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  The regulatory role of cell mechanics for migration of differentiating myeloid cells

Lautenschläger, F., Paschke, S., Schinkinger, S., Bruel, A., Beil, M., & Guck, J. (2009). The regulatory role of cell mechanics for migration of differentiating myeloid cells. Proceedings of the National Academy of Sciences (PNAS), 106(37), 15696-15701. doi:10.1073/pnas.0811261106.

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Lautenschläger, Franziska1, Autor
Paschke, Stephan1, Autor
Schinkinger, Stefan1, Autor
Bruel, Arlette1, Autor
Beil, Michael1, Autor
Guck, Jochen2, 3, 4, Autor           
Affiliations:
1External, ou_persistent22              
2Guck Division, Max Planck Institute for the Science of Light, Max Planck Society, ou_3164416              
3Max-Planck-Zentrum für Physik und Medizin, Max Planck Institute for the Science of Light, Max Planck Society, ou_3164414              
4Friedrich-Alexander-Universität Erlangen-Nürnberg, Department Physik, ou_persistent22              

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 Zusammenfassung: Migration of cells is important for tissue maintenance, immune response, and often altered in disease. While biochemical aspects, including cell adhesion, have been studied in detail, much less is known about the role of the mechanical properties of cells. Previous measurement methods rely on contact with artificial surfaces, which can convolute the results. Here, we used a non-contact, microfluidic optical stretcher to study cell mechanics, isolated from other parameters, in the context of tissue infiltration by acute promyelocytic leukemia (APL) cells, which occurs during differentiation therapy with retinoic acid. Compliance measurements of APL cells reveal a significant softening during differentiation, with the mechanical properties of differentiated cells resembling those of normal neutrophils. To interfere with the migratory ability acquired with the softening, differentiated APL cells were exposed to paclitaxel, which stabilizes microtubules. This treatment does not alter compliance but reduces cell relaxation after cessation of mechanical stress six-fold, congruent with a significant reduction of motility. Our observations imply that the dynamical remodeling of cell shape required for tissue infiltration can be frustrated by stiffening the microtubular system. This link between the cytokeleton, cell mechanics, and motility suggests treatment options for pathologies relying on migration of cells, notably cancer metastasis.

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 Datum: 2009-09-15
 Publikationsstatus: Erschienen
 Seiten: 6
 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1073/pnas.0811261106
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Titel: Proceedings of the National Academy of Sciences (PNAS)
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Washington D.C. : National Academy of Sciences (NAS) USA
Seiten: 6 Band / Heft: 106 (37) Artikelnummer: - Start- / Endseite: 15696 - 15701 Identifikator: -