This work was supported by grants from the Associazione Italiana per la Ricerca sul Cancro (AIRC, IG14593, MFAG13235), the Fondazione Cariplo (Grant 2010-0678 and NANOVAC) and the Fondazione Regionale per la Ricerca Biomedica.

Çalışma onayı: Deneysel protokoller decreto göre İtalyan Sağlık Bakanlığı (Roma, İtalya) tarafından onaylanmıştır n, 27 gennaio 1992 Legislativo. 116 &quot;Attuazione della direttiva n. 86/609 / CEE in materia di protezione degli animali utilizzati bir fini Sperimentali o reklam altri fini scientifici.&quot; 1. Cilt Örnekleri elde edilmesi <ol><li> servikal dislokasyon fare Euthanize. </li><li> Kulak: <ol><li> fare kulakları tüysüz bir bölümünü kesip. </li><li> forseps ile onları birbirinden çekerek ayrı dorsal ve ventral yüzü. forseps ile yavaşça kulak iç kısmı kazıyarak kalan kıkırdaklar çıkarın. </li></ol></li><li> Gövde cilt: <ol><li> Bir elektrikli tıraş makinesi ile ve narin tüy dökücü losyon ile hem hayvanın tüm cilt tıraş. </li><li> (2 cm 2 itibaren tüm hayvan derisi kadar) istenen deri örneği kesti. <ol><li> tüm dorsal keserek eğer ve ventral fare deri, sırt ve sonra fare gövdesi etrafında traş alan sınırları boyunca kesilmiş fare ortasında dikey kesim yapmak. </li><li> Yavaşça bir cerrahi makas veya neşter kapalı yuvarlak kenarlı ipuçları ile cilt örneği ayıran forseps ile yine deri örneği tutarak, periton ve sırt kasları cilt ayırmak. </li></ol></li><li> buz, 10 ml PBS ihtiva eden bir 100 aa hücre kültürü plakasının hazırlanması. </li><li> Adım 1.3.3 hazırlanan plaka PBS cilt örneği daldırarak ve forseps ile cilt örneği kazıyarak cilt altı yağ ortadan kaldırmak. </li></ol></li><li> Kuyruk: <ol><li> fare kuyruğu kesti. </li><li> Bir cerrahi makas veya cerrahi neşter, kuyruk tabanından başlayarak ve kuyruk ucuna kadar ulaşan kuyruk dikey kesim olun. </li><li> kuyruk Cildi ayırmak için forseps kullanabilir. kuyruk dibinde kesme kenarını tut ve tutarak ucuna doğru yavaşça çekinforseps ile kuyruk gövde. </li><li> nazikçe cilt örneği kazıyarak herhangi bir aşırı yağ çıkarmak. </li></ol></li><li> haydut <ol><li> cerrahi makas ile tüm fare ayak kesip. Herhangi bir saçlı deri kesme kaçınmak. </li><li> basamak başlangıcına bileği uzunlamasına ayak cildi kesin. </li><li> forseps ile cilt kapma sırasında forseps ile veya elle ayak bileği kemikleri tutun ve bir eldiven kalktıktan sanki basamak doğru cilt çekin. </li></ol></li></ol> 2. Sindirim <ol><li> Enzim karışımı (özellikler için Malzeme Listesi bakınız) 300 mg / ml, DNAse1 50 U / ml: Aşağıdaki reçete ile (Malzeme Listesi&#39;nde gibi hazırlandı) stok çözeltisinden sindirim kokteyl hazırlayın. RPMI% 5 FBS sulandırmak. </li><li> (Gövde ciltler için: Cilt 2 sindirimi Kokteyli ml her 2 cm 2, en fazla 3 ml toplam) Sindirim Kokteyli 2 ml ile 35 mm Petri kabı içine küçük parçalar halinde makas ile cilt örnekleri doğrayın. </li><li>90 dakika boyunca 37 ° C&#39;de inkübe edin. Yavaşça inkübasyon sırasında petri 1-2 kez çalkalayın. </li><li> RPMI1640% 5 FBS 1 ml içeren 66 mm Petri kabındaki 70 mikron hücre süzgecinden üzerinde sindirilmiş cilt örnekleri dökün. </li><li> RPMI 1640,% 5 FBS, 5 ml süzgeç yıkayın. </li><li> Bir şırınga pistonu ile hücre süzgecinden örnek sıkın. </li><li> Gömme piston, Petri kabı ve RPMI1640% 5 FBS, 20 ml süzgeç, 50 ml&#39;lik bir tüp içine aktarılır. </li></ol> 3. Antikorlar ve Etiketleme <ol><li> PBS% 1 FBS (ya da BSA), 5 ml ile iki kez elde edilen süspansiyon yıkayın. </li><li> istenen antikorlar için elde edilen hücre süspansiyonu etiketleyin. <ol><li> 100 ul numune yeniden süspanse / PBS% 1 FBS içerisinde seyreltilmiştir aCD16 / CD32 (klon 2.4G2) 2 ug / ml ihtiva eden bir karışım örneği. </li><li> Fc reseptörleri üzerinden arzu edilen antikorların spesifik olmayan bağlanma bloke etmek için, 4 ° C&#39;de 15 dakika boyunca inkübe edin. </li><li> Tablo l&#39;de gösterilen antikor ekleyin1. <ol><li> 4 ug / ml&#39;lik bir konsantrasyonda PBS% 1 FBS, 100 ul / numune içinde istenen antikorları seyreltilmesi bir karışım hazırlayın. </li><li> tüp içinde, 2 ug / ml&#39;lik bir nihai konsantrasyonda antikor karışımı 200 ul bir hacim olacak şekilde her numune için adım 3.2.3.1 hazırlanan karışımı 100 ul ekle. </li></ol></li><li> 4 ° C&#39;de 30 dakika süreyle inkübe edin ve ışıktan kapsamaktadır. </li></ol></li><li> 400 x g&#39;de 5 dakika boyunca PBS% 1 FBS, 1 ml santrifüj ile yıkayınız PBS% 1 FBS, 300 ul süpernatan ve tekrar süspansiyon atın. </li><li> 2 ug / ml&#39;lik bir son konsantrasyonda DAPI ekleyin ve 10 dakika için ışıktan korunan, 4 ° C&#39;de inkübe edin. </li><li> FACS ile elde edilen numunelerin analiz. <ol><li> lökositleri izole etmek için, aşağıda yolluk stratejisini kullanmak: <ol><li> İlk DAPI- nüfus yolluk herhangi ölü hücreleri ortadan kaldırır. </li><li> Şekil 1 &#39;de gösterildiği gibi FSC W çiziminde genel FSC A seç tekli </strong&gt;. </li><li> Kapı ilgi lökositlerin tipik büyüklüğü ve ayrıntı dayalı hücreler. </li><li> Şekil 1&#39;de gösterildiği gibi FSC-A CD45 arsa CD45 + hücreleri seçin. </li></ol></li><li> aşağıdaki gibi yüzey markerlerinin ifadesiyle lökositlerin farklı popülasyonlar ayırt: <ol><li> CD11c + MHC II + hücreleri gibi DC&#39;ler tanımlayın. Bunlar daha sonra CD207- Dermal DC&#39;lerden Langerhans hücreleri ve CD207 + Dermal DCler ayırt CD207 ekspresyonu için analiz edilebilir. </li><li> CD64 + F4 / 80 + hücreler olarak makrofajlar tanımlayın. </li><li> CD19 + MHC II + hücreleri gibi B hücreleri tanımlamak. </li><li> CD8 + ve CD4 + hücreleri gibi T hücrelerini belirlemek. </li></ol></li></ol></li></ol>

