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The nature of macrophage allows the possibility that this cell type could be used as drug delivery system to track therapeutic drug nanoparticles (NPs) in cancer. However, there is no existing research on the regulation between effective loading of NPs and targeted delivery of macrophages. Here, we investigated the important parameters of intracellular NP quantity and the vector migration rate. Macrophage loading capacity was obtained by comparing the uptake quantity of varisized NPs, and the delivery ability of loaded cells was determined by measuring vector migration rates. We observed a positive correlation between the size of NPs and directed macrophage migration. Our findings suggest that the molecular mechanism of migration vector rate regulation involved increased expression levels of colony-stimulating factor-1 (CSF-1) receptor and integrin induced by 100-nm and 500-nm particles. The ability of macrophages uptake to varisized NPs showed the opposite trend, with the increased vector rate of cell migration influenced by NPs. We are able to demonstrate the important balance between effective macrophage loading and targeted delivery. By adjusting the balance parameters, it will be possible to utilize NPs in macrophage-mediated disease diagnosis and therapy.  相似文献   
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有关山黧豆毒素ODAP的生物合成途径的前体物和合成程序已经证实,但其关键合成酶尚未分离与鉴定,因而无法克隆相应基因和利用反义RNA技术以控制其生物合成。研究表明,利用相应的抑制剂控制ODAP生物合成前体物可降低ODAP的积累量。山黧豆中ODAP含量与其抗逆性之间密切相关,这与其能有效地清除山黧豆中·OH自由基有关,外源ODAP处理获同样效果。此外,因ODAP既是含氮化合物,又是游离氨基酸,极易溶于水,可在逆境胁迫下与脯氨酸和多胺一样大量而迅速地积累,推测它也可能作为细胞渗透调节物质和防脱水剂,并在氮代谢和能量代谢方面起重要作用。对今后该领域的重点研究方向也进行了探讨。  相似文献   
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