Cell-type specific four-component hydrogel.
In the field of regenerative medicine we aim to develop implant matrices for specific tissue needs. By combining two per se, cell-permissive gel systems with enzymatic crosslinkers (gelatin/transglutaminase and fibrinogen/thrombin) to generate a blend (technical term: quattroGel), an unexpected cell...
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doaj-00ddbcb3a16d478685292aba7cf09baa2021-03-04T09:58:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8674010.1371/journal.pone.0086740Cell-type specific four-component hydrogel.Timo AberleKatrin FrankeElke RistKarin BenzBurkhard SchlosshauerIn the field of regenerative medicine we aim to develop implant matrices for specific tissue needs. By combining two per se, cell-permissive gel systems with enzymatic crosslinkers (gelatin/transglutaminase and fibrinogen/thrombin) to generate a blend (technical term: quattroGel), an unexpected cell-selectivity evolved. QuattroGels were porous and formed cavities in the cell diameter range, possessed gelation kinetics in the minute range, viscoelastic properties and a mechanical strength appropriate for general cell adhesion, and restricted diffusion. Cell proliferation of endothelial cells, chondrocytes and fibroblasts was essentially unaffected. In contrast, on quattroGels neither endothelial cells formed vascular tubes nor did primary neurons extend neurites in significant amounts. Only chondrocytes differentiated properly as judged by collagen isoform expression. The biophysical quattroGel characteristics appeared to leave distinct cell processes such as mitosis unaffected and favored differentiation of sessile cells, but hampered differentiation of migratory cells. This cell-type selectivity is of interest e.g. during articular cartilage or invertebral disc repair, where pathological innervation and angiogenesis represent adverse events in tissue engineering.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24475174/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Timo Aberle Katrin Franke Elke Rist Karin Benz Burkhard Schlosshauer |
spellingShingle |
Timo Aberle Katrin Franke Elke Rist Karin Benz Burkhard Schlosshauer Cell-type specific four-component hydrogel. PLoS ONE |
author_facet |
Timo Aberle Katrin Franke Elke Rist Karin Benz Burkhard Schlosshauer |
author_sort |
Timo Aberle |
title |
Cell-type specific four-component hydrogel. |
title_short |
Cell-type specific four-component hydrogel. |
title_full |
Cell-type specific four-component hydrogel. |
title_fullStr |
Cell-type specific four-component hydrogel. |
title_full_unstemmed |
Cell-type specific four-component hydrogel. |
title_sort |
cell-type specific four-component hydrogel. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2014-01-01 |
description |
In the field of regenerative medicine we aim to develop implant matrices for specific tissue needs. By combining two per se, cell-permissive gel systems with enzymatic crosslinkers (gelatin/transglutaminase and fibrinogen/thrombin) to generate a blend (technical term: quattroGel), an unexpected cell-selectivity evolved. QuattroGels were porous and formed cavities in the cell diameter range, possessed gelation kinetics in the minute range, viscoelastic properties and a mechanical strength appropriate for general cell adhesion, and restricted diffusion. Cell proliferation of endothelial cells, chondrocytes and fibroblasts was essentially unaffected. In contrast, on quattroGels neither endothelial cells formed vascular tubes nor did primary neurons extend neurites in significant amounts. Only chondrocytes differentiated properly as judged by collagen isoform expression. The biophysical quattroGel characteristics appeared to leave distinct cell processes such as mitosis unaffected and favored differentiation of sessile cells, but hampered differentiation of migratory cells. This cell-type selectivity is of interest e.g. during articular cartilage or invertebral disc repair, where pathological innervation and angiogenesis represent adverse events in tissue engineering. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24475174/?tool=EBI |
work_keys_str_mv |
AT timoaberle celltypespecificfourcomponenthydrogel AT katrinfranke celltypespecificfourcomponenthydrogel AT elkerist celltypespecificfourcomponenthydrogel AT karinbenz celltypespecificfourcomponenthydrogel AT burkhardschlosshauer celltypespecificfourcomponenthydrogel |
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