Systemic Injection of Neural Stem/Progenitor Cells in Mice with Chronic EAE

Podsumowanie

The transplantation of neural stem/progenitor cells (NPCs) holds great promises in regenerative neurology. The systemic delivery of NPCs has turned into effective, low invasive, and therapeutically very efficacious protocol to deliver stem cells in the brain and spinal cord of rodents and nonhuman primates affected by experimental chronic inflammatory damage of the central nervous system.

Streszczenie

Neural stem/precursor cells (NPCs) are a promising stem cell source for transplantation approaches aiming at brain repair or restoration in regenerative neurology. This directive has arisen from the extensive evidence that brain repair is achieved after focal or systemic NPC transplantation in several preclinical models of neurological diseases.

These experimental data have identified the cell delivery route as one of the main hurdles of restorative stem cell therapies for brain diseases that requires urgent assessment. Intraparenchymal stem cell grafting represents a logical approach to those pathologies characterized by isolated and accessible brain lesions such as spinal cord injuries and Parkinson's disease. Unfortunately, this principle is poorly applicable to conditions characterized by a multifocal, inflammatory and disseminated (both in time and space) nature, including multiple sclerosis (MS). As such, brain targeting by systemic NPC delivery has become a low invasive and therapeutically efficacious protocol to deliver cells to the brain and spinal cord of rodents and nonhuman primates affected by experimental chronic inflammatory damage of the central nervous system (CNS).

This alternative method of cell delivery relies on the NPC pathotropism, specifically their innate capacity to (i) sense the environment via functional cell adhesion molecules and inflammatory cytokine and chemokine receptors; (ii) cross the leaking anatomical barriers after intravenous (i.v.) or intracerebroventricular (i.c.v.) injection; (iii) accumulate at the level of multiple perivascular site(s) of inflammatory brain and spinal cord damage; and (i.v.) exert remarkable tissue trophic and immune regulatory effects onto different host target cells in vivo.

Here we describe the methods that we have developed for the i.v. and i.c.v. delivery of syngeneic NPCs in mice with experimental autoimmune encephalomyelitis (EAE), as model of chronic CNS inflammatory demyelination, and envisage the systemic stem cell delivery as a valuable technique for the selective targeting of the inflamed brain in regenerative neurology.

Wprowadzenie

Strong evidence has arisen from in vivo studies attesting to the therapeutic efficacy of the transplantation of somatic neural stem/precursor cells (NPCs) in animal models of CNS disorders^1-8. Nevertheless, a number of issues relating to the delivery of stem cells into the host require careful consideration before these experimental results can be translated into clinical applications. A particularly substantial hurdle towards the development of (nonhematopoietic) restorative stem cell therapies for multifocal, chronic inflammatory brain diseases is the identification of the ideal route of NPC injection. A firm understanding of the pathophysiology of the targeted disease (focal or multifocal; primary inflammatory or primary degenerative), and a cautious analysis of feasibility and risk issues associated with the delivery techniques are in identifying the optimal protocol for stem cell delivery.

While the focal (e.g. into the nervous system parenchyma) stem cell transplantation is a logical approach to the treatment of CNS diseases characterized by spatially confined areas of damage (e.g. Parkinson's and Huntington's disease, brain and spinal cord traumatic injuries, and stroke), the very same approach may prove to be practically not feasible in conditions such as MS, where a multifocal, chronic, and spatially disseminated CNS damage accumulates over time. In this latter case, targeting focal cell injections to individual lesions is also hindered by the limited capacity of transplanted NPCs to migrate over long distances within the CNS parenchyma, thus prompting the identification of alternative, more suitable methods of CNS targeting with less invasive NPC transplants.

