This work was financially supported by project SAF2017-82736-C2-1-R from Ministerio de Ciencia e Innovaci&#243;n to MTM-F and by Fundaci&#243;n Universidad Francisco de Vitoria to JS.

NOTE: Animal experimentation was approved by national and institutional bioethics committees.
1. ihOEG (Ts12 and Ts14) culture
NOTE: This procedure is done under sterile conditions in a tissue culture biosafety cabinet.
<ol>
	<li>Prepare 50 mL ME10 OEG culture medium as provided in Table 1.</li>
	<li>Prepare 5 mL of DMEM/F12-FBS, as provided in Table 1, in a 15 mL conical tube.</li>
	<li>Warm both media at 37 &#176;C in a clean wa...

<ol>
	<li>Kanno, H., Pearse, D. D., Ozawa, H., Itoi, E., Bunge, 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=Schwann+cell+transplantation+for+spinal+cord+injury+repair:+Its+significant+therapeutic+potential+and+prospectus.">Schwann cell transplantation for spinal cord injury repair: Its significant therapeutic potential and prospectus.</a> Reviews in the Neurosciences. 26 (2), 121-128 (2015).</li><li>Assinck, P., Duncan, G. J., Hilton, B. J., Plemel, J. R., Tetzlaff, W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cell+transplantation+therapy+for+spinal+cord+injury.">Cell transplantation therapy for spinal cord injury.</a> Nature Neuroscience. 20 (5), 637-647 (2017).</li><li>Lindsay, S. L., Toft, A., Griffin, J., Emraja, A. M. M., Barnett, S. C., Riddell, J. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Human+olfactory+mesenchymal+stromal+cell+transplants+promote+remyelination+and+earlier+improvement+in+gait+coordination+after+spinal+cord+injury.">Human olfactory mesenchymal stromal cell transplants promote remyelination and earlier improvement in gait coordination after spinal cord injury.</a> Glia. 65 (4), 639-656 (2017).</li><li>Moreno-Flores, M. T., 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=A+clonal+cell+line+from+immortalized+olfactory+ensheathing+glia+promotes+functional+recovery+in+the+injured+spinal+cord.">A clonal cell line from immortalized olfactory ensheathing glia promotes functional recovery in the injured spinal cord.</a> Molecular Therapy. 13 (3), 598-608 (2006).</li><li>Gilmour, A. D., Reshamwala, R., Wright, A. A., Ekberg, J. A. K., St. John, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optimizing+olfactory+ensheathing+cell+transplantation+for+spinal+cord+injury+repair.">Optimizing olfactory ensheathing cell transplantation for spinal cord injury repair.</a> Journal of Neurotrauma. 37 (5), 817-829 (2020).</li><li>Barraud, P., 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=Neural+crest+origin+of+olfactory+ensheathing+glia.">Neural crest origin of olfactory ensheathing glia.</a> Proceedings of the National Academy of Sciences of the United States of America. 107, 21040-21045 (2010).</li><li>Su, Z., He, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Olfactory+ensheathing+cells:+biology+in+neural+development+and+regeneration.">Olfactory ensheathing cells: biology in neural development and regeneration.</a> Progress in Neurobiology. 92 (4), 517-532 (2010).</li><li>Yao, R., 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=Olfactory+ensheathing+cells+for+spinal+cord+injury:+sniffing+out+the+issues.">Olfactory ensheathing cells for spinal cord injury: sniffing out the issues.</a> Cell Transplant. 27 (6), 879-889 (2018).</li><li>G&#243;mez, R. 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=Cell+therapy+for+spinal+cord+injury+with+olfactory+ensheathing+glia+cells+(OECs).">Cell therapy for spinal cord injury with olfactory ensheathing glia cells (OECs).</a> Glia. 66 (7), 1267-1301 (2018).</li><li>Plant, G. W., Harvey, A. R., Leaver, S. G., Lee, S. V. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Olfactory+ensheathing+glia:+repairing+injury+to+the+mammalian+visual+system.">Olfactory ensheathing glia: repairing injury to the mammalian visual system.</a> Experimental Neurology. 229 (1), 99-108 (2011).