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The authors declare that they have no competing financial interests.

Farklı fare derisi bölgelerden tek hücre süspansiyonları hazırlamak için bir yöntem tanımlanmıştır. Benimsedi¤imiz sindirim bir yöntem olup, yüksek verimler verir, aynı zamanda daha sonra FACS analizi için temel olan yüzey markerlerinin ifadesiyle, koruyor. kolajenaz I ve II termolizin bir karışımı içinde kullanımı, bu yöntem yüksek tekrarlanabilir hale enzim aktivitesinde toplu farklılıklar az toplu garanti eder. Diğer yayınlanmış yöntemler farklı enzim kokteyller güveniyor ama elimizde onlar ve daha da önemlisi, daha az tekrarlanabilir düşük verim verir. Bizim yöntemi, ancak, epidermise doldurmamak hücreler ve dermis doldurmamak hücreler arasında ayrım yapmaz. Birçok durumda bu iki farklı bölmeleri arasında ayrım yapmak yararlı olabilir bu yana, bu tür yöntemleri kullanan bu önceki çalışmalara okuyucuyu yönlendirir. 15 Bizim deneyim cilt Örneklemimizdekulak ve kuyruk ler deri altı yağ tabakası iyice enzim kokteyl dermis erişilebilir hale getirmek için kazınmalıdır gerekmektedir gövde cilt daha sindirimi kolaydır. de gres aşaması, hem de kesme hücre canlılığını korumak amacıyla hızlı bir şekilde ve yavaşça yapılmalıdır bile. Uzamış ya da çok kapsamlı yağ giderme adımı deride bağışıklık hücreleri ikamet hasara neden ve bu nedenle çok daha düşük verim ile sonuçlanabilir ve geri hücrelerin canlılığını azalmış olabilir. Ayrıca, yüzey markerlerinin bütünlüğünü korumak için dikkat edilmelidir, sindirim gibi β-merkaptoetanol gibi indirgeme maddeleri arasında orta yoksun yapılmalıdır. işaretçileri yüzey istenmeyen hasar görmesini önlemek için, inkübasyon süresi her durumda, mümkün olduğunca kısa gibi tutulmalıdır, en fazla 90 dakika boyunca uzatıldı değildir. hücreye sindirilmiş cilt örnekleri dökerken, özellikle bakım, aynı zamanda, alınmalıdırsüzgeç. İyice şırınga pistonu ile sindirilmiş örnek smashing önce kurtarılmış hücreleri yıkayacak için sindirilmiş cildi yıkamak önemlidir. Bu adım ile cilt örnek daha sonra herhangi bir daha fazla fiziksel stres uğramayan serbest bağışıklık hücrelerinden yıkanır. parçalanması, herhangi bir hücrelerini öldürmek için ve hücre süzgeci ve şırınga pistonu de iyice sonraki yıkama adımında yıkanmalıdır için yavaşça yapılmalıdır. Cilt sindirimi de 37 ° C &#39;de bir su banyosunda 50 ml Falcon gerçekleştirilebilir. Bu durumda cilt önceden doğranmış edilebilir ve daha sonra şahin tüpe koydu. deri örnekleri hep inkübasyon sırasında sindirim tampon batık edilmeli ve kulak-parçaları şahin tüpler yanlarına sopa unutmayın. şahin tüpleri kullanırken, bu nedenle, sindirim ortamında batık doğranmış cilt kalış parçaları emin olun. Bu yöntem MA yararlı olabilirny farklı deneysel ayarları olmayan iltihaplı cilt okuyan özellikle. enflamasyon sırasında, vazodilatasyon ve doku şişliği doku ve kandan bağışıklık hücrelerinin yapısı kitlesel cilde işe alınırlar gevşetin. hücresi geri kazanımı, verimlilik ve böylece, çok daha yüksektir. homeostatik koşullarda, dermişin sıkı bir kollajen matrisi sindirimi için etkili bir yol, aslında, deri doldurma karmaşık bir ağ oluşturan bir bağışıklık hücresi geri kazanmak için gereklidir. Okuyucu da kökenini ve farklı dendritik hücreler hem homeostatik ve inflamatuar koşullarda cildi doldurma makrofajların fenotip kapsayan kapsamlı bir inceleme ilginizi çekebilir. 16 Farklı deney ortamlarında fare derinin farklı kısımları muamele edilebilir. Örneğin, deri nakli modelinde, kuyruk bölümü bir alıcı hayvanın gövdede transplante edilebilir; okuyor ne zamanKulak sık DTH tahlili ile T hücre bellek değerlendirmek için kullanılır ise gr ödem oluşumu ya da bağışıklık prosedürleri, uyarı genellikle farelerin ayak tabanına enjekte edilmiştir. Bizim yöntemi ile biz verimli seçim deneysel ayarı için bizim yöntem yararlı hale farklı yerlerden deri ikamet bağışıklık hücrelerini ayıklamak.

