Name: preparation of single-cell suspensions from mouse spleen with the gentlemacs dissociator
Uploaded: 2008-12-11T00:00:00.000+00:00
Duration: 5 min 18 s
Description: Watch this Scientific Journal Video about Preparation of Single-Cell Suspensions from Mouse Spleen with the gentleMACS Dissociator at JoVE.com

Equipment Giriş <ol><li> Doku uygulanabilir tek hücre süspansiyonları içine menekşe C Tüpler kullanarak, hafifçe ayrışmış. </li><li> PBS / BSA EDTA tampon hücreleri ayırmak kullanılır. Tampon BSA Stok çözelti, EDTA içeren Çözüm Durulama autoMACS 20 kısım 1 kısım ekleyerek hazırlanır. </li><li> MACS Ön Ayırma Filtreler başarılı MACS ayrılması ve daha sonraki analiz teşvik ayrışmış doku örnekleri tüm hücre kümeleri, böylece kullanılır. </li></ol> Dalak hücreleri Dissociating <ol><li> Tüm dalak dalak gentleMACS Dissociator kullanarak tek hücre süspansiyonları disscociated. </li><li> Prosedürü başlatmak için, dalak, kitle göre tampon hacmi ile C Tüp yük. Genç bir yetişkin erkek BALB / c fare sağlıklı bir dalak 80-120 mg ağırlığındadır. Bu kitle her 1 ila 2 dalak 3 mL tampon gerektirir. Enfeksiyonları ile büyük hayvan veya hayvanların dalak genellikle büyük ve tampon tartılır olmalıdır. Tampon hacimleri buna göre ölçeklenmiş olmalıdır. 10 ml toplam tampon hacmi aşmayın. </li><li> 3 ml tampon içeren C Tüp disseke dalak ekleyin. </li><li> C Tüp kapağı sıkı olduğundan emin olun ve kapağı aşağı dissociator C Tüp takmak. </li><li> Dissociator kadar güç. 1-2 dalak için program m_spleen_01 seçin. Programını tamamlamak için 56 saniye sürer. Dalak, sayı büyükse, program m_spleen_04 kullanın, bu program 720 mg dalak doku için kullanılabilir. </li><li> Programın tamamlanmasından sonra yerli dalak doku splenocyte süspansiyon ayrışmış. </li><li> Yaklaşık 30 saniye boyunca oda sıcaklığında 300xg tüm hücre süspansiyonu aşağı spin. Bu rotor ve stator C Boru altında toplanan tüm hücreleri serbest olmasını sağlayacaktır. </li><li> 1000 mikrolitrelik pipetter kullanarak septum-C Tüp kapağı kapalı açılış ile örnek çıkarın. </li></ol> Filtrasyon adım <ol><li> Filtrasyon adım başlamak için, Pre-Ayırma Filtre ya da 30 mikron gözenek boyutu ile bir hücre süzgeç ayrışmış doku geçerlidir. Süzgeç fazla 2 dalak, 1-2 dalak ya da 50 ml tüp 15 ml tüp uygun olmalıdır. </li><li> Hücre süspansiyonu geçmesine izin verin. Daha sonra 5 ml tampon uygulayarak filtre yıkayın. </li><li> Şimdi, bir dalak hücre pelletini tüm splenositlerin toplamak için 10 dakika boyunca oda sıcaklığında, 300xg hücre süspansiyonu ile tüp santrifüj. </li><li> Şimdi, ayrışmış splenositlerin bir pelet, süpernatantı aspirat ve tamponu uygun bir miktarda hücre pelletini tekrar süspansiyon gerekir. </li></ol> Dalak ayrılma gentleMACS Dissociator kullanarak canlı splenositlerin MACSQuant Analyzer kullanarak flow sitometri gösterdiği yüksek bir yüzdesi verecektir. Ölü hücreler propidium iyodür tarafından lekeli. Verilen örnekte, ileri yan dağılım nokta arsa hazırlanan splenositlerin gösterir.

Tüm protokolleri ve veri sayfaları mevcuttur<a href="http://www.miltenyibiotec.com"&gt; Http://www.miltenyibiotec.com.</a&gt;.

