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Sci. STKE, 10 July 2007
Vol. 2007, Issue 394, p. tw242
[DOI: 10.1126/stke.3942007tw242]


Cell Migration Numb Cells Keep Moving

John F. Foley

Science’s STKE, AAAS, Washington, DC 20005, USA

Integrins are heterodimeric transmembrane receptors that bind to components of the extracellular matrix and are important for both cellular adhesion and migration. Clustering of activated integrins on the substrate-facing surface of the leading edge of a cell results in the recruitment of various proteins, including actin stress fibers, to form a focal adhesion complex (FAC). Cells migrate, in part, through the coordinated assembly of focal adhesions at the leading edge of a cell and the disassembly of such complexes at the rear of the cell. Integrins are thought to move from the rear of the cell to the front through recycling endosomes, although the mechanisms that mediate internalization of integrins are not fully understood. Numb is a cargo-specific adaptor protein that binds to several endocytic proteins and is perhaps best known for its role in down-regulating the signaling of Notch, a transmembrane receptor that affects cellular proliferation and differentiation. Nishimura et al. previously demonstrated that Numb localizes to the tips of growing axons in cultures of hippocampal neurons and that it plays a role in the internalization of the adhesion molecule L1, so they investigated a role for Numb in mediating integrin endocytosis and cell migration. The authors used immunohistochemistry to demonstrate the colocalization of Numb with clathrin-coated structures in various endothelial and epithelial cell cultures. Analysis of green fluorescent protein (GFP) fusions of wild-type and mutant Numb proteins showed that the {alpha}-adaptin-binding motif was necessary for the interaction of Numb with clathrin-coated structures. In a monolayer wounding assay, Numb polarized toward the leading edge of migrating cells (just behind the lamellipodium). Numb localized around focal adhesions, and this association was inhibited by disruption of polymerized actin (F-actin). Immunostaining demonstrated the colocalization of Numb and beta1-integrin at focal adhesions, and recombinant Numb protein coprecipitated beta1- and beta3-integrin but not other components of FACs. Depletion of Numb by siRNA reduced the number of beta1-integrin-positive endosomes in migrating HeLa cells and also markedly reduced the number of HeLa cells that migrated toward integrin ligands compared with control siRNA-treated HeLa cells. Coimmunoprecipitation experiments revealed that Numb bound to the PAR (for partitioning defective) polarization complex, PAR-3. This complex localizes to the leading edge of polarized migrating cells. One component of this complex, atypical protein kinase C (aPKC) phosphorylated Numb in vitro and in HeLa cells and, as a consequence, Numb no longer bound to integrins. The authors propose a model in which Numb binds to free integrin molecules (rather than disrupting FACs) and recruits them to clathrin-coated structures to initiate integrin recycling, and that the localization and function of Numb are negatively regulated by aPKC.

T. Nishimura, K. Kaibuchi, Numb controls integrin endocytosis for directional cell migration with aPKC and PAR-3. Dev. Cell 13, 15-28 (2007). [PubMed]

Citation: J. F. Foley, Numb Cells Keep Moving. Sci. STKE 2007, tw242 (2007).

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