This work was supported by the Australian National Health and Medical Research Council (NHMRC fellowship #454330 to JX, project grant #628761 to SM and APP1058647 to JX), Multiple Sclerosis Research Australia (MSRA #12070 to JX), the University of Melbourne Research Grant Support Scheme and Melbourne Research CI Fellowship to JX as well as Australia Postgraduate Scholarships to HP and AF.&#160;We would like to acknowledge the Operational Infrastructure Scheme of the Department of Innovation, Industry and Regional Development, Victoria Australia.

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The authors declare that there is no conflict of interest regarding this research.

Mielinizzazione di assoni è un processo fondamentale per il funzionamento ottimale di entrambi i sistemi nervoso centrale e periferico di vertebrati. La generazione e la manutenzione di assoni mielinizzati è un processo complesso e coordinato che coinvolge interazioni molecolari tra neuronale, gliale (dalle cellule di Schwann o oligodendrociti) e proteine ​​extracellulari della matrice. Il significato e l&#39;applicabilità di questo protocollo è che permette la manipolazione delle proteine ​​in un tipo di ce...

Mielinizzazione degli assoni è fondamentale per la trasmissione rapida ed efficiente dei potenziali d&#39;azione sia nel sistema nervoso centrale e periferico. Cellule specializzate, le cellule di Schwann nel sistema nervoso periferico e oligodendrociti nel sistema nervoso centrale, avvolgono e ensheathe assoni in mielina, efficace isolamento del nervo e facilitando la conduzione saltatory 1. Il processo di mielinizzazione può essere studiato in vitro utilizzando retina neuroni gangliari 2, nanofibre ingegnerizzati 3, o neuroni dei gangli delle radici dorsali co-coltura sia con le cellule di Schwann 4 o oligodendrociti 5-7. Il saggio mielinizzazione in vitro è un modello stabilito per lo studio mielinizzazione del sistema nervoso e si replica molti dei processi fondamentali che avvengono durante la mielinizzazione in vivo 5-8. Il test prevede la co-coltura di popolazioni purificate di dorsale Root Ganglion (DRG) neuroni, con OPC (per CNS mielinizzazione) o cellule di Schwann (per PNS mielinizzazione). In condizioni particolari queste cellule mielinizzanti ensheathe assoni DRG in ordinata, ultra strutturalmente verificato, scheda multi-lamellare di isolamento membrana plasmatica che esprimono lo stesso complemento di specifiche proteine ​​della mielina presenti in vivo. Il modello cellulare più comunemente usato di studiare CNS mielinizzazione in vitro è co-colture di neuroni DRG e OPC, che sono stati usati con successo per studiare l&#39;effetto che i fattori esogeni, quali le neurotrofine esercitano sul sistema nervoso centrale mielinizzazione in vitro 5,6. Fattori esogeni, quali fattori di crescita o piccole molecole inibitori farmacologici sono stati ampiamente utilizzati per studiare il ruolo delle vie di segnalazione nella mielinizzazione utilizzando il DRG-OPC modello coculture 7,9. Tuttavia, nelle impostazioni co-coltura miste contenenti sia i neuroni e oligodendrociti, rimase formalmente possibile che sia i fattori di crescita o il pharinibitori ve- avrebbero potuto esercitare effetti su entrambi i neuroni DRG e oligodendrociti (OL). Questo non offre la possibilità di sezionare specificamente i ruoli che le proteine ​​espresse solo DRG o oligodendroglia esercita su mielinizzazione con questo sistema a doppia cella. Per confermare in modo inequivocabile che il percorso di segnalazione in oligodendrogliale regola direttamente mielinizzazione, trasduzione lentivirale di OPC, prima della semina su neuroni DRG per il saggio mielinizzazione in vitro, ha dimostrato di essere un modo elegante per iperespressione sia wild-type e le proteine ​​mutanti, come pure come espressione atterramento di proteine ​​costitutivamente espresse da oligodendrociti. Così questo approccio offre un viale di interrogare in modo specifico e manipolare vie di segnalazione all&#39;interno oligodendrociti per studiare mielinizzazione 9,10. In questo lavoro, si segnala metodi che abbiamo sviluppato per iperespressione una proteina di interesse selettivamente in oligodendrociti mediante lentiviralapproccio per studiare mielinizzazione in vitro. La tecnica inizia con la generazione di vettori di espressione contenenti il ​​gene di interesse, sia esso in un ceppo selvatico, forma negativa costitutivamente attiva o dominante che vengono successivamente clonato nel vettore pENTR (pENTR L1-L2 pENTR4IRES2GFP). Questo vettore (contenente il gene di interesse), il donatore CMV promotore (pENTR L4-R1-pENTR pDNOR-CMV) e la lentivector 2K7 sono combinati in una reazione enzimatica per produrre un vettore contenente 2K7 CMV promoter, il gene di interesse, un sito interno ribosomiale ingresso e GFP (Figura 1). Questo Gateway clonato costrutto 2K7 combinata con la busta virus PMD2.G e il pacchetto di virus pBR8.91 può essere co-trasfettato in cellule HEK293T generare lentivirus che può essere successivamente utilizzato per trasdurre OPC. Una volta infettati con il lentivirus le OPC esprimono un alto livello della proteina di interesse. Questi OPC possono essere seminati in colture DRG neuroni e l&#39;effetto che l&#39;espressionedi elevati livelli della proteina desiderata esercita sulla mielinizzazione possono essere interrogato. Le co-colture sono valutati per l&#39;espressione delle proteine ​​della mielina mediante analisi western blot e visualizzati per la formazione di segmenti assonale mieliniche mediante immunocitochimica.