The skin is one of the largest organs of the body and its large surface is continuously exposed to the external environment. Therefore the skin has to protect the organism from potential threats in order to maintain homeostasis, both by physical means, and by providing active protection toward potential pathogen entry. In a similar way to the gut and lung mucosa, the skin homes a variety of immune cells that continuously interact with the epithelium in order to maintain immune surveillance. This complex system that involves both immune and non-immune cells of the skin has been acknowledged since the early days of immunology, when in 1978 the term "Skin-associated lymphoid tissue" (SALT) 1 was first coined to describe such complexity. 
The large number of immune cells residing in the skin helps the organism not only to fight potential invasions, but also to orchestrate wound healing and to maintain tolerance toward self-antigens and the skin microbiota 2,3. 
Amongst skin resident immune cells, Dendritic Cells (DCs) have a crucial role in shaping immune responses and maintaining homeostasis 4. Dermal DCs and Langerhans cells readily respond to pathogen invasions and, upon migration to lymph nodes activate T cells and induce the expression of skin homing receptors on the newly generated effector T cells 5. DCs also have a fundamental role in regulating skin homeostasis. DCs migrating from the dermis to the lymph nodes in homeostatic conditions transport skin sequestered antigens with the purpose of inducing T cell tolerance mostly through the differentiation of regulatory T cells (Tregs) specific for skin antigens 6-8. 
T cells represent the most abundant population of immune cells in the skin. Not only do they infiltrate the skin during an infection but they also represent a stable population among skin resident lymphocytes 9,10. Both CD8+ and CD4+ resident memory (rm)T cells reside in the skin and, following an infection, can respond long before effector T cells are recruited from the blood. In the skin, also resides a population of tissue resident Tregs capable of maintaining tolerance toward skin antigens and tissue homeostasis. These cells are rapidly and potently activated after exposure to their cognate antigen and have therefore been defined as memory Tregs 11,12. 
Along with DCs and T cells, many innate immune cells, such as NK cells, gamma delta T cells, group 2 ILCs 13, Mast Cells and Macrophages, populate the skin and contribute to host protection. To analyze such a complex environment, it is mandatory to obtain single-cell suspensions from skin specimens with high efficiency while at the same time preserving the expression of surface markers for flow cytofluorimetric analysis or sorting. 
Murine skin presents an outer epidermal layer, constituted mainly of keratinocytes, Langerhans cells and dendritic epidermal T cells; and the dermal layer beneath. The dermis homes most of the immune cells and is made by an extracellular matrix in which collagen fibers are the most abundant, especially collagen-I and collagen-IV. Unlike human skin, mouse skin is covered in fur, and thus more populated with hair follicles. It is, also, much thinner than human skin and contains a muscular layer, the panniculus carnosus, which helps wound healing 14. These characteristics render it more difficult to efficiently disrupt the collagen net of the dermis in order to get immune cells out.
In this paper we provide a suitable method for digesting the extracellular matrix that relies on a cocktail of high purity collagenase 1 and 2 and thermolysin. Moreover, since the analysis of skin from different regions requires different experimental procedures, we will show different methods to efficiently obtain skin samples from the footpad, tail, ear and trunk. We will then label the samples in order to evaluate the presence of DCs (MHCII+CD11c+CD45+) Macrophages (CD11b+F4/80+CD45+), CD8+, and CD4+ T cells.