</li><li>Xue, 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=Transplanted+olfactory+ensheathing+cells+restore+retinal+function+in+a+rat+model+of+light-induced+retinal+damage+by+inhibiting+oxidative+stress.">Transplanted olfactory ensheathing cells restore retinal function in a rat model of light-induced retinal damage by inhibiting oxidative stress.</a> Oncotarget. 8 (54), 93087-93102 (2017).</li><li>Pastrana, 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=Genes+associated+with+adult+axon+regeneration+promoted+by+olfactory+ensheathing+cells:+a+new+role+for+matrix+metalloproteinase+2.">Genes associated with adult axon regeneration promoted by olfactory ensheathing cells: a new role for matrix metalloproteinase 2.</a> The Journal of Neuroscience. 26, 5347-5359 (2006).</li><li>Pastrana, 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=BDNF+production+by+olfactory+ensheathing+cells+contributes+to+axonal+regeneration+of+cultured+adult+CNS+neurons.">BDNF production by olfactory ensheathing cells contributes to axonal regeneration of cultured adult CNS neurons.</a> Neurochemistry International. 50, 491-498 (2007).</li><li>Sim&#243;n, 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=Expression+of+plasminogen+activator+inhibitor-1+by+olfactory+ensheathing+glia+promotes+axonal+regeneration.">Expression of plasminogen activator inhibitor-1 by olfactory ensheathing glia promotes axonal regeneration.</a> Glia. 59, 1458-1471 (2011).</li><li>Lim, F., 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=Reversibly+immortalized+human+olfactory+ensheathing+glia+from+an+elderly+donor+maintain+neuroregenerative+capacity.">Reversibly immortalized human olfactory ensheathing glia from an elderly donor maintain neuroregenerative capacity.</a> Glia. 58, 546-558 (2010).</li><li>Garc&#237;a-Escudero, V., 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=Prevention+of+senescence+progression+in+reversibly+immortalized+human+ensheathing+glia+permits+their+survival+after+deimmortalization.">Prevention of senescence progression in reversibly immortalized human ensheathing glia permits their survival after deimmortalization.</a> Molecular Therapy. 18, 394-403 (2010).</li><li>Garc&#237;a-Escudero, V., 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=A+neuroregenerative+human+ensheathing+glia+cell+line+with+conditional+rapid+growth.">A neuroregenerative human ensheathing glia cell line with conditional rapid growth.</a> Cell Transplant. 20, 153-166 (2011).</li><li>Plaza, N., Sim&#243;n, D., Sierra, J., Moreno-Flores, M. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transduction+of+an+immortalized+olfactory+ensheathing+glia+cell+line+with+the+green+fluorescent+protein+(GFP)+gene:+Evaluation+of+its+neuroregenerative+capacity+as+a+proof+of+concept.">Transduction of an immortalized olfactory ensheathing glia cell line with the green fluorescent protein (GFP) gene: Evaluation of its neuroregenerative capacity as a proof of concept.</a> Neuroscience Letters. 612, 25-31 (2016).</li><li>Deumens, R., 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=Alignment+of+glial+cells+stimulates+directional+neurite+growth+of+CNS+neurons+in+vitro.">Alignment of glial cells stimulates directional neurite growth of CNS neurons in vitro.</a> Neuroscience. 125 (3), 591-604 (2004).</li><li>Chung, R. 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=Olfactory+ensheathing+cells+promote+neurite+sprouting+of+injured+axons+in+vitro+by+direct+cellular+contact+and+secretion+of+soluble+factors.">Olfactory ensheathing cells promote neurite sprouting of injured axons in vitro by direct cellular contact and secretion of soluble factors.</a> Cell and Molecular Life Sciences. 61 (10), 1238-1245 (2004).</li><li>Leaver, S. G., Harvey, A. R., Plant, G. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Adult+olfactory+ensheathing+glia+promote+the+long-distance+growth+of+adult+retinal+ganglion+cell+neurites+in+vitro.">Adult olfactory ensheathing glia promote the long-distance growth of adult retinal ganglion cell neurites in vitro.</a> Glia. 53 (5), 467-476 (2006).