Ringraziamo i membri del Laboratorio di Biologia phagosome per la lettura critica del manoscritto. Questo lavoro è supportato da una sovvenzione Helmholtz Young Investigator (Iniziativa e Networking fondi dell&#39;Associazione Helmholtz) e un programma di priorità SPP1580 Concessione del Consiglio per la ricerca tedesca (Deutsche Forschungsgemeinschaft, DFG).

<ol>
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S., Jaumouille, V., Grinstein, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+cell+biology+of+phagocytosis.">The cell biology of phagocytosis.</a> Annu. Rev. Pathol. 7, 61-98 (2012).</li><li>Vieira, O. V., Botelho, R. J., Grinstein, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phagosome+maturation:+aging+gracefully.">Phagosome maturation: aging gracefully.</a> Biochem. J. 366, 689-704 (2002).</li><li>Haas, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+phagosome:+compartment+with+a+license+to+kill.">The phagosome: compartment with a license to kill.</a> Traffic. 8, 311-330 (2007).</li><li>Flannagan, R. S., Cosio, G., Grinstein, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Antimicrobial+mechanisms+of+phagocytes+and+bacterial+evasion+strategies.">Antimicrobial mechanisms of phagocytes and bacterial evasion strategies.</a> Nat Rev Microbiol. 7, 355-366 (2009).</li><li>Luzio, J., Pryor, P., Bright, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Lysosomes:+fusion+and+function.">Lysosomes: fusion and function.</a> Nat. Rev. Mol. Cell Biol. 8, 622-632 (2007).</li><li>Huotari, J., Helenius, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endosome+maturation.">Endosome maturation.</a> EMBO J. 30, 3481-3500 (2011).</li><li>Luzio, J. 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=Lysosome-endosome+fusion+and+lysosome+biogenesis.">Lysosome-endosome fusion and lysosome biogenesis.</a> J. Cell. Sci. 113 (pt 9), 1515-1524 (2000).</li><li>Eissenberg, L., Goldman, W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fusion+of+lysosomes+with+phagosomes+containing+Histoplasma+capsulatum:+use+of+fluoresceinated+dextran).">Fusion of lysosomes with phagosomes containing Histoplasma capsulatum: use of fluoresceinated dextran).</a> Adv. Exp. Med. Biol. 239, 53-61 (1988).</li><li>de Souza Carvalho, C., 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=Internalization,+phagolysosomal+biogenesis+and+killing+of+mycobacteria+in+enucleated+epithelial+cells.">Internalization, phagolysosomal biogenesis and killing of mycobacteria in enucleated epithelial cells.</a> Cell. Microbiol. 13, 1234-1249 (2011).</li><li>Wang, Y. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differential+and+sequential+delivery+of+fluorescent+lysosomal+probes+into+phagosomes+in+mouse+peritoneal+macrophages.">Differential and sequential delivery of fluorescent lysosomal probes into phagosomes in mouse peritoneal macrophages.</a> J. Cell Biol. 104, 1749-1754 (1987).</li><li>Harrison, R. E., Bucci, C., Vieira, O. V., Schroer, T. A., Grinstein, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phagosomes+Fuse+with+Late+Endosomes+and/or+Lysosomes+by+Extension+of+Membrane+Protrusions+along+Microtubules:+Role+of+Rab7+and+RILP.">Phagosomes Fuse with Late Endosomes and/or Lysosomes by Extension of Membrane Protrusions along Microtubules: Role of Rab7 and RILP.</a> Mol. Cell. Biol. 23, 6494-6506 (2003).</li><li>Huynh, K. K., 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=LAMP+proteins+are+required+for+fusion+of+lysosomes+with+phagosomes.">LAMP proteins are required for fusion of lysosomes with phagosomes.</a> EMBO J. 26, 313-324 (2007).</li><li>Kasmapour, B., Gronow, A., Bleck, C., Hong, W., Gutierrez, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Size-dependent+mechanism+of+cargo+sorting+during+lysosome-phagosome+fusion+is+controlled+by+Rab34.">Size-dependent mechanism of cargo sorting during lysosome-phagosome fusion is controlled by Rab34.</a> Proc. Natl. Acad. Sci. U.S.A. 109, 20485-20490 (2012).</li><li>Snijder, B., 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=Population+context+determines+cell-to-cell+variability+in+endocytosis+and+virus+infection.">Population context determines cell-to-cell variability in endocytosis and virus infection.</a> Nature. 461, 520-523 (2009).</li><li>Knight, M., Roberts, S., Lee, D., Bader, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Live+cell+imaging+using+confocal+microscopy+induces+intracellular+calcium+transients+and+cell+death.">Live cell imaging using confocal microscopy induces intracellular calcium transients and cell death.</a> Am. J. Physiol. Cell Physiol. 284, 9 (2003).