Great promise emerged from the observations that NPCs target an intracranial tumor (e.g. glioma) in mice when injected intravascularly outside the CNS9. Following this seminal in vivo evidence of the stem cell pathotrophism¹⁰, extensive data have been accumulated pertaining to the feasibility and therapeutic efficacy of the systemic transplantation of NPCs in laboratory animals with experimental autoimmune encephalomyelitis (EAE), as a model of inflammatory CNS damage, via either intravenous (i.v.) or intracerebroventricular (i.c.v.) NPC injection^1,2,5,6,8.. We have first shown that this is dependent on the capability of transplanted NPCs to target and enter the inflamed CNS, and to subsequently engage multiple intercellular communications programs within specific microenvironments in vivo¹¹. In order to specifically target the CNS, NPCs are delivered directly into the cerebrospinal fluid (CSF) circulation by i.c.v. injection, or into the bloodstream via i.v. injection. Once entering either the bloodstream or CSF, transplanted NPCs actively interact with the blood brain (BBB) or blood cerebrospinal fluid (BCSFB) barriers and enter the CNS parenchyma. This interaction between the NPC graft and the BBB (or BCSFB) is regulated by specific set of NPC surface cell adhesion molecules (CAMs) and facilitated by the expression of high levels of CAM counter-ligands on activated endothelial/ependymal cells^12-14. Examples of these CAMs include the receptor for hyaluronate, CD44, and the intercellular adhesion molecule (ICAM)-1 ligand very late antigen (VLA)-4^5,15,16 (that, in leukocytes, are responsible of the interaction with activated ependymal and endothelial cells), and to a much lower extent Lymphocyte function-associated antigen (LFA)-1 and P-selectin glycoprotein ligand (PSGL)-1. NPCs also express a wide range of chemokine receptors, including CCR1, CCR2, CCR5, CXCR3, and CXCR4 (but do not express CCR3 and CCR7), which are functionally active, both in vitro and in vivo^5,16. Thus, systemically injected NPCs use these CAMs, along with G-protein coupled receptor (GPCRs), to accumulate at the level of the inflamed CNS. Conversely, NPCs injected systemically into healthy mice do not enter the CNS via vascular or cerebrospinal fluid space routes². CNS inflammation, or endothelial/ependymal cell activation following systemic cytokine or lypopolisaccharide (LPS) injection as a model of chemically induced encephalitis, is therefore necessary for the accumulation of systemically injected NPCs into the brain and spinal cord². Thus, successful targeting of the CNS with systemic NPC therapies is dependent on the identification of a disease specific window of Opportunity (WoO) in which the brain and spinal cord environment are conducive to the accumulation and transendothelial migration of NPCs. Such conditions generally arise in the context of acute and subacute inflammation¹⁷. Once having entered the CNS, transplanted undifferentiated NPCs have been shown to ameliorate the clinico-pathological features of mice as well as larger, nonhuman primates with EAE. This has been described to be dependent from minimal cell replacement² and remarkable secretion of immune regulatory and neuroprotective paracrine factors within perivascular CNS^2,5,6,18 vs non-CNS inflamed areas^19,20 (e.g. lymph nodes) in response to the inflammatory cell signaling elicited by infiltrating immune cells⁵.

Herein we describe the key methodological aspects of the systemic injection of somatic NPCs into a mouse model of chronic EAE. More specifically, we define the protocols that we have established to (i) derive, expand and prepare for transplantation somatic NPCs from the subventricular zone (SVZ) of adult C57BL/6 mice; (ii) induce chronic EAE in such mice and (iii) perform therapeutically efficacious systemic (i.v. or i.c.v) NPC transplantation into EAE mice.

Protokół

All procedures involving animals are performed according to the principles of laboratory animal care approved by the UK Home Office under the animals (scientific procedures) act 1986 (PPL No. 80/2457 to SP).

1. Derivation of Somatic Neural Stem/Progenitor Cells (NPCs) from the Subventricular Zone (SVZ) of the Brain of Adult Mice

1. Preparation of dissection instruments and media
   NB: These two solutions must be prepared 1-2 hr before dissections instruments are ready and prewarmed at 37 ºC at least 20-30 min before use (it helps to dilute papain and optimizes enzyme activity).
   