</li><li>Pellitteri, R., Spatuzza, M., Russo, A., Stanzani, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Olfactory+ensheathing+cells+exert+a+trophic+effect+on+the+hypothalamic+neurons+in+vitro.">Olfactory ensheathing cells exert a trophic effect on the hypothalamic neurons in vitro.</a> Neuroscience Letters. 417 (1), 24-29 (2007).</li><li>Pellitteri, R., Spatuzza, M., Russo, A., Zaccheo, D., Stanzani, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Olfactory+ensheathing+cells+represent+an+optimal+substrate+for+hippocampal+neurons:+an+in+vitro+study.">Olfactory ensheathing cells represent an optimal substrate for hippocampal neurons: an in vitro study.</a> International Journal of Developmental Neuroscience. 27 (5), 453-458 (2009).</li><li>Runyan, S. A., Phelps, P. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mouse+olfactory+ensheathing+glia+enhance+axon+outgrowth+on+a+myelin+substrate+in+vitro.">Mouse olfactory ensheathing glia enhance axon outgrowth on a myelin substrate in vitro.</a> Experimental Neurology. 216 (1), 95-104 (2009).</li><li>Witheford, M., Westendorf, K., Roskams, A. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Olfactory+ensheathing+cells+promote+corticospinal+axonal+outgrowth+by+a+L1+CAM-dependent+mechanism.">Olfactory ensheathing cells promote corticospinal axonal outgrowth by a L1 CAM-dependent mechanism.</a> Glia. 61 (11), 1873-1889 (2013).</li><li>Roloff, F., Ziege, S., Baumg&#228;rtner, W., Wewetzer, K., Bicker, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Schwann+cell-free+adult+canine+olfactory+ensheathing+cell+preparations+from+olfactory+bulb+and+mucosa+display+differential+migratory+and+neurite+growth-promoting+properties+in+vitro.">Schwann cell-free adult canine olfactory ensheathing cell preparations from olfactory bulb and mucosa display differential migratory and neurite growth-promoting properties in vitro.</a> BMC Neuroscience. 14, 141 (2013).</li><li>Khankan, R. R., Wanner, I. B., Phelps, P. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Olfactory+ensheathing+cell-neurite+alignment+enhances+neurite+outgrowth+in+scar-like+cultures.">Olfactory ensheathing cell-neurite alignment enhances neurite outgrowth in scar-like cultures.</a> Experimental Neurology. 269, 93-101 (2015).</li><li>Wigley, C. B., Berry, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regeneration+of+adult+rat+retinal+ganglion+cell+processes+in+monolayer+culture:+comparisons+between+cultures+of+adult+and+neonatal+neurons.">Regeneration of adult rat retinal ganglion cell processes in monolayer culture: comparisons between cultures of adult and neonatal neurons.</a> Brain Research. 470 (1), 85-98 (1988).</li><li>Sonigra, R. J., Brighton, P. C., Jacoby, J., Hall, S., Wigley, C. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Adult+rat+olfactory+nerve+ensheathing+cells+are+effective+promoters+of+adult+central+nervous+system+neurite+outgrowth+in+coculture.">Adult rat olfactory nerve ensheathing cells are effective promoters of adult central nervous system neurite outgrowth in coculture.</a> Glia. 25 (3), 256-269 (1999).</li><li>Hayat, S., Thomas, A., Afshar, F., Sonigra, R., Wigley, C. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Manipulation+of+olfactory+ensheathing+cell+signaling+mechanisms:+effects+on+their+support+for+neurite+regrowth+from+adult+CNS+neurons+in+coculture.">Manipulation of olfactory ensheathing cell signaling mechanisms: effects on their support for neurite regrowth from adult CNS neurons in coculture.</a> Glia. 44 (3), 232-241 (2003).</li><li>Kumar, R., Hayat, S., Felts, P., Bunting, S., Wigley, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Functional+differences+and+interactions+between+phenotypic+subpopulations+of+olfactory+ensheathing+cells+in+promoting+CNS+axonal+regeneration.">Functional differences and interactions between phenotypic subpopulations of olfactory ensheathing cells in promoting CNS axonal regeneration.</a> Glia. 50 (1), 12-20 (2005).</li><li>Moreno-Flores, M. T., Lim, F., Mart&#237;n-Bermejo, M. J., D&#237;az-Nido, J., Avila, J., Wandosell, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Immortalized+olfactory+ensheathing+glia+promote+axonal+regeneration+of+rat+retinal+ganglion+neurons.">Immortalized olfactory ensheathing glia promote axonal regeneration of rat retinal ganglion neurons.