</li><li>Hemmi, 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=A+Toll-like+receptor+recognizes+bacterial+DNA.">A Toll-like receptor recognizes bacterial DNA.</a> Nature. 408, 740-745 (2000).</li><li>Underhill, D., Ozinsky, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Toll-like+receptors:+key+mediators+of+microbe+detection.">Toll-like receptors: key mediators of microbe detection.</a> Curr. Opin. Immunol. 14, 103-110 (2002).</li><li>Bohdanowicz, M., Cos&#237;o, G., Backer, J., Grinstein, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Class+I+and+class+III+phosphoinositide+3-kinases+are+required+for+actin+polymerization+that+propels+phagosomes.">Class I and class III phosphoinositide 3-kinases are required for actin polymerization that propels phagosomes.</a> J. Cell Biol. 191, 999-1012 (2010).</li><li>Hoffmann, 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=Initial+receptor-ligand+interactions+modulate+gene+expression+and+phagosomal+properties+during+both+early+and+late+stages+of+phagocytosis.">Initial receptor-ligand interactions modulate gene expression and phagosomal properties during both early and late stages of phagocytosis.</a> Eur. J. Cell Biol. 89, 693-704 (2010).</li><li>Yates, R., Hermetter, A., Russell, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+kinetics+of+phagosome+maturation+as+a+function+of+phagosome/lysosome+fusion+and+acquisition+of+hydrolytic+activity.">The kinetics of phagosome maturation as a function of phagosome/lysosome fusion and acquisition of hydrolytic activity.</a> Traffic. 6, 413-420 (2005).</li><li>Savina, A., 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=NOX2+controls+phagosomal+pH+to+regulate+antigen+processing+during+crosspresentation+by+dendritic+cells.">NOX2 controls phagosomal pH to regulate antigen processing during crosspresentation by dendritic cells.</a> Cell. 126, 205-218 (2006).</li><li>Yates, R., Hermetter, A., Russell, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Recording+phagosome+maturation+through+the+real-time,+spectrofluorometric+measurement+of+hydrolytic+activities.">Recording phagosome maturation through the real-time, spectrofluorometric measurement of hydrolytic activities.</a> Methods Mol. Biol. 531, 157-171 (2009).</li><li>Russell, D., Vanderven, B., Glennie, S., Mwandumba, H., Heyderman, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+macrophage+marches+on+its+phagosome:+dynamic+assays+of+phagosome+function.">The macrophage marches on its phagosome: dynamic assays of phagosome function.</a> Nat. Rev. Immunol. 9, 594-600 (2009).</li><li>Hoffmann, 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=Autonomous+phagosomal+degradation+and+antigen+presentation+in+dendritic+cells.">Autonomous phagosomal degradation and antigen presentation in dendritic cells.</a> Proc. Natl. Acad. Sci. U.S.A. 109, 14556-14561 (2012).</li><li>Tan, S., Sukumar, N., Abramovitch, R., Parish, T., Russell, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mycobacterium+tuberculosis+Responds+to+Chloride+and+pH+as+Synergistic+Cues+to+the+Immune+Status+of+its+Host+Cell.">Mycobacterium tuberculosis Responds to Chloride and pH as Synergistic Cues to the Immune Status of its Host Cell.</a> PLoS Pathog. 9, (2013).</li><li>Aziz, M., Yang, W. -. L., Wang, P., Coliganet, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Measurement+of+phagocytic+engulfment+of+apoptotic+cells+by+macrophages+using+pHrodo+succinimidyl+ester.">Measurement of phagocytic engulfment of apoptotic cells by macrophages using pHrodo succinimidyl ester.</a> Current protocols in immunology. 14, (2013).</li><li>Rogers, L., Foster, 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+dynamic+phagosomal+proteome+and+the+contribution+of+the+endoplasmic+reticulum.">The dynamic phagosomal proteome and the contribution of the endoplasmic reticulum.</a> Proc. Natl. Acad. Sci. U.S.A. 104, 18520-18525 (2007).</li><li>Russell, D. G., Vanderven, B. C., Glennie, S., Mwandumba, H., Heyderman, R. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+macrophage+marches+on+its+phagosome:+dynamic+assays+of+phagosome+function.">The macrophage marches on its phagosome: dynamic assays of phagosome function.</a> Nat. Rev. Immunol. 9, 594-600 (2009).</li><li>Savina, A., Vargas, P., Guermonprez, P., Lennon, A. -. M., Amigorena, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Measuring+pH,+ROS+production,+maturation,+and+degradation+in+dendritic+cell+phagosomes+using+cytofluorometry-based+assays.">Measuring pH, ROS production, maturation, and degradation in dendritic cell phagosomes using cytofluorometry-based assays.</a> Methods. Mol. Biol. 595, 383-402 (2010).</li></ol>