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			<td height="81" style="height:81px;width:203px;">Supplemented RPMI 1640 medium&#160;</td>
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			<td style="width:276px;">RPMI1640 supplemented w/ L-glu, pen-strep w/o beta mercapto ethanol</td>
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		<tr height="22">
			<td height="22" style="height:22px;">100mm petri dishes</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">75um Cell Strainers</td>
			<td>BD</td>
			<td>352350</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Name</td>
			<td>Company</td>
			<td>Clone</td>
			<td>Label</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Antibodies</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">aCD45.2</td>
			<td></td>
			<td>104</td>
			<td>PE-Cy5.5</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">aCD11c</td>
			<td></td>
			<td>N418</td>
			<td>PE-Cy7</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">CD11b</td>
			<td></td>
			<td>M1/70</td>
			<td>FITC</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">F4/80</td>
			<td></td>
			<td>A 3-1</td>
			<td>APC-Cy7</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">aCD4</td>
			<td></td>
			<td>Gk1.5</td>
			<td>APC-Cy7</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">aCD8</td>
			<td></td>
			<td>53-6.7</td>
			<td>PE</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">aCD64</td>
			<td></td>
			<td>X54-5/7.1</td>
			<td>PE-Cy7</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">aCD207</td>
			<td></td>
			<td>4C7</td>
			<td>APC</td>
		</tr>
		<tr height="61">
			<td height="61" style="height:61px;">Name</td>
			<td>Company</td>
			<td>Catalog Number</td>
			<td>Comments</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Digestion cocktail</td>
			<td></td>
			<td></td>
			<td>Dilute in RPMI 5%FBS</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">LIberase TM&#160;</td>
			<td></td>
			<td></td>
			<td>300 ug/ml</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">DNAse1&#160;</td>
			<td></td>
			<td style="width:155px;"></td>
			<td>50 U/ml</td>
		</tr>
	</tbody>
</table>

preparation of single-cell suspensions for cytofluorimetric analysis from different mouse skin regions

The skin is a barrier organ that interacts with the external environment. Being continuously exposed to potential microbial invasion, the dermis and epidermis home a variety of immune cells in both homeostatic and inflammatory conditions. Tools to obtain skin cell release for cytofluorimetric analyses are, therefore, very useful in order to study the complex network of immune cells residing in the skin and their response to microbial stimuli. Here, we describe an efficient methodology for the digestion of mouse skin to rapidly and efficiently obtain single-cell suspensions. This protocol allows maintenance of maximum cell viability without compromising surface antigen expression. We also describe how to take and digest skin samples from different anatomical locations, such as the ear, trunk, tail, and footpad. The obtained suspensions are then stained and analyzed by flow cytometry to discriminate between different leukocyte populations.

vücudun farklı bölgeden Cilt belirtilen antikorlar ile tanımlanan ve lekeli protokole göre sindirilmiştir. Ayırıcı stratejisi ilk tekli (FSC W genel FSC A) ve lenfosit morfolojisi (SSC-A genel FSC A) hücreleri canlı sonra hücreler (DAPI- hücreleri), kapı seçmek Şekil 1&#39;de tasvir edilmiştir. Gösterdiğinde, hematopoietik kökenli CD45 + hücreler seçilir. DCler, anti-CD11c, -MHCII ve -CD45 antikorlar ile etiketlenir, makrofajlar olarak tanımlanan F4 / 80 + CD64 + CD45 + hücreleri, CD19 +, CD45 + MHCII + hücreleri gibi B hücreleri, CD4 + CD45 olarak CD4 + T lenfositleri + hücreler, ve CD8 + CD45 + hücreleri gibi CD8 + T lenfositleri (Şekil 2). Bu yöntem, guarantees incelendiğinde deri (Şekil 3A) bütün bölgelerinde toplam canlı hücre (DAPI-) arasında% 50&#39;den fazla ile sindirilmiş nüfusun yüksek mevcudiyetini göstermektedir. CD45 + hücrelerinin sayısının bir göstergesini Şekil 3B&#39;de gösterilmiştir cm2 başına verim. Fare derisinin 1 cm2 sindirimden elde edilen DH&#39;ler, makrofajlar, B hücreleri ve CD4 + veya CD8 + T hücrelerinin sayısı ile ilgili bir tahmin Şekil 3C&#39;de gösterilmiştir. <img alt="Şekil 1" src="/files/ftp_upload/52589/52589fig1.jpg" /> Deri, tek hücre süspansiyonları hematopoietik kökenli hücrelerin Şekil 1. tanımlanması. Tek hücre süspansiyonları, DAPI ve anti-CD45 antikoru ile lekelenmiş olan. canlı hücreler arasında (negatif DAPI), atlet (FSC-H vs FSC-A) lökosit ile hücreleri seçmek için analiz edilir<html> morfoloji (SSC-A vs FSC-A). Hematopoetik kaynaklı hücreler CD45 + olarak tanımlanır. <img alt="şekil 2" src="/files/ftp_upload/52589/52589fig2.jpg" /> +, Şekil 1 &#39;de gösterildiği gibi, farklı bölgelerden türetilen fare ciltte bulunan bağışıklık hücrelerinin Şekil 2. analizi. Hücreler. Kapılı DH&#39;ler CD11c + MHC II + CD45 + hücreleri olarak tanımlanmış, daha sonra Langerhans hücreleri ve CD207 ayırt CD207 ile boyanmış CD207 dermal DCler -; Makrofajlar CD64 + F4 / 80 + CD45 + hücreler olarak tanımlanır; T lenfositleri, CD8 +, CD45 + hücreleri ve CD4 + CD45 + hücreler ayrılır; B hücreleri, MHC II + CD19 + CD45 + hücreleri olarak tanımlanır. Yüzdeler toplam CD45 + hücreleri de ifade edilmektedir. &quot;&gt; <img alt="Şekil 3," src="/files/ftp_upload/52589/52589fig3.jpg" /> Farklı bölgelerden, fare ciltte bulunan bağışıklık hücrelerinin Şekil 3. nicel analizi uygulanabilir (A) yüzdesi. (DAPI -) Fare derisinin belirtilen bölgelerde türetilen hücreler. Fare derisinin farklı bölgelerinde (B) mutlak sayıları, CD45 + hücrelerinin deri cm2 başına hücre sayısı olarak ifade edilmiştir. DCler, MΦ, B hücreleri ve CD4 + ya da fare derisinin belirtilen bölgelerde cilt 1 cm2 türetilen CD8 + T hücrelerinin (C) tahmin sayısı. <table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always"><tbody><tr><td> Antikor </td><td> boyanma </td><td> konsantrasyon </td><td> Zaman </td><td> sıcaklık </td></tr><tr><td colspan="5"> DC&#39;lerkarıştırmak </td></tr><tr><td> CD11c </td><td> PE-Cy7 </td><td> 2 ug / ml </td><td> 30 dk </td><td> 4 ° C </td></tr><tr><td> MHC II </td><td> PE </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td> CD45 </td><td> PE-Cy5.5 </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td> CD207 </td><td> APC </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td colspan="5"> makrofajlar Mix </td></tr><tr><td> F4 / 80 </td><td> APC-Cy7 </td><td> 2 ug / ml </td><td> 30 dk </td><td> 4 ° C </td></tr><tr><td> MHC II </td><td> PE </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td> CD45 </td><td> PE-Cy5.5 </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td> CD64 </td><td> PE-Cy7 </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td colspan="5"> T ve B hücreleri karıştırın </td></tr><tr&gt; <td> CD8a </td><td> PE </td><td> 2 ug / ml </td><td> 30 dk </td><td> 4 ° C </td></tr><tr><td> CD4 </td><td> APC-Cy7 </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td> CD19 </td><td> APC </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr><tr><td> CD45 </td><td> PE-Cy5.5 </td><td> &quot; </td><td> &quot; </td><td> &quot; </td></tr></tbody></table> Tablo deri doldurma immün hücrelerin farklı popülasyonlarının boyama için 1. endikasyonları. Üç karışımları DH&#39;ler, makrofajlar ve lenfositler boyanması için endikedir.