GentleMACS Dissociator sıkıcı ve sıklıkla ağrılı manuel dissociations önlemek için, kontrollü ve tekrarlanabilir koşullar altında çok etkin bir şekilde doku ayırmak sağlar. Doku disosiasyon prosedürü yüksek canlılık oranı ile hücre ve verim hücre süspansiyonları yumuşaktır. C Tüpleri ile birlikte gentleMACS Dissociator, çeşitli dokuların tek hücre süspansiyonları hazırlanması için tasarlanmıştır. Cihaz fare dalak, karaciğer, akciğer veya sinir doku ayırmak önceden belirlenmiş programları bir dizi ile donatılmıştır. Çeşitli programların ve protokollerin ek dokuların sürekli kapsayacak şekilde genişletildi olacaktır.

<table><tbody><tr><td>gentleMACS&amp;#8482; Starting Kit</td><td>Miltenyi Biotec</td><td>130-093-235</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_709_763_gentleMACS_Dissociator.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_709_763_gentleMACS_Dissociator.aspx&lt;/a&gt;</td></tr><tr><td>C Tubes</td><td>Miltenyi Biotec</td><td>130-093-237</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_709_765_gentleMACS_C_Tubes.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_709_765_gentleMACS_C_Tubes.aspx&lt;/a&gt;</td></tr><tr><td>13 mL Tubes</td><td>Miltenyi Biotec</td><td>130-091-596</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_34_751_13_mL_Tubes_for_LS_Columns.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_34_751_13_mL_Tubes_for_LS_Columns.aspx&lt;/a&gt;</td></tr><tr><td>autoMACS&amp;#8482; Rinsing Solution </td><td>Miltenyi Biotec</td><td>130-091-222</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_134_155_autoMACS_Rinsing_Solution.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_134_155_autoMACS_Rinsing_Solution.aspx&lt;/a&gt;</td></tr><tr><td>MACS&amp;#174; BSA Stock Solution</td><td>Miltenyi Biotec</td><td>130-091-376</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_33_295_MACS_BSA_Stock_Solution.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_33_295_MACS_BSA_Stock_Solution.aspx&lt;/a&gt;</td></tr><tr><td>Pre-Separation Filters </td><td>Miltenyi Biotec</td><td>130-041-407</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_34_247_Pre_Separation_Filters.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_34_247_Pre_Separation_Filters.aspx&lt;/a&gt;</td></tr><tr><td>MACSQuant Analyzer</td><td>Miltenyi Biotec</td><td>130-092-197</td><td></td></tr><tr><td>Propidium Iodide Solution</td><td>Miltenyi Biotec</td><td>130-093-233</td><td>&lt;a href=&quot;http://www.miltenyibiotec.com/en/PG_337_744_Propidium_Iodide_Solution.aspx&quot;&gt;http://www.miltenyibiotec.com/en/PG_337_744_Propidium_Iodide_Solution.aspx&lt;/a&gt;</td></tr></tbody></table>

preparation of single-cell suspensions from mouse spleen with the gentlemacs dissociator

Tek hücre süspansiyonları hücre ayırma, hücre analizi ve hücre kültürü deneyleri için bir önkoşuldur. GentleMACS Dissociator sıkıcı ve sıklıkla ağrılı manuel dissociations önlemek için kontrollü ve tekrarlanabilir koşullar altında çok etkin bir şekilde doku ayırmak sağlar. GentleMACS Dissociator optimal, kullanıcı güvenliği ile zaman kazandıran ve standardizasyon birleştirerek, fare dalak ayrılabilir. Bu video gentleMACS Dissociator, mekanik, canlı hücre süspansiyonları üretmek için özel tüpler kullanılarak dokuların bozabilir otomatik bir tezgah üstü cihazı kullanarak fare dalak ayırmak anlatılmaktadır. Disosiasyon ardından, dalak, süzülür ve başka uygulamalar için yeniden süspanse.

Watch this Scientific Journal Video about Preparation of Single-Cell Suspensions from Mouse Spleen with the gentleMACS Dissociator at JoVE.com

Preparation of Single-Cell Suspensions from Mouse Spleen with the gentleMACS Dissociator

Bu video gentleMACS Dissociator kullanarak fare dalak tek hücre süspansiyonları hazırlamak için otomatik doku ayrılma için basit, zaman tasarrufu sağlayan bir teknik açıklar.

Fare Dalak gentleMACS Dissociator Tek Hücreli Cezalar hazırlanması

Single-cell suspensions are a prerequisite for experiments in cell separation, cell analysis and cell culture.  To avoid tedious and often painful manual ...