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Nella sezione seguente si discuterà fasi critiche del metodo presentato e le sue limitazioni. Inoltre, ci si collegherà alcuni dei problemi comuni con le loro soluzioni, introdurre eventuali modifiche e valutare i vantaggi del nostro metodo così come i metodi complementari adatti per questo approccio. La preparazione delle perline, compreso l&#39;accoppiamento di IgG di superficie delle sfere, è cruciale e l&#39;uso di preparati unfresh dovrebbe essere evitata. In aggiunta a ciò, è anc...

Fagociti professionali, tra macrofagi, svolgono un fondamentale nel sistema immunitario. Oltre ad essere la prima linea di difesa del sistema immunitario innato, ma anche svolgere un ruolo critico nella attivazione della immunità adattativa attraverso la loro segnalazione e presentanti l&#39;antigene ruolo 1-3. Mentre la funzione dei fagociti professionali è multiforme, phagosome maturazione è la spina dorsale critico della funzione di elaborazione battericida ed antigene dei fagociti professionali 4,5. Su engulfment recettore mediata e l&#39;assorbimento di un bersaglio fagocitaria, come batteri, phagosome nascente passa attraverso una sequenza complessa ed armonico di interazione e scambi con compartimenti della rete endocitosi e diversi altri organelli cellulari 6. La natura dei composti scambiate con queste entità cellulari, nonché il regolamento e la tempistica degli eventi di fusione determina il phagosomal milieu luminale e le phagoscomposizione OMAL membrana e, quindi 7, il destino del phagosome maturazione 8. La rilevanza fisiologica di phagosome maturazione è esemplificata dalle diverse strategie utilizzate dai vari agenti patogeni intracellulari di sfuggire, arresto o sovvertire phagosome maturazione 9. La maggior parte di queste strategie impediscono direttamente o indirettamente, la fase finale e critica del processo di maturazione phagosome: la fusione di phagosome con scomparti fine endosomal / lisosomiali, che conferisce loro la maggior parte degli enzimi idrolitici e fattori anti-batterici di un phagosome maturo 7 , 8,10. Analisi di questo passaggio finale e critico quindi ci può fornire con forti indicatori sullo stato di maturazione dei fagosomi e se lo stato fisiologico è essere positivamente o negativamente colpito sotto le impostazioni sperimentali particolari che vengono utilizzati. Il vano tardi endosomal / lisosomiales sono generalmente considerati essere i compartimenti terminali della via endocitosi, definiti e distinti dai primi compartimenti endocitici dalla presenza di vari, determinata fase, molecole marcatori. Per esempio enzimi idrolitici o componenti di membrana quali le proteine ​​di membrana lisosomiale associata (lampade) tra gli altri 11. Il terminale endocitica compartimenti-d&#39;ora in poi indicato semplicemente come lisosomi-servono anche come location principale per le fasi finali della digestione, alla fine della fagocitosi / endocytic percorso 12. In questo modo, non digeribili sonde possono essere caricati tramite endocitosi e macropinocitosi dall&#39;ambiente extracellulare e trasportati attraverso la via endocytic ai lisosomi, dove si accumula 13,14 dopo aver seguito un determinato ciclo di assorbimento e inseguimento. Sonde fluoroforo coniugato per la microscopia a fluorescenza come il destrano polimero organico nondigestible sono comunemente usati come endocyticprobes 15-17. <p class = &quot;jove_content&quot;&gt; In questo metodo, si descrive l&#39;utilizzo di microsfere IgG rivestite come carico fagocitica indagare phagosome maturazione analizzando la consegna di lisosomiale contenuto luminale a phagosomes. Utilizzando una sonda destrano fluoroforo coniugato come marcatore facilmente rilevabile dei lisosomi nel midollo osseo dal vivo macrofagi derivati ​​(BMM) e time-lapse video di imaging con un microscopio confocale a scansione laser, seguiamo il processo dinamico di consegna del carico in phagosomes con elevata risoluzione temporale. Abbiamo poi descrive come i dati di imaging time-lapse raccolti possono essere valutate utilizzando l&#39;open-source e software di analisi dell&#39;immagine liberamente disponibile, Fiji (o ImageJ), statisticamente analizzati utilizzando Microsoft Excel e presentata utilizzando il software GraphPad Prism 14,18. Dopo la descrizione del nostro metodo, esperimenti analoghi possono essere progettati utilizzando le impostazioni modificate e fattori di indagare la loro influenza sulla phagosome maturazione; qualsiasi otil suo tipo di fagociti primarie o linee cellulari aderenti, la perdita genetica degli esperimenti funzionali, tra cui gene knock-out e knock-down, mutanti o espressione delle proteine ​​di fusione, fagocitosi-obiettivi, composti di rivestimento microbead, sonde endosomal / lisosomiali e fattori quali una citochine, inibitori chimici o siRNA tra gli altri sono tutte variabili che possono essere applicate per l&#39;approccio di base di questo metodo. Definiamo l&#39;obiettivo e requisiti di base di questo metodo come segue: <ul type="disc"><li> Obiettivo del metodo: per consentire l&#39;osservazione diretta, quantitativa e qualitativa e l&#39;analisi di phagosome maturazione con alta risoluzione temporale nel vivere fagociti. </li><li> Carico dei fagociti: Un microparticelle opportunamente rivestiti o bersaglio biologico. Qui usiamo IgG-rivestito 3 micron microparticelle sferiche di polistirolo che sono prontamente interiorizzati attraverso il recettore Fc-γ fagocitosi mediata. In alternativa, qualsiasi microrganismo o un microfono patinataroparticle per i quali è presente un recettore fagocitica delle cellule può essere utilizzato. </li><li> Fagociti: fagociti aderenti esprimono gli appropriati recettori fagociti. Qui usiamo il mouse BMMs primari abbondantemente esprimono i recettori Fc-γ. In alternativa, potrebbero essere utilizzati cellule dendritiche (DC), monociti o cellule epiteliali fagocitarie o loro mutanti o varianti genetiche knock-out. </li><li> Lisosomiali cargo: Una sonda lisosomiale fluorescente. Qui, Texas Red-coniugato 70.000 kDa destrano (Dex70kD) è usato come il carico luminale dei lisosomi. In alternativa, qualsiasi marcatore fluorescente rilevabile di un compartimento cellulare o organello, o una sonda appropriata per le proprietà phagosomal come acidità o degradativa capacità, potrebbe essere utilizzata per studiare la progressione della phagosome maturazione. </li><li> Fattori che influenzano: Ad esempio, molecole di segnalazione, composti chimici, gene knock-down, o espressione transiente di proteine ​​mutanti potrebbe. Qui, abbiamo Förguno l&#39;uso di tale fattore per semplicità, ma per un esempio recente con l&#39;espressione della proteina mutante e di knock-down fattori che influenzano Si prega di vedere Kasmapour et al. 18 Qualsiasi fattore che può influenzare la fagocitosi o le circostanze e la mobilità dei phagosomes e / o compartimenti che interagiscono con phagosomes scadenza potrebbero essere utilizzati. </li></ul>

