The Department of Neurochemistry, Palladin Institute of Biochemistry, NAS of Ukraine, 9 Leontovicha Street, Kiev, 01601, Ukraine.
The Department of Neurochemistry, Palladin Institute of Biochemistry, NAS of Ukraine, 9 Leontovicha Street, Kiev, 01601, Ukraine ; The Biological Faculty, Taras Shevchenko National University of Kyiv, 64 Volodymyrska Str, Kiev, Ukraine.
Beilstein J Nanotechnol. 2014 Jun 4;5:778-88. doi: 10.3762/bjnano.5.90. eCollection 2014.
The manipulation of brain nerve terminals by an external magnetic field promises breakthroughs in nano-neurotechnology. D-Mannose-coated superparamagnetic nanoparticles were synthesized by coprecipitation of Fe(II) and Fe(III) salts followed by oxidation with sodium hypochlorite and addition of D-mannose. Effects of D-mannose-coated superparamagnetic maghemite (γ-Fe2O3) nanoparticles on key characteristics of the glutamatergic neurotransmission were analysed. Using radiolabeled L-[(14)C]glutamate, it was shown that D-mannose-coated γ-Fe2O3 nanoparticles did not affect high-affinity Na(+)-dependent uptake, tonic release and the extracellular level of L-[(14)C]glutamate in isolated rat brain nerve terminals (synaptosomes). Also, the membrane potential of synaptosomes and acidification of synaptic vesicles was not changed as a result of the application of D-mannose-coated γ-Fe2O3 nanoparticles. This was demonstrated with the potential-sensitive fluorescent dye rhodamine 6G and the pH-sensitive dye acridine orange. The study also focused on the analysis of the potential use of these nanoparticles for manipulation of nerve terminals by an external magnetic field. It was shown that more than 84.3 ± 5.0% of L-[(14)C]glutamate-loaded synaptosomes (1 mg of protein/mL) incubated for 5 min with D-mannose-coated γ-Fe2O3 nanoparticles (250 µg/mL) moved to an area, in which the magnet (250 mT, gradient 5.5 Т/m) was applied compared to 33.5 ± 3.0% of the control and 48.6 ± 3.0% of samples that were treated with uncoated nanoparticles. Therefore, isolated brain nerve terminals can be easily manipulated by an external magnetic field using D-mannose-coated γ-Fe2O3 nanoparticles, while the key characteristics of glutamatergic neurotransmission are not affected. In other words, functionally active synaptosomes labeled with D-mannose-coated γ-Fe2O3 nanoparticles were obtained.
外磁场对脑神经末梢的操控有望在纳米神经技术领域取得突破。通过共沉淀法制备了二糖甘露糖包覆的超顺磁纳米氧化铁颗粒,然后用过氧化氢进行氧化,并加入二糖甘露糖。分析了二糖甘露糖包覆的超顺磁磁赤铁矿(γ-Fe2O3)纳米颗粒对谷氨酸能神经传递的关键特征的影响。使用放射性标记的 L-[(14)C]谷氨酸,结果表明二糖甘露糖包覆的γ-Fe2O3 纳米颗粒不影响高亲和力 Na(+)-依赖性摄取、持续释放和分离的大鼠脑神经末梢(突触体)中 L-[(14)C]谷氨酸的细胞外水平。此外,由于应用二糖甘露糖包覆的 γ-Fe2O3 纳米颗粒,突触体的膜电位和突触小泡的酸化没有改变。这是通过使用电位敏感荧光染料罗丹明 6G 和 pH 敏感染料吖啶橙来证明的。该研究还集中于分析这些纳米颗粒用于通过外部磁场操控神经末梢的潜在用途。结果表明,与对照相比,在用二糖甘露糖包覆的 γ-Fe2O3 纳米颗粒(250μg/mL)孵育 5 分钟后,超过 84.3±5.0%的负载 L-[(14)C]谷氨酸的突触体(1mg 蛋白/mL)移动到磁场(250mT,梯度 5.5 Т/m)施加的区域,而对照的 33.5±3.0%和未经包覆的纳米颗粒处理的样品的 48.6±3.0%移动到磁场施加的区域。因此,使用二糖甘露糖包覆的 γ-Fe2O3 纳米颗粒可以很容易地通过外部磁场操控分离的脑神经末梢,而谷氨酸能神经传递的关键特征不受影响。换句话说,获得了用二糖甘露糖包覆的 γ-Fe2O3 纳米颗粒标记的功能活性突触体。