Biz yazının eleştirel okuma için fagosom Biyoloji Laboratuvarı üyelerine teşekkür ederim. Bu çalışma, bir Helmholtz Genç Araştırmacı hibe (Girişimi ve Helmholtz Derneği Ağ fonları) ve Öncelikli Programı Alman Araştırma Konseyi (Deutsche Forschungsgemeinschaft, DFG) içinde SPP1580 Grant tarafından desteklenmektedir.

<ol>
	<li>Greenberg, S., 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=Phagocytosis+and+innate+immunity.">Phagocytosis and innate immunity.</a> Curr. Opin. Immunol. 14, 136-145 (2002).</li><li>Jutras, I., Desjardins, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phagocytosis:+at+the+crossroads+of+innate+and+adaptive+immunity.">Phagocytosis: at the crossroads of innate and adaptive immunity.</a> Ann. Rev. Cell Dev. Biol. 21, 511-527 (2005).</li><li>Iwasaki, A., Medzhitov, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regulation+of+adaptive+immunity+by+the+innate+immune+system.">Regulation of adaptive immunity by the innate immune system.</a> Science. 327, 291-295 (2010).</li><li>Stuart, L., Ezekowitz, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phagocytosis:+elegant+complexity.">Phagocytosis: elegant complexity.</a> Immunity. 22, 539-550 (2005).</li><li>Blander, J. M., Medzhitov, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=On+regulation+of+phagosome+maturation+and+antigen+presentation.">On regulation of phagosome maturation and antigen presentation.</a> Nat. Immunol. 7, 1029-1035 (2006).</li><li>Flannagan, R. 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>

Yazarlar ifşa hiçbir şey yok.

Aşağıdaki bölümde sunulan yöntem ve sınırlamalar kritik adımları görüşecek. Ayrıca, biz, onların çözümleri ile yaygın sorunlardan bazıları bağlamak olası değişiklikler tanıtmak ve bizim yöntemin avantajları yanı sıra, bu yaklaşıma uygun tamamlayıcı yöntemler dikkate alacaktır. Boncuk yüzeye IgG bağlanması da dahil olmak üzere boncuklar, preparasyonu, önemlidir ve unfresh preparasyonlar kullanımından kaçınılmalıdır. Buna ilave olarak, dekstran t...