<table border="0" cellpadding="0" cellspacing="0" width="610">
	<tbody>
		<tr>
			<td>Dulbecco&#39;s Modified Eagles Medium (D-MEM)</td>
			<td>PAA, Austria</td>
			<td>E15-009</td>
			<td></td>
		</tr>
		<tr>
			<td>Dulbecco&#39;s Modified Eagles Medium without phenol red (D-MEM)</td>
			<td>PAA, Austria</td>
			<td>E15-047</td>
			<td></td>
		</tr>
		<tr>
			<td>Fetal Bovine Serum (FBS)</td>
			<td>PAA, Austria</td>
			<td>A15-151</td>
			<td></td>
		</tr>
		<tr>
			<td>L-Glutamine</td>
			<td>PAA, Austria</td>
			<td>M11-004</td>
			<td></td>
		</tr>
		<tr>
			<td>PBS</td>
			<td>PAA, Austria</td>
			<td>H15-002</td>
			<td></td>
		</tr>
		<tr>
			<td>Penicillin/Streptomycin</td>
			<td>PAA, Austria</td>
			<td>P11-010</td>
			<td></td>
		</tr>
		<tr>
			<td>WillCo-dish&#174; Glass bottom dish (35 mm &#8709;, #1.5)</td>
			<td>WillCo Wells, Netherlands</td>
			<td>GWSt-3522</td>
			<td></td>
		</tr>
		<tr>
			<td>CELLviewTM glass bottom dish, 35 mm</td>
			<td>Greiner Bio one, Germany</td>
			<td>627871</td>
			<td>Alternative: Available as segmented</td>
		</tr>
		<tr>
			<td>Carboxylated latex microspheres</td>
			<td>Polysciences, USA</td>
			<td>#09850</td>
			<td>Available in different diameters, we used 3 &#956;m</td>
		</tr>
		<tr>
			<td>Polystyrene microparticles</td>
			<td>Kisker Biotech, Germany</td>
			<td>PPs-3.0COOH</td>
			<td></td>
		</tr>
		<tr>
			<td>Triton-X 100</td>
			<td>ROTH, Germany</td>
			<td>305.1.3</td>
			<td></td>
		</tr>
		<tr>
			<td>mouse whole IgG</td>
			<td>Rockland, USA</td>
			<td>010-0102</td>
			<td></td>
		</tr>
		<tr>
			<td>EDAC crosslinker</td>
			<td>Sigma-Aldrich, USA</td>
			<td>E6383-1g</td>
			<td></td>
		</tr>
		<tr>
			<td>10 mM Tris</td>
			<td>Sigma-Aldrich,USA</td>
			<td>T1503</td>
			<td></td>
		</tr>
		<tr>
			<td>1-ml syringe Omnifix -F</td>
			<td>B.Braun, Germany</td>
			<td>9161406V</td>
			<td></td>
		</tr>
		<tr>
			<td>26&#160;G needle (0.45*25 mm)</td>
			<td>B.Baun, Germany</td>
			<td>4657683</td>
			<td></td>
		</tr>
		<tr>
			<td>RPMI 1640</td>
			<td>PAA, Austria</td>
			<td>E15-039</td>
			<td></td>
		</tr>
		<tr>
			<td>Horse Serum</td>
			<td>Gibco, USA</td>
			<td>16050-122</td>
			<td></td>
		</tr>
		<tr>
			<td>MES hydrate</td>
			<td>Sigma-Aldrich, USA</td>
			<td>M2933</td>
			<td></td>
		</tr>
		<tr>
			<td>0.2 &#956;M syringe mounted filter</td>
			<td>Sartorius, Germany</td>
			<td>83.1826.001</td>
			<td></td>
		</tr>
	</tbody>
</table>

study of phagolysosome biogenesis in live macrophages

Fagociti giocano un ruolo importante nel sistema immunitario innato rimuovendo ed eliminando microrganismi invasori nelle loro fagosomi. Phagosome maturazione è un processo complesso e strettamente regolata durante la quale un phagosome nascente subisce drastica trasformazione attraverso le interazioni ben orchestrate, con vari organuli cellulari e scomparti nel citoplasma. Questo processo, che è essenziale per la funzione fisiologica di fagociti dotando phagosomes con le loro proprietà litici e battericide, culmina nella fusione di phagosomes con i lisosomi e biogenesi dei phagolysosomes che è considerato come l&#39;ultimo e fondamentale fase di maturazione per phagosomes. In questo rapporto, descriviamo un metodo basato imaging cellulare dal vivo per l&#39;analisi qualitativa e quantitativa del processo dinamico di lisosomi per phagosome fornitura di contenuti, che è una caratteristica di fagolisosoma biogenesi. Questo approccio utilizza microsfere IgG rivestite come modello per phagocytosis e molecole di destrano fluoroforo coniugato come sonda carico lisosomiale luminale, per seguire la consegna di contenuto dinamico lysosmal ai fagosomi in tempo reale in macrofagi vivi usando time-lapse imaging e microscopia confocale. Qui si descrive nel dettaglio sullo sfondo, le fasi di preparazione e la configurazione step-by-step sperimentale per consentire la distribuzione facile e precisa di questo metodo in altri laboratori. Il nostro metodo descritto è semplice, robusta e, soprattutto, può essere facilmente adattato per studiare le interazioni phagosomal e maturazione in sistemi diversi e in varie impostazioni sperimentali, come l&#39;uso di vari tipi di fagociti, la perdita di funzione esperimenti, diverse sonde, e particelle fagociti.

