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载脂蛋白 E 修饰的纳米颗粒在血脑屏障模型中脑毛细血管内皮细胞上的摄取机制。

Uptake mechanism of ApoE-modified nanoparticles on brain capillary endothelial cells as a blood-brain barrier model.

机构信息

Department of Cell Biology and Applied Virology, Fraunhofer Institute for Biomedical Engineering, St. Ingbert, Germany.

出版信息

PLoS One. 2012;7(3):e32568. doi: 10.1371/journal.pone.0032568. Epub 2012 Mar 1.

Abstract

BACKGROUND

The blood-brain barrier (BBB) represents an insurmountable obstacle for most drugs thus obstructing an effective treatment of many brain diseases. One solution for overcoming this barrier is a transport by binding of these drugs to surface-modified nanoparticles. Especially apolipoprotein E (ApoE) appears to play a major role in the nanoparticle-mediated drug transport across the BBB. However, at present the underlying mechanism is incompletely understood.

METHODOLOGY/PRINCIPAL FINDINGS: In this study, the uptake of the ApoE-modified nanoparticles into the brain capillary endothelial cells was investigated to differentiate between active and passive uptake mechanism by flow cytometry and confocal laser scanning microscopy. Furthermore, different in vitro co-incubation experiments were performed with competing ligands of the respective receptor.

CONCLUSIONS/SIGNIFICANCE: This study confirms an active endocytotic uptake mechanism and shows the involvement of low density lipoprotein receptor family members, notably the low density lipoprotein receptor related protein, on the uptake of the ApoE-modified nanoparticles into the brain capillary endothelial cells. This knowledge of the uptake mechanism of ApoE-modified nanoparticles enables future developments to rationally create very specific and effective carriers to overcome the blood-brain barrier.

摘要

背景

血脑屏障(BBB)对大多数药物来说是一个难以逾越的障碍,从而阻碍了许多脑部疾病的有效治疗。克服这一障碍的一种解决方案是通过将这些药物与表面修饰的纳米颗粒结合来进行运输。特别是载脂蛋白 E(ApoE)似乎在纳米颗粒介导的药物通过 BBB 的运输中起主要作用。然而,目前其潜在机制尚不完全清楚。

方法/主要发现:在这项研究中,通过流式细胞术和共聚焦激光扫描显微镜研究了 ApoE 修饰的纳米颗粒进入脑毛细血管内皮细胞的摄取,以区分主动摄取和被动摄取机制。此外,还进行了不同的体外共孵育实验,使用各自受体的竞争配体。

结论/意义:本研究证实了一种主动的内吞摄取机制,并表明载脂蛋白 E 修饰的纳米颗粒进入脑毛细血管内皮细胞涉及到低密度脂蛋白受体家族成员,特别是低密度脂蛋白受体相关蛋白。对 ApoE 修饰的纳米颗粒摄取机制的了解,使未来的开发能够合理地创造出非常特异和有效的载体来克服血脑屏障。

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