Watch this Scientific Journal Video about Preparation of Single-cell Suspensions for Cytofluorimetric Analysis from Different Mouse Skin Regions at JoVE.com

Preparation of Single-cell Suspensions for Cytofluorimetric Analysis from Different Mouse Skin Regions

The skin is home to a complex immune cell network. We describe an efficient methodology for the digestion of mouse skin, from different parts of the animal's body, in order to obtain a single-cell suspension and analyze the different leukocyte populations resident in the skin by flow cytometry.

Farklı Fare Cilt Bölgelerinden sitoflüorimetrik analize için tek hücre süspansiyonları hazırlanması

The skin is a barrier organ that interacts with the external environment. Being continuously exposed to potential microbial invasion, the dermis and ...

preparation-single-cell-suspensions-for-cytofluorimetric-analysis

Nanyang Technological University

Research

JoVE Journal

Immunology and Infection

18.1K Görüntüleme.  University of Milano-Bicocca. The skin is home to a complex immune cell network. We describe an efficient methodology for the digestion of mouse skin, from different parts of the animal's body, in order to obtain a single-cell suspension and analyze the different leukocyte populations resident in the skin by flow cytometry. 

Video: Preparation of Single-cell Suspensions for Cytofluorimetric Analysis from Different Mouse Skin Regions

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

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

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

Deneysel Otoimmün hipofizitis İndüksiyon Fare Hipofiz İmmunogen hazırlanması

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

İmmünoloji ve Enfeksiyon

Preparation of Viral DNA from Nucleocapsids

Viruses are obligate cellular parasites, and thus the study of their DNA requires isolating viral material away from host cell contaminants and DNA. Several downstream applications require large quantities of pure viral DNA, which is provided by this protocol. These applications include viral genome sequencing, where the removal of host DNA is crucial to optimize data output for viral sequences, and the production of new viral recombinant strains, where co-transfection of purified plasmid and linear viral DNA facilitates recombination.1,2,3 
This procedure utilizes a combination of extractions and density-based centrifugation to isolate purified linear herpesvirus nucleocapsid DNA from infected cells.4,5 The initial purification steps aim to isolate purified viral capsids, which contain and protect the viral DNA during the extractions and centrifugation steps that remove cellular proteins and DNA. Lysis of nucleocapsids then releases viral DNA, and two final phenol-chloroform steps remove remaining proteins. The final DNA captured from solution is highly concentrated and pure, with an average OD260/280 of 1.90. Depending on the quantity of infected cells used, yields of viral DNA range from 150-800 &mu;g or more. The purity of this DNA makes it stable during long-term storage at 4C. This DNA is thus ideally suited for high-throughput sequencing, high fidelity PCR reactions, and transfections. 
Prior to beginning the protocol, it is important to know the average number of cells per dish (e.g. an average of 8 x 106 PK-15 cells in a confluent 15 cm dish), and the titer of the viral stock to be used (e.g. 1 x 108 plaque-forming units per ml). These are necessary to calculate the appropriate multiplicity of infection (MOI) for the protocol.6 For instance, to infect one 15 cm dish of PK-15 cells with the above viral stock, at an MOI of 5, you would use 400 &mu;l of viral stock and dilute it with 3.6 ml of medium (total inoculation volume of 4 ml for one 15 cm plate).
Multiple viral DNA preparations can be prepared at the same time. The number of simultaneous preparations is limited only by the number of tubes held by the ultracentrifuge rotor (one per virus; see step 3.9 below). Here we describe the procedure as though being done for one virus.

