Abstract
In mammals, the central nervous system (CNS) is constituted of various cellular elements, posing a challenge to isolating specific cell types to investigate their expression profile. As a result, tissue homogenization is not amenable to analyses of motor neurons profiling as these represent less than 10% of the total spinal cord cell population. One way to tackle the problem of tissue heterogeneity and obtain meaningful genomic, proteomic, and transcriptomic profiling is to use laser capture microdissection technology (LCM). In this chapter, we describe protocols for the capture of isolated populations of motor neurons from spinal cord tissue sections and for downstream transcriptomic analysis of motor neurons with RT-PCR. We have also included a protocol for the immunological confirmation that the captured neurons are indeed motor neurons. Although focused on spinal cord motor neurons, these protocols can be easily optimized for the isolation of any CNS neurons.
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Acknowledgement
This work was supported by a National Health and Medical Research Council NHMRC of Australia to Renée Morris.
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Morris, R., Mehta, P. (2018). The Isolation of Pure Populations of Neurons by Laser Capture Microdissection: Methods and Application in Neuroscience. In: Murray, G. (eds) Laser Capture Microdissection. Methods in Molecular Biology, vol 1723. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7558-7_12
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DOI: https://doi.org/10.1007/978-1-4939-7558-7_12
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Publisher Name: Humana Press, New York, NY
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Online ISBN: 978-1-4939-7558-7
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