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Hydration of hydrogels regulates vascularization in vivo

Abstract

The key barrier to clinical applications of tissue engineering scaffolds is the limitation of rapid and sufficient vascularization. Adipose-derived stem cells (ASCs), especially multicellular aggregates, exhibited a promising angiogenic activity. Herein, we designed a series of poly(L-glutamic acid) (PLGA)-based hydrogels with tunable hydration to control in situ formation of multicellular spheroids. Oligo(ethylene glycol)s (OEGs) were employed to regulate the hydration of hydrogels. The hydrogel cross-linked with ethylene glycol (OEG1) supported the most excellent adhesion and proliferation of human ASCs in vitro. However, the adherent ASCs were gradually replaced with multicellular spheroids in higher hydration of hydrogels. Moreover, the in situ formation of spheroids was more effective to upregulate hypoxia-adaptive signals (e.g., hypoxia-inducible factor-1α, HIF-1α) and enhance secretion of angiogenic factors (e.g., vascular endothelial growth and factor (VEGF) and fibroblast growth factor 2 (FGF-2)) compared to adherent cells in OEG1 hydrogels. The hydrogel cross-linked with oligo(ethylene glycol)400 (OEG9) carrying spheroids induced a high angiogenic response of host tissue in vivo, resulting in an improved system vascularization, compared to adherent cells in OEG1 hydrogel. These features indicated that the PLGA-based hydrogels were expected to be applied toward bone and fat tissue regeneration.

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Publication details

The article was received on 28 Mar 2017, accepted on 31 Aug 2017 and first published on 07 Sep 2017


Article type: Paper
DOI: 10.1039/C7BM00268H
Citation: Biomater. Sci., 2017, Accepted Manuscript
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    Hydration of hydrogels regulates vascularization in vivo

    J. Wu, K. Zhang, X. Yu, J. Ding, L. Cui and J. Yin, Biomater. Sci., 2017, Accepted Manuscript , DOI: 10.1039/C7BM00268H

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