Source:http://linkedlifedata.com/resource/pubmed/id/21247629
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2011-2-1
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pubmed:abstractText |
Synthetic hydrogels with tunable properties are appealing for regenerative medicine. A critical limitation in hydrogel design at low solids concentration is the formation of defects, which increase gelation times and swelling, and reduce elasticity. Here, we report that trifunctional cross-linking peptides applied to 4-arm poly-(ethylene glycol) (PEG) hydrogels decreased swelling and gelation time relative to bi-functional crosslinkers. In contrast to bi-functional peptides, the third cross-linking site on the peptide created a branch point if an intramolecular cross-link formed, which prevented non-functional "dangling-ends" in the hydrogel network and enhanced the number of elastically active cross-links. The improved network formation enabled mouse ovarian follicle encapsulation and maturation in vitro. Hydrogels with bi-functional crosslinkers resulted in cellular dehydration, likely due to osmosis during the prolonged gelation. For trifunctional crosslinkers, the hydrogels supported a 17-fold volumetric expansion of the tissue during culture, with expansion dependent on the ability of the follicle to rearrange its microenvironment, which is controlled through the sensitivity of the cross-linking peptide to the proteolytic activity of plasmin. The improved network design enabled ovarian follicle culture in a completely synthetic system, and can advance fertility preservation technology for women facing premature infertility from anticancer therapies.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/PL1 EB008542-04,
http://linkedlifedata.com/resource/pubmed/grant/PL1EB008542,
http://linkedlifedata.com/resource/pubmed/grant/T32 GM008449-17,
http://linkedlifedata.com/resource/pubmed/grant/U54 HD041857-08,
http://linkedlifedata.com/resource/pubmed/grant/U54HD41857
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1878-5905
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2524-31
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pubmed:dateRevised |
2011-6-14
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pubmed:meshHeading |
pubmed-meshheading:21247629-Animals,
pubmed-meshheading:21247629-Female,
pubmed-meshheading:21247629-Hydrogel,
pubmed-meshheading:21247629-Mice,
pubmed-meshheading:21247629-Mice, Inbred C57BL,
pubmed-meshheading:21247629-Osmotic Pressure,
pubmed-meshheading:21247629-Ovarian Follicle,
pubmed-meshheading:21247629-Tissue Culture Techniques,
pubmed-meshheading:21247629-Tissue Engineering,
pubmed-meshheading:21247629-Tissue Survival
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pubmed:year |
2011
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pubmed:articleTitle |
Hydrogel network design using multifunctional macromers to coordinate tissue maturation in ovarian follicle culture.
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pubmed:affiliation |
Department of Chemical and Biological Engineering, Northwestern University, 2170 Campus Dr, 3619 Silverman Hall, Evanston, IL 60208, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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