</a> Journal of Neurochemistry. 85 (4), 861-871 (2003).</li><li>Garc&#237;a-Escudero, V., 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=Patient-derived+olfactory+mucosa+cells+but+not+lung+or+skin+fibroblasts+mediate+axonal+regeneration+of+retinal+ganglion+neurons.">Patient-derived olfactory mucosa cells but not lung or skin fibroblasts mediate axonal regeneration of retinal ganglion neurons.</a> Neuroscience Letters. 509 (1), 27-32 (2012).</li><li>Sternberger, L. A., Sternberger, N. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Monoclonal+antibodies+distinguish+phosphorylated+and+nonphosphorylated+forms+of+neurofilaments+in+situ.">Monoclonal antibodies distinguish phosphorylated and nonphosphorylated forms of neurofilaments in situ.</a> Proceedings of the National Academy of Sciences of the United States of America. 80 (19), 6126-6130 (1983).</li><li>S&#225;nchez Martin, C., D&#237;az-Nido, J., Avila, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regulation+of+a+site-specific+phosphorylation+of+the+microtubule-associated+protein+2+during+the+development+of+cultured+neurons.">Regulation of a site-specific phosphorylation of the microtubule-associated protein 2 during the development of cultured neurons.</a> Neuroscience. 87 (4), 861-870 (1998).</li><li>Reshamwala, R., Shah, M., Belt, L., Ekberg, J. A. K., St. John, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Reliable+cell+purification+and+determination+of+cell+purity:+crucial+aspects+of+olfactory+ensheathing+cell+transplantation+for+spinal+cord+repair.">Reliable cell purification and determination of cell purity: crucial aspects of olfactory ensheathing cell transplantation for spinal cord repair.</a> Neural Regeneration Research. 15 (11), 2016-2026 (2020).</li></ol>

OEG transplantation at CNS injury sites is considered a promising therapy for CNS injury due to its constitutive pro-neuroregenerative properties7,8,9. However, depending on the tissue source&#8212;olfactory mucosa (OM-OEG) versus olfactory bulb (OB-OEG)&#8212;or the age of the donor, considerable variation exists in such capacity26,31,33</su...

Adult central nervous system (CNS) neurons have limited regenerative capacity after injury or disease. A common strategy to promote CNS regeneration is transplantation, at the injury site, of cell types that induce axonal growth such as stem cells, Schwann cells, astrocytes or olfactory ensheathing glia (OEG) cells1,2,3,4,5.
OEG derives from the neural crest6 and locates in the olfactory mucosa and in the olfactory bulb. In the adult, olfactory sensory neurons die regularly as the result of environmental exposure and they are replaced by newly differentiated neurons. OEG surrounds and guides these new olfactory axons to enter the olfactory bulb and to establish new synapses with their targets in the CNS7. Due to these physiological attributes, OEG has been used in models of CNS injury such as spinal cord or optic nerve injury and its neuroregenerative and neuroprotective properties become proven8,9,10,11. Several factors have been identified as responsible of the pro-regenerative characteristics of these cells, including extracellular matrix proteases production or secretion of neurotrophic and axonal growth factors12,13,14.
Given the technical limitations to expand primary OEG cells, we previously established and characterized reversible immortalized human OEG (ihOEG) clonal lines, which provide an unlimited supply of homogeneous OEG. These ihOEG cells derive from primary cultures, prepared from olfactory bulbs obtained in autopsies. They were immortalized by transduction of the telomerase catalytic subunit (TERT) and the oncogene Bmi-1 and modified with the SV40 virus large T antigen15,16,17,18. Two of these ihOEG cell lines are Ts14, which maintains the regenerative capacity of the original cultures and Ts12, a low regenerative line that is used as a low regeneration control in these experiments18.
