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MyJove Corporation, Journal of Visualized Experiments, 90, 2014

DOI: 10.3791/51835-v

MyJove Corporation, Journal of Visualized Experiments, 90, 2014

DOI: 10.3791/51835

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Organotypic Slice Cultures to Study Oligodendrocyte Dynamics and Myelination

Journal article published in 2014 by Robert A. Hill ORCID, Jelena Medved, Kiran D. Patel, Akiko Nishiyama
This paper is available in a repository.
This paper is available in a repository.

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Abstract

NG2 expressing cells (polydendrocytes, oligodendrocyte precursor cells) are the fourth major glial cell population in the central nervous system. During embryonic and postnatal development they actively proliferate and generate myelinating oligodendrocytes. These cells have commonly been studied in primary dissociated cultures, neuron cocultures, and in fixed tissue. Using newly available transgenic mouse lines slice culture systems can be used to investigate proliferation and differentiation of oligodendrocyte lineage cells in both gray and white matter regions of the forebrain and cerebellum. Slice cultures are prepared from early postnatal mice and are kept in culture for up to 1 month. These slices can be imaged multiple times over the culture period to investigate cellular behavior and interactions. This method allows visualization of NG2 cell division and the steps leading to oligodendrocyte differentiation while enabling detailed analysis of region-dependent NG2 cell and oligodendrocyte functional heterogeneity. This is a powerful technique that can be used to investigate the intrinsic and extrinsic signals influencing these cells over time in a cellular environment that closely resembles that found in vivo.