4.8 Article

In Situ Crosslinkable Gelatin Hydrogels for Vasculogenic Induction and Delivery of Mesenchymal Stem Cells

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 24, Issue 43, Pages 6771-6781

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201401110

Keywords

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Funding

  1. NSF DMR 1006558NSF CAREER CBET 1056046
  2. National Research Foundation of Korea - Ministry of Science
  3. ICT & Future Planning [NRF-2012R1A2A2A06046885]
  4. NIH [1S10RR027485-01, CA68485, DK20593, DK58404, HD15052, DK59637, EY08126]
  5. [NIH HL091465]
  6. [NIH 1UH2 TR000491]

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Clinical trials utilizing mesenchymal stem cells (MSCs) for severe vascular diseases have highlighted the need to effectively engraft cells and promote pro-angiogenic activity. A functional material accomplishing these two goals is an ideal solution as spatiotemporal and batch-to-batch variability in classical therapeutic delivery can be minimized, and tissue regeneration would begin rapidly at the implantation site. Gelatin may serve as a promising biomaterial due to its excellent biocompatibility, biodegradability, and non-immuno/antigenicity. However, the dissolution of gelatin at body temperature and quick enzymatic degradation in vivo have limited its use thus far. To overcome these challenges, an injectable, in situ crosslinkable gelatin was developed by conjugating enzymatically crosslinkable hydroxyphenyl propionic acid (GHPA). When MSCs are cultured in 3D in vitro or injected in vivo in GHPA, spontaneous endothelial differentiation occurs, as evidenced by marked increases in endothlelial cell marker expressions (Flk1, Tie2, ANGPT1, vWF) in addition to forming an extensive perfusable vascular network after 2-week subcutaneous implantation. Additionally, favorable host macrophage response is achieved with GHPA as shown by decreased iNOS and increased MRC1 expression. These results indicate GHPA as a promising soluble factor-free cell delivery template which induces endothelial differentiation of MSCs with robust neovasculature formation and favorable host response.

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