Optimized heterologous transfection of viable adult organotypic brain slices using an enhanced gene gun
© Arsenault and O’Brien; licensee BioMed Central Ltd. 2013
Received: 18 September 2013
Accepted: 16 December 2013
Published: 19 December 2013
Organotypic brain slices (OTBS) are an excellent experimental compromise between the facility of working with cell cultures and the biological relevance of using animal models where anatomical, morphological, and cellular function of specific brain regions can be maintained. The biological characteristics of OTBS can subsequently be examined under well-defined conditions. They do, however, have a number of limitations; most brain slices are derived from neonatal animals, as it is difficult to properly prepare and maintain adult OTBS. There are ample problems with tissue integrity as OTBS are delicate and frequently become damaged during the preparative stages. Notwithstanding these obstacles, the introduced exogenous proteins into both neuronal cells, and cells imbedded within tissues, have been consistently difficult to achieve.
Following the ex vivo extraction of adult mouse brains, mounted inside a medium-agarose matrix, we have exploited a precise slicing procedure using a custom built vibroslicer. To transfect these slices we used an improved biolistic transfection method using a custom made low-pressure barrel and novel DNA-coated nanoparticles (40 nm), which are drastically smaller than traditional microparticles. These nanoparticles also minimize tissue damage as seen by a significant reduction in lactate dehydrogenase activity as well as propidium iodide (PI) and dUTP labelling compared to larger traditional gold particles used on these OTBS. Furthermore, following EYFP exogene delivery by gene gun, the 40 nm treated OTBS displayed a significantly larger number of viable NeuN and EYFP positive cells. These OTBS expressed the exogenous proteins for many weeks.
Our described methodology of producing OTBS, which results in better reproducibility with less tissue damage, permits the exploitation of mature fully formed adult brains for advanced neurobiological studies. The novel 40 nm particles are ideal for the viable biolistic transfection of OTBS by reducing tissue stress while maintaining long term exogene expression.
Organotypic brain slices (OTBS) are viable segments of brain tissue that can be cultured in vitro. Improvements in brain slice methodology are required to permit this strategy to be utilized more frequently for a wide range of biological applications. Of particular advantage is the fact that OTBS maintain many characteristics of in vivo biology including functional synaptic circuitry and also preserve local brain architecture [1, 2]. Brain slices are increasingly being used for both basic and applied research, and have been proven successful for a number of pharmacological and genetic manipulations that investigate particular neurobiological functions [3–7]. Many biological questions can’t be sufficiently addressed using cell cultures while whole animal in vivo studies aren’t permissive to numerous biotechnological assays [6, 7]. OTBS maintain advantages of both.
OTBS have successfully been established on a variety of brain regions including hippocampus, hypothalamus, striatum, cortex, spinal cord, and cerebellum [8–14]. For further reading on the full range of OTBS regions studied please read the review by Lossi et al., 2009 . In addition, a range of tissue slice co-cultures have also been reported, which allow the assessment of neuronal intercommunication across brain regions. The utilities of these co-cultures have been well established with the examples of hippocampal, cortico-spinal, and cortico-striatal preparations [15–19] as well as testing OTBS under the effects of other cells such as carcinomas . Several methods have been developed to maintain thin OTBS under long-term culture [21, 22] based on the use of “roller tubes” or Maximov-type chambers, although preparing reproducible cultures using the conventional roller tube technique is especially demanding, and such cultures often display considerable experimental variability. Following these, a membrane interface culture method was described , which allows straightforward solution changes and easy access to the slices. This can be very advantageous, and many studies now use a modification of this membrane interface method. For a more indebt historical review of alternative neuronal culture methods please read Millet and Gillette, 2012 . However, the preparation of experimentally reliable slices is still a major obstacle, and successfully viable adult OTBS are exceptionally rare [2, 24–26].
Another major hurdle in the consistent use of OTBS is their intransigence with DNA transfection. Terminally differentiated cells such as neurons are difficult to transfect themselves, while cells within tissue aren’t easily exposed to the administered reagents. A potential solution to this is biolistic transfection, where genetic material, coated onto micro or nanoparticles, is fired through tissue, propelled by the pressurized gas of a “gene gun” . This, however, can cause considerable tissue damage, exacerbating what might already have arisen from the handling of delicate OTBS. For these reasons further advancements are thus required to expand the utility of OTBS.