   1. Autoclave one straight sharp scissor, one small surgical scissor and two small curved serrated forceps.
   2. ‘Digestion’ solution: Prepare two separate 50 ml tubes with:
      Solution #1: 25 ml Earle's Balanced Salt Solution (EBSS) + 10 mg ethylenediaminetetraacetic acid (EDTA) + 10 mg L-cysteine; and
      Solution #2: 25 ml EBSS + 50 mg papain.
   3. Prepare ‘Complete Growth Medium’ (CGM): complete mouse basal medium with mouse proliferation supplements, heparin 0.002%, basic fibroblast growth factor (bFGF; 10 ng/ml), epidermal growth factor (EGF; 20 ng/ml), and antibiotics (Pen/Strep).
2. Brain dissection
   NB: The removal of the temporal bones can easily damage the tissue because of their sharpness. To avoid this, firmly secure the bones with the forceps and pull out until the entire bone has been removed.
   
   1. For every preparation of NPCs, cull by cervical dislocation n= 5-7, 4-8 week old C57BL/6 mice.
   2. Cleanse with 70% ethanol (in water) the hair of the culled mice and cut behind the ears with the straight sharp scissor to remove the head;
   3. Make a midline incision using a small surgical scissor to cut the skin over the skull. Using the forceps, fold up the two patches of skin to expose the skull.
   4. With the small surgical scissor perform two little cuts at the base of the skull and remove the bones under the pons/medulla (ventral skull). Proceed by pulling out the temporal bones. With the same scissor perform a cut all along the skull, starting from the base to the bulbs, without damaging the surface of the brain. Also, perform a cut between the frontal bones and the eyes, to facilitate the removal of the parietal bones. With two forceps start removing the skull by pulling each of the parietal bones towards the outside. While pulling, pay attention to the meninges, which can damage the brain when the bones are being removed.
   5. Once the skull has been removed, slide the forceps between the brain and the skull to completely detach the meninges left. Gently lift up the brain from the skull. Cut the optic nerves to release the brain and finally collect the brain in a tube with cold phosphate buffered saline (PBS).
   6. Keep the tube on ice and repeat the same procedure for all the mice.
3. Dissection of the SVZ, neurosphere formation and maintenance assays
   Average number of cells x dilution factor x 10⁴
   
   Where 10⁴ represents the conversion of the total volume of the hematocytometer chamber (total volume = 0.1 mm³ -> 10-4 cm³ -> 10-4 ml). When considering the dilution factor, both the one done with CGM and with the vital stain have to be taken into consideration. As an example, if 160 cells have been counted in the 4 corner squares, the final density (cells/ml) of the cell suspension will be:
   