<table border="0" cellpadding="0" cellspacing="0" width="843">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:413px;">Item</td>
			<td style="width:148px;">Manufacturer</td>
			<td style="width:99px;">Catalog #</td>
			<td style="width:183px;">Notes</td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">2K7 lentivector&#160;</td>
			<td></td>
			<td></td>
			<td>Kind gift from Dr Suter9</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">5-Fluoro-2&#8242;-deoxyuridine</td>
			<td>Sigma-Aldrich</td>
			<td>F0503-100mg</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Alexa Fluor 488 Goat anti-mouse IgG</td>
			<td>Jackson Immunoresearch</td>
			<td>115545205</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Alexa Fluor 488 goat anti-rabbit IgG (H+L)</td>
			<td>Life Technologies</td>
			<td>A11008</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Alexa Fluor 594 goat anti-mouse IgG (H+L)</td>
			<td>Life Technologies</td>
			<td>A11005</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Alexa Fluor 594 goat anti-rabbit IgG (H+L)</td>
			<td>Life Technologies</td>
			<td>A11012</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Ampicillin</td>
			<td>Sigma-Aldrich</td>
			<td>A9518-5G</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">B27 - NeuroCul SM1 Neuronal Supplement</td>
			<td>Stem Cell Technologies&#160;</td>
			<td>5711</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">BDNF (Human)</td>
			<td>Peprotech</td>
			<td>PT450021000</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Biotin (d-Biotin)</td>
			<td>Sigma Aldrich</td>
			<td>B4639</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Bradford Reagent</td>
			<td>Sigma Aldrich</td>
			<td>B6916-500ML&#160;&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">BSA</td>
			<td>Sigma Aldrich</td>
			<td>A4161</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Chloramphenicol</td>
			<td>Sigma-Aldrich</td>
			<td>C0378-100G</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">CNTF</td>
			<td>Peprotech</td>
			<td>450-13020</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">DAKO fluoresence mounting media</td>
			<td>DAKO</td>
			<td>S302380-2</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">DMEM, High Glucose, Pyruvate, no Glutamine</td>
			<td>Life Technologies</td>
			<td>10313039</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">DNase</td>
			<td>Sigma-Aldrich</td>
			<td>D5025-375KU</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">DPBS</td>
			<td>Life Technologies</td>
			<td>14190250</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">DPBS, calcium, magnesium</td>
			<td>Life Technologies</td>
			<td>14040182</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">EBSS</td>
			<td>Life Technologies</td>
			<td>14155063</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">EcoRI-HF</td>
			<td>NEB</td>
			<td>R3101</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Entry vectors for promoter and gene of interest</td>
			<td></td>
			<td></td>
			<td>Generate as per protocols 1-2</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Fetal Bovine Serum</td>
			<td>Sigma-Aldrich</td>
			<td>12003C</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Forskolin&#160;</td>
			<td>Sigma Aldrich</td>
			<td>F6886-50MG</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Glucose (D-glucose)</td>
			<td>Sigma-Aldrich</td>
			<td>G7528</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Glycerol</td>
			<td>Chem Supply</td>
			<td>GL010-500M</td>
			<td>See stock solutions</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Goat Anti-Mouse IgG</td>
			<td>Jackson ImmunoResearch</td>
			<td>115005003</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Goat Anti-Mouse IgM&#160;</td>
			<td>Jackson ImmunoResearch</td>
			<td>115005020</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Goat Anti-Rat IgG</td>
			<td>Jackson ImmunoResearch</td>
			<td>112005167</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Hoechst 33342</td>
			<td>Life Technologies</td>
			<td>H3570</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Igepal</td>
			<td>Sigma Aldrich</td>
			<td>I3021-100ML&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Insulin&#160;</td>
			<td>Sigma Aldrich</td>
			<td>I6634&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Kanamycin</td>
			<td>Sigma-Aldrich</td>
			<td>60615</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Laminin&#160;</td>
			<td>Life Technologies</td>
			<td>23017015</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">LB Medium</td>
			<td></td>
			<td></td>
			<td>See stock solutions</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">LB-Agar</td>
			<td></td>
			<td></td>
			<td>See stock solutions</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">L-cysteine</td>
			<td>Sigma-Aldrich</td>
			<td>C-7477</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Leibovitz&#39;s L-15 Medium</td>
			<td>Life Technologies</td>
			<td>11415064</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">L-Glutamate</td>
			<td>Sigma-Aldrich</td>
			<td>G1626</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">L-Glutamine- 200mM (100X) liquid</td>
			<td>Life Technologies</td>
			<td>25030081</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">LR Clonase II Plus enzyme</td>
			<td>Life Technologies</td>
			<td>12538-120</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">MEM, NEAA, no Glutamine</td>
			<td>Life Technologies</td>
			<td>10370088</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Mouse &#945; &#946;III Tubulin&#160;</td>
			<td>Promega</td>
			<td>G7121</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Mouse &#945;MBP (monoclonal)</td>
			<td>Millipore</td>
			<td>MAB381</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Na pyruvate&#160;</td>