To assess OEG capacity to foster axonal regeneration after neural injury, several in vitro models have been implemented. In these models, OEG is applied to cultures of different neuronal origin and neurite formation and elongation&#8212;in response to glial coculture&#8212;are assayed. Examples of such neuronal sources are neonatal rat cortical neurons19, scratch wounds performed on rat embryonic neurons from cortical tissue20, rat retinal explants21, rat hypothalamic or hippocampal postnatal neurons22,23, postnatal rat dorsal root ganglion neurons24, postnatal mouse corticospinal tract neurons25, human NT2 neurons26, or postnatal cerebral cortical neurons on reactive astrocyte scar-like cultures27.
In these models, however, the regeneration assay relies on embryonic or postnatal neurons, which have an intrinsic plasticity that is absent in injured adult neurons. To overcome this drawback, we present a model of adult axonal regeneration in cocultures of OEG lines with adult retinal ganglion neurons (RGNs), based on the one originally developed by Wigley et al.28,29,30,31 and modified and used by our group12,13,14,15,16,17,18,32,33. Briefly, retinal tissue is extracted from adult rats and digested with papain. Retinal cell suspension is then plated on either polylysine-treated coverslips or onto Ts14 and Ts12 monolayers. Cultures are maintained for 96 h before they are fixed and then immunofluorescence for axonal (MAP1B and NF-H proteins)34 and somatodendritic (MAP2A and B)35 markers is performed. Axonal regeneration is quantified as a percentage of neurons with axon, with respect to the total population of RGNs and axonal regeneration index is calculated as the mean axonal length per neuron. This protocol is not only useful for assessing the neuroregenerative potential of ihOEG but can be extended to different sources of OEG or other glial cells.

<table>
	<tbody>
		<tr>
			<td>antibody 514</td>
			<td>Reference 34</td>
			<td></td>
			<td>Rabbit polyclonal antiserum, which recognizes MAP2A and B.</td>
		</tr>
		<tr>
			<td>antibody SMI-31</td>
			<td>BioLegend</td>
			<td>801601</td>
			<td>Monoclonal antibody against MAP1B and NF-H proteins</td>
		</tr>
		<tr>
			<td>anti-mouse Alexa Fluor 488 antibody</td>
			<td>ThermoFisher</td>
			<td>A-21202</td>
			<td></td>
		</tr>
		<tr>
			<td>anti-rabbit Alexa Fluor 594 antibody</td>
			<td>ThermoFisher</td>
			<td>A-21207</td>
			<td></td>
		</tr>
		<tr>
			<td>B-27 Supplement</td>
			<td>Gibco</td>
			<td>17504044</td>
			<td></td>
		</tr>
		<tr>
			<td>D,L-2-amino-5-phosphonovaleric acid</td>
			<td>Sigma</td>
			<td>283967</td>
			<td>NMDA receptor inhibitor</td>
		</tr>
		<tr>
			<td>DAPI</td>
			<td>Sigma</td>
			<td>D9542</td>
			<td>Nuclei fluorescent stain</td>
		</tr>
		<tr>
			<td>DMEM-F12</td>
			<td>Gibco</td>
			<td>11320033</td>
			<td>Cell culture medium</td>
		</tr>
		<tr>
			<td>FBS</td>
			<td>Gibco</td>
			<td>11573397</td>
			<td>Fetal bovine serum</td>
		</tr>
		<tr>
			<td>FBS-Hyclone</td>
			<td>Fisher Scientific</td>
			<td>16291082</td>
			<td>Fetal bovine serum</td>
		</tr>
		<tr>
			<td>Fluoromount</td>
			<td>Southern Biotech</td>
			<td>0100-01</td>
			<td>Mounting medium</td>
		</tr>
		<tr>
			<td>ImageJ</td>
			<td>National Institutes of Health (NIH-USA)</td>
			<td></td>
			<td>Image software</td>
		</tr>
		<tr>
			<td>L-Glutamine</td>
			<td>Lonza</td>