   160/4 x 5 (dilution with CGM) x 2 (dilution with vital stain) x 10⁴
   
   1. Turn on a dissection hood equipped with a dissecting microscope.
   2. Clean all the surfaces with 70% ethanol (in water), and spray with an anti Mycoplasma solution to lower the risk of contamination.
   3. Cover the bottom of a beaker with sterile gauze (to preserve sharpened instruments) and fill it with 70% ethanol (in water). Soak in the beaker two pairs of forceps, one pair of micro scissors and a surgical blade.
   4. Place the whole brain on the brain-slicer matrix.
   5. Using two razor blades perform a coronal sectioning 2 mm from the anterior pole of the brain, excluding the optic tracts, and 3 mm posterior to the previous cut; and place the tissue on a clean Petri dish.
   6. Under the dissecting microscope isolate the SVZ tissue and cut into 1 mm³ pieces using iridectomy scissors. Repeat for all the brains.
      1. Mix well the two solutions (section 1.1.2) above and filter through a 0.22 μm filter immediately after the brains are dissected and the SVZs are ready to be digested.
   7. Transfer the sections into 30 ml of ‘Digestion’ solution, gently resuspend with a10 ml pipette and incubate 30 min at 37 °C in 5% CO₂. Every 15 min gently shake the tube 2-3x.
   8. Centrifuge at 300 x g for 10 min.
   9. Remove the supernatant and resuspend the pellet in 200 μl of CGM by pipetting first with a P1000 and then with a P200 pipette (10-20x each), until obtaining a single cell suspension.
   10. Take the suspension up to 5 ml with CGM and transfer to a T25 cm² flask.
   11. After 5-7 days in vitro (DIV) neurospheres will form. Collect the suspension into a 15 ml tube and centrifuge 10 min at 150 x g.
   12. Remove the supernatant and resuspend the pellet into 200 μl of CGM.
       Dissociate the neurospheres mechanically by passaging the cells 100-150x with a P200 pipette, until obtaining a single cell suspension and take it up to 1 ml with CGM.
   13. Dilute the cell suspension, e.g. 10 μl of cell suspension in 40 μl of CGM to obtain a 1:5 dilution, and mix well. Mix 10 μl of the dilute cell suspension with 10 μl of a vital stain and mix well.
   14. Fill a hemocytometer counting chamber with 10 μl of a 1:1 cell suspension:vital stain solution. Separately count the number of live (white) and dead (blue) cells in the 4 corner squares. To determine the number of cells/ml, apply the following calculation:
   15. Resuspend 2 x 10⁵ cells in 5 ml of CGM and transfer to a T25 cm² flask;
   16. Repeat sections 1.3.11-1.3.12 every 4-5 DIV. From the second passage of expansion onwards, assess the cellular viability by vital stain exclusion and start building up a continuous growth curve by plating NPCs at clonal density (8,000 cells/cm2), as described²¹. Keep the cell numbers and repeat the procedure every 4-5 DIV. To generate a continuous growth curve, proceed as follows:
       NB: To have a good cell preparation, after 4-5 DIV spheres should have reached a diameter of 150-200 μm. To have a good estimate of the cell density, it is important to find an optimal dilution factor in order to have well distributed, nonoverlapping cells throughout the hematocytometer. Ideally, there should be between 50-200 total cells. When counting, only the cells comprised in the square without touching the borders have to be considered. Also, the viability of the cells is a crucial factor to have a healthy preparation. Importantly, it should be greater of 90%. A linear growth curve is another indicator of a healthy cell preparation.
       
       1. Count the number of live and dead cells (e.g. 1.3 x 10⁶).
       2. Define the growth rate dividing the number of live cells by the number of plated cells (e.g. 1.3 x 10⁶/2 x 10⁵= 6.5).
       3. Calculate the total number of cells by multiplying the growth rate for the total number of cells present at the previous time point (at the beginning= 2 x 10⁵).
       4. Report the mean ± standard deviation to build a linear trend line.
   17. Starting from passage 6, mechanical dissociation is replaced by enzymatic dissociation. After centrifugation at 150 x g for 10 min, remove the supernatant, resuspend the pellet in 200 μl of cell aggregate dissociation solution, resuspend 7-8x with a P200 and incubate 10 min at 37 °C, 5% CO_2.
   18. Resuspend 7-8x with a P200 to obtain a single cell suspension and add 800 μl of CGM. Count the cells (both live and dead) and establish their viability. Resuspend 2 x 10⁵ cells in 5 ml of CGM and transfer to a T25 cm² flask.
4. Viral transduction of NPCs for in vivo cell tracking
   NB: To verify the efficiency of viral transduction, build a parallel growth curve with transduced and nontransduced NPCs. In addition, the clonal efficiency, that is the absolute number of neurosphere forming cells present within a cell preparation or a cell cycle analysis by DNA content (with propidium iodide, PI), may be used as further indications of the cell status. If the percentage of infected cells should not be good, the protocol of viral transduction can be repeated a second time with the same population of cells. Once the level of infection is satisfactory and the growth curve is similar to that obtained with wild type cells, transduced NPCs can be expanded and/or transplanted.
   