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preparation-single-cell-suspensions-from-mouse-spleen-with-gentlemacs

Universidad San Sebastian

Research

JoVE Journal

Biology

37.7K Görüntüleme.  Miltenyi Biotec,GmbH.  中文 JapaneseVersion 

Video: Preparation of Single-Cell Suspensions from Mouse Spleen with the gentleMACS Dissociator

Preparing T Cell Growth Factor from Rat Splenocytes

Maintenance of antigen-specific T cell lines or clones in culture requires rounds of antigen-induced activation separated by phases of cell expansion 1,2. Addition of interleukin 2 to the culture media during the expansion phase is necessary to prevent cell death and sufficient to maintain short-term T cell lines but has been shown to increase Th1 polarization 3. Replacement of interleukin 2 by T cell growth factor (TCGF) which contains a mix of cytokines is more effective than interleukin 2 in maintaining long-term T cell lines in vitro 3. Moreover, TCGF can easily be prepared in large amounts in the laboratory and is much cheaper than recombinant interleukin 2. 
Here, we show how to prepare TCGF from rat splenocyte culture supernatants. For this procedure, we harvest spleens from naive Lewis rats euthanized for thymus and blood collection. We prepare single-cell suspensions from the spleens, lyze the red blood cells by osmotic shock, and seed the splenocytes in culture medium. The cells are stimulated with concanavalin A, a mitogen that non-selectively activates all rat T lymphocytes, inducing the production of cytokines. The culture supernantant is collected 48 hours later andexcess concanavalin A is bound to alpha methyl mannoside to prevent it from activating T cell lines to which TCGF will be added. The TCGF is then sterile-filtered, aliquoted, and stored at -20&deg;C.

We describe the preparation of T cell growth factor used for the in vitro expansion of antigen-specific rat T lymphocyte lines.

Rat splenositlerin T Hücre Büyüme Faktörü hazırlanması

Maintenance of antigen-specific T cell lines or clones in culture requires rounds of antigen-induced activation separated by phases of cell expansion 1,2. ...

Biyoloji

Standardized Preparation of Single-Cell Suspensions from Mouse Lung Tissue using the gentleMACS Dissociator

The preparation of single-cell suspensions from tissues is an important prerequisite for many experiments in cellular research. The process of dissociating whole organs requires specific parameters in order to obtain a high number of viable cells in a reproducible manner. The gentleMACS Dissociator optimizes this task with a simple, practical protocol. The instrument contains pre-programmed settings that are optimized for the efficient but gentle dissociation of a variety of tissue types, including mouse lungs. In this publication the use of the gentleMACS Dissociator on lung tissue derived from mice is demonstrated.

Dissociating cells from specific tissue types requires specific parameters for tissue agitation to obtain a high volume of viable, culturable cells. The Miltenyi gentleMACS dissociator optimizes this task with a simple, practical protocol. In this publication the use of this apparatus on lung tissue is explained.

Standardize Hazırlık gentleMACS Dissociator kullanarak Fare Akciğer Doku Tek Hücre Cezalar

The preparation of single-cell suspensions from tissues is an important prerequisite for many experiments in cellular research. The process of ...

Generation of Single-Cell Suspensions from Mouse Neural Tissue

Within the nervous system, hundreds of neuronal and glial cell types have been described. Each specific cell type in the brain or spinal cord has a repertoire of cell surface molecules, or molecular determinants, through which it can be identified and characterized. Currently, robust cell identification and separation technologies require single-cell preparations to be generated while simultaneously limiting cell death and destruction of characteristic surface protein. The gentleMACS Dissociator, when used in combination with trypsin or papain-based dissociation kits, can effectively and gently dissociate brain tissue while preserving antigen epitopes and limiting cell loss. Standardized preparation of single-cell suspensions is achieved using C Tubes and optimized, preset gentleMACS Programs. Once generated, single-cell suspensions can be treated with monoclonal conjugates like Anti-Prominin-1 MicroBeads, which identify neural progenitors, or purified further using Myelin Removal Beads.

Dissociating cells from specific tissue types requires specific parameters for tissue aggitation to obtain a high volume of viable, culturable cells. The Miltenyi gentleMACS Dissociator optimizes this task with a simple, practical protocol. In this publication the use of this apparatus on nerual tissue is explained.

Fare Sinir Doku Hücre Tek Cezalar Üretimi

Within the nervous system, hundreds of neuronal and glial cell types have been described. Each specific cell type in the brain or spinal cord has a ...