			<td>Life Technologies</td>
			<td>11360-070</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">NAC</td>
			<td>Sigma Aldrich</td>
			<td>A8199</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">NcoI-HF</td>
			<td>NEB</td>
			<td>R3193S</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">NEBuffer 4</td>
			<td>NEB</td>
			<td>B7004S</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Neurobasal medium</td>
			<td>Life Technologies</td>
			<td>21103049</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">NGF (mouse)</td>
			<td>Alomone Labs</td>
			<td>N-100</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">NT-3</td>
			<td>Peprotech</td>
			<td>&#160;450-03</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">O1 antibody - Mouse anti-O1</td>
			<td>Millipore</td>
			<td>MAB344</td>
			<td>Alternative if O1 hybridoma cells are unavailable</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">O1 hybridoma cells</td>
			<td></td>
			<td></td>
			<td>Conditioned medium containing anti-O1 antibody to be used for immunopanning</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">O4 antibody - Mouse anti-O4</td>
			<td>Millipore</td>
			<td>MAB345</td>
			<td>Alternative if O4 hybridoma cells are unavailable</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">O4 hybridoma cells</td>
			<td></td>
			<td></td>
			<td>Conditioned medium containing anti-O4 antibody to be used for immunopanning</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">&#160;Competent Cells</td>
			<td>Life Technologies</td>
			<td>A10460</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">One Shot Stbl competent cells</td>
			<td>Life Technologies</td>
			<td>C7373-03</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Papain Suspension</td>
			<td>Worthington/Cooper</td>
			<td>LS003126</td>
			<td></td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">pBR8.91</td>
			<td></td>
			<td></td>
			<td>Kind gift from Dr Denham10</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">PDGF-AA (Human)</td>
			<td>Peprotech</td>
			<td>PT10013A500&#160;&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Penicillin- Streptomycin 100X solution</td>
			<td>Life Technologies</td>
			<td>15140122</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">pENTRY4IRES2GFP</td>
			<td>Invitrogen</td>
			<td>11818-010&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">pMD2.G</td>
			<td>Addgene</td>
			<td>12259</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Poly-D-lysine</td>
			<td>Sigma</td>
			<td>P6407-5MG</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Polyethylenimine (PEI)&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>408727-100ML</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Poly-L-ornithine&#160;</td>
			<td>Sigma Aldrich&#160;</td>
			<td>P3655</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Progesterone&#160;</td>
			<td>Sigma Aldrich</td>
			<td>P8783</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Protease inhibitor tablet (Complete mini)</td>
			<td>Roche</td>
			<td>11836153001</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Proteinase K</td>
			<td></td>
			<td></td>
			<td>Supplied with Clonase enzyme</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Putrescine</td>
			<td>Sigma Aldrich</td>
			<td>P-5780</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Rabbit &#945; neurofilament</td>
			<td>Millipore</td>
			<td>AB1987&#160;&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Rabbit &#945;MBP (polyclonal)</td>
			<td>Millipore</td>
			<td>AB980</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Ran2 hybridoma cells</td>
			<td>ATCC</td>
			<td>TIB-119</td>
			<td>Conditioned medium containing anti-Ran2 antibody to be used for immunopanning</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Rat anti CD140A/PDGFRa antibody</td>
			<td>BD Pharmingen</td>
			<td>558774</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">SacII</td>
			<td>NEB</td>
			<td>R0157</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">SOC medium</td>
			<td></td>
			<td></td>
			<td>Supplied with competent bacteria</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Sodium selenite&#160;</td>
			<td>Sigma Aldrich</td>
			<td>S5261</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Spe I</td>
			<td>NEB</td>
			<td>R0133S</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">T4 DNA Ligase</td>
			<td>NEB</td>
			<td>M0202S</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">T4 DNA Ligase Buffer</td>
			<td>NEB</td>
			<td>B0202S</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">TE buffer pH8</td>
			<td></td>
			<td></td>
			<td>See stock solutions</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">TNE lysis buffer</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Trace Elements B</td>
			<td>Cellgro&#160;</td>
			<td>99-175-CI</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Transferrin (apo-Transferrin human)</td>
			<td>Sigma-Aldrich</td>
			<td>T1147</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Triton&#160;X-100</td>
			<td>Sigma-Aldrich</td>
			<td>T9284&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Trypsin</td>
			<td>Sigma-Aldrich</td>
			<td>T9201-1G</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Trypsin Inhibitor From Chicken Egg White</td>
			<td>Roche</td>
			<td>10109878001</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Trypsin-EDTA (1X), phenol red (0.05%)</td>
			<td>Life Technologies</td>
			<td>25300-054</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Unconjugated Griffonia Simplicifolia Lectin BSL-1</td>
			<td>Vector laboratories&#160;</td>
			<td>L-1100</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Uridine</td>
			<td>Sigma-Aldrich</td>
			<td>U3003-5G</td>
			<td></td>
		</tr>
	</tbody>
</table>

