We gratefully acknowledge Lydia Sorokin, who has shared her original in situ zymography protocol10 with us.&#160;

All studies were conducted under the guidelines according to the Swiss legislation on the protection of animals and were approved by the Veterinary Office of the Canton of Bern, Switzerland (permission numbers: BE 31/17 and BE 77/18).
1. Housing of C57BL/6 mice in specific pathogen free (SPF) conditions
<ol>
	<li>House mice in individual ventilated cages with a 12/12 h light-dark cycle. Provide food and water ad libidum.&#160;To supervise microbiological quality of the mice, the experimental cohort underwent quarterly health monitoring by dirty bedding sentinels following FELASA recommendations13.</li>
	<li>Use ear punches to individually mark 8-12 week old female C57BL/6 mice.</li>
</ol>
2. Immunization of C57BL/6 mice
<ol>
	<li>Preparation of solutions14:
	<ol>
		<li>For Complete Freund&#8217;s Adjuvant (CFA), mix 30 mL of Incomplete Freund&#8217;s Adjuvant with 120 mg of freshly pestled heat inactivated Mycobacterium tuberculosis (H37RA) under a fume hood. Store stock solution at 4 &#176;C.</li>
		<li>For the MOGaa35-55-peptide stock solution, dissolve MOGaa35-55-peptide in sterile PBS (4 mg/mL) and store at -80 &#176;C.</li>
		<li>Prepare the MOG-emulsion:&#160;
		<ol>
			<li>Dilute CFA 1:2 with MOG-peptide stock solution in a 2 mL microtube.&#160;</li>
			<li>Seal the microtube with sealing film and fix on a Vortex mixer by completely covering the tube with adhesive tape. Vortex emulsion for 4 h at 4 &#176;C.</li>
		</ol>
		</li>
		<li>Prepare syringes with stabile emulsion:&#160;
		<ol>
			<li>Take the microtube and quickly spin down the emulsion using a small table centrifuge. Collect emulsion into a syringe using a 18G x 1&#189;&#8217;&#8217; (1.2 mm x 40 mm) injection needle.&#160;</li>
			<li>According to the number of mice adjust the emulsion volume in the syringe (100 &#181;L/mouse) and replace the 18G needle with a 27G x &#190;&#8217;&#8217; (0.4 mm x 19 mm) injection needle. Seal the injection needle attached to the syringe with sealing film.&#160;</li>
		</ol>
		</li>
		<li>For the pertussis toxin (PTx) stock solution, dissolve 50 &#181;g of lyophilized PTx in 500 &#181;L of sterile PBS (100 ng/&#181;L). Store stock solution at 4 &#176;C.</li>
		<li>For the PTx working solution, mix 97 &#181;L of sterile PBS with 3 &#181;L of PTx stock solution (300 ng/100 &#181;L) per mouse (for intraperitoneal injection use a 30G x &#189;&#8217;&#8217; (0.3 mm x 13 mm) needle).</li>
	</ol>
	</li>
	<li>EAE induction
	<ol>
		<li>Anesthetize C57BL/6 mice with isofluorane using a vaporizer system. To induce anesthesia in mice, expose the mouse to 4.5% isofluorane in oxygen in a small incubation chamber before transferring the mouse to a facemask with 2.1% isofluorane.&#160;Use an anesthesia unit equipped with heating pad to prevent hypothermia of the mouse.</li>
		<li>Fix the anesthetized mouse in one hand and first inject 30 &#181;L of MOG35-55/CFA-emulsion subcutaneously into hind leg flanks (Figure 1: 1 + 2; in total 60 &#181;L; left flank 30 &#181;L and right flank 30 &#181;L) in close proximity to the inguinal lymph nodes.</li>
		<li>Place the mouse on its belly and inject 20 &#181;L of MOGaa35-55/CFA-emulsion into the left and right soft fatty tissue at the tail root (Figure 1: 3 + 4; in total 40 &#181;L; left side tail root 20 &#181;L and right side tail root 20 &#181;L) and a little droplet of MOGaa35-55/CFA-emulsion into the neck of the mouse (Figure 1: 5).</li>
		<li>Inject 100 &#181;L of PTx solution intraperitoneally into the mouse. Hold the head of the mouse below the body center avoiding injection into the intestine.&#160;</li>
		<li>Replace maintenance diet (extrudate major nutrients: crude protein 18.5%; crude fat 4.5%; crude fiber 4.5%; crude ash 6.5%; starch 35%; metabolic energy: 13.1 MJ/kg) to breeding diet (extrudate major nutrients: crude protein 23.5%; crude fat 5.5%; crude fiber 3%; crude ash 5.7%; starch 36%; metabolic energy: 14.3 MJ/kg) in order to provide the mice with food of higher energy content before and during the expected clinical disease.&#160;</li>
		<li>Remove the face mask and transfer the mouse to its home cage with a warming pad.&#160;Make sure the mouse is fully awake and motile after 10 minutes.&#160;</li>
		<li>Repeat the PTx injection (2.2.4) 48 h after the first treatment.</li>
	</ol>
	</li>
</ol>
3. Scoring of EAE mice
<ol>
	<li>Check the health status of EAE mice every morning by taking a look inside the cages.</li>
	<li>Score EAE mice every afternoon.</li>
	<li>Take every individual mouse included in the EAE experiment out of the cage and check whether the tail has tonus by moving it upward with a finger. A healthy mouse will keep its tail up (the tail has a tonus). If clinical EAE has started, the tail tonus will be lower, visible by a gradual drop of the tail. Eventually the mouse will not be able to lift its tail at all.&#160;</li>
	<li>Place every individual mouse included in the EAE experiment on the clean bench and observe and document the walking behavior. See Table 115&#160;for scoring criteria for the assessment of disease severity (the EAE score).</li>
	<li>Assess and document the weight of every mouse included in the experiment.</li>
	<li>To ensure adequate food and water uptake by mice displaying a clinical EAE score of 1 supply moistened food in a plastic dish on the bottom of the cage and refresh daily.</li>
</ol>
4. In vivo permeability assay
<ol>
	<li>Preparations of solutions:
	<ol>
		<li>For dextran stock solutions, dissolve 10 mg of 10 kDa Dextran Alexa Fluor 488 as well as 3 kDa Dextran Texas Red in 500 &#181;L of 0.9% sodium chloride solution (20 mg/mL).</li>
		<li>For the dextran working solution, just before injection pipet 55 &#181;L of 10 kDa Dextran Alexa Fluor 488 stock solution (20 mg/mL) onto a piece of sealing film and add 55 &#181;L of 3 kDa dextran Texas Red stock solution (20 mg/mL). Mix and collect 100 &#181;L into a disposable fine syringe (final concentration 2 mg/100 &#181;L).&#160;</li>
		<li>For the 10% formaldehyde (PFA) stock solution, combine 10 g of PFA extra pure powder, 100 mL of PBS, and 200 &#181;L of 1N NaOH in a clean glass beaker and heat up to precisely 56 &#176;C under stirring using a magnetic stirrer; keep at 56 &#176;C for 30 min until the PFA is completely dissolved; cool down to room temperature; adjust pH to 7.4; and filter through a paper filter. Store at - 20 &#176;C. The stock solution can be diluted further using PBS.</li>
	</ol>
	</li>
	<li>Shortly anesthetize healthy C57BL/6 mice or C57BL/6 mice suffering from EAE with isoflurane (the mouse will be sedated for approximately 1 min). Use an automated system as in step 2.2.1 (mice will be exposed to 4.5% isoflurane in oxygen in an induction chamber and then transferred to a facemask with 2.1% isoflurane).</li>
	<li>Place the anesthetized mouse in lateral position on the table, then intravenously (e.g. retro-orbitally) inject 100 &#181;L of fluorescent tracers into the mouse before the mouse wakes up.</li>
	<li>Immediately remove the facemask and make sure the mouse is fully awake and motile after the short anesthesia. Let the tracer circulate for 15 min.</li>
	<li>Proceed with step 5.1.</li>
</ol>
5. Perfusion of mice
<ol>
	<li>For in vivo permeability assessment:
	<ol>
		<li>Begin the procedure 15 min after fluorescent tracer injection by inducing deep isoflurane anesthesia.&#160;To induce deep anesthesia in mice use 2.3% of isoflurane in oxygen.&#160;Use the paw withdrawal reflex to judge the depth of the anesthesia (pinch the skin between the toes; a lack of flexion indicates a sufficient depth), and probe the reflexes of both the forelimb and the hindlimb in mice subjected to EAE.&#160;</li>
		<li>Fix the mouse on its back and spray the belly with ethanol. Open the thorax using a scissor and remove the diaphragm. Open the right atrium of the beating heart using a scissor and perfuse the mouse through the left ventricle of the heart with 10 mL of PBS followed by 10 mL of 4% PFA in PBS.&#160; 
		CAUTION: To avoid inhaling PFA, perfuse the mouse in a fume hood.</li>
		<li>Proceed to section 6.&#160;</li>
	</ol>
	</li>
	<li>For in situ zymography:&#160;
	<ol>