Makrofajlar dahil olmak üzere, profesyonel fagositlerin, bağışıklık sisteminde önemli bir oyun. Doğuştan gelen bağışıklık sistemindeki ilk savunma hattı olmasının yanı sıra, aynı zamanda bir rol 1-3 sunulması da sinyalizasyon ve antijen ile edinilmiş bağışıklık aktivasyonunda kritik bir rol oynamaktadır. Profesyonel fagositlerin işlevi çok yönlü iken, fagosom olgunlaşma profesyonel fagositlerin 4,5 bakterisit ve antijen işleme fonksiyonlarının kritik bir omurgadır. Reseptör aracılı yutulma ve bakteriler gibi bir fagositik hedef, alımından sonra, olgunlaşmamış fagosom etkileşim ve endositik ağ bölümlerinde ve çeşitli diğer hücresel organel 6 değişim karmaşık ve iyi ayarlanmış bir dizisi boyunca geçer. Bileşiklerin yapısı, bu hücresel varlıklar olarak düzenlenmesi ile değiştirilir ve füzyon olayların zamanlama luminal phagosomal ortamı ve phagos belirleromal membran bileşimi ve böylece 7, olgunlaşan fagozomun 8 kaderi. Fagosom olgunlaşma fizyolojik alaka, kaçmak tutuklama veya fagosom olgunlaşmasını 9 yıkmak için çeşitli hücre içi patojenler tarafından istihdam çeşitli stratejiler ile örneklenmiştir. Hidrolitik enzim ve olgun fagozomun 7 arasında anti-bakteriyel faktörler bir kısmı ile endows geç endozomal / lızozomal bölmeli fagozomun füzyon: Bu stratejilerin çoğu doğrudan ya da dolaylı olarak fagosom olgunlaşma sürecinin son ve kritik aşamaya önlemek , 8,10. Doğal fizyolojik bir durum kullanılan ediliyor, özellikle deneysel ayarları altında etkilenen olumlu ya da olumsuz olması halinde, bu nihai ve kritik adım Analizi nedenle phagosomes olgunlaşma durumu hakkında güçlü göstergeler ile bize sağlayabilir ve. Geç endozomal / lizozomal bölmesis genellikle çeşitli varlığı ile erken endositik bölmelerden tanımlanmış ve ayırt edici endositik yolunun terminal bölmeleri, spesifik, marker moleküllerin sahne olduğu kabul edilmektedir. Örneğin, diğerleri 11 arasında Lizozomal ilişkili membran proteinleri (lambalar) gibi hidrolitik enzimler veya membran bileşenleri için. Terminal endositik bölmeleri-bundan böyle lizozomlar-da fagositik / endositik yolunun 12 sonunda sindirim son aşamaları için ana konum olarak hizmet basitçe olarak anılacaktır. Bu şekilde, sindirilemez sondalar hücre dışı ortamdan endositoz ve makropinositoz yoluyla yüklenebilir ve alımı ve Chase belirlenmiş bir döngü takip sonra 13,14 birikir lizozomlara endositik yolu aracılığıyla taşınır. 15-17 endocyticprobes gibi organik sindirilemez polimer dekstran gibi floresan mikroskobu için fluorofor-konjuge problar yaygın olarak kullanılmaktadır. <p clasBu yöntemde, s = &quot;jove_content&quot;&gt; biz phagosomes için lızozomal luminal içerik teslim analiz ederek fagosom olgunlaşmasını araştırmak fagositik kargo olarak IgG kaplı mikroboncuk kullanımını tarif eder. Canlı kemik iliği kaynaklı makrofajlar (BMM) ve konfokal lazer tarama mikroskobu ile time-lapse video görüntülemede lizozomların bir kolaylıkla saptanabilir marker olarak flüorofor-konjuge dekstran prob kullanarak, yüksek olan phagosomes içine kargo teslim dinamik sürecini takip zamansal çözünürlük. Daha sonra istatistiksel olarak Microsoft Excel kullanarak analiz ve GraphPad yazılımı 14,18 kullanarak sunulan, toplanan time-lapse görüntüleme verileri, açık kaynak kodlu ve serbestçe kullanılabilir görüntü analiz yazılımı, Fiji (veya ImageJ) kullanılarak değerlendirilebilir anlatacağız. Bizim yöntemin açıklaması ardından, benzer deneyler fagosom olgunlaşması üzerindeki etkilerini araştırmak için modifiye ayarları ve faktörler kullanılarak dizayn edilebilir; hemen her otyapışık birincil veya hücre hattı fagositik hücrelerin kendi türü de dahil olmak üzere fonksiyon deneyler genetik kaybı gen nakavt ve knock-down, mutantlar veya füzyon proteinleri, fagositik-hedefler, microbead kaplama bileşikleri, endozomal / lizozomal sondaları ve faktörlerin böyle bir ifade diğerleri arasında sitokinler, kimyasal inhibitörleri veya siRNA bu yöntemin temel yaklaşım uygulanabilir tüm değişkenlerdir. Biz aşağıdaki gibi bu yöntemin hedefi ve temel gereksinimlerini tanımlar: <ul type="disc"><li> Yöntemin Hedef: fagositik canlı hücreler yüksek zamansal çözünürlüğe sahip fagosom olgunlaşma, doğrudan nicel ve nitel gözlem ve analiz sağlamaktır. </li><li> Fagositik yük: Bir uygun şekilde kaplanmış mikro parçacık veya biyolojik hedef. Burada kolayca Fc-γ reseptörü aracılığıyla fagositoz ile içselleştirilir 3 um küresel polistiren mikro-IgG kaplı kullanın. Seçenek olarak ise, bir mikroorganizma ya da kaplanmış mikrofon, retina reseptör hücrelerde mevcut olduğu için roparticle kullanılabilir. </li><li> Fagositik hücreler: Uygun fagositik reseptörlerini sentezleyen Yapışık fagositik hücreler. Burada bol Fc-γ reseptörlerini ifade fare primer BMMs kullanın. Alternatif olarak, dendritik hücreler (DC), monositler veya fagositik epitel hücreleri ya da bunların mutantlan ya da genetik knock-out varyantlar kullanılabilir. </li><li> Lizozomal kargo: Bir floresan etiketli lizozomal prob. Burada, Texas Red-konjüge edilmiş dekstran 70,000 kiloDalton (Dex70kD) lizozomlara luminal yük olarak kullanılır. Alternatif olarak, bu asitlik veya indirgeyici kapasitesi phagosomal özellikleri için bir hücre bölmesi veya organel ya da uygun bir prob, floresan bir saptanabilir marker ile etiketlenebilir fagosom olgunlaşma ilerlemesini incelemek için kullanılabilir. </li><li> Örneğin, molekülleri, kimyasal bileşikler, gen knock-down, ya da olabilir mutant proteinlerin geçici ifadesini sinyalizasyon: etkileyen faktörler. Burada, biz Förg varbasitlik uğruna böyle bir faktör biri kullanılması, ancak mutant protein ifade ve Kasmapour vd. 18. phagosomes fagositozunu veya şartlar ve hareketlilik etkileyebilir ve / olabilir Herhangi bir faktör bakın lütfen knock-down etkileyen faktörler ile yeni bir örnek ya da olgunlaşma phagosomes etkileşim bölmeleri potansiyel olarak kullanılabilir. </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

