Abstract
Recent discoveries have brought mitochondria functions in focus of the neuroscience research community and greatly stimulated the demand for approaches to study mitochondria dysfunction in neurodegenerative diseases. Many mouse disease models have been generated, but studying mitochondria isolated from individual mouse brain regions is a challenge because of small amount of the available brain tissue. Conventional techniques for isolation and purification of mitochondria from mouse brain subregions, such as ventral midbrain, hippocampus, or striatum, require pooling brain tissue from six to nine animals for a single mitochondrial preparation. Working with pooled tissue significantly decreases the quality of data because of the time required to dissect several brains. It also greatly increases the labor intensity and the cost of experiments as several animals are required per single data point.
We describe a method for isolation of brain mitochondria from mouse striata or other 7–12 mg brain samples. The method utilizes a refrigerated table-top microtube centrifuge, and produces research grade quality mitochondria in amounts sufficient for performing multiple enzymatic and functional assays, thereby eliminating the necessity for pooling mouse brain tissue. We also include a method of measuring ADP-ATP exchange rate as a function of mitochondrial membrane potential (ΔΨm) in small amounts of isolated mitochondria, adapted to a plate reader format.
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Acknowledgments
This work was supported by the Országos Tudományos Kutatási Alapprogram-Nemzeti Kutatási és Technológiai Hivatal (OTKA-NKTH) grant NF68294 and OTKA NNF78905 grant and Egeszsegügyi Tudományos Tanács (ETT) grant to C.C., the NIH grant 5POAG014930-11 to A.A.S. and NIH grants NS060885 and NS062165 to B.T.
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Chinopoulos, C., Zhang, S.F., Thomas, B., Ten, V., Starkov, A.A. (2011). Isolation and Functional Assessment of Mitochondria from Small Amounts of Mouse Brain Tissue. In: Manfredi, G., Kawamata, H. (eds) Neurodegeneration. Methods in Molecular Biology, vol 793. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-328-8_20
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DOI: https://doi.org/10.1007/978-1-61779-328-8_20
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Publisher Name: Humana Press, Totowa, NJ
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