		<li>Induce deep isoflurane anesthesia&#160;using 2.3% isoflurane in oxygen&#160;in a mouse suffering from EAE, and check the depth of anesthesia as in step 5.1.1.</li>
		<li>Next, fix the mouse on its back and spray the belly with ethanol. Open the thorax using a scissor and remove the diaphragm. Open the right atrium of the beating heart using a scissor and perfuse the mouse through the left ventricle of the heart with 20 mL of PBS.</li>
		<li>Proceed to section 6.</li>
	</ol>
	</li>
</ol>
6. Dissection and freezing of brains
<ol>
	<li>Preparation of cooling bath:
	<ol>
		<li>Fill a flat dewar container with crushed dry ice and add 2-methylbutane (Isopentane) until the liquid reaches about 1 cm above the dry ice pack. Cover with a loose lid &#8211; e.g., an ice bucket cover.</li>
	</ol>
	</li>
	<li>Clip off the head of the perfused mouse with sharp scissors and remove skin and ears using a smaller set of scissors.</li>
	<li>Carefully dissect the skullcap by cutting from the foramen magnum towards the front at the left and the right side allowing to upfold the skullcap over the brain. Then, carefully lift out the intact brain from the base of the skull while severing the optical nerves using a flat metal spatula.&#160;</li>
	<li>Place brain on aluminum foil and cut the brain in three pieces (frontal brain, middle brain, and cerebellum + brain stem) by placing two coronal cuts.</li>
	<li>Fill a cryomold (25 mm x 20 mm x 5 mm) to the first quarter with optimum temperature cutting (O.C.T.) matrix, place brain slices with the anterior side of each brain piece facing downwards into the cryomold, and cover tissue completely with O.C.T. matrix.</li>
	<li>Place the cryomold with the tissue in a horizontal orientation into the 2-Methylbutane bath and make sure that the tissue freezes from the bottom to the top within 1 minute by avoiding dipping the entire tissue block into the bath.</li>
	<li>Transfer frozen tissue to -80 &#176;C for storage and proceed with section 7.</li>
</ol>
7. Preparation of frozen tissue sections
<ol>
	<li>Equilibrate temperature from frozen tissue from -80 &#176;C to -20 &#176;C in the cryostat for 30 min.</li>
	<li>Remove tissue block from the cryomold and mount on the cryostat tissue holder (set to -15 &#176;C) using O.C.T. matrix.</li>
	<li>Trim the edges of the tissue block on the holder of the cryostat with a sharp scalpel, and start cutting into the tissue block by removing 20 &#181;m sections with the cryostat knife until the tissue is visible.</li>
	<li>For the analysis of in vivo BBB permeability:
	<ol>
		<li>Cut 6-10 &#181;m tissue sections, collect them on adhesion glass slides, and immediately image the sections covered with a cover slip using a fluorescence microscope.&#160;</li>
		<li>Assess appearance of blood vessels in the brain (pay attention to sharp borders of non-leaky blood vessels compared to diffuse fluorescence patterns observed for leaky blood vessels). As positive control, verify the leakage of the tracer into the stroma of the circumventricular organs or the choroid plexus which lack a BBB.</li>
	</ol>
	</li>
	<li>For in situ zymography:
	<ol>
		<li>Cut 6 &#181;m tissue sections using a cryostat, collect them on adhesion glass slides, and freeze tissue sections at -20 &#176;C in a freezing box containing silica gel in the lid.</li>
	</ol>
	</li>
</ol>
8. In situ zymography combined with laminin/CD45 immunofluorescence staining
<ol>
	<li>Prepare solutions:
	<ol>
		<li>Prepare embedding solution:&#160;
		<ol>
			<li>Mix 6 g of glycerol (analytical grade), 2.4 g of poly(vinyl alcohol), 6 mL of ddH2O, and 12 mL of 0.2 M Tris buffer, pH 8, and stir (magnetic stirrer) the solution for 4 h at RT.&#160;</li>
			<li>Transfer the solution to a 50 mL centrifuge tube and let it rest for 2 h at RT. Subsequently incubate the solution for 10 min at 50 &#176;C (water bath) and centrifuge for 20 min at 2,700 x g at room temperature.&#160;</li>
			<li>Take the supernatant and freeze in aliquots at -20 &#176;C.&#160;</li>
		</ol>
		</li>
		<li>Prepare cold gelatin solution:&#160;
		<ol>
			<li>Dissolve 0.1 g of cold gelatin from bovine skin in 10 mL of ddH2O.</li>
			<li>Let it soak for at least 1 day and store aliquots at 4 &#176;C.</li>
		</ol>
		</li>
		<li>Prepare ice-cold methanol (-20 &#176;C):&#160;
		<ol>
			<li>Put 100% methanol in a coplin jar and cool down to -20 &#176;C.</li>
		</ol>
		</li>
		<li>Prepare 10% sodium azide stock solution:&#160;
		<ol>
			<li>Add 1 g of sodium azide to 10 mL of ddH2O and store at room temperature.</li>
		</ol>
		</li>
		<li>Prepare 0.1% sodium azide working solution:&#160;
		<ol>
			<li>Mix 99 &#181;L of ddH2O with 1 &#181;L of 10% sodium azide stock solution.</li>
		</ol>
		</li>
		<li>Dissolve 1 mg of fluorescein conjugated dye-quenched (DQ) gelatin from pig skin in 1 mL of sodium azide working solution and store 100 &#181;L aliquots protected from light at 4 &#176;C.</li>
		<li>Dissolve 30 mg of 1,10-phenanthroline monohydrate in 76 &#181;L of ethanol and store at -20 &#176;C.</li>
		<li>Prepare 25x protease inhibitor solution:&#160;
		<ol>
			<li>Add 1 tablet of EDTA free protease inhibitor to 2 mL of ddH2O. Store at -20 &#176;C.</li>
		</ol>
		</li>
		<li>Just before use, prepare reaction solution (150 &#181;L/section):&#160;
		<ol>
			<li>Centrifuge the 1 mg/mL DQ gelatin solution for 5 min at 13,300 x g.&#160;</li>
			<li>Mix 127.2 &#181;L of ddH2O, 15 &#181;L of 10x reaction buffer (Gelatinase/Collagenase Assay Kit; see Table of Materials), 0.3 &#181;L of 20 mg/mL cold gelatin, 1.5 &#181;L of 1 mg/mL DQ gelatin, and 6 &#181;L of 25x protease inhibitor solution.</li>
		</ol>
		</li>
		<li>Just before use, prepare phenantroline negative control reaction solution (150 &#181;L/section):&#160;
		<ol>
			<li>Mix 125.2 &#181;L of ddH2O, 15 &#181;L of 10x reaction buffer, 0.3 &#181;L of 20 mg/mL cold gelatin, 1.5 &#181;L of 1 mg/mL DQ gelatin, 6 &#181;L of 25x protease inhibitor EDTA free, and 2 &#181;L of 2 M 1,10-phenantroline (MMP inhibitor).</li>
		</ol>
		</li>
		<li>Just before use, prepare cold gelatin (non-fluorescent) negative control reaction solution (150 &#181;L/section):
		<ol>
			<li>Mix 128.7 &#181;L of ddH2O, 15 &#181;L of 10x reaction buffer, 0.3 &#181;L of 20 mg/mL cold gelatin, and 6 &#181;L of EDTA-free 25x protease inhibitor.&#160;</li>
		</ol>
		</li>
		<li>Prepare primary antibody cocktail for counterstaining, for example, 0.95 &#181;g/mL polyclonal rabbit anti-laminin antibody and 10 &#181;g/mL polyclonal rat anti-CD45 antibody in 1% BSA in PBS, and prepare appropriate isotype control primary antibody cocktails.</li>
		<li>Prepare secondary antibody solution, for example, 7.5 &#181;g/mL Cy3 goat anti-rat + 15 &#181;g/mL AMCA anti-rabbit in 1% BSA in PBS (protect from light).</li>
	</ol>
	</li>
	<li>Thaw 6 &#181;m non-fixed brain tissue sections from EAE mice inside the plastic freezing box containing silica gel in the lid in a fume hood to avoid retention of water to the tissue and separate 2 tissue sections on one slide by drawing lines with a water repelling pen</li>
	<li>Prepare reaction solutions (steps 8.1.9-8.1.11), centrifuge for 5 min at 13,400 x g at room temperature, and pre-warm to 37 &#176;C using a water bath.</li>
	<li>Rehydrate the tissue sections for 5 min at 37 &#176;C using 1x reaction buffer. Then, pour off the 1x reaction buffer, add reaction solution on the tissue sections, and incubate for 4 h at 37 &#176;C. Wash slides 5 times in ddH2O.</li>
	<li>Fix sections for 5 min with ice-cold methanol at -20 &#176;C and afterwards wash sections once with PBS at room temperature.</li>
	<li>Add 1% BSA in PBS to the sections and incubate for 20 min at room temperature (protect from light). Then, discard 1% BSA in PBS from the sections by flipping the slides on tissue, add primary antibody cocktail, and incubate for 1 h at room temperature (protect from light).</li>
	<li>Wash sections twice with PBS, add secondary antibody cocktail, and incubate for 1 h at room temperature (protect from light).</li>
	<li>Wash sections twice with PBS, mount the slides with embedding solution, let mounted sections dry over night at room temperature (protect from light). Finally, analyze stained tissue sections using a fluorescent microscope.</li>
</ol>

