Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells

One of the most common regenerative therapies is autologous fat grafting, which frequently suffers from unexpected volume loss. One approach is to deliver adipose stem cells encapsulated in the engineered hydrogels supportive of cell survival, differentiation, and integration after transplant. We de...

Full description

Bibliographic Details
Main Authors: Tracy N Clevenger, Gabriel Luna, Daniel Boctor, Steven K Fisher, Dennis O Clegg
Format: Article
Language:English
Published: SAGE Publishing 2016-09-01
Series:Journal of Tissue Engineering
Online Access:https://doi.org/10.1177/2041731416670482
_version_ 1818441805605109760
author Tracy N Clevenger
Gabriel Luna
Daniel Boctor
Steven K Fisher
Dennis O Clegg
author_facet Tracy N Clevenger
Gabriel Luna
Daniel Boctor
Steven K Fisher
Dennis O Clegg
author_sort Tracy N Clevenger
collection DOAJ
description One of the most common regenerative therapies is autologous fat grafting, which frequently suffers from unexpected volume loss. One approach is to deliver adipose stem cells encapsulated in the engineered hydrogels supportive of cell survival, differentiation, and integration after transplant. We describe an encapsulating, biomimetic poly(ethylene)-glycol hydrogel, with embedded peptides for attachment and biodegradation. Poly(ethylene)-glycol hydrogels containing an Arg–Gly–Asp attachment sequence and a matrix metalloprotease 3/10 cleavage site supported adipose stem cell survival and showed remodeling initiated by adipogenic differentiation. Arg–Gly–Asp–matrix metalloprotease 3/10 cleavage site hydrogels showed an increased number and area of lacunae or holes after adipose stem cell differentiation. Image analysis of adipose stem cells in Arg–Gly–Asp–matrix metalloprotease 3/10 cleavage site hydrogels showed larger Voronoi domains, while cell density remained unchanged. The differentiated adipocytes residing within these newly remodeled spaces express proteins and messenger RNAs indicative of adipocytic differentiation. These engineered scaffolds may provide niches for stem cell differentiation and could prove useful in soft tissue regeneration.
first_indexed 2024-12-14T18:34:05Z
format Article
id doaj.art-68578eb8d79b4b28a3b5263e80479c01
institution Directory Open Access Journal
issn 2041-7314
language English
last_indexed 2024-12-14T18:34:05Z
publishDate 2016-09-01
publisher SAGE Publishing
record_format Article
series Journal of Tissue Engineering
spelling doaj.art-68578eb8d79b4b28a3b5263e80479c012022-12-21T22:51:40ZengSAGE PublishingJournal of Tissue Engineering2041-73142016-09-01710.1177/204173141667048210.1177_2041731416670482Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cellsTracy N Clevenger0Gabriel Luna1Daniel Boctor2Steven K Fisher3Dennis O Clegg4Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, CA, USACenter for Bio-Image Informatics, University of California, Santa Barbara, CA, USANeuroscience Research Institute, University of California, Santa Barbara, CA, USACenter for Bio-Image Informatics, University of California, Santa Barbara, CA, USADepartment of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, CA, USAOne of the most common regenerative therapies is autologous fat grafting, which frequently suffers from unexpected volume loss. One approach is to deliver adipose stem cells encapsulated in the engineered hydrogels supportive of cell survival, differentiation, and integration after transplant. We describe an encapsulating, biomimetic poly(ethylene)-glycol hydrogel, with embedded peptides for attachment and biodegradation. Poly(ethylene)-glycol hydrogels containing an Arg–Gly–Asp attachment sequence and a matrix metalloprotease 3/10 cleavage site supported adipose stem cell survival and showed remodeling initiated by adipogenic differentiation. Arg–Gly–Asp–matrix metalloprotease 3/10 cleavage site hydrogels showed an increased number and area of lacunae or holes after adipose stem cell differentiation. Image analysis of adipose stem cells in Arg–Gly–Asp–matrix metalloprotease 3/10 cleavage site hydrogels showed larger Voronoi domains, while cell density remained unchanged. The differentiated adipocytes residing within these newly remodeled spaces express proteins and messenger RNAs indicative of adipocytic differentiation. These engineered scaffolds may provide niches for stem cell differentiation and could prove useful in soft tissue regeneration.https://doi.org/10.1177/2041731416670482
spellingShingle Tracy N Clevenger
Gabriel Luna
Daniel Boctor
Steven K Fisher
Dennis O Clegg
Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells
Journal of Tissue Engineering
title Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells
title_full Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells
title_fullStr Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells
title_full_unstemmed Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells
title_short Cell-mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells
title_sort cell mediated remodeling of biomimetic encapsulating hydrogels triggered by adipogenic differentiation of adipose stem cells
url https://doi.org/10.1177/2041731416670482
work_keys_str_mv AT tracynclevenger cellmediatedremodelingofbiomimeticencapsulatinghydrogelstriggeredbyadipogenicdifferentiationofadiposestemcells
AT gabrielluna cellmediatedremodelingofbiomimeticencapsulatinghydrogelstriggeredbyadipogenicdifferentiationofadiposestemcells
AT danielboctor cellmediatedremodelingofbiomimeticencapsulatinghydrogelstriggeredbyadipogenicdifferentiationofadiposestemcells
AT stevenkfisher cellmediatedremodelingofbiomimeticencapsulatinghydrogelstriggeredbyadipogenicdifferentiationofadiposestemcells
AT dennisoclegg cellmediatedremodelingofbiomimeticencapsulatinghydrogelstriggeredbyadipogenicdifferentiationofadiposestemcells