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 JoVE Biology

Neuronal Nuclei Isolation from Human Postmortem Brain Tissue

1, 1

1Psychiatry, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School

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    Summary

    The cellular heterogeneity of brain tissue poses a significant limitation for the study of epigenetic markings in chromatin because most assays lack single cell resolution. Neurons typically are intermingled with glia and other non-neuronal cells. We provide a protocol to extract and collect neuronal nuclei from human brain.

    Date Published: 10/01/2008, Issue 20; doi: 10.3791/914

    Cite this Article

    Matevossian, A., Akbarian, S. Neuronal Nuclei Isolation from Human Postmortem Brain Tissue. J. Vis. Exp. (20), e914, doi:10.3791/914 (2008).

    Abstract

    Neurons in the human brain become postmitotic largely during prenatal development, and thus maintain their nuclei throughout the full lifespan. However, little is known about changes in neuronal chromatin and nuclear organization during the course of development and aging, or in chronic neuropsychiatric disease. However, to date most chromatin and DNA based assays (other than FISH) lack single cell resolution. To this end, the considerable cellular heterogeneity of brain tissue poses a significant limitation, because typically various subpopulations of neurons are intermingled with different types of glia and other non-neuronal cells. One possible solution would be to grow cell-type specific cultures, but most CNS cells, including neurons, are ex vivo sustainable, at best, for only a few weeks and thus would provide an incomplete model for epigenetic mechanisms potentially operating across the full lifespan. Here, we provide a protocol to extract and purify nuclei from frozen (never fixed) human postmortem brain. The method involves extraction of nuclei in hypotonic lysis buffer, followed by ultracentrifugation and immunotagging with anti-NeuN antibody. Labeled neuronal nuclei are then collected separately using fluorescence-activated sorting. This method should be applicable to any brain region in a wide range of species and suitable for chromatin immunoprecipitation studies with site- and modification-specific anti-histone antibodies, and for DNA methylation and other assays.

    Protocol

    Nuclei Extraction

    1. Put 250 mg of frozen postmortem brain tissue in 5 mL Lysis Buffer1 in a douncer and place it on ice. To receive about 5 million nuclei after FACS sorting, we usually use 1000 mg of tissue per sample.
    2. Once the tissue has thawed, dounce the tissue for 1 minute while on ice.
    3. Take the homogenized tissue and place it into a 15 mL clear ultracentrifuge tube. Put the tube on ice.
    4. Take 9 mL of Sucrose Solution2 with a pipette, put the pipette at the bottom of the clear ultracentrifuge tube, and release the Sucrose Solution2 to create a concentration gradient with the homogenized tissue solution on top of the Sucrose Solution2.
    5. Weigh the ultracentrifuge tubes to make sure that they will all be balanced while rotating within the ultracentrifuge. Make any adjustments to the weight by adding Lysis Buffer1 to the top layer.
    6. After the tubes have been weighed, place them into the rotor's buckets.
    7. Place all buckets into a SW28 rotor and carefully place the rotor into the ultracentrifuge.
    8. Ultracentrifuge the samples at 107163.6 RCF for 2.5 hours at 4°C.
    9. Once the centrifugation is complete, remove the supernatant, along with the layer of debris found at the concentration gradient, with the use of a vacuum, while being careful not to disturb the pellet containing the nuclei at the bottom of the tube.
    10. Add 500 µL of 1X PBS to each pellet and let sit on ice for 20 minutes. This allows the pellet to dissolve a little on its own, making it easier to later mechanically dissolve it by pipetting up and down, which lessens the amount of stress the nuclei experience.
    11. After the nuclei have incubated on ice for 20 minutes, mechanically pipette up and down to completely dissolve the nuclei within 1XPBS.
    12. Remove the nuclei-containing solution from the ultracentrifuge tubes and combine the contents of two tubes into a single 2 mL microcentrifuge tube. Again, place the samples on ice.