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D., Karpus, W. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Experimental+autoimmune+encephalomyelitis+in+the+mouse.">Experimental autoimmune encephalomyelitis in the mouse.</a> Current Protocols in Immunology. 15, (2007).</li><li>Sobel, R. A., Tuohy, V. K., Lu, Z. J., Laursen, R. A., Lees, M. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Acute+experimental+allergic+encephalomyelitis+in+SJL/J+mice+induced+by+a+synthetic+peptide+of+myelin+proteolipid+protein.">Acute experimental allergic encephalomyelitis in SJL/J mice induced by a synthetic peptide of myelin proteolipid protein.</a> Journal of Neuropathology &amp; Experimental Neurology. 49, 468-479 (1990).</li><li>Westarp, M. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=T+lymphocyte+line-mediated+experimental+allergic+encephalomyelitis--a+pharmacologic+model+for+testing+of+immunosuppressive+agents+for+the+treatment+of+autoimmune+central+nervous+system+disease.">T lymphocyte line-mediated experimental allergic encephalomyelitis--a pharmacologic model for testing of immunosuppressive agents for the treatment of autoimmune central nervous system disease.</a> Journal of Pharmacology and Experimental Therapeutics. 242, 614-620 (1987).</li><li>Klotz, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=B7-H1+shapes+T-cell-mediated+brain+endothelial+cell+dysfunction+and+regional+encephalitogenicity+in+spontaneous+CNS+autoimmunity.">B7-H1 shapes T-cell-mediated brain endothelial cell dysfunction and regional encephalitogenicity in spontaneous CNS autoimmunity.</a> Proceedings of the National Academy of Sciences of the United States of America. 113, E6182-E6191 (2016).</li><li>Tietz, S. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=MK2+and+Fas+receptor+contribute+to+the+severity+of+CNS+demyelination.">MK2 and Fas receptor contribute to the severity of CNS demyelination.</a> PLoS One. 9, e100363 (2014).</li><li>Coisne, C., Mao, W., Engelhardt, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cutting+edge:+Natalizumab+blocks+adhesion+but+not+initial+contact+of+human+T+cells+to+the+blood-brain+barrier+in+vivo+in+an+animal+model+of+multiple+sclerosis.">Cutting edge: Natalizumab blocks adhesion but not initial contact of human T cells to the blood-brain barrier in vivo in an animal model of multiple sclerosis.</a> Journal of Immunology. 182, 5909-5913 (2009).</li><li>Korner, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Critical+points+of+tumor+necrosis+factor+action+in+central+nervous+system+autoimmune+inflammation+defined+by+gene+targeting.">Critical points of tumor necrosis factor action in central nervous system autoimmune inflammation defined by gene targeting.</a> Journal of Experimental Medicine. 186, 1585-1590 (1997).</li><li>Krueger, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Blood-brain+barrier+breakdown+involves+four+distinct+stages+of+vascular+damage+in+various+models+of+experimental+focal+cerebral+ischemia.">Blood-brain barrier breakdown involves four distinct stages of vascular damage in various models of experimental focal cerebral ischemia.</a> Journal of Cerebral Blood Flow &amp; Metabolism. 35, 292-303 (2015).</li><li>Hawkins, B. T., Egleton, R. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fluorescence+imaging+of+blood-brain+barrier+disruption.">Fluorescence imaging of blood-brain barrier disruption.</a> Journal of Neuroscience Methods. 151, 262-267 (2006).</li><li>Graesser, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Altered+vascular+permeability+and+early+onset+of+experimental+autoimmune+encephalomyelitis+in+PECAM-1-deficient+mice.">Altered vascular permeability and early onset of experimental autoimmune encephalomyelitis in PECAM-1-deficient mice.</a> Journal of Clinical Investigation. 109, 383-392 (2002).</li><li>Engelhardt, B., Sorokin, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+blood-brain+and+the+blood-cerebrospinal+fluid+barriers:+function+and+dysfunction.">The blood-brain and the blood-cerebrospinal fluid barriers: function and dysfunction.</a> Seminars in Immunopathology. 31, 497-511 (2009).</li><li>Owens, T., Bechmann, I., Engelhardt, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Perivascular+spaces+and+the+two+steps+to+neuroinflammation.">Perivascular spaces and the two steps to neuroinflammation.</a> Journal of Neuropathology &amp; Experimental Neurology. 67, 1113-1121 (2008).</li><li>Sixt, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endothelial+cell+laminin+isoforms,+laminins+8+and+10,+play+decisive+roles+in+T+cell+recruitment+across+the+blood-brain+barrier+in+experimental+autoimmune+encephalomyelitis.">Endothelial cell laminin isoforms, laminins 8 and 10, play decisive roles in T cell recruitment across the blood-brain barrier in experimental autoimmune encephalomyelitis.</a> Journal of Cell Biology. 153, 933-946 (2001).</li><li>Grewal, I. S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CD62L+is+required+on+effector+cells+for+local+interactions+in+the+CNS+to+cause+myelin+damage+in+experimental+allergic+encephalomyelitis.">CD62L is required on effector cells for local interactions in the CNS to cause myelin damage in experimental allergic encephalomyelitis.</a> Immunity. 14, 291-302 (2001).</li></ol>

