用于递送靶向CCR5的反义γ - pna低聚物的纳米颗粒。

Raman Bahal, Nicole Ali McNeer, Danith H Ly, W Mark Saltzman, Peter M Glazer
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引用次数: 32

摘要

一类新的肽核酸(PNAs),即γ - PNAs (γ - PNAs)的发展,需要一种通用而有效的方法将其传递到细胞中,以调节哺乳动物细胞中的基因表达。在这里,我们报告了最近开发的亲水性和生物相容性的二甘醇(miniPEG)为基础的伽马肽核酸的反义活性,称为mp - γ pnas通过其传递聚丙交酯-羟基乙酸酯(PLGA)为基础的纳米颗粒系统。我们发现,与常规PNA低聚物相比,mp - γPNA低聚物结合到趋化因子受体5 (CC R5)转录物的选择区域,可诱导有效的序列特异性反义效应。此外,PLGA纳米颗粒递送mp - γ pnas对细胞无毒。本研究结果提供了一种结合γ - pna技术和基于plga的纳米颗粒递送方法,通过反义机制调节活细胞中的基因表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanoparticle for delivery of antisense γPNA oligomers targeting CCR5.

The development of a new class of peptide nucleic acids (PNAs), i.e., gamma PNAs (γPNAs), creates the need for a general and effective method for its delivery into cells for regulating gene expression in mammalian cells. Here we report the antisense activity of a recently developed hydrophilic and biocompatible diethylene glycol (miniPEG)-based gamma peptide nucleic acid called MPγPNAs via its delivery by poly(lactide-co-glycolide) (PLGA)-based nanoparticle system. We show that MPγPNA oligomers designed to bind to the selective region of chemokine receptor 5 (CC R5) transcript, induce potent and sequence-specific antisense effects as compared with regular PNA oligomers. In addition, PLGA nanoparticle delivery of MPγPNAs is not toxic to the cells. The findings reported in this study provide a combination of γPNA technology and PLGA-based nanoparticle delivery method for regulating gene expression in live cells via the antisense mechanism.

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