Combination scaffolds of salmon fibrin, hyaluronic acid, and laminin for human neural stem cell and vascular tissue engineering

被引:125
作者
Arulmoli, Janahan [1 ,2 ]
Wright, Heather J. [2 ,3 ]
Phan, Duc T. T. [3 ]
Sheth, Urmi [2 ]
Que, Richard A. [1 ]
Botten, Giovanni A. [4 ]
Keating, Mark [1 ]
Botvinick, Elliot L. [1 ,8 ]
Pathak, Medha M. [2 ,5 ]
Zarembinski, Thomas I. [6 ]
Yanni, Daniel S. [7 ]
Razorenova, Olga V. [2 ,3 ]
Hughes, Christopher C. W. [1 ,3 ,8 ]
Flanagan, Lisa A. [1 ,2 ,9 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Sue & Bill Gross Stem Cell Res Ctr, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[4] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[5] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92697 USA
[6] BioTime Inc, 1301 Harbor Pkwy, Alameda, CA 94502 USA
[7] Disc Comfort Inc, 351 Hosp Rd,Suite 202, Newport Beach, CA 92663 USA
[8] Univ Calif Irvine, Edwards Lifesci Ctr Adv Cardiovasc Technol, Irvine, CA 92697 USA
[9] Univ Calif Irvine, Dept Neurol, 3030 Gross Hall,845 Hlth Sci Rd, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
Neural stem cell; Biomaterial scaffold; Hydrogel; Neural tissue engineering; Integrin; Co-culture; Salmon fibrin; Hyaluronic acid; Laminin; Neurovascular niche; Matrix mechanics; ENDOTHELIAL GROWTH-FACTOR; SPINAL-CORD-INJURY; PROGENITOR CELLS; EXTRACELLULAR-MATRIX; IN-VITRO; NEURONAL DIFFERENTIATION; ARTICULAR-CARTILAGE; NEURITE OUTGROWTH; HOST VASCULATURE; PRECURSOR CELLS;
D O I
10.1016/j.actbio.2016.07.043
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
Human neural stem/progenitor cells (hNSPCs) are good candidates for treating central nervous system (CNS) trauma since they secrete beneficial trophic factors and differentiate into mature CNS cells; however, many cells die after transplantation. This cell death can be ameliorated by inclusion of a biomaterial scaffold, making identification of optimal scaffolds for hNSPCs a critical research focus. We investigated the properties of fibrin-based scaffolds and their effects on hNSPCs and found that fibrin generated from salmon fibrinogen and thrombin stimulates greater hNSPC proliferation than mammalian fibrin. Fibrin scaffolds degrade over the course of a few days in vivo, so we sought to develop a novel scaffold that would retain the beneficial properties of fibrin but degrade more slowly to provide longer support for hNSPCs. We found combination scaffolds of salmon fibrin with interpenetrating networks (IPNs) of hyaluronic acid (HA) with and without laminin polymerize more effectively than fibrin alone and generate compliant hydrogels matching the physical properties of brain tissue. Furthermore, combination scaffolds support hNSPC proliferation and differentiation while significantly attenuating the cell-mediated degradation seen with fibrin alone. HNSPCs express two fibrinogen-binding integrins, alpha V beta 1 and alpha 5 beta 1, and several laminin binding integrins (alpha 7 beta 1, alpha 6 beta 1, alpha 3 beta 1) that can mediate interaction with the scaffold. Lastly, to test the ability of scaffolds to support vascularization, we analyzed human cord blood-derived endothelial cells alone and in co-culture with hNSPCs and found enhanced vessel formation and complexity in co-cultures within combination scaffolds. Overall, combination scaffolds of fibrin, HA, and laminin are excellent biomaterials for hNSPCs. Statement of Significance Interest has increased recently in the development of biomaterials as neural stem cell transplantation scaffolds to treat central nervous system (CNS) injury since scaffolds improve survival and integration of transplanted cells. We report here on a novel combination scaffold composed of fibrin, hyaluronic acid, and laminin to support human neural stem/progenitor cell (hNSPC) function. This combined biomaterial scaffold has appropriate physical properties for hNSPCs and the CNS, supports hNSPC proliferation and differentiation, and attenuates rapid cell-mediated scaffold degradation. The hNSPCs and scaffold components synergistically encourage new vessel formation from human endothelial cells. This work marks the first report of a combination scaffold supporting human neural and vascular cells to encourage vasculogenesis, and sets a benchmark for biomaterials to treat CNS injury. (C) 2016 Acta Materialia Inc. Published by Elsevier Ltd.
引用
收藏
页码:122 / 138
页数:17
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