   1. Harvest the neurospheres and obtain a single cell suspension. Plate the cells at high density (1.5 x 10⁶ cells in a T75 cm² flask) in 10 ml CGM.
   2. After 12 hr add 3 x 10⁶ T.U./ml of a third generation lentiviral vector pRRLsin. PPT-hCMV engineered with the E. coli-derived β-galactosidase (lacZ) or with green fluorescent protein (GFP).
   3. 48 hr later, harvest the cells, centrifuge at 300 x g for 10 min and replate the cells at a 1:1 ratio.
   4. After 3 passages in vitro verify the efficiency of the infection. Flow cytometry is commonly used to test infection efficacy, and the satisfactory level of infection is commonly accepted to be in the range of 75-95% of positive cells. Check again the efficiency of the infection after 3 further passages of expansion to verify the maintenance of the marker expression.
5. Neurosphere freezing
   1. Harvest the neurospheres from a T25 cm² flask, centrifuge at 300 x g for 10 min, and discard the supernatant.
   2. Resuspend the pellet with 1 ml of freezing medium (CGM with 10% dimethyl sulfoxide (DMSO).
   3. Place the cryovials at -80 °C within a freezing container.
   4. After at least 24 hr move the cells to a cryobox and store at -80 °C for months, or bring to liquid nitrogen (N₂) for longer storage.
6. Neurosphere thawing
   NB: To avoid the toxic effects of prolonged contact of NPCs with DMSO, the thawing process must be as fast as possible.
   
   1. Remove the cryovial from the -80 °C/N₂ and keep it on dry ice.
   2. Quickly thaw the vial on a water bath, until almost all the cell suspension is defrosted and only a small piece of iced suspension remains.
   3. Resuspend the cell suspension with 5 ml of prewarmed fresh CGM.
   4. Centrifuge at 300 x g for 10 min.
   5. Remove the supernatant, resuspend gently with 5 ml of fresh CGM and plate the cell suspension in a clean, untreated T25 cm² flask.
7. 1.7) NPC characterization
   NB: The last wash PBS can be replaced with 0.05% sodium azide-PBS to prevent fungal growth or contaminations, and coverslides are stored at 4 °C for 2-3 weeks.
   
   NB: To stain for intracellular markers add a permeabilizing agent to PBS in the blocking solution. If the source of the primary antibody is goat, bovine serum albumin (BSA) or serum of other than goat should be used.
   
   NB: To stain for intracellular markers use a permeabilizing agent in the primary antibody solution.
   
   1. Place a 13 mm glass coverslide on the bottom of a 24 well plate. Add 150 μl of coating solution on the top of each coverslide to create a small drop. Incubate for at least 30 min at 37 °C, 5% CO_2.
   2. Harvest the neurospheres and dissociate to obtain a single cell suspension.
   3. Count live cells and dilute to obtain 80,000 cells/35 μl. Remove the excess of coating solution from the coverslide by gentle aspiration, and plate the 35 μl of cell suspension.
   4. Incubate 25 min at 37 °C, 5% CO₂. Quickly check at the contrast phase microscope if the cells have started to adhere.
   5. Prepare the differentiation medium by mixing basal mouse medium with the appropriate supplements (see Table 1) and antibiotics (Pen/Strep).
   6. Add 400 μl of differentiation medium and incubate at 37 °C, 5% CO_2.
   7. After 3 DIV, change half of the medium with fresh differentiation medium.
   8. After 6 DIV, remove the medium and wash once with PBS. Under a chemical hood remove the PBS and add 300 μl of prewarmed 4% paraformaldehyde (PFA) 4% sucrose. Incubate for 5 min at room temperature (RT). Remove the PFA and wash 3x with PBS.
   9. To proceed with immunocytochemistry, remove the PBS and block with PBS 10% normal goat serum (NGS) (blocking solution), and incubate 1 hr at RT.
   10. Remove the blocking solution and add the desired primary antibody diluted with PBS 1% NGS. Incubate at 4 °C O/N or, alternatively, 120 min at RT.
   11. After the incubation, wash 2x with PBS. Incubate with the appropriate secondary antibody diluted with PBS 1%NGS. Incubate 60 min at RT.
   12. Wash 2x with PBS and counter-stain the nuclei with 4',6-diamidino-2-phenylindole (DAPI) diluted 1:20,000 with PBS permeabilizing agent for 3 min at RT in the dark. Wash twice with PBS and once with distilled water.
   13. Put a drop of mounting medium on a glass tissue slide and with forceps mount the coverslide with the cells facing the mounting medium. Gently press the coverslide to squeeze out the excess of mounting medium. Leave the coverslide in the dark at RT until the mounting medium is dried and store at 4 °C.

