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1.
J Biomed Mater Res A ; 105(8): 2129-2138, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28371423

ABSTRACT

The physical properties of substrates can have profound effects on the structure and function of cultured cells. In this study, we aimed to examine the viability, adherence, and morphological and functional variations between SH-SY5Y human neuroblastoma cells cultured on SU-8 surfaces compared with control surfaces composed of borosilicate glass, which are routinely used for cell culture. The SU-8 polymer has been extensively studied for its biocompatibility, but there has been little investigation into the characteristic differences between cells cultured on SU-8 when compared with glass. SH-SY5Y cells were cultured within polydimethylsiloxane wells on both SU-8 and glass substrates for up to 72 h after which flow cytometry and enzyme-linked immunosorbent assay analysis was performed to examine cell viability and neurotoxicity. Immunocytochemistry was also performed to analyze the morphological and functional characteristics of the cells. Atomic force microscopy was performed to measure surface roughness and to map cell-substrate interactions. Nanoindentation testing was used to characterize the mechanical properties of polymer surface. Results showed that SH-SY5Y cells grown on SU-8 have significantly improved viability and increased morphological and functional characteristics of neurodevelopment. The results from this study suggest that the mechanical properties of the polymer are optimal for the study of cultured cell lines, which could account for the increased viability, adherence, and morphological and functional characteristics of neurodevelopment. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 2129-2138, 2017.


Subject(s)
Biocompatible Materials/chemistry , Cell Proliferation , Epoxy Compounds/chemistry , Glass/chemistry , Neurons/cytology , Polymers/chemistry , Cell Adhesion , Cell Culture Techniques , Cell Line, Tumor , Cell Survival , Humans , Neuroblastoma/metabolism , Neurons/metabolism
2.
Prog Neurobiol ; 123: 18-36, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25291406

ABSTRACT

The impact of central nervous system (CNS) disorders on the human population is significant, contributing almost €800 billion in annual European healthcare costs. These disorders not only have a disabling social impact but also a crippling economic drain on resources. Developing novel therapeutic strategies for these disorders requires a better understanding of events that underlie mechanisms of neural circuit physiology. Studying the relationship between genetic expression, synapse development and circuit physiology in CNS function is a challenging task, involving simultaneous analysis of multiple parameters and the convergence of several disciplines and technological approaches. However, current gold-standard techniques used to study the CNS have limitations that pose unique challenges to furthering our understanding of functional CNS development. The recent advancement in nanotechnologies for biomedical applications has seen the emergence of nanoscience as a key enabling technology for delivering a translational bridge between basic and clinical research. In particular, the development of neuroimaging and electrophysiology tools to identify the aetiology and progression of CNS disorders have led to new insights in our understanding of CNS physiology and the development of novel diagnostic modalities for therapeutic intervention. This review focuses on the latest applications of these nanotechnologies for investigating CNS function and the improved diagnosis of CNS disorders.


Subject(s)
Biosensing Techniques/instrumentation , Brain/anatomy & histology , Brain/physiology , Contrast Media , Image Enhancement/methods , Nanoparticles , Nanotechnology/instrumentation , Animals , Biosensing Techniques/methods , Contrast Media/chemistry , Humans , Nanoparticles/chemistry , Nanoparticles/ultrastructure , Particle Size
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