La corretta preparazione delle cellule e le perline per l&#39;imaging è critica. Figura 1 mostra il profilo della semina, sonda-loading e gradini di imaging iniziale, in questo metodo, basato sulla nostra protocollo ottimizzato per BMMs. È pertanto indispensabile che i parametri di protocollo testati e ottimizzati a seconda del tipo di cellule e sonde che devono essere utilizzati. Dopo l&#39;aggiunta delle perline rivestite con IgG verso le cellule precaricati, è importan...

Watch this Scientific Journal Video about Study of Phagolysosome Biogenesis in Live Macrophages at JoVE.com

Study of Phagolysosome Biogenesis in Live Macrophages

Studio di fagolisosoma Biogenesis nei macrofagi in diretta

Phagocytic cells play a major role in the innate immune system by removing and eliminating invading microorganisms in their phagosomes. Phagosome ...

study-of-phagolysosome-biogenesis-in-live-macrophages

Research

JoVE Journal

Immunology and Infection

14.3K Views.  Helmholtz Centre for Infection Research. Studio di fagolisosoma Biogenesis nei macrofagi in diretta

Video: Study of Phagolysosome Biogenesis in Live Macrophages

In vivo Imaging of Transgenic Leishmania Parasites in a Live Host

Distinct species of Leishmania, a protozoan parasite of the family Trypanosomatidae, typically cause different human disease manifestations. The most common forms of disease are visceral leishmaniasis (VL) and cutaneous leishmaniasis (CL). Mouse models of leishmaniasis are widely used, but quantification of parasite burdens during murine disease requires mice to be euthanized at various times after infection. Parasite loads are then measured either by microscopy, limiting dilution assay, or qPCR amplification of parasite DNA. The in vivo imaging system (IVIS) has an integrated software package that allows the detection of a bioluminescent signal associated with cells in living organisms. Both to minimize animal usage and to follow infection longitudinally in individuals, in vivo models for imaging Leishmania spp. causing VL or CL were established. Parasites were engineered to express luciferase, and these were introduced into mice either intradermally or intravenously. Quantitative measurements of the luciferase driving bioluminescence of the transgenic Leishmania parasites within the mouse were made using IVIS. Individual mice can be imaged multiple times during longitudinal studies, allowing us to assess the inter-animal variation in the initial experimental parasite inocula, and to assess the multiplication of parasites in mouse tissues. Parasites are detected with high sensitivity in cutaneous locations. Although it is very likely that the signal (photons/second/parasite) is lower in deeper visceral organs than the skin, but quantitative comparisons of signals in superficial versus deep sites have not been done. It is possible that parasite numbers between body sites cannot be directly compared, although parasite loads in the same tissues can be compared between mice. Examples of one visceralizing species (L. infantum chagasi) and one species causing cutaneous leishmaniasis (L. mexicana) are shown. The IVIS procedure can be used for monitoring and analyzing small animal models of a wide variety of Leishmania species causing the different forms of human leishmaniasis.

In vivo Imaging of Transgenic Leishmania Parasites in a Live Host

An in vivo imaging system is used to generate quantitative measurements of murine infection with the Trypanosomatid protozoan Leishmania. This is a non-invasive and non-lethal method for detecting parasites expressing luciferase within many tissues throughout the course of chronic Leishmania spp. infection.

Imaging in vivo del transgenico parassiti Leishmania in un host live

Distinct species of Leishmania, a protozoan parasite of the family Trypanosomatidae, typically cause different human disease manifestations. The most ...

Ricerca

Immunologia e infezioni

Use of an Optical Trap for Study of Host-Pathogen Interactions for Dynamic Live Cell Imaging