Fagositik hücreler kaldırma ve phagosomes istila mikroorganizmaları ortadan kaldırarak, doğuştan gelen bağışıklık sisteminde önemli bir rol oynamaktadır. Fagosom olgunlaşma olgunlaşmamış bir fagosom sitoplazmada çeşitli hücresel organellere ve bölmeleri ile iyi yönetilen bir etkileşimler yoluyla köklü dönüşüme uğrar sırasında karmaşık ve sıkı düzenlenmiş bir süreçtir. Onların litik ve bakterisidal özellikleri ile phagosomes donatarak fagositik hücrelerin fizyolojik fonksiyonu için gerekli olan bu süreç, lizozomlar ve phagosomes için olgunlaşma son ve kritik aşama olarak kabul edilir fagolizozomları arasında biyotekvinin ile phagosomes füzyonu sona eriyor. Bu raporda, biz phagolysosome biyotekvinin bir özelliğidir içerik dağıtım, fagosom için lizozoma dinamik süreci kalitatif ve kantitatif analiz için canlı hücre görüntüleme bazlı yöntem açıklanmaktadır. Bu yaklaşım, phagocy için bir model olarak IgG kaplı mikro-boncuklar kullanırbir lizozomal luminal yük prob olarak apoptosisi ve fluorofor ile konjüge edilmiş dekstran molekülleri, zaman atlamalı görüntüleme ve konfokal lazer tarama mikroskobu kullanılarak canlı makrofajlarda gerçek zamanlı olarak phagosomes için lysosmal dinamik içerik teslim takip etmek amacıyla. Burada ayrıntılı olarak arka plan, hazırlık aşamaları ve diğer laboratuvarlar bu yöntemin kolay ve hassas bir dağıtım sağlamak için adım adım bir deney düzeneği tarif. Bizim tanımlanan metot basit, sağlam, ve en önemlisi, kolayca farklı sistemlerde ve örneğin çeşitli fagositik hücreler türleri, kayıp-fonksiyon deneyleri, farklı prob kullanımı gibi çeşitli deneysel ayarları altında phagosomal etkileşimleri ve olgunlaşmasını çalışmak için adapte edilebilir, ve Fagositik parçacıklar.