We describe the process of isolating high purity herpesvirus nucleocapsid DNA from infected cells. The final DNA captured from solution is of high concentration and purity, making it ideally suited for high-throughput sequencing, high fidelity PCR reactions, and transfections to produce new viral recombinants.

Nucleocapsids gelen Viral DNA hazırlanması

Viruses are obligate cellular parasites, and thus the study of their DNA requires isolating viral material away from host cell contaminants and DNA. ...

Single-cell Analysis of Bacillus subtilis Biofilms Using Fluorescence Microscopy and Flow Cytometry

Biofilm formation is a general attribute to almost all bacteria 1-6. When bacteria form biofilms, cells are encased in extracellular matrix that is mostly constituted by proteins and exopolysaccharides, among other factors 7-10. The microbial community encased within the biofilm often shows the differentiation of distinct subpopulation of specialized cells 11-17. These subpopulations coexist and often show spatial and temporal organization within the biofilm 18-21.
Biofilm formation in the model organism Bacillus subtilis requires the differentiation of distinct subpopulations of specialized cells. Among them, the subpopulation of matrix producers, responsible to produce and secrete the extracellular matrix of the biofilm is essential for biofilm formation 11,19. Hence, differentiation of matrix producers is a hallmark of biofilm formation in B. subtilis.
We have used fluorescent reporters to visualize and quantify the subpopulation of matrix producers in biofilms of B. subtilis 15,19,22-24. Concretely, we have observed that the subpopulation of matrix producers differentiates in response to the presence of self-produced extracellular signal surfactin 25. Interestingly, surfactin is produced by a subpopulation of specialized cells different from the subpopulation of matrix producers 15.
We have detailed in this report the technical approach necessary to visualize and quantify the subpopulation of matrix producers and surfactin producers within the biofilms of B. subtilis. To do this, fluorescent reporters of genes required for matrix production and surfactin production are inserted into the chromosome of B. subtilis. Reporters are expressed only in a subpopulation of specialized cells. Then, the subpopulations can be monitored using fluorescence microscopy and flow cytometry (See Fig 1).
The fact that different subpopulations of specialized cells coexist within multicellular communities of bacteria gives us a different perspective about the regulation of gene expression in prokaryotes. This protocol addresses this phenomenon experimentally and it can be easily adapted to any other working model, to elucidate the molecular mechanisms underlying phenotypic heterogeneity within a microbial community.

Single-cell Analysis of Bacillus subtilis Biofilms Using Fluorescence Microscopy and Flow Cytometry

Microbial biofilms are generally constituted by distinct subpopulations of specialized cells. Single-cell analysis of these subpopulations requires the use of fluorescent reporters. Here we describe a protocol to visualize and monitor several subpopulationswithin B. subtilis biofilms using fluorescence microscopy and flow cytometry.

Tek hücreli Analizi Bacillus subtilis</emFloresan Mikroskobu ve Akım Sitometri Kullanma> Biyofilmler

Biofilm formation is a general attribute to almost all bacteria 1-6. When bacteria form biofilms, cells are encased in extracellular matrix that is mostly ...

Granulocyte-dependent Autoantibody-induced Skin Blistering

Autoimmune phenomena occur in healthy individuals, but when self-tolerance fails, the autoimmune response may result in specific pathology. According to Witebsky's postulates, one of the criteria in diagnosing a disease as autoimmune is the reproduction of the disease in experimental animals by the passive transfer of autoantibodies. For epidermolysis bullosa acquisita (EBA), a prototypic organ-specific autoimmune disease of skin and mucous membranes, several experimental models were recently established. In the animal model described in our present work, purified IgG antibodies against a stretch of 200 amino acids (aa 757-967) of collagen VII are injected repeatedly into mice reproducing the blistering phenotype as well as the histo- and immunopathological features characteristic to human EBA 1. Full-blown widespread disease is usually seen 5-6 days after the first injection and the extent of the disease correlates with the dose of the administered collagen VII-specific IgG. The tissue damage (blister formation) in the experimental EBA is depending on the recruitment and activation of granulocytes by tissue-bound autoantibodies 2,-4. Therefore, this model allows for the dissection of the granulocyte-dependent inflammatory pathway involved in the autoimmune tissue damage, as the model reproduces only the T cell-independent phase of the efferent autoimmune response. Furthermore, its value is underlined by a number of studies demonstrating the blister-inducing potential of autoantibodies in vivo and investigating the mechanism of the blister formation in EBA 1,3,-6. Finally, this model will greatly facilitate the development of new anti-inflammatory therapies in autoantibody-induced diseases. Overall, the passive transfer animal model of EBA is an accessible and instructive disease model and will help researchers to analyze not only EBA pathogenesis but to answer fundamental biologically and clinically essential autoimmunity questions.

In the animal model described in our present work, purified IgG antibodies against a stretch of 200 amino acids (aa 757-967) of collagen VII are injected repeatedly into mice reproducing the blistering phenotype as well as the histo- and immunopathological features characteristic to human epidermolysis bullosa acquisita (EBA)1.

