Volume 12, Issue 26 pp. 3559-3567
Full Paper

The Age of Cortical Neural Networks Affects Their Interactions with Magnetic Nanoparticles

Andy Tay

Andy Tay

Department of Bioengineering, University of California, Los Angeles, CA, 90095 USA

Department of Biomedical Engineering, National University of Singapore, 4 Engineering Drive 3, Singapore, 117583 Singapore

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Anja Kunze

Anja Kunze

Department of Bioengineering, University of California, Los Angeles, CA, 90095 USA

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Dukwoo Jun

Dukwoo Jun

Department of Civil and Environmental Engineering, University of California, Los Angeles, CA, 90095 USA

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Eric Hoek

Eric Hoek

Department of Civil and Environmental Engineering, University of California, Los Angeles, CA, 90095 USA

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Dino Di Carlo

Corresponding Author

Dino Di Carlo

Department of Bioengineering, University of California, Los Angeles, CA, 90095 USA

California Nanosystems Institute, University of California, Los Angeles, CA, 90095 USA

Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA, 90095 USA

E-mail: [email protected]Search for more papers by this author
First published: 27 May 2016
Citations: 20

Abstract

Despite increasing use of nanotechnology in neuroscience, the characterization of interactions between magnetic nanoparticles (MNPs) and primary cortical neural networks remains underdeveloped. In particular, how the age of primary neural networks affects MNP uptake and endocytosis is critical when considering MNP-based therapies for age-related diseases. Here, primary cortical neural networks are cultured up to 4 weeks and with CCL11/eotaxin, an age-inducing chemokine, to create aged neural networks. As the neural networks are aged, their association with membrane-bound starch-coated ferromagnetic nanoparticles (fMNPs) increases while their endocytic mechanisms are impaired, resulting in reduced internalization of chitosan-coated fMNPs. The age of the neurons also negates the neuroprotective effects of chitosan coatings on fMNPs, attributing to decreased intracellular trafficking and increased colocalization of MNPs with lysosomes. These findings demonstrate the importance of age and developmental stage of primary neural cells when developing in vitro models for fMNP therapeutics targeting age-related diseases.

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