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首页> 外文期刊>Biomacromolecules >Role of Biophysical Parameters on ex Vivo and in Vivo Gene Transfer to the Airway Epithelium by Polyethylenimine/Albumin Complexes
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Role of Biophysical Parameters on ex Vivo and in Vivo Gene Transfer to the Airway Epithelium by Polyethylenimine/Albumin Complexes

机译:聚乙烯亚胺/白蛋白复合物在体外和体内基因转移到气道上皮中的生物物理参数的作用

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摘要

Efficient gene transfer to the airways by nonviral vectors is a function of different parameters,among which the size and the charge of the transfecting particles.The aim of this study was to determine the transfection efficiency of polyethylenimine (PEI)/albumin polyplexes in ex vivo and in vivo models of respiratory epithelium and to correlate it with biophysical characteristics of the particles.Complexes were obtained by adding different amounts of human serum albumin (HSA) to PEI polyplexes preformed in saline.The presence of HSA caused the formation of bigger and more negative polyplexes and increased PEI transfection efficiency in primary respiratory epithelial cells by 4-6-fold.For in vivo administration to the lung,PEI polyplexes were formed in water and optimized with respect to the NIP ratio.PEI/pC-Luc complexes gave the highest luciferase expression at NIP 15 when administered through the trachea.At this NIP ratio,the size and the surface charge of albumin-containing polyplexes were not different as compared with plain PEI polyplexes.Formulation of PEI polyplexes in the presence of HSA or murine serum albumin (MSA) resulted in a 2-fold increase in luciferase expression.In mice treated with PEI or PEI/MSA polyplexes containing the nuclear beta-gal gene,X-gal staining revealed that transfected cells localized at the bronchiolar epithelium and that PEI/MSA transfected four times as many cells as PEI (p < 0.05).Finally,double administration of PEI/MSA polyplexes resulted in a further enhancement of transfection of the lung.Our data show that serum albumin enhances PEI-mediated gene transfer to airway epithelial cells in vivo,likely facilitating the uptake of polyplexes,and indicate that this formulation would fulfill the requirement of repeated administration,as necessary in chronic lung diseases like cystic fibrosis.
机译:非病毒载体有效地将基因转移至气道是不同参数的函数,其中包括转染颗粒的大小和电荷。本研究的目的是确定聚乙烯亚胺(PEI)/白蛋白复合物在体外的转染效率。通过将不同量的人血清白蛋白(HSA)加入到盐水中形成的PEI多聚体中来获得复合物.HSA的存在导致越来越大的形成PEI / pC-Luc复合物可产生负的多聚体,并使初级呼吸道上皮细胞的PEI转染效率提高4-6倍。通过气管给药时,NIP 15的荧光素酶表达最高。在此NIP比率下,含白蛋白的息肉的大小和表面电荷与普通的PEI多聚体相比,xes没有差异。在存在HSA或鼠血清白蛋白(MSA)的情况下配制PEI多聚体导致萤光素酶表达增加2倍。核β-gal基因,X-gal染色显示,转染的细胞位于细支气管上皮,PEI / MSA转染的细胞是PEI的四倍(p <0.05)。最后,重复施用PEI / MSA复合物导致我们的数据显示,血清白蛋白可增强PEI介导的基因在体内向气道上皮细胞的转移,促进多聚体的摄取,并表明该制剂可满足重复给药的需要,在体内慢性肺部疾病如囊性纤维化。

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