2. Myelin Oligodendrocyte Glycoprotein (MOG)-induced Experimental Autoimmunity in C57Bl/6 Mice

1. Preparation of emulsion
   1. On a glass beaker prepare an emulsion composed of Incomplete Freund’s adjuvant containing 4 mg/ml of Mycobacterium tuberculosis [otherwise defined as Complete Freund’s Adjuvant (CFA)] and 200 μg of MOG (peptide 35-55), considering that the total amount of emulsion per mouse will be 300 μl.
      NB: Appropriate controls of MOG-immunized mice in CFA are mice immunized with CFA only. The expected variance of disease onset in MOG-immunized mice is 11.3 (±1.8) dpi.
      
      NB: When calculating the total volume of emulsion needed, consider twice as much volume as the number of mice to immunize. Glassware should be preferred to plasticware to minimize the waste of part of the emulsion.
      
      1. With a glass syringe holding a 19 G needle blend for about 30 min, always keeping the emulsion on ice.
      2. To verify if the emulsion is ready, drop a small amount of emulsion on water. The emulsion is ready to be injected only if the drop remains as it is and does not disperse.
      3. Immunize the control group of mice with CFA only. Treat experimental mice (MOG immunized) with MOG in CFA. The expected variance of disease onset in MOG immunized mice is 11.3 (±1.8) dpi.
   2. Transfer the 19 G needle to a 1 ml plastic syringe and aspirate the emulsion. Avoid bubbles, change the needle with a 25 G and leave the syringe on ice. Syringes filled with the emulsion are ready to be used and should be kept on ice for a couple of hr.
2. Immunization
   1. Place the mice (6-8 weeks old, female) into a warming box and wait for about 10 min to allow the tail vein to dilate.
   2. Transfer one mouse from the warming box to a mouse restrainer. Close the restrainer to avoid any movement of the mouse.
   3. Fill a 1 ml insulin syringe with 100 µl of pertussis toxin (5 μg/ml) avoiding making bubbles. Slowly inject the solution in the tail vein. Remove the needle and press for a few seconds with a piece of paper to plug the bleeding.
   4. Place the mouse back in the cage and repeat the same procedure for all the mice.
   5. Anesthetize a mouse with continuous isoflurane inhalation (1-2%, 2 L/min) and inject 100 µl of the emulsion subcutaneously at the level of the two flanks and the base of the tail (300 μl emulsion/mouse). Slowly remove the syringe, avoiding the leakage of the emulsion.
   6. Mark the mouse with an ear puncher, place the mice in the cage and check until full recovery. Repeat for all the mice.
   7. After 48 hr (2 days post immunization, dpi) repeat section 2.2.3.
3. Behavioral analysis of EAE mice
   1. Starting from 5 dpi, weigh the mice daily and monitor their locomotor performances by using the scale scoring system described in Table 1.

3. Injection of Neural Stem/Progenitor Cells into the Tail Vein (i.v.)

1. Cell preparation
   1. Harvest neurospheres by centrifugation at 300 x g for 10 min.
   2. Remove the supernatant and add 200 μl of cell aggregate dissociation solution. Incubate 10 min at 37 °C, 5% CO_2.
   3. Gently resuspend 10-12x (avoiding bubbles) with a P200 until obtaining a single cell suspension and take to 800 μl with basal medium without Ca²⁺ and Mg²⁺.
   4. Count the cells by using a vital stain to assay cell viability and dilute the suspension with basal medium without Ca²⁺ and Mg²⁺ to obtain a final density of 10⁶ cells/150 μl. Keep the cell suspension on ice until use.
2. NPC i.v. injection
   NB: The ideal dissociation into single cell suspension and the absence of air bubbles are two key aspects to consider to reduce the risk of either clumps/aggregates vs emboli formation which might result in vein occlusion and consequent death.
   
