In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells
Gelatin is a hydrolyzed and denatured form of collagen, which comprises the majority of extracellular matrix. Despite its numerous advantages for tissue engineering, its use as a thermostable hydrogel has been achieved only recently by conjugating hydroxyphenyl propionic acid to the gelatin backbone...
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ndltd-VANDERBILT-oai-VANDERBILTETD-etd-12062013-1525512013-12-13T05:05:21Z In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells Lee, Sue Hyun Biomedical Engineering Gelatin is a hydrolyzed and denatured form of collagen, which comprises the majority of extracellular matrix. Despite its numerous advantages for tissue engineering, its use as a thermostable hydrogel has been achieved only recently by conjugating hydroxyphenyl propionic acid to the gelatin backbone, resulting in injectable in situ crosslinking hydrogels through a H2O2- and peroxidase-mediated reaction. Gelatin hydrogels gelled rapidly, and exhibited excellent biocompatibility in vitro where mesenchymal stem cells (MSCs) were encapsulated over 15 days. Furthermore, MSCs organized into tubular network and differentiated into an endothelial lineage purely by material effects. Finally, 2-week long subcutaneous implantation of gelatin hydrogels delivering MSCs in vivo confirmed the vasculogenic and angiogenic effect where implanted MSCs expressed Flk-1, an endothelial cell marker, and increased blood vessel formation was observed via microangiography. Histology showed no fibrous capsule formation around the gelatin hydrogel, and qPCR also confirmed favorable host macrophage responses by up-regulating MRC1, a reparative/regenerative macrophage marker, and down-regulating iNOS, an inflammatory macrophage marker. Based on these observations, we conclude that injectable in situ crosslinking gelatin hydrogel is a promising biomaterial for tissue engineering/regenerative medicine where robust angiogenesis and favorable host immune response are required. Pampee Young Hak-Joon Sung VANDERBILT 2013-12-12 text application/pdf http://etd.library.vanderbilt.edu/available/etd-12062013-152551/ http://etd.library.vanderbilt.edu/available/etd-12062013-152551/ en restrictone I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Vanderbilt University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
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Biomedical Engineering Lee, Sue Hyun In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells |
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Gelatin is a hydrolyzed and denatured form of collagen, which comprises the majority of extracellular matrix. Despite its numerous advantages for tissue engineering, its use as a thermostable hydrogel has been achieved only recently by conjugating hydroxyphenyl propionic acid to the gelatin backbone, resulting in injectable in situ crosslinking hydrogels through a H2O2- and peroxidase-mediated reaction. Gelatin hydrogels gelled rapidly, and exhibited excellent biocompatibility in vitro where mesenchymal stem cells (MSCs) were encapsulated over 15 days. Furthermore, MSCs organized into tubular network and differentiated into an endothelial lineage purely by material effects. Finally, 2-week long subcutaneous implantation of gelatin hydrogels delivering MSCs in vivo confirmed the vasculogenic and angiogenic effect where implanted MSCs expressed Flk-1, an endothelial cell marker, and increased blood vessel formation was observed via microangiography. Histology showed no fibrous capsule formation around the gelatin hydrogel, and qPCR also confirmed favorable host macrophage responses by up-regulating MRC1, a reparative/regenerative macrophage marker, and down-regulating iNOS, an inflammatory macrophage marker. Based on these observations, we conclude that injectable in situ crosslinking gelatin hydrogel is a promising biomaterial for tissue engineering/regenerative medicine where robust angiogenesis and favorable host immune response are required. |
author2 |
Pampee Young |
author_facet |
Pampee Young Lee, Sue Hyun |
author |
Lee, Sue Hyun |
author_sort |
Lee, Sue Hyun |
title |
In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells |
title_short |
In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells |
title_full |
In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells |
title_fullStr |
In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells |
title_full_unstemmed |
In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells |
title_sort |
in situ crosslinkable gelatin hydrogels for vasculogenic delivery of mesenchymal stem cells |
publisher |
VANDERBILT |
publishDate |
2013 |
url |
http://etd.library.vanderbilt.edu/available/etd-12062013-152551/ |
work_keys_str_mv |
AT leesuehyun insitucrosslinkablegelatinhydrogelsforvasculogenicdeliveryofmesenchymalstemcells |
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