No conflicts of interest declared.

Here, we present a protocol to induce and monitor EAE in female C57BL/6 mice. Females are preferentially chosen, and there is a incidence of women : men of 3:1 in MS. To assess the severity of EAE, we made use of a 3-point scoring sheet. EAE severity is generally scored with respect to the severity of motor dysfunctions. Mice with advanced stages of EAE, i.e. exhibiting a score above 2 should be sacrificed to avoid unnecessary suffering of the animals. Thus, it is recommended to score the mice at close intervals e.g. twi...

The central nervous system (CNS) coordinates all body and mental functions in vertebrates, and CNS homeostasis is essential for a proper communication of neurons. CNS homeostasis is warranted by the neurovascular unit (NVU), which protects the CNS from the changing milieu of the blood stream. The NVU is composed of CNS microvascular endothelial cells, which are biochemically unique and establish the blood-brain barrier (BBB) in continuous crosstalk with pericytes, astrocytes, neurons, and extracellular matrix (ECM) components, establishing two distinct basement membranes1. The endothelial basement membrane that ensheathes the abluminal aspect of the BBB endothelial cells harbors a high number of pericytes and is composed of laminin &#945;4 and laminin &#945;5, in addition to other ECM proteins2. In contrast, the parenchymal basement membrane consists of laminin &#945;1 and laminin &#945;2 and is embraced by astrocytic end-feet. The parenchymal basement membrane together with the astrocyte end-feet composes the glia limitans that segregates the CNS neuronal network from the cerebrospinal fluid filled perivascular or subarachnoid spaces3. Due to the unique architecture of the NVU, immune cell trafficking into the CNS is distinct from that into peripheral tissues as it requires a two-step process with the immune cells, first breaching the endothelial BBB and subsequently the glia limitans in order to reach the CNS parenchyma.&#160;
Multiple sclerosis (MS) is a common neuroinflammatory disease of the CNS, in which a large number of circulating immune cells enter the CNS and cause neuroinflammation, demyelination, and focal loss of BBB integrity4. Loss of BBB integrity is an early hallmark of MS, as indicated by the presence of gadolinium contrast enhancing lesions in the CNS as visualized by magnetic resonance imaging (MRI)5. Leukocyte extravasation into the CNS occurs at the level of postcapillary venules; however, the precise mechanisms involved in immune cell diapedesis across the BBB basement membrane and subsequently the glial barrier remain to be explored. Experimental autoimmune encephalomyelitis (EAE) serves as an animal model for MS and has significantly contributed to our current knowledge about MS pathogenesis. For instance, using the EAE model it has been discovered that leukocyte extravasation occurs in a multistep process, including an initial capture and rolling step mediated by selectins and mucin-like molecules such as P-selectin glycoprotein ligand (PSGL)-1, followed by integrin-dependent firm arrest and crawling of T cells on BBB endothelial cells to permissive sides for diapedesis6.&#160;
Once T cells have crossed the endothelial BBB and the endothelial basement membrane, they need to encounter their cognate antigen on macrophages or dendritic cells strategically localized in the leptomeningeal or perivascular spaces. This interaction induces focal production of pro-inflammatory mediators that trigger the subsequent mechanisms required for CNS tissue invasion of immune cells via the glia limitans7,8,9. Focal activation of matrix-metalloproteinases (MMP) -2 and MMP-9 alters chemokine activation and induces degradation of extracellular matrix receptors on astrocyte end-feet, which is a prerequisite for immune cell migration across the glia limitans into the CNS parenchyma and to induce the onset of clinical symptoms of EAE10,11.&#160;
Combining detection of CNS infiltrating immune cell with BBB leakage and gelatinase activity in CNS tissue sections provides valuable information about the functional integrity of the endothelial and glial barrier in the context of neuroinflammation. For instance, we recently investigated the constitutive loss of the endothelial tight junction molecule junctional adhesion molecule (JAM)-B in immune cell trafficking into the CNS in the context of EAE. Compared to healthy wild-type C57BL/6 mice, healthy JAM-B-deficient littermates showed no impairment of BBB integrity as shown by in vivo permeability assessment using endogenous as well as exogenous tracers12. In the context of EAE, JAM-B-deficient C57BL/6 mice showed ameliorated disease symptoms, which was associated with inflammatory cell trapping in the leptomeningeal and perivascular spaces12. To examine this phenomenon we applied in situ zymography, allowing identification of gelatinase activity in order to test if lack of gelatinase activity in JAM-B-deficient mice may be responsible for the reduced numbers of immune cells able to breach the glia limitans12.&#160;&#160;
Given the availability of different genetically modified mouse models lacking, e.g., different BBB tight junction molecules that might cause changes in BBB function, methodologies for investigating BBB integrity are important. In addition, newly developed drugs could impact on NVU barriers. Here we show how to induce EAE in C57BL/6 mice by active immunization with the myelin oligodendrocyte glycoprotein (MOG)-peptide aa35-55 in complete Freund&#8217;s adjuvants. We then explain how to localize immune cell infiltration across the endothelial and glial barriers of the NVU and how to study in vivo endothelial and glial barrier integrity by in situ detection of exogenous tracers and gelatinase activity, respectively.&#160;&#160;