production and use of lentivirus to selectively transduce primary oligodendrocyte precursor cells for in vitro myelination assays

Mielinizzazione è un processo complesso che coinvolge sia i neuroni e la mielina che formano le cellule gliali, oligodendrociti nel sistema nervoso centrale (SNC) e le cellule di Schwann nel sistema nervoso periferico (PNS). Usiamo una vitro mielinizzazione test in un modello stabilito per lo studio del sistema nervoso centrale mielinizzazione in vitro. Per fare questo, le cellule precursori degli oligodendrociti (OPC) vengono aggiunti i primari roditore dorsale radice gangli (DRG) neuroni purificati per formare co-culture mielinizzanti. Per interrogare specificamente i ruoli che particolari proteine ​​espresse da oligodendrociti esercitano su di mielinizzazione abbiamo sviluppato protocolli che trasducono selettivamente OPC con il lentivirus overexpressing wild type, proteine ​​negativi costitutivamente attive o dominanti prima di essere testa di serie sui neuroni DRG. Questo ci permette di interrogare in particolare il ruolo di queste proteine ​​nella regolazione oligodendrogliali mielinizzazione. I protocolli possono essere applicati anche nello studio di otsuoi tipi cellulari, fornendo così un metodo che permette la manipolazione selettiva di proteine ​​espresse da un tipo cellulare desiderato, come oligodendrociti per lo studio mirato di segnalazione e meccanismi di compensazione. In conclusione, combinando la mielinizzazione test in vitro con lentivirali infettato OPC fornisce uno strumento strategico per l&#39;analisi dei meccanismi molecolari coinvolti nella mielinizzazione.

Il segnale legate chinasi 1 (Flag-Erk1) costrutto usato per la produzione di lentivirus è verificato da enzima di restrizione digerire dei costrutti utilizzati, inclusi sia i costrutti 2K7 ei costrutti packaging e accessori necessari per la produzione di virus extracellulare (Figura 3) flag-tagged . <img alt="Figura 3" src="/files/ftp_upload/52179/52179fig3highres.jpg" /> Figura 3: verifica costrutto DNA. Tutti i c...

Watch this Scientific Journal Video about Production and Use of Lentivirus to Selectively Transduce Primary Oligodendrocyte Precursor Cells for In Vitro Myelination Assays at JoVE.com

Production and Use of Lentivirus to Selectively Transduce Primary Oligodendrocyte Precursor Cells for In Vitro Myelination Assays

Here we present protocols that offer a flexible and strategic foundation for virally manipulating oligodendrocyte precursor cells to overexpress proteins of interest in order to specifically interrogate their role in oligodendrocytes via the in vitro model of central nervous system myelination.

Produzione e l&#39;uso di Lentivirus a celle selettivamente trasdurre primaria Oligodendrocyte precursore<em&gt; In Vitro</em&gt; Saggi mielinizzazione

Myelination is a complex process that involves both neurons and the myelin forming glial cells, oligodendrocytes in the central nervous system (CNS) and ...

production-use-lentivirus-to-selectively-transduce-primary

Research

JoVE Journal

Developmental Biology

Production and Use of Lentivirus to Selectively Transduce Primary Oligodendrocyte Precursor Cells for In Vitro Myelination Assays

14.4K Views.  The University of Melbourne. Here we present protocols that offer a flexible and strategic foundation for virally manipulating oligodendrocyte precursor cells to overexpress proteins of interest in order to specifically interrogate their role in oligodendrocytes via the in vitro model of central nervous system myelination.

