1. Academic Validation
  2. Effect of PEGylated Magnetic PLGA-PEI Nanoparticles on Primary Hippocampal Neurons: Reduced Nanoneurotoxicity and Enhanced Transfection Efficiency with Magnetofection

Effect of PEGylated Magnetic PLGA-PEI Nanoparticles on Primary Hippocampal Neurons: Reduced Nanoneurotoxicity and Enhanced Transfection Efficiency with Magnetofection

  • ACS Appl Mater Interfaces. 2019 Oct 16;11(41):38190-38204. doi: 10.1021/acsami.9b15014.
Yanna Cui 1 Xiao Li 1 2 Kristina Zeljic 1 3 Shifang Shan 1 Zilong Qiu 1 3 Zheng Wang 1 3 4 5
Affiliations

Affiliations

  • 1 Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience , CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences , 320 Yueyang Road , Shanghai 200031 , China.
  • 2 School of Basic Medical Science , Fudan University , 138 Yixueyuan Road , Shanghai 200032 , China.
  • 3 University of Chinese Academy of Sciences , 19 Yuquan Road , Beijing 100049 , China.
  • 4 Kunming Institute of Zoology, Chinese Academy of Sciences , 32 Jiaochang East Road , Kunming , Yunnan 650223 , China.
  • 5 Shanghai Research Center for Brain Science and Brain-inspired Intelligence Technology , 100 Haike Road , Shanghai 201210 , China.
Abstract

Despite broad application of nanotechnology in neuroscience, the nanoneurotoxicity of magnetic nanoparticles in primary hippocampal neurons remains poorly characterized. In particular, understanding how magnetic nanoparticles perturb neuronal calcium homeostasis is critical when considering magnetic nanoparticles as a nonviral vector for effective gene therapy in neuronal diseases. Here, we address the pressing need to systematically investigate the neurotoxicity of magnetic nanoparticles with different surface charges in primary hippocampal neurons. We found that unlike negative and neutral nanoparticles, positively charged magnetic nanoparticles (magnetic poly(lactic-co-glycolic acid) (PLGA)-polyethylenimine (PEI) nanoparticles, MNP-PLGA-PEI NPs) rapidly elevated cytoplasmic calcium levels in primary hippocampal neurons, mainly via extracellular calcium influx regulated by voltage-gated calcium channels. We went on to show that this perturbation of intracellular calcium homeostasis elicited serious cytotoxicity in primary hippocampal neurons. However, our next experiment demonstrated that PEGylation on the surface of MNP-PLGA-PEI NPs shielded the surface charge, thereby preventing the perturbation of intracellular calcium homeostasis. That is, PEGylated MNP-PLGA-PEI NPs reduced nanoneurotoxicity. Importantly, biocompatible PEGylated MNP-PLGA-PEI NPs under an external magnetic field enhanced transfection efficiency (>7%) of plasmid DNA encoding GFP in primary hippocampal neurons compared to NPs without external magnetic field mediation. Moreover, under an external magnetic field, this system achieved gene transfection in the hippocampus of the C57 mouse. Overall, this study is the first to successfully employ biocompatible PEGylated MNP-PLGA-PEI NPs for transfection using a magnetofection strategy in primary hippocampal neurons, thereby providing a nanoplatform as a new perspective for treating neuronal diseases or modulating neuron activities.

Keywords

PEGylation; intracellular calcium homeostasis; magnetic PLGA-PEI nanoparticles; nanoneurotoxicity; primary hippocampal neurons.

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