Department of Neurological Surgery, University of California at San Francisco San Francisco, CA, USA.
Department of Materials Science & Engineering, University of California at Berkeley Berkeley, CA, USA.
Front Neuroanat. 2014 Mar 17;8:9. doi: 10.3389/fnana.2014.00009. eCollection 2014.
When nanoparticles/proteins are infused into the brain, they are often transported to distal sites in a manner that is dependent both on the characteristics of the infusate and the region targeted. We have previously shown that adeno-associated virus (AAV) is disseminated within the brain by perivascular flow and also by axonal transport. Perivascular distribution usually does not depend strongly on the nature of the infusate. Many proteins, neutral liposomes and AAV particles distribute equally well by this route when infused under pressure into various parenchymal locations. In contrast, axonal transport requires receptor-mediated uptake of AAV by neurons and engagement with specific transport mechanisms previously demonstrated for other neurotropic viruses. Cerebrospinal fluid (CSF) represents yet another way in which brain anatomy may be exploited to distribute nanoparticles broadly in the central nervous system. In this study, we assessed the distribution and perivascular transport of nanoparticles of different sizes delivered into the parenchyma of rodents and CSF in non-human primates.
当纳米颗粒/蛋白质被注入大脑时,它们通常以依赖于注入物特征和目标区域的方式被运输到远端部位。我们之前已经表明,腺相关病毒 (AAV) 通过血管周围流和轴突运输在大脑内传播。血管周围分布通常不太依赖于注入物的性质。当以压力将许多蛋白质、中性脂质体和 AAV 颗粒注入各种实质部位时,它们通过这种途径同样均匀地分布。相比之下,轴突运输需要神经元通过受体介导的 AAV 摄取,并与先前证明的其他神经病毒的特定运输机制结合。脑脊液 (CSF) 是另一种可以利用脑解剖结构将纳米颗粒广泛分布在中枢神经系统中的方式。在这项研究中,我们评估了不同大小的纳米颗粒在啮齿动物和非人类灵长类动物脑实质和脑脊液中的分布和血管周围运输。