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr >
			<td >AMCA anti-rabbit antibody</td>
			<td >Jackson ImmunoResearch</td>
			<td >111-156-045</td>
			<td >Store at 4 &#176;C; protect from light</td>
		</tr>
		<tr >
			<td >Anti-CD45 Antibody (30F11)</td>
			<td >Pharmingen</td>
			<td >07-1401</td>
			<td >Store at 4 &#176;C</td>
		</tr>
		<tr >
			<td >Anti-Laminin Antibody</td>
			<td >DAKO</td>
			<td >Z0097</td>
			<td >Store at 4 &#176;C</td>
		</tr>
		<tr >
			<td >Breeding food</td>
			<td >e.g. PROVIMI KLIBA SA</td>
			<td >3336</td>
			<td ></td>
		</tr>
			<tr >
			<td >Individually ventilated cages, Blue line Type II or III</td>
			<td >e.g. Tecniplast	</td>
			<td >1145T, 1285L</td>
			<td ></td>
		</tr>	
		<tr >
			<td >BSA fraction V</td>
			<td >Applichem</td>
			<td >A1391</td>
			<td >Store at 4 &#176;C</td>
		</tr>
		<tr >
			<td >Cold gelatine</td>
			<td >Sigma-Aldrich</td>
			<td >G 9391</td>
			<td ></td>
		</tr>
		<tr >
			<td >Coplin jar + rack</td>
			<td >e.g. Carl Roth GmbH + Co. KG</td>
			<td >H554.1; H552.1</td>
			<td ></td>
		</tr>
		<tr >
			<td >Cy3 anti-rat antibody</td>
			<td >Jackson ImmunoResearch</td>
			<td >111-156-144</td>
			<td >Store at 4 &#176;C; protect from light</td>
		</tr>
		<tr >
			<td >Cover slips 24 x 40 mm # 1</td>
			<td >e.g. Thermo Scientific</td>
			<td >85-0186-00</td>
			<td></td>
		</tr>
		<tr >
			<td >Dextran Alexa Fluor 488 (10,000 MW)</td>
			<td >e.g. Molecular probes</td>
			<td >D22910</td>
			<td >Store at -20 &#176;C; protect from light</td>
		</tr>
		<tr >
			<td >Dextran Texas Red (3000 MW)</td>
			<td >Invitrogen</td>
			<td >D3328</td>
			<td >Store at -20 &#176;C; protect from light</td>
		</tr>
		<tr >
			<td >EnzChek Gelatinase/Collagenase Assay Kit&#160;</td>
			<td >Thermo Fisher Scientific; EnzCheck</td>
			<td >E12055</td>
			<td >Store at -20 &#176;C; protect form light</td>
		</tr>
		<tr >
			<td >Female C57BL/6J mice (8-12 weeks)</td>
			<td >e.g. Janvier Labs</td>
			<td ></td>
			<td >Females, 8-12 weeks</td>
		</tr>
		<tr >
			<td >Freezing box for histology slides</td>
			<td >e.g. Carl Roth GmbH + Co. KG</td>
			<td >2285.1</td>
			<td ></td>
		</tr>
		<tr >
			<td >18G x 1&#189;&#8217;&#8217; (1.2mm x 40mm) injection needle</td>
			<td >e.g. BD, BD Microlance 3</td>
			<td >304622</td>
			<td ></td>
		</tr>
		<tr >
			<td >27G x &#190;&#8217;&#8217; &#8211; Nr. 20 (0.4mm x 19mm) injection needle</td>
			<td >e.g. BD, BD Microlance 3</td>
			<td >302200</td>
			<td ></td>
		</tr>
		<tr >
			<td >30G x &#189;&#8217;&#8217; (0.3 mm x 13 mm) injection needle</td>
			<td >e.g. BD, BD Microlance 3</td>
			<td >304000</td>
			<td ></td>
		</tr>
		<tr >
			<td >Incomplete Freund&#8217;s adjuvant (IFA)</td>
			<td >e.g. Santa Cruz Biotechnology</td>
			<td >sc-24648</td>
			<td >Store at 4&#176;C</td>
		</tr>
		<tr >
			<td >Maintenance food</td>
			<td >e.g. PROVIMI KLIBA SA</td>
			<td >3436</td>
			<td ></td>
		</tr>
		<tr >
			<td >MOGaa35-55 peptide</td>
			<td >e.g. GenScript</td>
			<td ></td>
			<td >Store at -80 &#176;C</td>
		</tr>
		<tr >
			<td >microscope slides (Superfrost Plus )</td>
			<td >Thermo Scientific</td>
			<td >J1800AMNZ</td>
			<td ></td>
		</tr>
		<tr >
			<td >Mycobacterium tuberculosis H37RA</td>
			<td >e.g. BD</td>
			<td >231141</td>
			<td >Store at 4 &#176;C&#160;</td>
		</tr>
		<tr >
			<td >NaCl 0.9 %</td>
			<td >B. Braun</td>
			<td >3535789</td>
			<td ></td>
		</tr>
		<tr >
			<td >O.C.T. compound (Tissue-Tek )</td>
			<td >Sakura</td>
			<td >4583</td>
			<td ></td>
		</tr>
		<tr >
			<td >Omnican 50 30G x &#189;&#8217;&#8217;</td>
			<td >B. Braun</td>
			<td >9151125S</td>
			<td></td>
		</tr>
		<tr >
			<td >Paraformaldehyde</td>
			<td >Merck</td>
			<td >30525-89-4</td>
			<td ></td>
		</tr>
		<tr >
			<td >Pertussis toxin</td>
			<td >e.g. List biological laboratories, Inc.</td>
			<td >180</td>
			<td >Store at 4 &#176;C</td>
		</tr>
		<tr >
			<td >poly(vinyl alcohole) (Mowiol 4-88)</td>
			<td >Sigma-Aldrich</td>
			<td >81381</td>
			<td ></td>
		</tr>
		<tr >
			<td >Protease Inhibitor EDTA free (Roche)</td>
			<td >Sigma-Aldrich</td>
			<td >4693132001</td>
			<td >Store at 4 &#176;C</td>
		</tr>
		<tr >
			<td >repelling pen e.g. DAKO Pen</td>
			<td >e.g. DAKO</td>
			<td >S2002</td>
			<td ></td>
		</tr>
		<tr >
			<td >sealing film e.g. Parafilm M</td>
			<td >e.g Sigma-Aldrich</td>
			<td >P7793</td>
			<td ></td>
		</tr>
		<tr >
			<td >Silica gel</td>
			<td >e.g. Carl Roth GmbH + Co. KG</td>
			<td >9351.1</td>
			<td ></td>
		</tr>
		<tr >
			<td >Stitch scissor</td>
			<td >F.S.T</td>
			<td >15012-12</td>
			<td ></td>
		</tr>
		<tr >
			<td >syringe 1 ml</td>
			<td >e.g. PRIMO</td>
			<td >62.1002</td>
			<td ></td>
		</tr>
		<tr >
			<td >syringe 10 ml</td>
			<td >e.g. CODAN Medical ApS</td>
			<td >2022-05</td>
			<td ></td>
		</tr>
		<tr >
			<td >vaporizer system Univentor 400</td>
			<td >UNO.BV</td>
			<td ></td>
			<td></td>
		</tr>
	</tbody>
</table>