The Use of Flow Cytometry to Assess the State of Chromatin in T Cells

During a proper immune response, quiescent T cells become activated upon antigen presentation to their antigen-specific T cell receptor. This leads to clonal proliferation of only those T cells that bear a receptor that recognizes the antigen. Chromatin decondensation is a hallmark of T cell activation and is required for T cells to acquire the ability to proliferate after antigen engagement. This change in chromatin condensation can be detected using antibodies raised against histone proteins. These antibodies cannot bind to their epitopes in na&#239;ve T cells as well as they can in activated T cells. We describe how to simultaneously stain T cell-specific surface markers, track viability with a fixable dead cell stain, and measure chromatin status via intracellular staining of Histone H3 proteins. Stained cells are analyzed by flow cytometry and chromatin condensation status is measured as the mean fluorescence intensity (MFI) of the Histone H3 stain. Chromatin decondensation during T cell activation is demonstrated as an increase in the MFI

Flow cytometry can be utilized to assess the state of chromatin within T cells. This protocol allows scientists to interpret evidence of chromatin decondensation during T cell activation demonstrated by an increase in the mean florescence intensity (MFI) of fluorescent Histone H3 antibodies

Akış Sitometrinin Kullanımı T Hücrelerinde Kromatin Devleti değerlendirmek için

During a proper immune response, quiescent T cells become activated upon antigen presentation to their antigen-specific T cell receptor. This leads to ...

İmmünoloji ve Enfeksiyon

Isolation of Murine Spermatogenic Cells using a Violet-Excited Cell-Permeable DNA Binding Dye

Isolation of meiotic spermatocytes is essential to investigate molecular mechanisms underlying meiosis and spermatogenesis. Although there are established cell isolation protocols using Hoechst 33342 staining in combination with fluorescence-activated cell sorting, it requires cell sorters equipped with an ultraviolet laser. Here we describe a cell isolation protocol using the DyeCycle Violet (DCV) stain, a low cytotoxicity DNA binding dye structurally similar to Hoechst 33342. DCV can be excited by both ultraviolet and violet lasers, which improves the flexibility of equipment choice, including a cell sorter not equipped with an ultraviolet laser. Using this protocol, one can isolate three live-cell subpopulations in meiotic prophase I, including leptotene/zygotene, pachytene, and diplotene spermatocytes, as well as post-meiotic round spermatids. We also describe a protocol to prepare single-cell suspension from mouse testes. Overall, the procedure requires a short time to complete (4-5 hours depending on the number of needed cells), which facilitates many downstream applications.

Here we present a simple and efficient method to isolate live meiotic and post-meiotic germ cells from adult mouse testes. Using a low-cytotoxicity, violet-excited DNA binding dye and fluorescence-activated cell sorting, one can isolate highly enriched spermatogenic cell populations for many downstream applications.

Mor-Heyecanlı Hücre-Geçirgen DNA Bağlayıcı Boya Kullanılarak Murine Spermatojenik Hücrelerin İzolasyon

Isolation of meiotic spermatocytes is essential to investigate molecular mechanisms underlying meiosis and spermatogenesis. Although there are established ...

Gelişim Biyolojisi

Basement Membrane Matrix Encapsulated Cell Aggregation for Investigating Murine Spleen Tissue Formation

The spleen is an immune organ that plays a key role in blood-borne immune responses. The anatomical or functional loss of this tissue increases susceptibility to severe blood infections and sepsis. Auto-transplantation of spleen slices has been used clinically to replace lost tissue and restore immune function. However, the mechanism driving robust and immunologically functional spleen tissue regeneration has not been fully elucidated. Here, we aim to develop a method for aggregating and encapsulating spleen cells within a semi-solid matrix in order to investigate the cellular requirements for spleen tissue formation. Basement membrane matrix encapsulated cell constructs are amenable to both in vitro tissue culture of three-dimensional organoids as well as transplantation under the kidney capsule to directly assess in vivo tissue formation. By manipulating the input cells for aggregation and encapsulation, we demonstrate that graft-derived PDGFR&#946;+MAdCAM-1- neonatal stromal cells are required for spleen tissue regeneration under animal transplantation models.

This article describes a protocol for aggregating and encapsulating spleen cells within a semi-solid basement membrane matrix. Basement membrane matrix constructs can be used in three-dimensional culture for studying organoid development, or for in vivo transplantation and tissue regeneration studies.