Granülosit-bağımlı otoantikor indüklenen Cilt Kabarcıklanma

Autoimmune phenomena occur in healthy individuals, but when self-tolerance fails, the autoimmune response may result in specific pathology. According to ...

Quantitative High-throughput Single-cell Cytotoxicity Assay For T Cells

Cancer immunotherapy can harness the specificity of immune response to target and eliminate tumors. Adoptive cell therapy (ACT) based on the adoptive transfer of T cells genetically modified to express a chimeric antigen receptor (CAR) has shown considerable promise in clinical trials1-4. There are several advantages to using CAR+ T cells for the treatment of cancers including the ability to target non-MHC restricted antigens and to functionalize the T cells for optimal survival, homing and persistence within the host; and finally to induce apoptosis of CAR+ T cells in the event of host toxicity5.
Delineating the optimal functions of CAR+ T cells associated with clinical benefit is essential for designing the next generation of clinical trials. Recent advances in live animal imaging like multiphoton microscopy have revolutionized the study of immune cell function in vivo6,7. While these studies have advanced our understanding of T-cell functions in vivo, T-cell based ACT in clinical trials requires the need to link molecular and functional features of T-cell preparations pre-infusion with clinical efficacy post-infusion, by utilizing in vitro assays monitoring T-cell functions like, cytotoxicity and cytokine secretion. Standard flow-cytometry based assays have been developed that determine the overall functioning of populations of T cells at the single-cell level but these are not suitable for monitoring conjugate formation and lifetimes or the ability of the same cell to kill multiple targets8.
Microfabricated arrays designed in biocompatible polymers like polydimethylsiloxane (PDMS) are a particularly attractive method to spatially confine effectors and targets in small volumes9. In combination with automated time-lapse fluorescence microscopy, thousands of effector-target interactions can be monitored simultaneously by imaging individual wells of a nanowell array. We present here a high-throughput methodology for monitoring T-cell mediated cytotoxicity at the single-cell level that can be broadly applied to studying the cytolytic functionality of T cells.

We describe a single-cell high-throughput assay to measure cytotoxicity of T cells when incubated with tumor target cells. This method employs a dense, elastomeric array of sub-nanoliter wells (~100,000 wells/array) to spatially confine the T cells and target cells at defined ratios and is coupled to fluorescence microscopy to monitor effector-target conjugation and subsequent apoptosis.

T Hücreleri İçin Kantitatif Yüksek throughput Tek hücreli Sitotoksisite Testi

Cancer immunotherapy can harness the specificity of  immune response to target and eliminate tumors. Adoptive cell therapy (ACT)  based on the adoptive ...

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture

Human skin has an important barrier function and contains various immune cells that contribute to tissue homeostasis and protection from pathogens. As the skin is relatively easy to access, it provides an ideal platform to study peripheral immune regulatory mechanisms. Immune resident cells in healthy skin conduct immunosurveillance, but also play an important role in the development of inflammatory skin disorders, such as psoriasis. Despite emerging insights, our understanding of the biology underlying various inflammatory skin diseases is still limited. There is a need for good quality (single) cell populations isolated from biopsied skin samples. So far, isolation procedures have been seriously hampered by a lack of obtaining a sufficient number of viable cells. Isolation and subsequent analysis have also been affected by the loss of immune cell lineage markers, due to the mechanical and chemical stress caused by the current dissociation procedures to obtain single cell suspension. Here, we describe a modified method to isolate T cells from both healthy and involved psoriatic human skin by combining mechanical skin dissociation using an automated tissue dissociator and collagenase treatment. This methodology preserves expression of most immune lineage markers such as CD4, CD8, Foxp3 and CD11c upon the preparation of single cell suspensions. Examples of successful CD4+ T cell isolation and subsequent phenotypic and functional analysis are shown.

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture

We describe a protocol to efficiently isolate skin resident T cells from human skin biopsies. This protocol yields sufficient numbers of viable human skin resident lymphocytes for flow cytometric analysis and ex vivo culture.

Fenotipik Analizi ve İnsan Cilt lenfosit izolasyonu<em&gt; Ex Vivo</em&gt; Hücre Kültürü

Human skin has an important barrier function and contains various immune cells that contribute to tissue homeostasis and protection from pathogens. As the ...

Isolation of Infiltrating Leukocytes from Mouse Skin Using Enzymatic Digest and Gradient Separation

Dissociating murine skin into a single cell suspension is essential for downstream cellular analysis such as the characterization of infiltrating immune cells in rodent models of skin inflammation. Here, we describe a protocol for the digestion of mouse skin in a nutrient-rich solution with collagenase D, followed by separation of hematopoietic cells using a discontinuous density gradient. Cells thus obtained can be used for in vitro studies, in vivo transfer, and other downstream cellular and molecular analyses including flow cytometry. This protocol is an effective and economical alternative to expensive mechanical dissociators, specialized separation columns, and harsher trypsin- and dispase-based digestion methods, which may compromise cellular viability or density of surface proteins relevant for phenotypic characterization or cellular function. As shown here in our representative data, this protocol produced highly viable cells, contained specific immune cell subsets, and had no effect on integrity of common surface marker proteins used in flow cytometric analysis.

