Cortactin

Template:PBB Cortactin (from “cortical actin binding protein”) is a monomeric protein located in the cytoplasm of cells that can be activated by external stimuli to promote polymerization and rearrangement of the actin cytoskeleton, especially the actin cortex around the cellular periphery. It is present in all cell types. When activated, it will recruit Arp2/3 complex proteins to existing actin microfilaments, facilitating and stabilizing nucleation sites for actin branching. Cortactin is important in promoting lamellipodia formation, invadopodia formation, cell migration, and endocytosis.

Structure

Cortactin is a thin, elongated monomer that consists of an amino-terminal acidic (NTA) region; 37-residue-long segments that are highly conserved among cortactin proteins of all species and which are repeated up to 6.5 times in tandem (“cortactin repeats”); a proline-rich region; and an SH3 domain. This basic structure is highly conserved among all species that express cortactin (Daly, 2004).

Activation and Binding

Cortactin is activated via phosphorylation, by tyrosine kinases or serine/threonine kinases, in response to extracellular signals like growth factors, adhesion sites, or pathogenic invasion of the epithelial layer.

The SH2 domain of certain tyrosine kinases, such as the oncogene Src kinase, binds to cortactin’s proline-rich region and phosphorylates it on Tyr421, Tyr466, and Tyr482. Once activated in this way, it can bind to filamentous actin (F-actin) with the fourth of its cortactin repeats (Daly, 2004). As the concentration of phosphorylated cortactin increases in specific regions within the cell, the monomers each begin to recruit an Arp2/3 complex to F-actin. It binds to Arp2/3 with an aspartic acid-aspartic acid-tryptophan (DDW) sequence in its NTA region, a motif that is often seen in other actin nucleation-promoting factors (NPFs) (Weed et al., 2000).

Certain serine/threonine kinases, such as ERK, can phosphorylate cortactin on Ser405 and Ser418 in the SH3 domain (Daly, 2004). Activated like this, it still associates with Arp2/3 and F-actin, but will also allow other actin NPFs, most importantly N-WASp (Neuronal Wiskott-Aldrich syndrome protein), to bind to the complex as well; when phosphorylated by tyrosine kinases, other NPFs are excluded (Martinez-Quiles et al., 2004). The ability of these other NPFs to bind the Arp2/3 complex while cortactin is also bound could come from new interactions with cortactin’s SH3 domain, which is in a different conformation when phosphorylated by Ser/Thr kinases and thus may be more open to interactions with other NPFs (Martinez-Quiles et al., 2004). Having other NPFs bind to the Arp2/3 complex at the same time as cortactin may enhance nucleation site stability (Daly, 2004).

Location and Functions in the Cell

Inactive cortactin is diffuse throughout the cytoplasm, but upon phosphorylation, the protein begins to target certain areas in the cell. Cortactin-assisted Arp2/3-nucleated actin branches are most prominent in the actin cortex, around the periphery of the cell (Weaver et al., 2001). A phosphorylated cortactin monomer binds to, activates, and stabilizes an Arp2/3 complex on preexisting F-actin, which provides a nucleation site for a new actin branch to form from the “mother” filament. Branches formed from cortactin-assisted nucleation sites are very stable; cortactin has been shown to inhibit debranching (Weaver et al., 2001). Thus, polymerization and branching of actin is promoted in areas of the cell where cortactin is localized.

Cortactin is very active in lamellipodia, protrusions of the cell membrane formed by actin polymerization and treadmilling that propel the cell along a surface as it migrates towards some target (Weed et al., 2001). Cortactin acts as a link between extracellular signals and lamellipodial “steering.” When a receptor tyrosine kinase on the cell membrane binds to an adhesion site, for example, cortactin will be phosphorylated locally to the area of binding, activate and recruit Arp2/3 to the actin cortex in that region, and thus stimulate cortical actin polymerization and movement of the cell in that direction. Macrophages, highly mobile immune cells that engulf cellular debris and pathogens, are propelled by lamellipodia and identify/migrate toward a target via chemotaxis; thus, cortactin must also be activated by receptor kinases that pick up a large variety of chemical signals (Weed et al., 2001).