Here we describe an improved method of preparing adult OTBS with increased ease of preparation. These adult OTBS were then used to explore the efficiency of a modified biolistic transfection procedure using novel and less damaging, nanometer-sized DNA bound gold particles fired by a lower pressure and more precise barrel. These fired nano-particles, while concomitantly heightening the precision of the transfected area (~3 mm diameter) compared to traditional gene gun, preserve cellular viability and also elevate transfection yields within these difficult to transfect cells.
Agarose-embedded brain slices
Additional file 1:Organotypic brain slice preparation using the vibroslicer. The brain mounted inside the DMEM-agarose matrix was glued onto the copper platform. The blade was then properly aligned as described in the methods section. Ice-cold PBS containing P/S was added to the recipient covering both the blade and imbedded brain. Once activated, the vibroslicer, at predetermined slicing amplitude and frequency, cuts OTBS of precise thickness. These OTBS, contrasted by the phenol red in the DMEM, can easily be seen. They are then lifted by the blade, scooped, and transferred to the appropriate medium. (MOV 6 MB)
Nanoparticle mediated biolistic transfection and cell survival
Efficient transfection of OTBS is difficult using traditional techniques but we have previously shown that biolistic transfection using a modified gene gun (Figure 1B-D) can result in efficient and precisely localized gene expression . However, we and others have showed that biolistic transfection can cause tissue damage, which is a significant problem for these delicate adult OTBS, see  and refs therein.
Lineage quantification within the OTBS and exogene expression
Transfection rates as determined by the number of EYFP positive cells over the total amount of DAPI positive cells were also more elevated in the 40 nm particle treated OTBS compared to 1 μm particles and this expression can still be abundantly observed in terminally differentiated neuronal cells (Figure 2E). This expression pattern can be seen at 5, 14, and 21 days for the 40 nm and 1 μm particle treated OTBS in Figure 3B.
Highly detailed images of fully formed adult neurons
Biolistic transfection using 40 nm EYFP-DNA gold particles, which resulted in significantly reduced tissue damage compared to microparticles, showed brilliant expression patterns in whole cells.
Here we describe an improved method of preparing OTBS for biolistic transfection. The efficient medium-agarose embedded strategy, results in excellent viability due to ease of handling, and thus can be used for both immature and myelinated adult brains. We also demonstrate that using biolistic transfection with smaller, nanometer-sized particles combined with the modified gun barrel, also minimizes the damage to OTBS, which ultimately heightens exogenous protein expression inside cells that have consistently been shown refractory to DNA transfection.
Typically OTBS are prepared from the brains of animals at postnatal days 3–9. These brains show a high degree of plasticity and resistance to mechanical trauma during the preparation, which has proved important to obtain viable and healthy cultures. Although at this age basic synaptic connections have been established in a number of brain regions (e.g. in the CA1 area of the hippocampus), the mature synapses have not yet fully developed [31, 32]. Thus using pup brain is less than ideal to study many aspects of synaptic physiology where adult brain would be necessary, e.g. “connectomics”, age-related neurodegeneration, adult neurogenesis [33–36].
Even in neonatal OTBS that maintain sufficient viability, there arises a gradual loss of morphological characteristics that therefore doesn’t sufficiently represent the brain regions under long-term study . This loss of characteristics might be due to the more pronounced cellular de-differentiation occurring in neonatal cultures compared to older animal OTBS — a hypothesis supported by several studies [38, 39]. Reproducible adult OTBS are difficult to obtain, but the DMEM-agarose embedding procedures in combination with a stable vibroslicer promote the use of adult OTBS. The vibroslicer greatly facilitates the cutting of the brain into slices which are then effortlessly separated during the slicing procedure, as opposed to a tissue chopper where difficulties in separating very thin (150 μm) and sticky adult OTBS often occurs (slices can adhere both to the blade and to themselves while using a tissue chopper). This reduced thickness of the OTBS that facilitates the absorption of nutrient from the medium was also supported by other studies . Variations of culture medium supplementation for adult OTBS have also been shown encouraging . The vibroslicer essentially minimizes any additional stresses to the tissue. Although our instrument was custom designed, there are now great quality commercially available vibroslicers (e.g. World Precision Instruments Model No. NVSL and Leica VT 1000S). Since it was impossible to prepare adult 150 μm OTBS using a tissue chopper, the comparison between slicing methods could not be addressed in this study. Nevertheless, ease of manipulation inherently reduces stresses to, and promotes the preservation of, these fragile tissues.