Video: Production and Use of Lentivirus to Selectively Transduce Primary Oligodendrocyte Precursor Cells for In Vitro Myelination Assays

Characterization of Thymic Settling Progenitors in the Mouse Embryo Using In Vivo and In Vitro Assays

Characterizing thymic settling progenitors is important to understand the pre-thymic stages of T cell development, essential to devise strategies for T cell replacement in lymphopenic patients. We studied thymic settling progenitors from murine embryonic day 13 and 18 thymi by two complementary in vitro and in vivo techniques, both based on the &#8220;hanging drop&#8221; method. This method allowed colonizing irradiated fetal thymic lobes with E13 and/or E18 thymic progenitors distinguished by CD45 allotypic markers and thus following their progeny. Colonization with mixed populations allows analyzing cell autonomous differences in biologic properties of the progenitors while colonization with either population removes possible competitive selective pressures. The colonized thymic lobes can also be grafted in immunodeficient male recipient mice allowing the analysis of the mature T cell progeny in vivo, such as population dynamics of the peripheral immune system and colonization of different tissues and organs. Fetal thymic organ cultures revealed that E13 progenitors developed rapidly into all mature CD3+ cells and gave rise to the canonical &#947;&#948; T cell subset, known as dendritic epithelial T cells. In comparison, E18 progenitors have a delayed differentiation and were unable to generate dendritic epithelial T cells. The monitoring of peripheral blood of thymus-grafted CD3-/- mice further showed that E18 thymic settling progenitors generate, with time, larger numbers of mature T cells than their E13 counterparts, a feature that could not be appreciated in the short term fetal thymic organ cultures.

Characterization of Thymic Settling Progenitors in the Mouse Embryo Using In Vivo and In Vitro Assays

This article describes in vivo and in vitro methodology to characterize the thymic settling progenitors by the analysis of the kinetics of generation, phenotype and numbers of their T cell progeny.

Caratterizzazione di timica assestamento Progenitori nell&#39;embrione mouse Uso<em&gt; In Vivo</em&gt; E<em&gt; In Vitro</em&gt; Saggi

Characterizing thymic settling progenitors is important to understand the pre-thymic stages of T cell development, essential to devise strategies for T ...

Ricerca

Biologia dello sviluppo

In Vitro Colony Assays for Characterizing Tri-potent Progenitor Cells Isolated from the Adult Murine Pancreas

Stem and progenitor cells from the adult pancreas could be a potential source of therapeutic beta-like cells for treating patients with type 1 diabetes. However, it is still unknown whether stem and progenitor cells exist in the adult pancreas. Research strategies using cre-lox lineage-tracing in adult mice have yielded results that either support or refute the idea that beta cells can be generated from the ducts, the presumed location where adult pancreatic progenitors may reside. These in vivo cre-lox lineage-tracing methods, however, cannot answer the questions of self-renewal and multi-lineage differentiation-two criteria necessary to define a stem cell. To begin addressing this technical gap, we devised 3-dimensional colony assays for pancreatic progenitors. Soon after our initial publication, other laboratories independently developed a similar, but not identical, method called the organoid assay. Compared to the organoid assay, our method employs methylcellulose, which forms viscous solutions that allow the inclusion of extracellular matrix proteins at low concentrations. The methylcellulose-containing assays permit easier detection and analyses of progenitor cells at the single-cell level, which are critical when progenitors constitute a small sub-population, as is the case for many adult organ stem cells. Together, results from several laboratories demonstrate in vitro self-renewal and multi-lineage differentiation of pancreatic progenitor-like cells from mice. The current protocols describe two methylcellulose-based colony assays to characterize mouse pancreatic progenitors; one contains a commercial preparation of murine extracellular matrix proteins and the other an artificial extracellular matrix protein known as a laminin hydrogel. The techniques shown here are 1) dissociation of the pancreas and sorting of CD133+Sox9/EGFP+ ductal cells from adult mice, 2) single cell manipulation of the sorted cells, 3) single colony analyses using microfluidic qRT-PCR and whole-mount immunostaining, and 4) dissociation of primary colonies into single-cell suspensions and re-plating into secondary colony assays to assess self-renewal or differentiation.

In Vitro Colony Assays for Characterizing Tri-potent Progenitor Cells Isolated from the Adult Murine Pancreas

In vitro colony assays to detect self-renewal and differentiation of progenitor cells isolated from adult murine pancreas are devised. In these assays, pancreatic progenitors give rise to cell colonies in 3-dimensional space in methylcellulose-containing semi-solid medium. Protocols for handling single cells and characterization of individual colonies are described.

In Vitro Colony saggi per Caratterizzazione Tri-potenti cellule progenitrici isolato dal adulti murini Pancreas

Stem and progenitor cells from the adult pancreas could be a potential source of therapeutic beta-like cells for treating patients with type 1 diabetes. ...

