Receptor-mediated gene delivery into human mesenchymal stem cells using hyaluronic acid-shielded polyethylenimine/pDNA nanogels

被引:38
作者
Park, Ji Sun [1 ]
Yi, Se Won [1 ]
Kim, Hye Jin [1 ]
Park, Keun-Hong [1 ]
机构
[1] CHA Univ, Dept Biomed Sci, Coll Life Sci, Songnam 463400, South Korea
基金
新加坡国家研究基金会;
关键词
PEI; Hyaluronic acid; hMSCs; CD44; SOX9; EXTRACELLULAR-MATRIX; MSC CHONDROGENESIS; PLGA NANOPARTICLES; BREAST-CANCER; HYDROGELS; DIFFERENTIATION; CD44; REGENERATION; ALGINATE; MODULATE;
D O I
10.1016/j.carbpol.2015.09.053
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Polyethylenimine (PEI) has been used as a vehicle to deliver genes to cancer cells and somatic cells. In this study, cationic polymers of PEI were shielded with anionic polymers of hyaluronic acid (HA) to safely and effectively deliver genes into human mesenchymal stem cells (hMSCs). HA interacted with CD44 in the plasma membranes of hMSCs to facilitate the internalization of HA-shielded PEI/pDNA complexes. The HA-shielded PEI/pDNA nanogels were confirmed by size changes, zeta-potential, and gel retardation assays. HA-shielded nanogels were easily internalized by hMSCs, and this was reduced by pretreatment with a specific monoclonal antibody that blocked CD44. By shielding PEI/pDNA complexes with HA, nanogels were easily internalized to hMSCs when it did not blocked by anti-CD44. These shielded nanogels were also easily internalized by HeLa cells, and this was reduced by pretreatment with an anti-CD44 monoclonal antibody. Following internalization of the SOX9 gene, chondrogenesis of hMSCs was increased, as determined by RT-PCR, real-time quantitative PCR, and histological analyses. (C) 2015 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:791 / 802
页数:12
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