    Immunostaining for FACS

    1. At this point, make an immunostaining mixture composed of primary and secondary antibody, and Blocking Mix. For each sample, combine 300 µL of 1XPBS containing 1.2 µL of NeuN antibody, 100 µL of Blocking Mix, which contains 0.5% BSA and 10% Normal Goat Serum in 1XPBS, and 1 µL of Alexa Fluor 488. For the control samples, exclude the primary antibody NeuN and, instead, just add more 1XPBS.
    2. Vortex the immunostaining mixture and incubate for 5 minutes at room temperature in the dark.
    3. While the staining mixture is incubating, make the controls for the samples. For FACS sorting, a sample, containing nuclei alone, called the "unstained control" is needed; a second sample, a negative control, containing the nuclei with the secondary antibody Alexa Fluor 488 without the primary antibody NeuN is also needed.
    4. Aliquot 20 µL of the nuclei containing solution into a 2 mL microcentrifuge tube containing 1XPBS for the unstained control, and another 20 µL into another 2 mL tube containing 980 uL of 1XPBS for the negative control. Raise the volume of the nuclei-containing sample back up to 1 mL with 1XPBS. All samples are placed back on ice.
    5. Now that the immunostaining mixture has finished incubating, add its contents of 401 µL into the appropriate samples. The nuclei sample will receive the mixture containing both NeuN and Alexa Fluor 488, while the negative sample will receive the mixture containing only the secondary antibody Alexa Fluor 488.
    6. Take the samples into the cold room to rotate in the dark for 45 minutes.
    7. After the samples have incubated in the dark for 45 minutes, put them on ice and bring them to the FACS facility. During the transport to the FACS facility, the samples should be kept on ice and in the dark.

    FACS

    1. At the FACS facility, filter the samples through a 40 um filter. Then, run them through the instrument for a few minutes, while being kept cold, in order to get some preliminary data before sorting.
    2. At this point, it is necessary to set the appropriate gates required for sorting. Several different gates are used to sort samples. The first gate gives an idea of the size of the different nuclei found within the sample, and allows separatation of debris from actual nuclei. The second gate allows us to sort nuclei individually. Discard any aggregates are discarded at this point. Finally, the third gate is set to a specific fluorescence wavelength, matching that of the fluorochrome found in our secondary antibody. Placing this gate allows us to sort and separate NeuN +, hence neuronal nuclei from NeuN - nuclei.
    3. After all the gates are chosen, the nuclei can be sorted into 1XPBS.
    4. Once the whole sample has gone through, check the purity of the sort by running an aliquot of the sorted sample through the instrument. Make sure that the sample's fluorescence is not spread out, but rather is contained within a single quadrant. It is best to choose samples which are over 90% pure.

    After FACS

    1. Once the sample has been sorted, processing of the nuclei can begin. Take 10 mL of sorted sample and add to it 2 mL of Sucrose Solution2, 50 uL of 1M CaCl2 and 30 ul of 1m Mg(Ace)2. As a reminder, always be sure to keep the sample on ice since the nuclei are unfixed.
    2. If there is less than 10 mL of sorted sample, raise the volume up to 10 mL by adding 1XPBS, or adjust the additional materials accordingly.
    3. Invert the sample several times and place on ice for 15 minutes.
    4. After the samples have incubated on ice for 15 minutes, centrifuge them in a swing bucket rotor at 1786 RCF for 15 minutes at 4°C.
    5. Discard the supernatant with the use of a vacuum, without disturbing the white pellet found at the bottom of the tube.
    6. Dissolve the pellet in 200 µl of whatever solution you require for the proceeding experiments, and pipette up and down.
    7. Transfer the solution into a smaller tube and place it into the -80°C freezer until further use.

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    Discussion

    The protocol presented here should be particularly useful for studies focused on epigenetic changes of neuronal chromatin and, more generally, on the molecular phenotype of the neuronal nucleus, during normal developing and aging, or in neurological or psychiatric disease. The method is of particular advantage when the cellular heterogeneity of brain tissue, including potential shifts in neuron-to-glia ration during the course of aging or due to disease are a concern 1. For example, by combining the present sorting protocol with chromatin immunoprecipitation techniques, we recently described neuron-specific histone methylation patterns at the brain derived neurotrophic factor (BDNF) gene promoter, and for additional neuronal genes 2. A similar method had been used previously to collect neurons from adult cerebral cortex for retrospective birth dating 3. The sorting technique was also employed in mouse brain 2, and because of the stability of nuclei in frozen-then-thawed tissue, we anticipate that the approach presented here is applicable to a wide range of species. Because chromatin immunoprecipitation from as little as 10,000 cells for is now feasible even for a more comprehensive genome coverage 4, it may be possible to use much less than the 1000 mg of starting material that we recommended above.