Preparation and Culture of Myogenic Precursor Cells/Primary Myoblasts from Skeletal Muscle of Adult and Aged Humans

Skeletal muscle homeostasis depends on muscle growth (hypertrophy), atrophy and regeneration. During ageing and in several diseases, muscle wasting occurs. Loss of muscle mass and function is associated with muscle fiber type atrophy, fiber type switching, defective muscle regeneration associated with dysfunction of satellite cells, muscle stem cells, and other pathophysiological processes. These changes are associated with changes in intracellular as well as local and systemic niches. In addition to most commonly used rodent models of muscle ageing, there is a need to study muscle homeostasis and wasting using human models, which due to ethical implications, consist predominantly of in vitro cultures. Despite the wide use of human Myogenic Progenitor Cells (MPCs) and primary myoblasts in myogenesis, there is limited data on using human primary myoblast and myotube cultures to study molecular mechanisms regulating different aspects of age-associated muscle wasting, aiding in the validation of mechanisms of ageing proposed in rodent muscle. The use of human MPCs, primary myoblasts and myotubes isolated from adult and aged people, provides a physiologically relevant model of molecular mechanisms of processes associated with muscle growth, atrophy and regeneration. Here we describe in detail a robust, inexpensive, reproducible and efficient protocol for the isolation and maintenance of human MPCs&#160;and their progeny&#160;&#8212; myoblasts and myotubes from human muscle samples using enzymatic digestion. Furthermore, we have determined the passage number at which primary myoblasts from adult and aged people undergo senescence in an in vitro culture. Finally, we show the ability to transfect these myoblasts and the ability to characterize their proliferative and differentiation capacity and propose their suitability for performing functional studies of molecular mechanisms of myogenesis and muscle wasting in vitro.

This protocol describes a robust, reproducible and simple method of isolation and culture of myoblast progenitor cells from the skeletal muscle of adult and aged people. The muscles used here include foot and leg muscles. This approach enables the isolation of an enriched population of primary myoblasts for functional studies.

Preparazione e la cultura di cellule miogeniche Precursore / mioblasti primari dal muscolo scheletrico di adulti e esseri umani invecchiati

Skeletal muscle homeostasis depends on muscle growth (hypertrophy), atrophy and regeneration. During ageing and in several diseases, muscle wasting ...

Reprogramming Primary Amniotic Fluid and Membrane Cells to Pluripotency in Xeno-free Conditions

Autologous cell-based therapies got a step closer to reality with the introduction of induced pluripotent stem cells. Fetal stem cells, such as amniotic fluid and membrane mesenchymal stem cells, represent a unique type of undifferentiated cells with promise in tissue engineering and for reprogramming into iPSC for future pediatric interventions and stem cell banking. The protocol presented here describes an optimized procedure for extracting and culturing primary amniotic fluid and membrane mesenchymal stem cells and generating episomal induced pluripotent stem cells from these cells in fully chemically defined culture conditions utilizing human recombinant vitronectin and the E8 medium. Characterization of the new lines by applying stringent methods &#8211; flow cytometry, confocal imaging, teratoma formation and transcriptional profiling &#8211; is also described. The newly generated lines express markers of embryonic stem cells &#8211; Oct3/4A, Nanog, Sox2, TRA-1-60, TRA-1-81, SSEA-4 &#8211; while being negative for the SSEA-1 marker. The stem cell lines form teratomas in scid-beige mice in 6-8 weeks and the teratomas contain tissues representative of all three germ layers. Transcriptional profiling of the lines by submitting global expression microarray data to a bioinformatic pluripotency assessment algorithm deemed all lines pluripotent and therefore, this approach is an attractive alternative to animal testing. The new iPSC lines can readily be used in downstream experiments involving the optimization of differentiation and tissue engineering.

This protocol describes the reprogramming of primary amniotic fluid and membrane mesenchymal stem cells into induced pluripotent stem cells using a non-integrating episomal approach in fully chemically defined conditions. Procedures of extraction, culture, reprogramming, and characterization of the resulting induced pluripotent stem cells by stringent methods are detailed.

Riprogrammazione primario del liquido amniotico e le celle a membrana di pluripotenza in condizioni prive di Xeno

Autologous cell-based therapies got a step closer to reality with the introduction of induced pluripotent stem cells. Fetal stem cells, such as amniotic ...

Rapid Detection of Neurodevelopmental Phenotypes in Human Neural Precursor Cells (NPCs)

