An MEK-cofilin signalling module controls migration of human T cells in 3D but not 2D environments

T cells infiltrate peripheral tissues to execute immunosurveillance and effector functions. For this purpose, T cells first migrate on the two-dimensional (2D) surface of endothelial cells to undergo transendothelial migration. Then they change their mode of movement to undergo migration within the...

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Hauptverfasser: Klemke, Martin (VerfasserIn) , Kramer, Elisabeth (VerfasserIn) , Konstandin, Mathias (VerfasserIn) , Wabnitz, Guido H. (VerfasserIn) , Samstag, Yvonne (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 30 July 2010
In: The EMBO journal
Year: 2010, Jahrgang: 29, Heft: 17, Pages: 2915-2929
ISSN:1460-2075
DOI:10.1038/emboj.2010.153
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1038/emboj.2010.153
Verlag, lizenzpflichtig, Volltext: https://www.embopress.org/doi/full/10.1038/emboj.2010.153
Volltext
Verfasserangaben:Martin Klemke, Elisabeth Kramer, Mathias H Konstandin, Guido H Wabnitz and Yvonne Samstag

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520 |a T cells infiltrate peripheral tissues to execute immunosurveillance and effector functions. For this purpose, T cells first migrate on the two-dimensional (2D) surface of endothelial cells to undergo transendothelial migration. Then they change their mode of movement to undergo migration within the three-dimensional (3D)-extracellular matrix of the infiltrated tissue. As yet, no molecular mechanisms are known, which control migration exclusively in either 2D or 3D environments. Here, we describe a signalling module that controls T-cell chemotaxis specifically in 3D environments. In chemotaxing T cells, Ras activity is spatially restricted to the lamellipodium. There, Ras initiates activation of MEK, which in turn inhibits LIM-kinase 1 activity, thereby allowing dephosphorylation of the F-actin-remodelling protein cofilin. Interference with this MEK-cofilin module by either inhibition of MEK or by knockdown of cofilin reduces speed and directionality of chemotactic migration in 3D-extracellular matrices, but not on 2D substrates. This MEK-cofilin module may have an important function in the tissue positioning of T cells during an immune response. 
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