Studies have implicated cortactin in both clathrin-mediated endocytosis (Samaj et al., 2004) and clathrin-independent endocytosis (Sauvonnet et al., 2004). In both kinds of endocytosis, it has long been known that actin localizes to sites of vesicle invagination and is a vital part of the endocytic pathway, but the actual mechanisms by which actin facilitates endocytosis are still unclear. Recently, however, it has been found that dynamin, the protein responsible for breaking the newly formed vesicular bud off the inside of the plasma membrane, can associate with the SH3 domain of cortactin. Since cortactin recruits the Arp2/3 complexes that lead to actin polymerization, this suggests that it may play an important part in linking vesicle formation to the as yet unknown functions actin has in endocytosis (Zhu et al., 2005).

Related Diseases

Amplification of the genes encoding cortactin—in humans, EMS1—has been found to occur in certain tumors. Overexpression of cortactin can lead to highly-active lamellipodia in tumor cells, dubbed “invadopodia.” These cells are especially invasive and migratory, making them very dangerous, for they can easily spread cancer across the body into other tissues (Weaver, 2006).

References

• Daly, Roger J. (2004). "Cortactin Signalling and Dynamic Actin Networks". Biochemistry Journal. 382: 13–25. doi:10.1042/BJ20040737. {{cite journal}}: Cite has empty unknown parameters: |month= and |coauthors= (help)
• Martinez-Quiles, Narcisa (2004). "Erk/Src Phosphorylation of Cortactin Acts as a Switch On-Switch Off Mechanism That Controls Its Ability To Activate N-WASP". Molecular and Cellular Biology. 24 (12): 5269–5280. doi:10.1128/MCB.24.12.5269-5280.2004. {{cite journal}}: Cite has empty unknown parameters: |month= and |coauthors= (help)
• Samaj, Jozef (2004). "Endocytosis, Actin Cytoskeleton, and Signaling". Plant Physiology. 135: 1150–1161. {{cite journal}}: Cite has empty unknown parameter: |month= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
• Sauvonnet, Nathalie (2004). "Cortactin and dynamin are required for the clathrin-independent endocytosis of gamma-c cytokine receptor". JCB. 168 (1): 155–163. {{cite journal}}: Cite has empty unknown parameter: |month= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
• Weaver, Alissa M. (2001). "Cortactin promotes and stabilizes Arp2/3-induced actin filament network formation". Current Biology. 11 (5): 370–374. {{cite journal}}: Cite has empty unknown parameter: |month= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
• Weaver, Alissa M. (2006). "Invadopodia: specialized cell structures for cancer invasion". Clin Exp Metastasis. 23: 97–105. {{cite journal}}: Cite has empty unknown parameters: |month= and |coauthors= (help)
• Weed, Scott A. (2000). "Cortactin Localization to Sites of Actin Assembly in Lamellipodia Requires Interactions with F-Actin and the Arp2/3 Complex". Journal of Cell Biology. 151 (1): 29–40. {{cite journal}}: Cite has empty unknown parameter: |month= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
• Weed, Scott A. (2001). "Cortactin: coupling membrane dynamics to cortical actin assembly". Oncogene. 20 (44): 6418–6434. doi:10.1038/sj.onc.1204783. {{cite journal}}: Cite has empty unknown parameter: |month= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
• Zhu, Jianwei (2005). "Regulation of cortactin/dynamin interaction by actin polymerization during the fission of clathrin-coated pits". Journal of Cell Science. 118: 807–817. {{cite journal}}: Cite has empty unknown parameter: |month= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)

See also

• actin
• gelsolin
• transferrin
• villin

External links

• Cortactin at the U.S. National Library of Medicine Medical Subject Headings (MeSH)