Human brain development proceeds through a series of precisely orchestrated processes, with earlier stages distinguished by proliferation, migration, and neurite outgrowth; and later stages characterized by axon/dendrite outgrowth and synapse formation. In neurodevelopmental disorders, often one or more of these processes are disrupted, leading to abnormalities in brain formation and function. With the advent of human induced pluripotent stem cell (hiPSC) technology, researchers now have an abundant supply of human cells that can be differentiated into virtually any cell type, including neurons. These cells can be used to study both normal brain development and disease pathogenesis. A number of protocols using hiPSCs to model neuropsychiatric disease use terminally differentiated neurons or use 3D culture systems termed organoids. While these methods have proven invaluable in studying human disease pathogenesis, there are some drawbacks. Differentiation of hiPSCs into neurons and generation of organoids are lengthy and costly processes that can impact the number of experiments and variables that can be assessed. In addition, while post-mitotic neurons and organoids allow the study of disease-related processes, including dendrite outgrowth and synaptogenesis, they preclude the study of earlier processes like proliferation and migration. In neurodevelopmental disorders, such as autism, abundant genetic and post-mortem evidence indicates defects in early developmental processes. Neural precursor cells (NPCs), a highly proliferative cell population, may be a suitable model in which to ask questions about ontogenetic processes and disease initiation. We now extend methodologies learned from studying development in mouse and rat cortical cultures to human NPCs. The use of NPCs allows us to investigate disease-related phenotypes and define how different variables (e.g., growth factors, drugs) impact developmental processes including proliferation, migration, and differentiation in only a few days. Ultimately, this toolset can be used in a reproducible and high-throughput manner to identify disease-specific mechanisms and phenotypes in neurodevelopmental disorders.

Rapid Detection of Neurodevelopmental Phenotypes in Human Neural Precursor Cells NPCs

Neurodevelopmental processes such as proliferation, migration, and neurite outgrowth are often perturbed in neuropsychiatric diseases. Thus, we present protocols to rapidly and reproducibly assess these neurodevelopmental processes in human iPSC-derived NPCs. These protocols also allow the assessment of the effects of relevant growth factors and therapeutics on NPC development.

Rilevamento rapido dei fenotipi di Neurodevelopmental in cellule precursori neurali umane (NPC)

Human brain development proceeds through a series of precisely orchestrated processes, with earlier stages distinguished by proliferation, migration, and ...

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

Studying the cell biological processes during converting the identities of specific cell types provides important insights into mechanism that maintain and protect cellular identities. The conversion of germ cells into specific neurons in the nematode Caenorhabditis elegans (C. elegans) is a powerful tool for performing genetic screens in order to dissect regulatory pathways that safeguard established cell identities. Reprogramming of germ cells to a specific type of neurons termed ASE requires transgenic animals that allow broad over-expression of the Zn-finger transcription factor (TF) CHE-1. Endogenous CHE-1 is expressed exclusively in two head neurons and is required to specify the glutamatergic ASE neurons fate, which can easily be visualized by the gcy-5prom::gfp reporter. A trans gene containing the heat-shock promoter-driven che-1 gene expression construct allows broad mis-expression of CHE-1 in the entire animal upon heat-shock treatment. The combination of RNAi against the chromatin-regulating factor LIN-53 and heat-shock-induced che-1 over-expression leads to reprogramming of germ cell into ASE neuron-like cells. We describe here the specific RNAi procedure and appropriate conditions for heat-shock treatment of transgenic animals in order to successfully induce germ cell to neuron conversion.

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

This protocol describes how to study cellular processes during cell fate conversion in Caenorhabditis elegans in vivo. Using transgenic animals, allowing heat-shock promoter-driven overexpression of the neuron fate-inducing transcription factor CHE-1 and RNAi-mediated depletion of the chromatin-regulating factor LIN-53 germ cell to neuron reprogramming can be observed in vivo.

Applicazione di RNAi ed espressione di fattore di trascrizione indotta da calore-shock per riprogrammare le cellule germinali ai neuroni in c. elegans

Studying the cell biological processes during converting the identities of specific cell types provides important insights into mechanism that maintain ...

Single-cell Photoconversion in Living Intact Zebrafish

Animal and plant tissue is composed of distinct populations of cells. These cells interact over time to build and maintain the tissue and can cause disease when disrupted. Scientists have developed clever techniques to investigate characteristics and natural dynamics of these cells within intact tissue by expressing fluorescent proteins in subsets of cells. However, at times, experiments require more selected visualization of cells within the tissue, sometimes at the single-cell or population-of-cells manner. To achieve this and visualize single cells within a population of cells, scientists have utilized single-cell photoconversion of fluorescent proteins. To demonstrate this technique, we show here how to direct UV light to an Eos-expressing cell of interest in an intact, living zebrafish. We then image those photoconverted Eos+ cells 24 h later to determine how they changed in the tissue. We describe two techniques: single cell photoconversion and photoconversions of populations of cell. These techniques can be used to visualize cell-cell interactions, cell-fate and differentiation, and cell migrations, making it a technique that is applicable in numerous biological questions.

Here, we present a protocol to show how cell photoconversion is achieved through UV exposure to specific areas expressing the fluorescent protein, Eos, in living animals.

Cella singola fotoconversione in Zebrafish intatto vivente

Animal and plant tissue is composed of distinct populations of cells. These cells interact over time to build and maintain the tissue and can cause ...