Görüntüleme için hücrelerin ve boncukların doğru hazırlama kritik önem taşır. Şekil 1 BMMs için Optimize edilen protokolüne bağlı olarak tohumlama, prob yükleme ve bu yöntemde ilk görüntüleme adımlar, ana hatlarını göstermektedir. Bu protokol parametreleri hücreleri ve kullanılacak olan sondaların türüne bağlı olarak test edilmiş ve optimize edilmesi bu nedenle önemlidir. Önceden yüklenmiş hücrelere IgG kaplı boncuk ilave edildikten son...

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

Study of Phagolysosome Biogenesis in Live Macrophages

Canlı Makrofagların içinde Phagolysosome Biogenesis&#39;den Çalışması

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 Görüntüleme.  Helmholtz Centre for Infection Research. Canlı Makrofagların içinde Phagolysosome Biogenesis'den Çalışması

Video: Study of Phagolysosome Biogenesis in Live Macrophages

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.

Dinamik Canlı Hücre Görüntüleme Konukçu-Patojen Etkileşimleri Çalışma Optik Tuzak

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

İmmünoloji ve Enfeksiyon

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.

Farelerde Makrofajlar tükenmesi ve Sulandırma

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.

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.

Kullanımı<em&gt; Shigella flexneri</em&gt; Otofaji-Sitoiskelet Etkileşimleri Okumak

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.

2D Elektroforez ile Makrofagların proteomik Profil

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

Quantification of Cytosolic vs. Vacuolar Salmonella in Primary Macrophages by Differential Permeabilization

Intracellular bacterial pathogens can replicate in the cytosol or in specialized pathogen-containing vacuoles (PCVs). To reach the cytosol, bacteria like Shigella flexneri and Francisella novicida need to induce the rupture of the phagosome. In contrast, Salmonella typhimurium replicates in a vacuolar compartment, known as Salmonella-containing vacuole (SCV). However certain mutants of Salmonella fail to maintain SCV integrity and are thus released into the cytosol. The percentage of cytosolic vs. vacuolar bacteria on the level of single bacteria can be measured by differential permeabilization, also known as phagosome-protection assay. The approach makes use of the property of detergent digitonin to selectively bind cholesterol. Since the plasma membrane contains more cholesterol than other cellular membranes, digitonin can be used to selectively permeabilize the plasma membrane while leaving intracellular membranes intact. In brief, following infection with the pathogen expressing a fluorescent marker protein (e.g. mCherry among others), the plasma membrane of host cells is permeabilized with a short incubation in digitonin containing buffer. Cells are then washed and incubated with a primary antibody (coupled to a fluorophore of choice) directed against the bacterium of choice (e.g. anti-Salmonella-FITC) and washed again. If unmarked bacteria are used, an additional step can be done, in which all membranes are permeabilized and all bacteria stained with a corresponding antibody. Following the staining, the percentage of vacuolar and cytosolic bacteria can be quantified by FACS or microscopy by counting single or double-positive events. Here we provide experimental details for use of this technique with the bacterium Salmonella typhimurium. The advantage of this assay is that, in contrast to other assay, it provides a quantification on the level of single bacteria, and if analyzed by microscopy provides the exact number of cytosolic and vacuolar bacteria in a given cell.

Quantification of Cytosolic vs. Vacuolar Salmonella in Primary Macrophages by Differential Permeabilization

We describe the quantification of cytosolic and vacuolar Salmonella typhimurium in bone-marrow derived macrophages using differential digitonin permeabilization.

Koful genel Sitosolik kantifikasyonu<em&gt; Salmonella</em&gt; Diferansiyel permeabilizasyon tarafından İlköğretim Makrofagların içinde

Intracellular bacterial pathogens can replicate in the cytosol or in specialized pathogen-containing vacuoles (PCVs). To reach the cytosol, bacteria like ...

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.

HIV-1 ile infekte Canlı İlköğretim İnsan Makrofagların Ölçülen fagosom Göç ve Hız

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.

Salmonella typhimuriumyalıtım-makrofajlar üzerinden Phagosomes içeren

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.

Yalıtım ve fare ve insan alveoler makrofajlar Vitro kültürü

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.

Akış sitometrik ölçüm makrofajlar FcγR Cross-linking yanıt ROS üretim

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