Publication date: Available online 15 November 2017
Source:Journal of Neuroscience Methods
Author(s): Mustafa S. Kassem, Sandra Y.Y. Fok, Kristie L. Smith, Michael Kuligowski, Bernard W. Balleine
BackgroundHigh resolution neuronal information is extraordinarily useful in understanding the brain's functionality. The development of the Golgi-Cox stain allowed observation of the neuron in its entirety with unrivalled detail. Recently tissue clearing techniques, e.g., CLARITY and CUBIC, provide the potential to observe entire neuronal circuits intact within tissue and without previous restrictions with regard to section thickness.New MethodHere we describe an improved Golgi-Cox stain method, optimized for use with CLARITY and CUBIC, that stains within 48hrs and that can be used in both fresh and fixed tissue.ResultsUsing this method, we were able to observe neurons in their entirety within a fraction of the time traditionally taken to clear tissue (48hrs). We were also able to show for the first-time that Golgi stained tissue is fluorescent when visualized using a multi-photon microscope, allowing us to image synaptic spines with a detail previously unachievable.Comparison with Existing MethodsThese novel methods provide cheap and easy to use techniques to investigate the morphology of cellular processes in the brain at a new-found depth, speed, utility and detail, without previous restrictions of time, tissue type and section thickness.ConclusionsThis is the first application of a Golgi-Cox stain to cleared brain tissue, it is investigated and discussed in detail, describing different methodologies that may be used, a comparison between the different clearing techniques and lastly the novel interaction of these techniques with this ultra-rapid stain.
Graphical abstract
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