   1. At the peak of the disease (16-18 dpi), weigh and score the mice. Distribute the mice according to their score in order to have homogeneous groups.
   2. Place the mice into a warming box and wait for about 10 min to allow the tail vein to dilate.
   3. Transfer one mouse from the warming box to a mouse restrainer. Close the restrainer to avoid any movement of the mouse.
   4. Fill a 1 ml insulin syringe with 150 μl of cell suspension and make sure to remove all the bubbles. Slowly inject the solution into the tail vein. Remove the needle and press for a few seconds with a piece of paper to plug the bleeding (Figures 6A and 6B).
   5. Place the mouse in the cage and check until recovery. Repeat the same procedure for all the mice.

4. Injection of Neural Stem/Progenitor Cells into the Cisterna Magna (i.c.v)

1. Cell preparation
   1. Harvest NPCs by centrifuging at 300 x g for 10 min.
   2. Remove the supernatant and add 200 μl of cell aggregate dissociation solution. Incubate 10 min at 37 °C, 5% CO_2.
   3. Gently resuspend 10-12x with a P200 until obtaining a single cell suspension and take to 800 μl with basal medium without Ca²⁺ and Mg²⁺.
   4. Count the cells and dilute the suspension with basal medium without Ca²⁺ and Mg²⁺ to obtain the desired cell density. Keep the cell suspension on ice until use.
2. 4.2) NPC i.c.v. injection
   1. At the peak of the disease (16-18 dpi), weigh and score the mice. Distribute the mice according to their score in order to have homogeneous groups.
   2. Place the mouse on a stereotaxic apparatus under continuous isoflurane inhalation (1-2%, 2 L/min). Secure the head of the mouse with the ear bars. Then adjust both the mouth and nose pieces. Make sure the head of the mouse is flat and fixed.
   3. Swab the head of the mouse with Povidone-iodine (PVP-I) and make an incision to cut the skin in the posterior portion of the head to expose the skull.
   4. Using a micromanipulator, insert the tip of a microliter syringe into the cleft between the occiput and the atlas vertebra through the intact muscles and ligaments in the midline at the back of the neck. The bent part of the needle is kept in close contact with the internal surface of the occiput for the entire length, as described²².
   5. Slowly insert the needle and wait a few sec. The operator is meant to learn to recognize the feeling of the needle being "hooked" to the mouse skull, prior to start injecting the cell preparation. Slowly inject the volume of cells (within 3-5 min). Leave the needle in place for additional few seconds after the injection and remove slowly the syringe.
   6. Stitch up the skin and place the mouse into a recovery cage until full recovery.

5. Tissue Processing

1. Deeply anaesthetize the mice with a mixture of 0.5 ml ketamine (100 mg/ml), 0.25 ml xylazine (23.32 mg/ml) and 4.25 ml sterile water and transcardically perfuse, washing with saline-EDTA and fixing with 4% PFA. Remove both the vertebral columns and brains and postfix in 4% PFA for 12 hr at 4 °C. Wash the tissue in PBS, remove the spinal cords from the bones and leave the tissue at least 48 hr in 30% sucrose (in PBS) at 4 °C. Embed the tissues in optimal cutting temperature (OCT) compound and snap freeze with liquid nitrogen, as described².
2. Use a microtome to cut the tissues in 10-12 μm thick slices.
3. Alternatively, embed fresh tissue in agarose and cut tissue using a vibratome 50-80 μm thick slices.
4. In both the cases, incubate O/N at 37 °C in 5-bromo-4-chloro-3-indolyl-β D-galactopyranoside (X-gal) solution to detect nuclear β-galactosidase activity.
5. Recut sections containing β-gal+ cells into 5 µm slices and double stain using antiglial fibrillary acidic protein (GFAP) for astrocytes (50 μg/ml), antineuronal nuclear antigen (NeuN) for neurons (1μg/ml) and antiNestin for undifferentiated neural cells (10 μg/ml).
6. Proceed as described in sections 1.7.11 and 1.7.12. For multiple stainings make sure to use secondary antibodies conjugated with different fluorophores.
7. For tissues containing GFP labeled cells proceed as explained in steps 5.1-5.3 and proceed with the multiple stainings.
8. Add some drops of mounting medium to the slides and cover with a tissue coverslip.
9. For sections stained with biotin conjugated antibodies prepare a solution of avidin biotin complex (ABC solution, see Table 2) and leave in agitation for 45 min.
10. Incubate the slices 5 min with 1% H₂O₂ to block the activity of endogenous peroxidase.
11. Wash twice with PBS.
12. Incubate with ABC solution for 1hr at RT.
13. Wash twice with PBS.
14. Incubate with 3,3'-diaminobenzidine solution and 0.3% H₂O₂. Monitor the reaction under a microscope and wash with PBS as soon as the slice start getting brown (usually around 5-10 min).
15. Wash twice with PBS and proceed as described in step 5.7.

