%0 Journal Article %1 mosiewicz2013manipulation %A Mosiewicz, Katarzyna A. %A Kolb, Laura %A van der Vlies, André J. %A Martino, Mikaël M. %A Lienemann, Philipp S. %A Hubbell, Jeffrey A. %A Ehrbar, Martin %A Lutolf, Matthias P. %D 2013 %I Nature Publishing Group %J Nat Mater %K hydrogel migration phd stemcell %N 11 %P 1072--1078 %T In situ cell manipulation through enzymatic hydrogel photopatterning %U http://dx.doi.org/10.1038/nmat3766 %V 12 %X The physicochemical properties of hydrogels can be manipulated in both space and time through the controlled application of a light beam. However, methods for hydrogel photopatterning either fail to maintain the bioactivity of fragile proteins and are thus limited to short peptides, or have been used in hydrogels that often do not support three-dimensional (3D) cell growth. Here, we show that the 3D invasion of primary human mesenchymal stem cells can be spatiotemporally controlled by micropatterning the hydrogel with desired extracellular matrix (ECM) proteins and growth factors. A peptide substrate of activated transglutaminase factor XIII (FXIIIa)—a key ECM crosslinking enzyme—is rendered photosensitive by masking its active site with a photolabile cage group. Covalent incorporation of the caged FXIIIa substrate into poly(ethylene glycol) hydrogels and subsequent laser-scanning lithography affords highly localized biomolecule tethering. This approach for the 3D manipulation of cells within gels should open up avenues for the study and manipulation of cell signalling.

@article{mosiewicz2013manipulation, abstract = {The physicochemical properties of hydrogels can be manipulated in both space and time through the controlled application of a light beam. However, methods for hydrogel photopatterning either fail to maintain the bioactivity of fragile proteins and are thus limited to short peptides, or have been used in hydrogels that often do not support three-dimensional (3D) cell growth. Here, we show that the 3D invasion of primary human mesenchymal stem cells can be spatiotemporally controlled by micropatterning the hydrogel with desired extracellular matrix (ECM) proteins and growth factors. A peptide substrate of activated transglutaminase factor XIII (FXIIIa)—a key ECM crosslinking enzyme—is rendered photosensitive by masking its active site with a photolabile cage group. Covalent incorporation of the caged FXIIIa substrate into poly(ethylene glycol) hydrogels and subsequent laser-scanning lithography affords highly localized biomolecule tethering. This approach for the 3D manipulation of cells within gels should open up avenues for the study and manipulation of cell signalling.}, added-at = {2015-07-31T13:17:30.000+0200}, author = {Mosiewicz, Katarzyna A. and Kolb, Laura and van der Vlies, André J. and Martino, Mikaël M. and Lienemann, Philipp S. and Hubbell, Jeffrey A. and Ehrbar, Martin and Lutolf, Matthias P.}, biburl = {https://www.bibsonomy.org/bibtex/2c46842be823682412c2feb6f55f081ab/bkoch}, description = {In situ cell manipulation through enzymatic hydrogel photopatterning : Nature Materials : Nature Publishing Group}, interhash = {0e91229fcfe8f23dbd610562844f9e06}, intrahash = {c46842be823682412c2feb6f55f081ab}, issn = {14761122}, journal = {Nat Mater}, keywords = {hydrogel migration phd stemcell}, month = nov, number = 11, pages = {1072--1078}, publisher = {Nature Publishing Group}, timestamp = {2015-07-31T13:17:30.000+0200}, title = {In situ cell manipulation through enzymatic hydrogel photopatterning}, url = {http://dx.doi.org/10.1038/nmat3766}, volume = 12, year = 2013 }