in N-syndecan-dependent neurite outgrowth.
Kinnunen, T., Kaksonen, M., Saarinen, J., Kalkkinen, N., Peng, H. B., & Rauvala, H. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.17.10702 · Cited by 234
Cao, H., Weller, S., Orth, J. D., Chen, J., Huang, B., Chen, J.-L., Stamnes, M., & McNiven, M. A. (2005) · Nature Cell Biology · doi:10.1038/ncb1246 · Cited by 169
Cited by
Physiology of cell volume regulation in vertebrates
Hoffmann, E. K., Lambert, I. H., & Pedersen, S. F. (2009) · Physiological Reviews · doi:10.1152/physrev.00037.2007 · Cited by 1,441
Regulation of Actin Assembly Associated With Protrusion and Adhesion in Cell Migration
Le Clainche, C., & Carlier, M.-F. (2008) · Physiological Reviews · doi:10.1152/physrev.00021.2007 · Cited by 849
Arp2/3 complex interactions and actin network turnover in lamellipodia
Lai, F. P., Szczodrak, M., Block, J., Faix, J., Breitsprecher, D., Mannherz, H. G., Stradal, T. E., Dunn, G. A., Small, J. V., & Rottner, K. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.34 · Cited by 300
Chen, Y.-K., & Hsueh, Y.-P. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4405-11.2012 · Cited by 90
β-Pix modulates actin-mediated recruitment of synaptic vesicles to synapses
Sun, Y., & Bamji, S. X. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2359-11.2011 · Cited by 63
Metadata
- Authors
- Cosen-Binker, L. I., & Kapus, A.
- Venue
- Physiology
- Publisher
- American Physiological Society
- Published
- 2006-10
- Volume
- 21
- Issue
- 5
- Pages
- 352-361
- ISSN
- 0886-1714 (ISSN-L)
- 1548-9213
- 1548-9221
- OpenAlex
- W2160713438
- Cited by
- 187
- References
- 5
- FWCI
- 4.99
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