Isolation of Human Endometrial Stromal Cells for In Vitro Decidualization

The differentiation of human endometrial stromal cells (HESC) from fibroblast-like appearance into secretory decidua is a transformation required for embryo implantation into the uterine lining of the maternal womb. Improper decidualization has been established as a root cause for implantation failure and subsequent early embryo miscarriage. Therefore, understanding the molecular mechanisms underlying decidualization is advantageous to improving the rate of successful births. In vivo based studies of artificial decidualization are often limiting due to ethical dilemmas associated with human research, as well as translational complications within animal models. As a result, in vitro assays through primary cell culture are often utilized to explore the modulation of decidualization via hormones. This study provides a detailed protocol for the isolation of HESC and subsequent artificial decidualization via the supplementation of hormones to the culturing medium. Further, this study provides a well-designed method to knockdown any gene of interest by utilizing lipid-based siRNA transfections. This protocol permits the optimization of culture purity as well as product yield, thereby maximizing the ability to utilize this model as a reliable method to understand the molecular mechanisms underlying decidualization, and the subsequent quantification of secreted agents by decidualized endometrial stromal cells.

Isolation of Human Endometrial Stromal Cells for In Vitro Decidualization

This study presents a validated and optimized procedure for the isolation and culture of human endometrial stromal cells to conduct in vitro decidualization assay. Further, this study provides a detailed method to efficiently knockdown a specific gene using siRNAs in human endometrial stromal cells.

Isolamento delle cellule stromali dell'endometrio umane per In Vitro decidualizzazione

The differentiation of human endometrial stromal cells (HESC) from fibroblast-like appearance into secretory decidua is a transformation required for ...

Computational Analysis of the Caenorhabditis elegans Germline to Study the Distribution of Nuclei, Proteins, and the Cytoskeleton

The Caenorhabditis elegans (C. elegans) germline is used to study several biologically important processes including stem cell development, apoptosis, and chromosome dynamics. While the germline is an excellent model, the analysis is often two dimensional due to the time and labor required for three-dimensional analysis. Major readouts in such studies are the number/position of nuclei and protein distribution within the germline. Here, we present a method to perform automated analysis of the germline using confocal microscopy and computational approaches to determine the number and position of nuclei in each region of the germline. Our method also analyzes germline protein distribution that enables the three-dimensional examination of protein expression in different genetic backgrounds. Further, our study shows variations in cytoskeletal architecture in distinct regions of the germline that may accommodate specific spatial developmental requirements. Finally, our method enables automated counting of the sperm in the spermatheca of each germline. Taken together, our method enables rapid and reproducible phenotypic analysis of the C. elegans germline.

Computational Analysis of the Caenorhabditis elegans Germline to Study the Distribution of Nuclei, Proteins, and the Cytoskeleton

We present an automated method for three-dimensional reconstruction of the Caenorhabditis elegans germline. Our method determines the number and position of each nucleus within the germline and analyses germline protein distribution and cytoskeletal structure.

Analisi computazionale della linea germinale Caenorhabditis elegans di studiare la distribuzione dei Nuclei, le proteine ed il citoscheletro

The Caenorhabditis elegans (C. elegans) germline is used to study several biologically important processes including stem cell development, apoptosis, and ...

Induction and Validation of Cellular Senescence in Primary Human Cells

Cellular senescence is a state of permanent cell cycle arrest activated in response to different damaging stimuli. Activation of cellular senescence is a hallmark of various pathophysiological conditions including tumor suppression, tissue remodeling and aging. The inducers of cellular senescence in vivo are still poorly characterized. However, a number of stimuli can be used to promote cellular senescence ex vivo. Among them, most common senescence-inducers are replicative exhaustion, ionizing and non-ionizing radiation, genotoxic drugs, oxidative stress, and demethylating and acetylating agents. Here, we will provide detailed instructions on how to use these stimuli to induce fibroblasts into senescence. This protocol can easily be adapted for different types of primary cells and cell lines, including cancer cells. We also describe different methods for the validation of senescence induction. In particular, we focus on measuring the activity of the lysosomal enzyme Senescence-Associated &#946;-galactosidase (SA-&#946;-gal), the rate of DNA synthesis using 5-ethynyl-2&#39;-deoxyuridine (EdU) incorporation assay, the levels of expression of the cell cycle inhibitors p16 and p21, and the expression and secretion of members of the Senescence-Associated Secretory Phenotype (SASP). Finally, we provide example results and discuss further applications of these protocols.

Here, we discuss a series of protocols for induction and validation of cellular senescence in cultured cells. We focus on different senescence-inducing stimuli and describe the quantification of common senescence-associated markers. We provide technical details using fibroblasts as a model, but the protocols can be adapted to various cellular models.

Induzione e convalida della senescenza cellulare in cellule umane primarie

Cellular senescence is a state of permanent cell cycle arrest activated in response to different damaging stimuli. Activation of cellular senescence is a ...

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