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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Main Authors: Timo Aberle, Katrin Franke, Elke Rist, Karin Benz, Burkhard Schlosshauer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24475174/?tool=EBI
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spelling 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
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AT katrinfranke celltypespecificfourcomponenthydrogel
AT elkerist celltypespecificfourcomponenthydrogel
AT karinbenz celltypespecificfourcomponenthydrogel
AT burkhardschlosshauer celltypespecificfourcomponenthydrogel
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