			<td>BE17-605F</td>
			<td></td>
		</tr>
		<tr>
			<td>Neurobasal Medium</td>
			<td>Gibco</td>
			<td>21103049</td>
			<td>Neuronal cells culture medium</td>
		</tr>
		<tr>
			<td>Papain Dissociation System</td>
			<td>Worthington Biochemical Corporation</td>
			<td>LK003150</td>
			<td>For use in neural cell isolation</td>
		</tr>
		<tr>
			<td>PBS</td>
			<td>Home made</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>PBS-EDTA</td>
			<td>Lonza</td>
			<td>H3BE02-017F</td>
			<td></td>
		</tr>
		<tr>
			<td>Penicillin/Streptomycin/Amphotericin B</td>
			<td>Lonza</td>
			<td>17-745E</td>
			<td>Bacteriostatic and bactericidal</td>
		</tr>
		<tr>
			<td>Pituitary extract</td>
			<td>Gibco</td>
			<td>13028014</td>
			<td>Bovine pituitary extract</td>
		</tr>
		<tr>
			<td>Poly -L- lysine (PLL)</td>
			<td>Sigma</td>
			<td>A-003-M</td>
			<td></td>
		</tr>
	</tbody>
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coculture of axotomized rat retinal ganglion neurons with olfactory ensheathing glia, as an in vitro model of adult axonal regeneration

Olfactory ensheathing glia (OEG) cells are localized all the way from the olfactory mucosa to and into the olfactory nerve layer (ONL) of the olfactory bulb. Throughout adult life, they are key for axonal growing of newly generated olfactory neurons, from the lamina propria to the ONL. Due to their pro-regenerative properties, these cells have been used to foster axonal regeneration in spinal cord or optic nerve injury models.
We present an in vitro model to assay and measure OEG neuroregenerative capacity after neural injury. In this model, reversibly immortalized human OEG (ihOEG) is cultured as a monolayer, retinas are extracted from adult rats and retinal ganglion neurons (RGN) are cocultured onto the OEG monolayer. After 96 h, axonal and somatodendritic markers in RGNs are analyzed by immunofluorescence and the number of RGNs with axon and the mean axonal length/neuron are quantified.
This protocol has the advantage over other in vitro assays that rely on embryonic or postnatal neurons, that it evaluates OEG neuroregenerative properties in adult tissue. Also, it is not only useful for assessing the neuroregenerative potential of ihOEG but can be extended to different sources of OEG or other glial cells.

In this protocol, we present an in vitro model to assay OEG neuroregenerative capacity after neuronal injury. As shown in Figure 1, the OEG source is a reversible immortalized human OEG clonal cell line -Ts14 and Ts12-, which derives from primary cultures, prepared from olfactory bulbs obtained in autopsies15,17,18. Retinal tissue is extracted from adult rats, digested, and retinal ganglion neurons ...

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Coculture of Axotomized Rat Retinal Ganglion Neurons with Olfactory Ensheathing Glia, as an In Vitro Model of Adult Axonal Regeneration

We present an in vitro model to assess olfactory ensheathing glia (OEG) neuroregenerative capacity, after neural injury. It is based on a coculture of axotomized adult retinal ganglion neurons (RGN) on OEG monolayers and subsequent study of axonal regeneration, by analyzing RGN axonal and somatodendritic markers.

Olfactory ensheathing glia (OEG) cells are localized all the way from the olfactory mucosa to and into the olfactory nerve layer (ONL) of the olfactory ...