visualizing impairment of the endothelial and glial barriers of the neurovascular unit during experimental autoimmune encephalomyelitis in vivo

The neurovascular unit (NVU) is composed of microvascular endothelial cells forming the blood-brain barrier (BBB), an endothelial basement membrane with embedded pericytes, and the glia limitans composed by the parenchymal basement membrane and astrocytic end-feed embracing the abluminal aspect of central nervous system (CNS) microvessels. In addition to maintaining CNS homeostasis the NVU controls immune cell trafficking into the CNS. During immunosurveillance of the CNS low numbers of activated lymphocytes can cross the endothelial barrier without causing BBB dysfunction or clinical disease. In contrast, during neuroinflammation such as in multiple sclerosis or its animal model experimental autoimmune encephalomyelitis (EAE) a large number of immune cells can cross the BBB and subsequently the glia limitans eventually reaching the CNS parenchyma leading to clinical disease. 
Immune cell migration into the CNS parenchyma is thus a two-step process that involves a sequential migration across the endothelial and glial barrier of the NVU employing distinct molecular mechanisms. If following their passage across the endothelial barrier, T cells encounter their cognate antigen on perivascular antigen-presenting cells their local reactivation will initiate subsequent mechanisms leading to the focal activation of gelatinases, which will enable the T cells to cross the glial barrier and enter the CNS parenchyma. Thus, assessing both, BBB permeability and MMP activity in spatial correlation to immune cell accumulation in the CNS during EAE allows to specify loss of integrity of the endothelial and glial barriers of the NVU. 
We here show how to induce EAE in C57BL/6 mice by active immunization and how to subsequently analyze BBB permeability in vivo using a combination of exogenous fluorescent tracers. We further show, how to visualize and localize gelatinase activity in EAE brains by in situ zymogaphy coupled to immunofluorescent stainings of BBB basement membranes and CD45+ invading immune cells.

Assessment of the clinical course of EAE in C57BL/6 mice should result in a disease curve as depicted in Figure 2A and changes in the mouse body weight as presented in Figure 2B. C57BL/6 mice immunized with MOGaa35-55 usually start to develop disease symptoms around day 10-12 after active immunization (Figure 1A). Typically, immunized mice show a transient drop of body weight the day after the injection of the emulsion and the first...

Watch this Scientific Journal Video about Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo at JoVE.com

Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo

Here, we present protocols to investigate impairment of the neurovascular unit during experimental autoimmune encephalomyelitis in vivo. We specifically address how to determine blood-brain barrier permeability and gelatinase activity involved in leukocyte migration across the glia limitans.&#160;

The neurovascular unit (NVU) is composed of microvascular endothelial cells forming the blood-brain barrier (BBB), an endothelial basement membrane with ...

visualizing-impairment-endothelial-glial-barriers-neurovascular-unit

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JoVE Journal

Immunology and Infection

7.6K Views.  University of Bern. Here, we present protocols to investigate impairment of the neurovascular unit during experimental autoimmune encephalomyelitis in vivo. We specifically address how to determine blood-brain barrier permeability and gelatinase activity involved in leukocyte migration across the glia limitans. 

Video: Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo

Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis

Autoimmune hypophysitis is a chronic inflammation of the pituitary gland caused or accompanied by autoimmunity1. It has traditionally been considered a rare disease but reporting has increased markedly in recent years. Hypophysitis, in fact, develops not uncommonly as a "side effect" in cancer patients treated with antibodies that block inhibitory receptors expressed on T lymphocytes, such as CTLA-42 and PD-1 receptors. Autoimmune hypophysitis can be induced experimentally by injecting mice with pituitary proteins mixed with an adjuvant3. In this video article we demonstrate how to extract proteins from mouse pituitary glands and how to prepare them in a form suitable for inducing autoimmune hypophysitis in SJL mice.

Autoimmune hypophysitis can be reproduced in mice by injecting an extract of mouse pituitary proteins.

Autoimmune hypophysitis is a chronic inflammation of the pituitary gland caused or accompanied by autoimmunity1.  It has traditionally been considered a ...

Induction of Experimental Autoimmune Hypophysitis in SJL Mice

Autoimmune hypophysitis can be reproduced experimentally by the injection of pituitary proteins mixed with an adjuvant into susceptible mice1. Mouse models allow us to study how diseases unfold, often providing a good replica of the same processes occurring in humans. For some autoimmune diseases, like type 1A diabetes, there are models (the NOD mouse) that spontaneously develop a disease similar to the human counterpart. For many other autoimmune diseases, however, the model needs to be induced experimentally. A common approach in this regard is to inject the mouse with a dominant antigen derived from the organ being studied. For example, investigators interested in autoimmune thyroiditis inject mice with thyroglobulin2, and those interested in myasthenia gravis inject them with the acetylcholine receptor3. If the autoantigen for a particular autoimmune disease is not known, investigators inject a crude protein extract from the organ targeted by the autoimmune reaction. For autoimmune hypophysitis, the pathogenic autoantigen(s) remain to be identified4, and thus a crude pituitary protein preparation is used. In this video article we demonstrate how to induce experimental autoimmune hypophysitis in SJL mice.

This video shows how to induce autoimmune hypophysitis in SJL mice and how to assess its severity by histopathology.

Autoimmune hypophysitis can be reproduced experimentally by the injection of pituitary proteins mixed with an adjuvant into susceptible mice1. Mouse ...