This protocol describes enzymatic digestion of mouse skin in nutrient-rich medium followed by gradient separation to isolate leukocytes. Cells thus derived can be used for diverse downstream applications. This is an effective, economical, and improved alternative to tissue dissociation machines and harsher trypsin and dispase-based tissue digestion protocols.

Enzimatik Digest ve Gradient Ayırma kullanma Fare Skin gelen sızan lökositlerin İzolasyonu

Dissociating murine skin into a single cell suspension is essential for downstream cellular analysis such as the characterization of infiltrating immune ...

Isolation and Flow Cytometric Analysis of Immune Cells from the Ischemic Mouse Brain

Ischemic stroke initiates a robust inflammatory response that starts in the intravascular compartment and involves rapid activation of brain resident cells. A key mechanism of this inflammatory response is the migration of circulating immune cells to the ischemic brain facilitated by chemokine release and increased endothelial adhesion molecule expression. Brain-invading leukocytes are well-known contributing to early-stage secondary ischemic injury, but their significance for the termination of inflammation and later brain repair has only recently been noticed.
Here, a simple protocol for the efficient isolation of immune cells from the ischemic mouse brain is provided. After transcardial perfusion, brain hemispheres are dissected and mechanically dissociated. Enzymatic digestion with Liberase&#160;is followed by density gradient (such as Percoll) centrifugation to remove myelin and cell debris. One major advantage of this protocol is the single-layer density gradient procedure which does not require time-consuming preparation of gradients and can be reliably performed. The approach yields highly reproducible cell counts per brain hemisphere and allows for measuring several flow cytometry panels in one biological replicate. Phenotypic characterization and quantification of brain-invading leukocytes after experimental stroke may contribute to a better understanding of their multifaceted roles in ischemic injury and repair.

Inflammation plays a central role in the pathogenesis of ischemic stroke. Increasing evidence suggests that it acts as a double-edged sword which exacerbates early brain injury, but also contributes to later repair. This protocol describes the isolation of immune cells from the ischemic brain and their subsequent flow cytometric phenotyping.

İskemik Fare Beyin gelen Bağışıklık Hücreleri İzolasyon ve Akım Sitometrisi Analizi

Ischemic stroke initiates a robust inflammatory response that starts in the intravascular compartment and involves rapid activation of brain resident ...

Preparation of CD4+ T Cells for Analysis of GD3 and GD2 Ganglioside Membrane Expression by Microscopy

The methods described herein for activation of na&#239;ve CD4+ T cells in suspension and their adherence in coverslips for confocal microscopy analysis allow the spatial localization and visualization of gangliosides involved in CD4+ T cell activation, that complement expression profiling experiments such as flow cytometry, western blotting or real-time PCR. The quantification of ganglioside expression through flow cytometry and their cellular localization through microscopy can be obtained by the use of anti-ganglioside antibodies with high affinity and specificity. Nonetheless, an adequate handling of cells in suspension involves the treatment of culture plates to promote the necessary adherence required for fluorescence or confocal microscopy acquisition. In this work, we describe a protocol for determining GD3 and GD2 ganglioside expression and colocalization with the TCR during na&#239;ve CD4+ T cell activation. Also, real-time PCR experiments using &#60;40,000 cells are described for the determination of the GD3 and GM2/GD2 synthase genes, demonstrating that gene analysis experiments can be performed with a low number of cells and without the need of additional low input RNA kits.

Preparation of CD4+ T Cells for Analysis of GD3 and GD2 Ganglioside Membrane Expression by Microscopy

We describe a standard antibody staining protocol for use in microscopy to determine the membrane expression and localization of gangliosides in resting and activated human na&#239;ve CD4+ T cells. Also described are real-time PCR experiments using &#60;40,000 cells that do not require additional low input RNA kits.

CD4 hazırlanması<sup&gt; +</sup&gt; Mikroskopi GD3 ve GD2 Gangliozidleri Membran İfade Analizi T hücreleri

The methods described herein for activation of na&#239;ve CD4+ T cells in suspension and their adherence in coverslips for confocal microscopy analysis ...

Single-cell Analysis of Immunophenotype and Cytokine Production in Peripheral Whole Blood via Mass Cytometry

Cytokines play a pivotal role in the pathogenesis of autoimmune diseases. Hence, the measurement of cytokine levels has been the focus of multiple studies in an attempt to understand the precise mechanisms that lead to the breakdown of self-tolerance and subsequent autoimmunity. Approaches thus far have been based on the study of one specific aspect of the immune system (a single or few cell types or cytokines), and do not offer a global assessment of complex autoimmune disease. While patient sera-based studies have afforded important insights into autoimmunity, they do not provide the specific cellular source of the dysregulated cytokines detected. A comprehensive single-cell approach to evaluate cytokine production in multiple immune cell subsets, within the context of &#34;intrinsic&#34; patient-specific plasma circulating factors, is described here. This approach enables monitoring of the patient-specific immune phenotype (surface markers) and function (cytokines), either in its native &#34;intrinsic pathogenic&#34; disease state, or in the presence of therapeutic agents (in vivo or ex vivo).

Here we describe a single-cell proteomic approach to evaluate immune phenotypic and functional (intracellular cytokine induction) alterations in peripheral whole blood samples, analyzed via mass cytometry.

Tek hücreli Immunophenotype ve sitokin üretimde kitle sitometresi ile periferik tam kan analizi

Cytokines play a pivotal role in the pathogenesis of autoimmune diseases. Hence, the measurement of cytokine levels has been the focus of multiple studies ...