Our protocol is a simple and reproducible model to assess olfactory ensheathing capacity to foster adult axonal regeneration This is a quantitative technique that allows the evaluation of olfactory ensheathing glia regenerative capacity that can also be extended to other glial cell types. This technique is the first step to study olfactory ensheathing glia as a candidate for cell therapy in nervous system injuries before translation to in vivo or clinical studies. Demonstrating the procedure will be Maria Portela, a PhD student from our laboratory.To begin, prepare all the required media as described in the text manuscript. After sacrificing the rat, place its head in a 100 milliliter Petri dish and spray it with 70%ethanol before placing it in a laminar flow hood. Cut the rat's whiskers with scissors so they do not interfere with the eye manipulation.Grip the optic nerve with forceps to pull out the eyeball enough to be able to make an incision across the eye with a scalpel. Remove the lens and vitreous humor and pull out the retina, keeping the remaining layers of the eye inside. Place the retina in a previously prepared P60 cell culture dish with five milliliters of cold EBSS, then transfer it to a P60 cell culture dish with reconstituted papain plus 50 microliters of APV and 250 microliters of DNAs plus five microliters of APV.Cut the retina into small pieces with a scalpel. Transfer the pieces to a 15 milliliter plastic tube and incubate them for 30 minutes in a humidified incubator at 37 degrees Celsius under 5%carbon dioxide, agitating every 10 minutes. Dissociate cell clumps by pipetting up and down with a glass pasture pipette.Then centrifuge the cell suspension at 200 times G for five minutes. Discard supernatant and re-suspend the cell pellet in albumin OVO mucoid protease inhibitor with 150 microliters of DNAs and 30 microliters of APV. Carefully add the cell suspension on five milliliters of albumin OVO mucoid protease inhibitor and repeat the centrifugation.While centrifuging, completely remove the EMI 10 medium from an OEG 24 well plate and replace it with 500 microliters of NBB 27 medium per well. Discard the supernatant and re-suspend the cells in two milliliters of NB B27 medium. Plate 100 microliters of retinal cell suspension into each well of the M 24 plate onto PLL-treated or OEG monolayer cover slips.Maintain cultures at 37 degrees Celsius with 5%carbon dioxide for 96 hours in NB B27 medium. After 96 hours, fix the cells for 10 minutes by adding the same volume of 4%PFA in PBS to the culture medium. Discard the fixing solution and wash the cells three times with PBS for five minutes per wash, then block with PBS TS for 30 to 40 minutes.Prepare the primary antibodies in PBS TS buffer as described in the text manuscript and add them to the cocultures. Incubate the cells overnight at four degrees Celsius. On the next day, discard the antibodies and wash the cover slips three times with PBS for five minutes per wash.Add the corresponding fluorescent secondary antibodies and incubate the cover slips for one hour at room temperature in the dark. Then wash the cover slips three times with PBS for five minutes per wash in the dark. Mount the cover slips with mounting medium and keep them at four degrees Celsius.Use a 40 times objective of an epi fluorescence microscope to quantify axonal regeneration. Quantify the percentage of neurons with axons relative to the total population of retinal ganglion neurons. Use the neuron J plugin in image J to quantify the axonal regeneration index or mean Ono length, which is the sum of the lengths of all identified axons divided by the total number of counted neurons, whether they presented in axon or not.After opening the image, click on analyze and set scale according to microscope settings, working in pixels per micrometer. Select add tracings to begin axon tracking then track the axons from the soma to the end. Click on measure tracings, display tracing measurements, and run.Neuroregenerative capacity of olfactory ensheathing glia after neuronal injury was investigated using a reversible immortalized human OEG clonal cell line. TS14 OEG identity was assessed by immunostaining within sheath and glioma markers, such as S 100 beta and vimentin. GFAP expression was also analyzed to discard astrocyte contamination.In the axonal regeneration assay, TS14 regenerative capacity was compared to TS12 in RGN OEG cocultures using PLL substrate as a negative control. Representative images show a lack of capacity of RGN to regenerate their axons over PLL or TS12 cells. Well TS14 stimulates the outgrowth of axons in RGN.Both the percentage of cells with axons, as well as the average length of the regenerated axons were significantly higher in neurons cocultured on TS14 monolayers compared to neurons plated on either TS12 cells or PLL. This protocol can be used to elucidate the molecular mechanisms responsible of the neuroregenerative capacities of olfactory ensheathing glia.

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3.7K vistas.  Universidad Francisco de Vitoria. Our protocol is a simple and reproducible model to assess olfactory ensheathing capacity to foster adult axonal regeneration This is a quantitative technique that allows the evaluation of olfactory ensheathing glia regenerative capacity that can also be extended to other glial cell types. This technique is the first step to study olfactory ensheathing glia as a candidate for cell therapy in nervous system injuries before translation to in vivo or clinical studies. Demonstrating the procedure ...