Multifunctional biomimetic hydrogel systems to boost the immunomodulatory potential of mesenchymal stromal cells

被引:53
作者
Gonzalez-Pujana, Ainhoa [1 ,2 ]
Vining, Kyle H. [3 ,4 ]
Zhang, David K. Y. [3 ,4 ]
Santos-Vizcaino, Edorta [1 ,2 ]
Igartua, Manoli [1 ,2 ]
Maria Hernandez, Rosa [1 ,2 ]
Mooney, David J. [3 ,4 ]
机构
[1] Univ Basque Country, UPV EHU, Sch Pharm, NanoBioCel Grp,Lab Pharmaceut, Vitoria, Spain
[2] Biomed Res Networking Ctr Bioengn Biomat & Nanome, Vitoria, Spain
[3] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[4] Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
MSCs; Immunomodulation; Interferon; Extracellular matrix; Hydrogel; Alginate; INTERFERON-GAMMA; STEM-CELLS; INDOLEAMINE 2,3-DIOXYGENASE; CHRONIC INFLAMMATION; DENDRITIC CELLS; SUPPRESSION; PROSTAGLANDIN-E2; PROLIFERATION; MACROPHAGES; SPHEROIDS;
D O I
10.1016/j.biomaterials.2020.120266
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Mesenchymal stromal cells (MSCs) hold great therapeutic potential, in part because of their immunomodulatory properties. However, these properties can be transient and depend on multiple factors. Here, we developed a multifunctional hydrogel system to synergistically enhance the immunomodulatory properties of MSCs, using a combination of sustained inflammatory licensing and three-dimensional (3D) encapsulation in hydrogels with tunable mechanical properties. The immunomodulatory extracellular matrix hydrogels (iECM) consist of an interpenetrating network of click functionalized-alginate and fibrillar collagen, in which interferon gamma (IFN-gamma) loaded heparin-coated beads are incorporated. The 3D microenvironment significantly enhanced the expression of a wide panel of pivotal immunomodulatory genes in bone marrow-derived primary human MSCs (hMSCs), compared to two-dimensional (2D) tissue culture. Moreover, the inclusion of IFN-gamma loaded heparin-coated beads prolonged the expression of key regulatory genes upregulated upon licensing, including indoleamine 2,3-dioxygenase 1 (IDO1) and galectin-9 (GAL9). At a protein level, iECM hydrogels enhanced the secretion of the licensing responsive factor Gal-9 by hMSCs. Its presence in hydrogel conditioned media confirmed the correct release and diffusion of the factors secreted by hMSCs from the system. Furthermore, co-culture of iECMencapsulated hMSCs and activated human T cells resulted in suppressed proliferation, demonstrating direct regulation on immune cells. These data highlight the potential of iECM hydrogels to enhance the immunomodulatory properties of hMSCs in cell therapies.
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页数:12
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