| Literature DB >> 29132248 |
Yukinobu Kodama1,2, Hiroki Hanamura2, Takahiro Muro1, Hiroo Nakagawa1, Tomoaki Kurosaki1, Tadahiro Nakamura1, Takashi Kitahara1, Shigeru Kawakami3, Mikiro Nakashima2, Hitoshi Sasaki1.
Abstract
Fetuin is a biocompatible plasma protein and strongly enhances phagocytosis of bacteria, DNA and apoptotic cells by peripheral blood cells such as monocytes, macrophages and dendritic cells. We developed a novel gene delivery system: ternary complexes constructed with pDNA, polyethylenimine (PEI) and fetuin. Without covalent binding, fetuin was able to coat pDNA-PEI complexes, and stable anionic nanoparticles formed at a weight ratio greater than 30. Optimised pDNA-PEI-fetuin complexes significantly decreased the cytotoxicity of pDNA-PEI complexes in the melanoma cell line B16F10. Furthermore, the pDNA-PEI-fetuin complexes had higher transgene efficiency compared to that of commercial lipofectin previously reported in B16F10 cells despite an anionic surface. The pDNA-PEI-fetuin complexes did not agglutinate with erythrocytes. The pDNA-PEI-fetuin complexes had high gene expression in the spleen after intravenous administration in mice. Thus, the pDNA-PEI-fetuin complexes were a useful in vivo gene delivery system with tropism for the spleen.Entities:
Keywords: Fetuin; gene delivery; plasmid DNA; ternary complex
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Year: 2017 PMID: 29132248 DOI: 10.1080/1061186X.2017.1405425
Source DB: PubMed Journal: J Drug Target ISSN: 1026-7158 Impact factor: 5.121