The efficient transfection of genetic material into OTBS has tremendous potential, yet, lacking in sufficient advancement, this approach has had limited success. There are many methods of inserting DNA into cultured cells, including lipofection, electroporation, viral transduction, and microinjection [40–42]. However, none of these are ideal for OTBS, largely due to the poor DNA uptake into the nucleus of terminally differentiated cells such as neurones, and this is further compounded by the lack of access to cells deep within the tissue. Biolistic transfection overcome both hindrances, but can cause significant tissue damage, which can be exasperatingly problematic with delicate adult OTBS. Our recent work  suggested that nanometer sized DNA coated particles are as efficient as the widely used micrometer sized particles do deliver genetic material, yet could minimize incidental damages, suggested that this approach would be ideal for OTBS and other preparations. Our current data supports this hypothesis and shows improved viability of the cells in the OTBS following genetic delivery. These adult OTBS also showed exquisite details of neural architecture that were preserved and these can subsequently be meticulously investigated. The observed morphology of these neuronal cells can thus be analysed by various methods such as measuring neurites or using a combination of fluophores, stochastically delivered, to visualise intercellular synaptic networks [7, 43, 44]. Overall these results show that this improved protocol to prepare adult OTBS are ideal for biolistic transfection, that the 40 nm DNA coated gold particles minimizing cell and tissue damage, and that the exogene can remains expressed for weeks.
This improved method of producing finely sliced adult OTBS for biolistic transfection and exploiting novel nanometer-sized particles allows for the efficient expression of exogenous proteins while minimizing tissue damage, which is essential to properly visualize the morphological, anatomical, and cellular functions within fully formed adult brains structures. These improvements in OTBS preparation in conjunction with the modified gene gun becomes a useful platform for in vitro transfection of ex vivo organotypic slices and enhances their possible applications for subsequent genetic and biochemical manipulations. These results also encourage further translational expansion of the biolistic delivery methods for medical and bio-technological applications.
Six week old C57 Black 6 mice were sacrificed according to ethical committee approval and their brains dissected as previously described . A solution of 2% LMP agarose was prepared in Dulbecco’s modified eagles medium (DMEM) supplemented with 100 U/ml penicillin and 100 μg/ml streptomycin (P/S), and cooled (4-10°C). The freshly removed brain was then placed in a plastic mould and covered with the agarose solution; the mould was then rapidly cooled to 4°C on ice. When the agarose set (5–10 min), the medium-agarose embedded brain (Figure 1A) was removed from the mould, trimmed if necessary, and then super glued (Loctite) to a copper base platform. This was then placed into the vibroslicer chamber that contained ice-cold phosphate buffered saline (PBS: 137 mM NaCl, 2.7 mM KCl, 8.1 mM Na2HPO4, 1.76 mM, KH2PO4, pH 7.4).
Slices were prepared using a vibroslicer as previously described . The vibroslicer was constructed by the engineers at the Laboratory of Molecular Biology’s mechanical workshop using these specifications . Briefly, the oscillation frequency was 90 Hz, the amplitude 1.5-2.0 mm, and the cutting blade positioned at a 15° angle to the horizontal plane; the mounting block bearing the medium-agarose embedded brain was set to move at 1.7 mm/min towards the blade. Sections (150 ± 1.5 μm) were collected into a falcon containing ice-cold culture media (DMEM, 1% P/S, and 10% Fetal Calf Serum (FCS)). See Additional file 1: video. The slices were then placed into 0.4 μm, 30 mm diameter cell culture inserts (Milli Cell) in a 6 multi-well tray with culture media on the outside of the insert, and incubated in a humidified incubator at 37°C with 5% CO2. The coronal brain slices were carefully positioned in the centre of the insert and the insert positioned to orient the brain’s dorsal region the same way in each well.
