Enhanced survival and engraftment of transplanted stem cells using growth factor sequestering hydrogels

被引:96
作者
Jha, Amit K. [1 ,2 ]
Tharp, Kevin M. [3 ]
Ye, Jianqin [4 ]
Santiago-Ortiz, Jorge L. [5 ]
Jackson, Wesley M. [1 ]
Stahl, Andreas [3 ]
Schaffer, David V. [1 ,5 ]
Yeghiazarians, Yerem [4 ,6 ,7 ]
Healy, Kevin E. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Nutr Sci & Toxicol, Berkeley, CA 94720 USA
[4] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[5] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[6] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
[7] Univ Calif San Francisco, Inst Cardiovasc Res, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
Stem cell transplantation; Hyaluronic acid hydrogel; Growth factor sequestration; Neovascularization; Heparin; TGF beta 1; CONTROLLED-RELEASE; IN-VIVO; FIBRIN MATRICES; DELIVERY; DIFFERENTIATION; CARDIOMYOCYTES; TGF-BETA-1; MIGRATION; REPAIR; ASSAY;
D O I
10.1016/j.biomaterials.2014.12.043
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
We have generated a bioinspired tunable system of hyaluronic acid (HyA)-based hydrogels for Matrix-Assisted Cell Transplantation (MACT). With this material, we have independently evaluated matrix parameters such as adhesion peptide density, mechanical properties, and growth factor sequestering capacity, to engineer an environment that imbues donor cells with a milieu that promotes survival and engraftment with host tissues after transplantation. Using a versatile population of Sca-1(+)/CD45(-) cardiac progenitor cells (CPCs), we demonstrated that the addition of heparin in the HyA hydrogels was necessary to coordinate the presentation of TGF beta 1 and to support the trophic functions of the CPCs via endothelial cell differentiation and vascular like tubular network formation. Presentation of exogenous TGF beta 1 by binding with heparin improved differentiated CPC function by sequestering additional endogenously-produced angiogenic factors. Finally, we demonstrated that TGF beta 1 and heparin-containing HyA hydrogels can promote CPC survival when implanted subcutaneously into murine hind-limbs and encouraged their participation in the ensuing neovascular response, which included blood vessels that had anastomosed with the host's blood vessels. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 12
页数:12
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