Dynamic live cell imaging allows direct visualization of real-time interactions between cells of the immune system1, 2; however, the lack of spatial and temporal control between the phagocytic cell and microbe has rendered focused observations into the initial interactions of host response to pathogens difficult. Historically, intercellular contact events such as phagocytosis3 have been imaged by mixing two cell types, and then continuously scanning the field-of-view to find serendipitous intercellular contacts at the appropriate stage of interaction. The stochastic nature of these events renders this process tedious, and it is difficult to observe early or fleeting events in cell-cell contact by this approach. This method requires finding cell pairs that are on the verge of contact, and observing them until they consummate their contact, or do not. To address these limitations, we use optical trapping as a non-invasive, non-destructive, but fast and effective method to position cells in culture.
Optical traps, or optical tweezers, are increasingly utilized in biological research to capture and physically manipulate cells and other micron-sized particles in three dimensions4. Radiation pressure was first observed and applied to optical tweezer systems in 19705, 6, and was first used to control biological specimens in 19877. Since then, optical tweezers have matured into a technology to probe a variety of biological phenomena8-13.
We describe a method14 that advances live cell imaging by integrating an optical trap with spinning disk confocal microscopy with temperature and humidity control to provide exquisite spatial and temporal control of pathogenic organisms in a physiological environment to facilitate interactions with host cells, as determined by the operator. Live, pathogenic organisms like Candida albicans and Aspergillus fumigatus, which can cause potentially lethal, invasive infections in immunocompromised individuals15, 16 (e.g. AIDS, chemotherapy, and organ transplantation patients), were optically trapped using non-destructive laser intensities and moved adjacent to macrophages, which can phagocytose the pathogen. High resolution, transmitted light and fluorescence-based movies established the ability to observe early events of phagocytosis in living cells. To demonstrate the broad applicability in immunology, primary T-cells were also trapped and manipulated to form synapses with anti-CD3 coated microspheres in vivo, and time-lapse imaging of synapse formation was also obtained. By providing a method to exert fine spatial control of live pathogens with respect to immune cells, cellular interactions can be captured by fluorescence microscopy with minimal perturbation to cells and can yield powerful insight into early responses of innate and adaptive immunity.

A method is described to individually select, manipulate, and image live pathogens using an optical trap coupled to a spinning disk microscope. The optical trap provides spatial and temporal control of organisms and places them adjacent to host cells. Fluorescence microscopy captures dynamic intercellular interactions with minimal perturbation to cells.

L&#39;uso di una trappola ottica per lo Studio delle interazioni ospite-patogeno per Dynamic Imaging Live Cell

Dynamic live cell imaging allows direct visualization of real-time interactions between cells of the immune system1, 2; however, the lack of spatial and ...

Depletion and Reconstitution of Macrophages in Mice

Macrophages are critical players in the innate immune response to infectious challenge or injury, initiating the innate immune response and directing the acquired immune response. Macrophage dysfunction can lead to an inability to mount an appropriate immune response and as such, has been implicated in many disease processes, including inflammatory bowel diseases. Macrophages display polarized phenotypes that are broadly divided into two categories. Classically activated macrophages, activated by stimulation with IFN&gamma; or LPS, play an essential role in response to bacterial challenge whereas alternatively activated macrophages, activated by IL-4 or IL-13, participate in debris scavenging and tissue remodeling and have been implicated in the resolution phase of inflammation. During an inflammatory response in vivo, macrophages are found amid a complex mixture of infiltrating immune cells and may participate by exacerbating or resolving inflammation. To define the role of macrophages in situ in a whole animal model, it is necessary to examine the effect of depleting macrophages from the complex environment. To ask questions about the role of macrophage phenotype in situ, phenotypically defined polarized macrophages can be derived ex vivo, from bone marrow aspirates and added back to mice, with or without prior depletion of macrophages. In the protocol presented here clodronate-containing liposomes, versus PBS injected controls, were used to deplete colonic macrophages during dextran sodium sulfate (DSS)-induced colitis in mice. In addition, polarized macrophages were derived ex vivo and transferred to mice by intravenous injection. A caveat to this approach is that clodronate-containing liposomes deplete all professional phagocytes, including both dendritic cells and macrophages so to ensure the effect observed by depletion is macrophage-specific, reconstitution of phenotype by adoptive transfer of macrophages is necessary. Systemic macrophage depletion in mice can also be achieved by backcrossing mice onto a CD11b-DTR background, which is an excellent complementary approach. The advantage of clodronate-containing liposome-mediated depletion is that it does not require the time and expense involved in backcrossing mice and it can be used in mice regardless of the background of the mice (C57BL/6, BALB/c, or mixed background).

Macrophages play a central role in homeostasis and pathology in many tissues. The protocol presented here describes methods for depleting macrophages in vivo, deriving polarized macrophages from bone marrow aspirates, and adoptively transferring macrophages into mice. These techniques allow determination of the role that polarized macrophages play in health and disease.

Esaurimento e Ricostituzione dei macrofagi nei topi

Macrophages are critical players in the innate  immune response to infectious challenge or injury, initiating the innate immune  response and directing ...

Establishment of an In vitro System to Study Intracellular Behavior of Candida glabrata in Human THP-1 Macrophages

A cell culture model system, if a close mimic of host environmental conditions, can serve as an inexpensive, reproducible and easily manipulatable alternative to animal model systems for the study of a specific step of microbial pathogen infection. A human monocytic cell line THP-1 which, upon phorbol ester treatment, is differentiated into macrophages, has previously been used to study virulence strategies of many intracellular pathogens including Mycobacterium tuberculosis. Here, we discuss a protocol to enact an in vitro cell culture model system using THP-1 macrophages to delineate the interaction of an opportunistic human yeast pathogen Candida glabrata with host phagocytic cells. This model system is simple, fast, amenable to high-throughput mutant screens, and requires no sophisticated equipment. A typical THP-1 macrophage infection experiment takes approximately 24 hr with an additional 24-48 hr to allow recovered intracellular yeast to grow on rich medium for colony forming unit-based viability analysis. Like other in vitro model systems, a possible limitation of this approach is difficulty in extrapolating the results obtained to a highly complex immune cell circuitry existing in the human host. However, despite this, the current protocol is very useful to elucidate the strategies that a fungal pathogen may employ to evade/counteract antimicrobial response and survive, adapt, and proliferate in the nutrient-poor environment of host immune cells.