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    Disclosures

    Acknowledgements

    The authors appreciate the advice and technical support provided by Dr. Richard Konz and staff at the Flow Cytometry Core facility at the University of Massachusetts Medical School. Core resources supported by the Diabetes Endocrinology Research Center Grant DK032520 were also used. This work is supported by grants from the National Institute of Mental Health (NIMH), the National Institute of Drug Abuse (NIDA) and the National Institute of Child Health and Human Development.

    Materials

    Reagents:

    1. Lysis Buffer
    0.32MSucrose5.47 g
    5 mMCaCl2250 μl
    3 mMMg(Acetate)2150 μl
    0.1 mMEDTA10 μl
    10mMTris-HCl, pH8 500 μl
    1 mM DTT17 μl
    0.1%Triton X-10050 μl
    Adjust volume to 50 ml with Autoclaved water
    2. Sucrose Solution
    1.8 MSucrose30.78 g
    3 mM Mg(Acetate)2150 μl
    1 mMDTT17 μl
    10 mMTris-HCl, pH8500 μl
    Adjust volume to 50 ml with Autoclaved water
    3. Dounce buffer
    10 mMTris0.242 g
    4 mMMgCl20.163 g
    1 mMCaCl20.03 g
    Adjust pH to 7.5 and volume to 200 ml with Autoclaved water

    References

    1. Siegmund, K.D., Connor, C.M., Campan, M., Long, T.I., Weisenberger, D.J., Biniszkiewicz, D., Jaenisch, R., Laird, P.W. and Akbarian, S. (2007) DNA methylation in the human cerebral cortex is dynamically regulated throughout the life span and involves differentiated neurons. PLoS ONE, 2, e895.

    2. Jiang, Y., Matevossian, A., Huang, H.S., Straubhaar, J. and Akbarian, S. (2008) Isolation of neuronal chromatin from brain tissue. BMC Neurosci, 9, 42.

    3. Spalding, K.L., Bhardwaj, R.D., Buchholz, B.A., Druid, H. and Frisen, J. (2005) Retrospective birth dating of cells in humans. Cell, 122, 133-43.

    4. Acevedo, L.G., Iniguez, A.L., Holster, H.L., Zhang, X., Green, R. and Farnham, P.J. (2007) Genome-scale ChIP-chip analysis using 10,000 human cells. Biotechniques, 43, 791-797.

    Comments

    7 Comments

    your method of isolating brain nuclei is practical straight forword and I am happy that I have across your paper and demonstration. I am interested to isolate intact nuclei. How do I know the isolated nuclei are intact? Do you have a suggestion for me to "test" my nuclei are intact? thank you in advance for your help
    Reply

    Posted by: AnonymousApril 27, 2009, 12:50 PM

    The quickest way is to stain with NeuN and check under the fluorescent microscope.
    Reply

    Posted by: AnonymousDecember 9, 2011, 12:00 PM

    Hello,
    thanks for your nice protocol for nuclei isolation and sorting. I tried the approach but had a problem with nuclei aggregates, can you tell how one can improve this?
    Reply

    Posted by: AnonymousNovember 16, 2011, 12:40 PM

    At what stage in the process do you encounter aggregates? If it is after the ultracentrifugation, then spending more time re-suspending the nuclei pellet will result in better separation during FACS.
    Reply

    Posted by: AnonymousDecember 9, 2011, 12:03 PM

    Thanks again for the video. In the meantime, aggregate formation is not an isse anymore. With regard to stainings: Did you test for other nuclear protein antibodies to distinguish neuronal/glial subtypes. If yes, can you tell which ab are suitable?
    Thanks in advance again for the video and your response!
    Reply

    Posted by: AnonymousDecember 10, 2011, 8:45 AM

    Thank you for the video. Have you checked to see whether you can extract RNA for microarray or RNA-seq from these nuclei post-FACS?
    Reply

    Posted by: AnonymousJanuary 9, 2012, 7:57 AM

    How do you keep the nuclei from clumping other than filter them with 40um filter? Thanks.
    Reply

    Posted by: Tao K.October 2, 2012, 3:00 PM

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