Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT
Zur Ablage hinzufügen
  Lokale TagsFreigabegeschichteDetailsÜbersicht

Freigegeben
Zeitschriftenartikel

Differential adhesion of fibroblast and neuroblastoma cells on size- and geometry-controlled nanofibrils of the extracellular matrix

MPG-Autoren
/persons/resource/persons75646

Kaiser,  Peter
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons76135

Spatz,  Joachim P.
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;
Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany;

Externe Ressourcen

http://pubs.rsc.org/en/content/articlepdf/2010/sm/b911461k
(beliebiger Volltext)

https://dx.doi.org/10.1039/B911461K
(beliebiger Volltext)

Volltexte (beschränkter Zugriff)
Für Ihren IP-Bereich sind aktuell keine Volltexte freigegeben.
Volltexte (frei zugänglich)
Es sind keine frei zugänglichen Volltexte in PuRe verfügbar
Ergänzendes Material (frei zugänglich)
Es sind keine frei zugänglichen Ergänzenden Materialien verfügbar
Zitation

Kaiser, P., & Spatz, J. P. (2010). Differential adhesion of fibroblast and neuroblastoma cells on size- and geometry-controlled nanofibrils of the extracellular matrix. Soft Matter, 6(1), 113-119. doi:10.1039/b911461k.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0010-3B42-5
Zusammenfassung
We present a universal method to produce highly regular arrays of nanofibrils constituted by the extracellular matrix (ECM) proteins fibronectin (FN), collagen I (COL I) and EHS laminin (EHS LN). Adjusting the de-wetting parameters of a protein solution on a hydrophobic silicon micropillar structure, we control the mean nanofibril diameter between 20 nm and 160 nm. Array geometry predetermines nanofibril diameter, while protein concentration and de-wetting speed have to be adapted to yield high regularity. ECM nanofibrils span the space between adjacent pillars and immunofluorescence labelling of LN and FN nanofibrils allows us to discriminate both species in mixed networks. The biological function of ECM nanofibrils was verified in cell adhesion experiments after transfer of the nanofibrils onto non-adhesive polyethylene glycol (PEG) hydrogels. Co-cultures of fibroblasts and neuroblastoma cells on vertically arranged nanofibrils of FN and LN showed differential adhesion of the distinct cell types.