Establishment of an In vitro System to Study Intracellular Behavior of Candida glabrata in Human THP-1 Macrophages

The current article outlines a protocol to establish an in vitro cell culture model system to study the interaction of a facultative intracellular human fungal pathogen Candida glabrata with human macrophages which will be a useful tool to advance our knowledge of fungal virulence mechanisms.

Istituzione di un<em&gt; In vitro</em&gt; Sistema per studiare intracellulare Comportamento<em&gt; Candida glabrata</em&gt; In umani THP-1 macrofagi

A cell culture model system, if a close mimic of host environmental conditions, can serve as an inexpensive, reproducible and easily manipulatable ...

Use of Shigella flexneri to Study Autophagy-Cytoskeleton Interactions

Shigella flexneri is an intracellular pathogen that can escape from phagosomes to reach the cytosol, and polymerize the host actin cytoskeleton to promote its motility and dissemination. New work has shown that proteins involved in actin-based motility are also linked to autophagy, an intracellular degradation process crucial for cell autonomous immunity. Strikingly, host cells may prevent actin-based motility of S. flexneri by compartmentalizing bacteria inside &#8216;septin cages&#8217; and targeting them to autophagy. These observations indicate that a more complete understanding of septins, a family of filamentous GTP-binding proteins, will provide new insights into the process of autophagy. This report describes protocols to monitor autophagy-cytoskeleton interactions caused by S. flexneri in vitro using tissue culture cells and in vivo using zebrafish larvae. These protocols enable investigation of intracellular mechanisms that control bacterial dissemination at the molecular, cellular, and whole organism level.

Use of Shigella flexneri to Study Autophagy-Cytoskeleton Interactions

To counteract pathogen dissemination, host cells reorganize their cytoskeleton to compartmentalize bacteria and induce autophagy. Using Shigella infection of tissue culture cells, host and pathogen determinants underlying this process are identified and characterized. Using zebrafish models of Shigella infection, the role of discovered molecules and mechanisms are investigated in vivo.

Uso di<em&gt; Shigella flexneri</em&gt; Per studiare le interazioni autofagia-Citoscheletro

Shigella flexneri is an intracellular pathogen that can escape from phagosomes to reach the cytosol, and polymerize the host actin cytoskeleton to promote ...

Proteomic Profiling of Macrophages by 2D Electrophoresis

The goal of the two-dimensional (2D) electrophoresis protocol described here is to show how to analyse the phenotype of human cultured macrophages. The key role of macrophages has been shown in various pathological disorders such as inflammatory, immunological, and infectious diseases. In this protocol, we use primary cultures of human monocyte-derived macrophages that can be differentiated into the M1 (pro-inflammatory) or the M2 (anti-inflammatory) phenotype. This in vitro model is reliable for studying the biological activities of M1 and M2 macrophages and also for a proteomic approach. Proteomic techniques are useful for comparing the phenotype and behaviour of M1 and M2 macrophages during host pathogenicity. 2D gel electrophoresis is a powerful proteomic technique for mapping large numbers of proteins or polypeptides simultaneously. We describe the protocol of 2D electrophoresis using fluorescent dyes, named 2D Differential Gel Electrophoresis (DIGE). The M1 and M2 macrophages proteins are labelled with cyanine dyes before separation by isoelectric focusing, according to their isoelectric point in the first dimension, and their molecular mass, in the second dimension. Separated protein or polypeptidic spots are then used to detect differences in protein or polypeptide expression levels. The proteomic approaches described here allows the investigation of the macrophage protein changes associated with various disorders like host pathogenicity or microbial toxins.

Macrophages are the key cells involved in host pathogenicity. Macrophages display phenotypic and functional diversity that can be analysed and detected by proteomic analysis. This article describes how to perform 2D electrophoresis of primary cultures of human macrophages differentiated into M1 or M2 phenotype.

Proteomica Profiling dei macrofagi da 2D elettroforesi

The goal of the two-dimensional (2D) electrophoresis protocol described here is to show how to analyse the phenotype of human cultured macrophages. The ...

Phagosome Migration and Velocity Measured in Live Primary Human Macrophages Infected with HIV-1

Macrophages are phagocytic cells that play a major role at the crossroads between innate and specific immunity. They can be infected by the human immunodeficiency virus (HIV)-1 and because of their resistance to its cytopathic effects they can be considered to be persistent viral reservoirs. In addition, HIV-infected macrophages exhibit defective functions that contribute to the development of opportunistic diseases.
The exact mechanism by which HIV-1 impairs the phagocytic response of macrophages was unknown. We had previously shown that the uptake of various particulate material by macrophages was inhibited when they were infected with HIV-1. This inhibition was only partial and phagosomes did form within HIV-infected macrophages. Therefore, we focused on analyzing the fate of these phagosomes. Phagosome maturation is accompanied by migration of these compartments towards the cell center, where they fuse with lysosomes, generating phagolysosomes, responsible for degradation of the ingested material. We used IgG-opsonized Sheep Red Blood Cells as a target for phagocytosis. To measure the speed of centripetal movement of phagosomes in individual HIV-infected macrophages, we used a combination of bright field and fluorescence confocal microscopy. We established a method to calculate the distance of phagosomes towards the nucleus, and then to calculate the velocity of the phagosomes. HIV-infected cells were identified thanks to a GFP-expressing virus, but the method is applicable to non-infected cells or any type of infection or treatment.