Overcoming Unresponsiveness in Experimental Autoimmune Encephalomyelitis (EAE) Resistant Mouse Strains by Adoptive Transfer and Antigenic Challenge

Experimental autoimmune encephalomyelitis (EAE) is an inflammatory disease of the central nervous system (CNS) and has been used as an animal model for study of the human demyelinating disease, multiple sclerosis (MS). EAE is characterized by pathologic infiltration of mononuclear cells into the CNS and by clinical manifestation of paralytic disease. Similar to MS, EAE is also under genetic control in that certain mouse strains are susceptible to disease induction while others are resistant. Typically, C57BL/6 (H-2b) mice immunized with myelin basic protein (MBP) fail to develop paralytic signs. This unresponsiveness is certainly not due to defects in antigen processing or antigen presentation of MBP, as an experimental protocol described here had been used to induce severe EAE in C57BL/6 mice as well as other reputed resistant mouse strains. In addition, encephalitogenic T cell clones from C57BL/6 and Balb/c mice reactive to MBP had been successfully isolated and propagated.
The experimental protocol involves using a cellular adoptive transfer system in which MBP-primed (200 &mu;g/mouse) C57BL/6 donor lymph node cells are isolated and cultured for five days with the antigen to expand the pool of MBP-specific T cells. At the end of the culture period, 50 million viable cells are transferred into naive syngeneic recipients through the tail vein. Recipient mice so treated normally do not develop EAE, thus reaffirming their resistant status, and they can remain normal indefinitely. Ten days post cell transfer, recipient mice are challenged with complete Freund adjuvant (CFA)-emulsified MBP in four sites in the flanks. Severe EAE starts to develop in these mice ten to fourteen days after challenge. Results showed that the induction of disease was antigenic specific as challenge with irrelevant antigens did not induce clinical signs of disease. Significantly, a titration of the antigen dose used to challenge the recipient mice showed that it could be as low as 5 &mu;g/mouse. In addition, a kinetic study of the timing of antigenic challenge showed that challenge to induce disease was effective as early as 5 days post antigenic challenge and as long as over 445 days post antigenic challenge. These data strongly point toward the involvement of a "long-lived" T cell population in maintaining unresponsiveness. The involvement of regulatory T cells (Tregs) in this system is not defined.

Overcoming Unresponsiveness in Experimental Autoimmune Encephalomyelitis EAE Resistant Mouse Strains by Adoptive Transfer and Antigenic Challenge

Certain mouse strains are able to resist induction of experimental autoimmune encephalomyelitis (EAE) with myelin basic protein. Described here is a simple immunization protocol that reverses the unresponsiveness and induces paralytic disease in several typical EAE resistant mouse stains.

Experimental autoimmune encephalomyelitis (EAE) is an inflammatory disease of the central nervous system (CNS) and has been used as an animal model for ...

Myelin Oligodendrocyte Glycoprotein (MOG35-55) Induced Experimental Autoimmune Encephalomyelitis (EAE) in C57BL/6 Mice

Multiple sclerosis is a chronic neuroinflammatory demyelinating disorder of the central nervous system with a strong neurodegenerative component. While the exact etiology of the disease is yet unclear, autoreactive T lymphocytes are thought to play a central role in its pathophysiology. MS therapy is only partially effective so far and research efforts continue to expand our knowledge on the pathophysiology of the disease and to develop novel treatment strategies. Experimental autoimmune encephalomyelitis (EAE) is the most common animal model for MS sharing many clinical and pathophysiological features. There is a broad diversity of EAE models which reflect different clinical, immunological and histological aspects of human MS. Actively-induced EAE in mice is the easiest inducible model with robust and replicable results. It is especially suited for investigating the effects of drugs or of particular genes by using transgenic mice challenged by autoimmune neuroinflammation. Therefore, mice are immunized with CNS homogenates or peptides of myelin proteins. Due to the low immunogenic potential of these peptides, strong adjuvants are used. EAE susceptibility and phenotype depends on the chosen antigen and rodent strain. C57BL/6 mice are the commonly used strain for transgenic mouse construction and respond among others to myelin oligodendrocyte glycoprotein (MOG). The immunogenic epitope MOG35-55 is suspended in complete Freund's adjuvant (CFA) prior to immunization and pertussis toxin is applied on the day of immunization and two days later. Mice develop a "classic" self-limited monophasic EAE with ascending flaccid paralysis within 9-14 days after immunization. Mice are evaluated daily using a clinical scoring system for 25-50 days. Special considerations for care taking of animals with EAE as well as potential applications and limitations of this model are discussed.

Myelin Oligodendrocyte Glycoprotein MOG35-55 Induced Experimental Autoimmune Encephalomyelitis EAE in C57BL/6 Mice

Experimental autoimmune encephalomyelitis (EAE) is an established animal model of multiple sclerosis. C57BL/6 mice are immunized with myelin oligodendrocyte glycoprotein (MOG) peptide 35-55 (MOG35-55), resulting in an ascending flaccid paralysis caused by autoreactive immune cells in the central nervous system. Protocols for disease induction and monitoring will be discussed.

Multiple sclerosis is a chronic neuroinflammatory demyelinating disorder of the central nervous system with a strong neurodegenerative component. While ...

Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues

Multiple sclerosis is presumed to be an inflammatory autoimmune disease, which is characterized by lesion formation in the central nervous system (CNS) resulting in cognitive and motor impairment. Experimental autoimmune encephalomyelitis (EAE) is a useful animal model of MS, because it is also characterized by lesion formation in the CNS, motor impairment and is also driven by autoimmune and inflammatory reactions. One of the EAE models is induced with a peptide derived from the myelin oligodendrocyte protein (MOG)35-55 in mice. The EAE mice develop a progressive disease course. This course is divided into three phases: the preclinical phase (day 0 - 9), the disease onset (day 10 - 11) and the acute phase (day 12 - 14). MS and EAE are induced by autoreactive T cells that infiltrate the CNS. These T cells secrete chemokines and cytokines which lead to the recruitment of further immune cells. Therefore, the immune cell distribution in the spinal cord during the three disease phases was investigated. To highlight the time point of the disease at which the activation/proliferation/accumulation of T cells, B cells and monocytes starts, the immune cell distribution in lymph nodes, spleen and blood was also assessed. Furthermore, the levels of several cytokines (IL-1&#946;, IL-6, IL-23, TNF&#945;, IFN&#947;) in the three disease phases were determined, to gain insight into the inflammatory processes of the disease. In conclusion, the data provide an overview of the functional profile of immune cells during EAE pathology.

This manuscript describes the methods for induction and scoring of the experimental autoimmune encephalomyelitis (EAE) model, together with the assessment of immune cell distribution and mRNA cytokine levels in lymph nodes, spleen, blood and spinal cord using flow cytometry and quantitative PCR, respectively, at various disease phases.

Multiple sclerosis is presumed to be an inflammatory autoimmune disease, which is characterized by lesion formation in the central nervous system (CNS) ...

Determining Immune System Suppression versus CNS Protection for Pharmacological Interventions in Autoimmune Demyelination

A major hallmark of the autoimmune demyelinating disease multiple sclerosis (MS) is immune cell infiltration into the brain and spinal cord resulting in myelin destruction, which not only slows conduction of nerve impulses, but causes axonal injury resulting in motor and cognitive decline. Current treatments for MS focus on attenuating immune cell infiltration into the central nervous system (CNS). These treatments decrease the number of relapses, improving quality of life, but do not completely eliminate relapses so long-term disability is not improved. Therefore, therapeutic agents that protect the CNS are warranted. In both animal models as well as human patients with MS, T cell entry into the CNS is generally considered the initiating inflammatory event. In order to assess if a drug protects the CNS, any potential effects on immune cell infiltration or proliferation in the periphery must be ruled out. This protocol describes how to determine whether CNS protection observed after drug intervention is a consequence of attenuating CNS-infiltrating immune cells or blocking death of CNS cells during inflammatory insults. The ability to examine MS treatments that are protective to the CNS during inflammatory insults is highly critical for the advancement of therapeutic strategies since current treatments reduce, but do not completely eliminate, relapses (i.e., immune cell infiltration), leaving the CNS vulnerable to degeneration.