Preparation of micro/nano particles
Particles were prepared as described  using 1 μm or 40 nm diameter gold particles. Briefly, 50 μl of 0.05 M spermidine and 10 μl DNA at 1 mg/ml (pEYFP-N1; Clontech, USA) were added to 10 mg of particles. These were mixed while adding 50 μl of 1 M CaCl2 in 10–15 μl drops. After 5 min with occasional mixing, the supernatant was removed by centrifugation (1,000 × g for 30 s) and the gold pellet resuspended in 3.5 ml 0.075 M polyvinylpyrrollidone (PVP; Sigma). This suspension was then inserted into Tefzel tubing (0.1 mm internal diameter; Bio-Rad) using a syringe. The tubing was placed in the tubing preparation station (Bio-Rad), the gold particles were allowed to settle, and the supernatant removed with a syringe. Then the tubing was rotated to ensure an even spread of gold particles, which were subsequently dried under nitrogen flow. To create bullets, the tubing was cut using a tubing cutter (Bio-Rad) into 1 cm lengths, which were either immediately inserted into the gene gun cartridge, or kept desiccated at 4°C until required.
Brain slices were transfected with biolistics as previously described  using a gas pressure of 50 psi at a distance of 10 mm (Figure 1B and C). Briefly, an alignment rod, which can be placed alongside the wall of the well periphery, was used as a distance and angle control. A stand support was also used to help maintain perpendicular alignment. Modified gene gun barrel was constructed by, and can be obtained from the MRC-LMB mechanical workshop. The distribution pattern was aimed to concentrate around the CA1 area of the hippocampus (Figure 1D). The affected diameter was previously determined to be approximately 3 mm .
Survival assays and confocal microscopy
OTBS were then cultured for a further 24 h, or as otherwise noted. Lactate dehydrogenase (LDH) assay was used to determine cell survival following treatments according to manufacturers protocol (Clontech). Briefly, the colorimetric conversion of a tetrazolium salt added to the culture medium supernatant that absorbs at 490 nm is proportional to the number of lysed cells. The signal was normalized to untreated OTBS. Triton X-100 was used as a positive assay control to define maximal absorbance (i.e. equal to 0% survival). Survival was calculated as 1 - (sampled medium - negative control)/(positive control - negative control) and presented as a%.
As the epicentre of biolistic delivery was aimed to the CA1 region, this regio-selective targeting was confirmed by EYFP signal. Targeting using the modified barrel was shown very reproducible from a 10 mm targeting distance using our method, yet any misaligned OTBS delivery was excluded from the subsequent analyses. Damaged cells were also identified using a Terminal deoxynucleotide transferase dUTP nick end labelling (TUNEL) assay (Click-iT® TUNEL Alexa Fluor® Imaging Assay; Invitrogen) , which detects fragments of DNA from apoptotic and necrotic cells. dUTP solution was added to the OTBS as per manufacturers protocol. Propidium Iodide (PI) was also used to monitor the number of exposed nuclei. A final concentration of PI of 1.5 μM was added to the OTBS and incubated for 30 min then washed three times with PBS.
The slices were subsequently fixed with 4% paraformaldehyde (PFA; Sigma-Aldrich). For lineage differentiation, antibodies rabbit anti-NeuN (Merck; MAB377) and guinea pig anti-GFAP (Abcam; 4674) at 1:1000 and 1:500 dilutions respectively were incubated with the OTBS for 1 h. Following three PBS washes, the secondary donkey alexa fluor 488 anti-rabbit (Life technologies) and goat alexa fluor 547 anti-guinea pig (Life technologies) were used at 1:1000 and incubated 30 min. Cells were counterstained with diamidino-2-phenylindole (DAPI) for 30 min then washed three times with PBS. Following corresponding labelling OTBS were mounted in Vectashield. Brain slices were examined using an upright Bio-Rad Radiance 2100 confocal microscope and the numbers of labelled cells were counted. Only comparative brain areas were evaluated between conditions and the same magnification, pinhole size (1 AU), and gain intensity were maintained for each test. Labelled cells were counted from confocal images taken completely within these brain regions.
Experiments were performed in at least three independent experiments. Results are presented as mean ± standard deviation (SD). Data analysis was performed using Graphpad Prism 5.0 (La Jolla, USA). The unpaired 2-tailed Student’s t test was used for comparison of the average total amount of counted cells per representative image or the average absorbance measurements. A p value of < 0.05 was considered statistically significant.
This work was supported by the Medical Research Council Laboratory of Molecular Biology. Video was filmed and edited by the MRC LMB visual aids department. Vibroslicer and modified gene gun barrel was constructed by the MRC LMB mechanical workshop department. We would like to thank SC Lummis for her help with the manuscript.
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