We describe a method to measure the velocity of phagosomes moving towards the cell center in living cells infected with or without the human immunodeficiency virus (HIV) type 1, using spinning disk confocal fluorescence microscopy to identify fluorescent infected cells and bright field microscopy to detect phagosomes.

Migrazione phagosome e velocità misurata in Live primarie macrofagi umani infettati con HIV-1

Macrophages are phagocytic cells that play a major role at the crossroads between innate and specific immunity. They can be infected by the human ...

Isolation of Salmonella typhimurium-containing Phagosomes from Macrophages

Salmonella typhimurium is a facultative intracellular bacterium that causes gastroenteritis in humans. After invasion of the lamina propria, S. typhimurium bacteria are quickly detected and phagocytized by macrophages, and contained in vesicles known as phagosomes in order to be degraded. Isolation of S. typhimurium-containing phagosomes have been widely used to study how S. typhimurium infection alters the process of phagosome maturation to prevent bacterial degradation. Classically, the isolation of bacteria-containing phagosomes has been performed by sucrose gradient centrifugation. However, this process is time-consuming, and requires specialized equipment and a certain degree of dexterity. Described here is a simple and quick method for the isolation of S. typhimurium-containing phagosomes from macrophages by coating the bacteria with biotin-streptavidin-conjugated magnetic beads. Phagosomes obtained by this method can be suspended in any buffer of choice, allowing the utilization of isolated phagosomes for a broad range of assays, such as protein, metabolite, and lipid analysis. In summary, this method for the isolation of S. typhimurium-containing phagosomes is specific, efficient, rapid, requires minimum equipment, and is more versatile than the classical method of isolation by sucrose gradient-ultracentrifugation.

Isolation of Salmonella typhimurium-containing Phagosomes from Macrophages

We describe here a simple and quick method for the isolation of Salmonella typhimurium-containing phagosomes from macrophages by coating the bacteria with biotin and streptavidin.

Isolamento di Salmonella typhimurium-contenente fagosomi dai macrofagi

Salmonella typhimurium is a facultative intracellular bacterium that causes gastroenteritis in humans. After invasion of the lamina propria, S. ...

Isolation and In Vitro Culture of Murine and Human Alveolar Macrophages

Alveolar macrophages are terminally differentiated, lung-resident macrophages of prenatal origin. Alveolar macrophages are unique in their long life and their important role in lung development and function, as well as their lung-localized responses to infection and inflammation. To date, no unified method for identification, isolation, and handling of alveolar macrophages from humans and mice exists. Such a method is needed for studies on these important innate immune cells in various experimental settings. The method described here, which can be easily adopted by any laboratory, is a simplified approach to harvesting alveolar macrophages from bronchoalveolar lavage fluid or from lung tissue and maintaining them in vitro. Because alveolar macrophages primarily occur as adherent cells in the alveoli, the focus of this method is on dislodging them prior to harvest and identification. The lung is a highly vascularized organ, and various cell types of myeloid and lymphoid origin inhabit, interact, and are influenced by the lung microenvironment. By using the set of surface markers described here, researchers can easily and unambiguously distinguish alveolar macrophages from other leukocytes, and purify them for downstream applications. The culture method developed herein supports both human and mouse alveolar macrophages for in vitro growth, and is compatible with cellular and molecular studies.

Isolation and In Vitro Culture of Murine and Human Alveolar Macrophages

This communication describes methodologies for isolation and culture of alveolar macrophages from humans and murine models for experimental purposes.

Isolamento e coltura In Vitro dei macrofagi alveolari murini ed umani

Alveolar macrophages are terminally differentiated, lung-resident macrophages of prenatal origin. Alveolar macrophages are unique in their long life and ...

Flow Cytometric Measurement Of ROS Production In Macrophages In Response To Fc&#947;R Cross-linking

The oxidative or respiratory burst is used to describe the rapid consumption of oxygen and generation of reactive oxygen species (ROS) by phagocytes in response to various immune stimuli. ROS generated during immune activation exerts potent antimicrobial activity primarily through the ability of ROS to damage DNA and proteins, causing death of microorganisms. Being able to measure ROS production reproducibly and with ease is necessary in order to assess the contribution of various pathways and molecules to this mechanism of host defense. In this paper, we demonstrate the use of fluorescent probes and flow cytometry to detect ROS production. Although widely used, fluorescent measurement of ROS is notoriously problematic, especially with regards to measurement of ROS induced by specific and not mitogenic stimuli. We present a detailed methodology to detect ROS generated as a result of specific Fc&#947;R stimulation beginning with macrophage generation, priming, staining, Fc&#947;R cross-linking, and ending with flow cytometric analysis.

This study demonstrates the use of flow cytometry to detect reactive oxygen species (ROS) production resulting from activation of the Fc&#947;R. This method can be used to assess changes in the antimicrobial and redox signaling function of phagocytes in response to immune complexes, opsonized microorganisms, or direct Fc&#947;R cross-linking.

Misurazione del flusso Cytometric di produzione di ROS nei macrofagi In risposta a FcγR cross-linking

The oxidative or respiratory burst is used to describe the rapid consumption of oxygen and generation of reactive oxygen species (ROS) by phagocytes in ...

Studio di fagolisosoma Biogenesis nei macrofagi in diretta

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