This protocol describes how to determine whether pharmacological treatments for experimental autoimmune encephalomyelitis show CNS protection as a consequence of suppressing immune cell infiltration or are neuroprotective during the onslaught of immune cell infiltration.

A major hallmark of the autoimmune demyelinating disease multiple sclerosis (MS) is immune cell infiltration into the brain and spinal cord resulting in ...

Simple and Efficient Production and Purification of Mouse Myelin Oligodendrocyte Glycoprotein for Experimental Autoimmune Encephalomyelitis Studies

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS), thought to occur as a result of autoimmune responses targeting myelin. Experimental autoimmune encephalomyelitis (EAE) is the most common animal model of CNS autoimmune disease, and is typically induced via immunization with short peptides representing immunodominant CD4+ T cell epitopes of myelin proteins. However, B cells recognize unprocessed protein directly, and immunization with short peptide does not activate B cells that recognize the native protein. As recent clinical trials of B cell-depleting therapies in MS have suggested a role for B cells in driving disease in humans, there is an urgent need for animal models that incorporate B cell-recognition of autoantigen. To this end, we have generated a new fusion protein containing the extracellular domain of the mouse version of myelin oligodendrocyte glycoprotein (MOG) as well as N-terminal fusions of a His-tag for purification purposes and the thioredoxin protein to improve solubility (MOGtag). A tobacco etch virus (TEV) protease cleavage site was incorporated to allow the removal of all tag sequences, leaving only the pure MOG1-125 extracellular domain. Here, we describe a simple protocol using only standard laboratory equipment to produce large quantities of pure MOGtag or MOG1-125. This protocol consistently generates over 200 mg of MOGtag protein. Immunization with either MOGtag or MOG1-125 generates an autoimmune response that includes pathogenic B cells that recognize the native mouse MOG.

We describe a simple protocol using only basic lab equipment to generate and purify large quantities of a fusion protein that contains mouse Myelin Oligodendrocyte Glycoprotein. This protein can be used to induce experimental autoimmune encephalomyelitis driven by both T and B cells.

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS), thought to occur as a result of autoimmune responses ...

Visualizing the Effects of Sputum on Biofilm Development Using a Chambered Coverglass Model

Biofilms consist of groups of bacteria encased in a self-secreted matrix. They play an important role in industrial contamination as well as in the development and persistence of many health related infections. One of the most well described and studied biofilms in human disease occurs in chronic pulmonary infection of cystic fibrosis patients. When studying biofilms in the context of the host, many factors can impact biofilm formation and development. In order to identify how host factors may affect biofilm formation and development, we used a static chambered coverglass method to grow biofilms in the presence of host-derived factors in the form of sputum supernatants. Bacteria are seeded into chambers and exposed to sputum filtrates. Following 48 hr of growth, biofilms are stained with a commercial biofilm viability kit prior to confocal microscopy and analysis. Following image acquisition, biofilm properties can be assessed using different software platforms. This method allows us to visualize key properties of biofilm growth in presence of different substances including antibiotics.

This protocol describes the visualization of biofilm development following exposure to host-factors using a slide chamber model. This model allows for direct visualization of biofilm development as well as analysis of biofilm parameters using computer software programs.

Biofilms consist of groups of bacteria encased in a self-secreted matrix. They play an important role in industrial contamination as well as in the ...

Screening Assays to Characterize Novel Endothelial Regulators Involved in the Inflammatory Response

The endothelial layer is essential for maintaining homeostasis in the body by controlling many different functions. Regulation of the inflammatory response by the endothelial layer is crucial to efficiently fight against harmful inputs and aid in the recovery of damaged areas. When the endothelial cells are exposed to an inflammatory environment, such as the outer component of gram-negative bacteria membrane, lipopolysaccharide (LPS), they express soluble pro-inflammatory cytokines, such as Ccl5, Cxcl1 and Cxcl10, and trigger the activation of circulating leukocytes. In addition, the expression of adhesion molecules E-selectin, VCAM-1 and ICAM-1 on the endothelial surface enables the interaction and adhesion of the activated leukocytes to the endothelial layer, and eventually the extravasation towards the inflamed tissue. In this scenario, the endothelial function must be tightly regulated because excessive or defective activation in the leukocyte recruitment could lead to inflammatory-related disorders. Since many of these disorders do not have an effective treatment, novel strategies with a focus on the vascular layer must be investigated. We propose comprehensive assays that are useful to the search of novel endothelial regulators that modify leukocyte function. We analyze endothelial activation by using specific expression targets involved in leukocyte recruitment (such as, cytokines, chemokines, and adhesion molecules) with several techniques, including: real-time quantitative polymerase chain reaction (RT-qPCR), western-blot, flow cytometry and adhesion assays. These approaches determine endothelial function in the inflammatory context and are very useful to perform screening assays to characterize novel endothelial inflammatory regulators that are potentially valuable for designing new therapeutic strategies.

Vascular endothelium tightly controls leukocyte recruitment. Inadequate leukocyte extravasation contributes to human inflammatory diseases. Therefore, searching for novel regulatory elements of endothelial activation is necessary to design improved therapies for inflammatory disorders. Here, we describe a comprehensive methodology to characterize novel endothelial regulators that can modify leukocyte trafficking during inflammation.

The endothelial layer is essential for maintaining homeostasis in the body by controlling many different functions. Regulation of the inflammatory ...

Flow Cytometric Analysis of Lymphocyte Infiltration in Central Nervous System during Experimental Autoimmune Encephalomyelitis

Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) caused by the combination of environmental factors and susceptible genetic background. Experimental autoimmune encephalomyelitis (EAE) is a typical disease model of MS widely used for investigating the pathogenesis in which T lymphocytes specific for myelin antigens initiate an inflammatory reaction in CNS. It is very important to assess how lymphocytes in the CNS regulate the development of disease. However, the approach for measuring the quantity and quality of infiltrated lymphocytes in the CNS is very limited due to the difficulties in isolating and detecting infiltrated lymphocytes from the brain. This manuscript presents a protocol for that is useful for the isolation, identification, and characterization of infiltrated lymphocytes from the CNS and will be helpful for our understanding of how lymphocytes are involved in the development of the CNS autoimmune disease.

This manuscript presents a protocol to induce active experimental autoimmune encephalomyelitis (EAE) in mice. A method for the isolation and characterization of the infiltrated lymphocytes in the central nervous system (CNS) is also presented to show how lymphocytes are involved in the development of CNS autoimmune disease.

Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) caused by the combination of environmental factors and susceptible ...