Towards a Novel Patch Material for Cardiac Applications: Tissue-Specific Extracellular Matrix Introduces Essential Key Features to Decellularized Amniotic Membrane

被引:38
作者
Becker, Matthias [1 ,2 ]
Maring, Janita A. [1 ,2 ]
Schneider, Maria [1 ,2 ]
Martin, Aaron X. Herrera [1 ,3 ]
Seifert, Martina [1 ,2 ]
Klein, Oliver [1 ,2 ]
Braun, Thorsten [4 ]
Falk, Volkmar [2 ,5 ,6 ]
Stamm, Christof [1 ,2 ,5 ,6 ]
机构
[1] Humboldt Univ, Freie Univ Berlin, Charite Univ Med Berlin, D-13353 Berlin, Germany
[2] Berlin Brandenburg Ctr Regenerat Therapies BCRT, D-13353 Berlin, Germany
[3] Julius Wolff Inst Biomech & Musculoskeletal Regen, D-13353 Berlin, Germany
[4] Charite Med Univ, Dept Obstet & Gynecol, D-13353 Berlin, Germany
[5] German Ctr Cardiovasc Res DZHK, Partner Site Berlin, D-13316 Berlin, Germany
[6] Deutsch Herzzentrum Berlin DHZB, Augustenburger Pl 1, D-13353 Berlin, Germany
关键词
extracellular matrix; hydrogel; cardioprotection; patch; epicardium; amnion; immunocompatibility; PLURIPOTENT STEM-CELLS; HEART REGENERATION; ECM HYDROGEL; CARDIOMYOCYTES; PROMOTES; DELIVERY; DIFFERENTIATION; POLARIZATION; PLATFORM; SCAFFOLD;
D O I
10.3390/ijms19041032
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
There is a growing need for scaffold material with tissue-specific bioactivity for use in regenerative medicine, tissue engineering, and for surgical repair of structural defects. We developed a novel composite biomaterial by processing human cardiac extracellular matrix (ECM) into a hydrogel and combining it with cell-free amniotic membrane via a dry-coating procedure. Cardiac biocompatibility and immunogenicity were tested in vitro using human cardiac fibroblasts, epicardial progenitor cells, murine HL-1 cells, and human immune cells derived from buffy coat. Processing of the ECM preserved important matrix proteins as demonstrated by mass spectrometry. ECM coating did not alter the mechanical characteristics of decellularized amniotic membrane but did cause a clear increase in adhesion capacity, cell proliferation and viability. Activated monocytes secreted less pro-inflammatory cytokines, and both macrophage polarization towards the pro-inflammatory M1 type and T cell proliferation were prevented. We conclude that the incorporation of human cardiac ECM hydrogel shifts and enhances the bioactivity of decellularized amniotic membrane, facilitating its use in future cardiac applications.
引用
收藏
页数:20
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