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低分子量透明质酸对DNA/PEI复合物的屏蔽作用有助于其通过CD44受体介导进入人角膜上皮细胞。

Low molecular weight hyaluronan shielding of DNA/PEI polyplexes facilitates CD44 receptor mediated uptake in human corneal epithelial cells.

作者信息

Hornof Margit, de la Fuente Maria, Hallikainen Marjut, Tammi Raija H, Urtti Arto

机构信息

Drug Discovery and Development Technology Center DDTC, University of Helsinki, Finland.

出版信息

J Gene Med. 2008 Jan;10(1):70-80. doi: 10.1002/jgm.1125.

Abstract

AIM

It was the aim of this study to prepare purified DNA/PEI polyplexes, which are coated with hyaluronan to facilitate CD44 receptor mediated uptake of the DNA/PEI polyplex and to reduce unspecific interactions of the complex with negatively charged extracellular matrix components on the ocular surface.

METHODS

Hyaluronans of different molecular weights (<10 kDa, 10-30 kDa and 30-50 kDa) were isolated after enzymatic degradation of high molecular weight hyaluronan via ultrafiltration by centrifugation. The influence of the different hyaluronans used for coating on the stability and transfection efficiency of the complexes was evaluated in vitro. Transfection and uptake studies were performed in human corneal epithelial (HCE) cells. CD44 receptor expression of this cell model was evaluated by immunohistochemistry.

RESULTS

Coating of purified DNA/PEI polyplexes with low molecular weight hyaluronan (<10 kDa) facilitated receptor-mediated uptake via the CD44 receptor in HCE cells, increased complex stability in vitro, and effectively shielded the positive surface charges of the polyplex without decreasing its transfection efficiency. Higher molecular weights and larger amounts of hyaluronan in the complexes resulted in lesser improvements in the stability and transfection efficacy of the complexes.

CONCLUSIONS

Coating of polyplexes with low molecular weight hyaluronan is a promising strategy for gene delivery to the ocular surface, where CD44 receptor mediated uptake decreased cytotoxicity and reduced non-specific interactions with the negatively charged extracellular matrix components are considered beneficial for increased transfection efficiency of non-viral vectors.

摘要

目的

本研究旨在制备纯化的DNA/聚乙烯亚胺(PEI)多聚体,其表面包被有透明质酸,以促进CD44受体介导的DNA/PEI多聚体摄取,并减少该复合物与眼表带负电荷的细胞外基质成分的非特异性相互作用。

方法

通过离心超滤法对高分子量透明质酸进行酶解后,分离出不同分子量(<10 kDa、10 - 30 kDa和30 - 50 kDa)的透明质酸。体外评估用于包被的不同透明质酸对复合物稳定性和转染效率的影响。在人角膜上皮(HCE)细胞中进行转染和摄取研究。通过免疫组织化学评估该细胞模型的CD44受体表达。

结果

用低分子量(<10 kDa)透明质酸包被纯化的DNA/PEI多聚体,可促进HCE细胞中通过CD44受体介导的摄取,提高复合物在体外的稳定性,并有效屏蔽多聚体的正表面电荷,而不降低其转染效率。复合物中较高分子量和较大量的透明质酸对复合物稳定性和转染效果的改善较小。

结论

用低分子量透明质酸包被多聚体是一种有前景的眼表基因递送策略,其中CD44受体介导的摄取降低细胞毒性以及减少与带负电荷的细胞外基质成分的非特异性相互作用,被认为有利于提高非病毒载体的转染效率。

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