Comprehensive list of materials and reagents is shown in Table 2.

Wyniki

NPC derivation and characterization
SVZ dissections are performed on pools (n= 5-7 mice/pool) of 6-8 week old C57Bl/6 mice by means of mechanical and enzymatic dissociation (Figure 1A). After a few days of culturing in CGM, free-floating neurospheres begin forming (Figures 1A and 1B). Primary spheres are collected and mechanically passaged every 4-5 DIV. Upon passaging, numbers of live and dead cells are ascertained and cumulative cell numbers plotted to generate a...

Dyskusje

Somatic stem cell based therapies are emerging as one of the most promising strategies for treating chronic inflammatory CNS disorders such as MS2¹¹. While the mechanisms sustaining their therapeutic effects still need to be completely elucidated, the significant impact of NPC transplantation in different experimental models of neurodegenerative diseases has given rise to the somewhat provocative belief that stem cells may soon be applied into human studies. However, before envisaging any potential human appli...

Materiały

Name	Company	Catalog Number	Comments
Cell culture
EBSS	Sigma	E2888
L-Cystein	Sigma Aldrich	C7352
Papain	Worthington	30H11965
EDTA	Fisher Scientific	D/0700/50
Mouse NeuroCult basal medium	Stem Cell Technologies	05700
NeuroCult proliferation supplements	Stem Cell Technologies	05701
Heparin	Sigma	H3393
Basic fibroblast growth factor	Peprotech	100-18B-1000
Epidermal growth factor	Peprotech	AF-100-15-1000
Pen/Strep	Invitrogen	1514012
Matrigel (coating solution)	BD Biosciences	354230
NeuroCult® Differentiation Kit (Mouse)	Stem Cell Technologies	05704
Accumax	eBioscience	00-4666-56
Dulbecco's PBS (DPBS) (10x) without Ca and Mg	PAA Laboratories	H15-011
Myco trace	PAA Laboratories	Q052-020
Dimethyl sulfoxide (DMSO)	Sigma	D2650
Immunofluorescence
Normal goat serum	PAA Laboratories	B11-035
Polyethylene glycol p-(1,1,3,3-tetramethylbutyl)-phenyl ether	Sigma Aldrich	T8787
Mouse anti Nestin	Abcam	ab11306
Rabbit anti GFAP	DAKO	203344
Mouse anti Histone H3 (phospho S10)	Abcam	ab14955
Rabbit anti MAP-2	Abcam	ab32454
Rat anti MBP	AbD SEROTEC	MCA409S
Anti-O4 Antibody, clone 81 | MAB345	Millipore	MAB345
DAPI	Invitrogen	D1306
Mounting solution	DAKO	S3023
EAE
Freund's Adjuvant Incomplete	Sigma Aldrich	F5506
Mycobacterium tuberculosis	DIFCO	H37Ra
MOG(35–55)	Espikem
Pertussis toxin	List Biological Laboratories	181
Tissue processing
Iris scissor straight	Fine Sciences Tools	14060-09
Blunt/bended forceps	Fine Sciences Tools	11080-02
Brain slicer	Zivic Instruments	BSMAS005-1
Surgical blades	Swann-Morton	324
P200, P1000 pipettes
Ketamine (Vetalar)	Boehringer Ingelheim	01LC0030
Xylazine (Rompun)	Bayer	32371
Stereotaxic frame	KOPF	Model 900
Hamilton syringe	Hamilton	7762-04
Paraformaldehyde (PFA)	Sigma	158127
VECTASTAIN Elite ABC Kit	Vector Laboratories	PK-6100