Murin Dalak Dokusu Oluşumunu Araştırmak için Bazal Membran Matris Kapsüllü Hücre Agregasyonu

The spleen is an immune organ that plays a key role in blood-borne immune responses. The anatomical or functional loss of this tissue increases ...

Isolation and Adoptive Transfer of High Salt Treated Antigen-presenting Dendritic Cells

Excess dietary salt intake contributes to inflammation and plays a vital role in the development of hypertension. We previously found that antigen-presenting dendritic cells (DCs) can sense elevated extracellular sodium leading to the activation of the NADPH oxidase and formation of isolevuglandin (IsoLG)-protein adducts. These IsoLG-protein adducts react with self-proteins and promote an autoimmune-like state and hypertension. We have developed and optimized state-of-the-art methods to study DC function in hypertension. Here, we provide a detailed protocol for isolation, in vitro treatment with elevated sodium, and adoptive transfer of murine splenic CD11c+ cells into recipient mice to study their role in hypertension.

Here, we present a protocol to isolate dendritic cells from murine spleens by magnetic cell sorting and subsequent adoptive transfer into na&#239;ve mice. The model of high-salt activated dendritic cells was chosen to explain the step-by-step procedures of adoptive transfer and flow cytometry.

Yalıtım ve yüksek tuz evlat edinen Transfer dendritik hücreler antijen sunan tedavi

Excess dietary salt intake contributes to inflammation and plays a vital role in the development of hypertension. We previously found that ...

Flow Cytometric Characterization of Murine B Cell Development

Extensive studies have characterized the development and differentiation of murine B cells in secondary lymphoid organs. Antibodies secreted by B cells have been isolated and developed into well-established therapeutics. Validation of murine B cell development, in the context of autoimmune prone mice, or in mice with modified immune systems, is a crucial component of developing or testing therapeutic agents in mice and is an appropriate use of flow cytometry. Well established B cell flow cytometric parameters can be used to evaluate B cell development in the murine peritoneum, bone marrow, and spleen, but a number of best practices must be adhered to. In addition, flow cytometric analysis of B cell compartments should also complement additional readouts of B cell development. Data generated using this technique can further our understanding of wild type, autoimmune prone mouse models as well as humanized mice that can be used to generate antibody or antibody-like molecules as therapeutics.

We describe herein a simple analysis of the heterogeneity of the murine immune B cell compartment in the peritoneum, spleen, and bone marrow tissues by flow cytometry. The protocol can be adapted and extended to other mouse tissues.

Murine B Hücre Gelişiminin Akış Sitometrik Karakterizasyonu

Extensive studies have characterized the development and differentiation of murine B cells in secondary lymphoid organs. Antibodies secreted by B cells ...

<meta charset="utf8"></head><body>Murin Dalak Kaynaklı Eksozom İzolasyonu için Rafine Etme Teknikleri

Isolation and Characterization of Exosomes Derived from Mouse Spleen Tissues

Exosomes (Exo) are lipid-bilayer structures secreted by various cells, including those of animals, plants, and prokaryotes. Previous studies have revealed that Exo derived from humoral or cell-supernatant are promising targets for novel diagnostic or prognostic biomarkers, underscoring their significant role in disease pathogenesis. Tissue-derived Exo (Ti-Exo) have attracted increasing attention due to its ability to accurately reflect tissue specificity and the microenvironment. Ti-Exo, present in interstitial space, play crucial roles in intercellular communication and cross-organ signaling. Despite their recognized value in elucidating disease mechanisms, isolating Ti-Exo remains challenging due to the complexity of tissue matrices and variability in extraction methods. In this study, we developed a practical protocol for isolating exosomes from mice spleen tissue, providing a reproducible technique for subsequent identification analysis and functional studies. We used Type I collagenase digestion combined with differential ultracentrifugation to isolate spleen-derived Exo. The characteristics of isolated Exo were determined through electron microscopy, the nano-flow cytometer, and the western blot. The isolated spleen-derived Exo displayed the typical morphology of lipid bilayer vesicles, with particle sizes ranging from 30 nm to 150 nm. In addition, the expression profile of exosome markers confirmed the presence and purity of exosomes. Taken together, we successfully established a practical protocol for isolating spleen-derived Exo in mice.

<meta charset="utf8"></head><body>Fare Dalak Dokularından Elde Edilen Eksozomların İzolasyonu ve Karakterizasyonu

Here, we present a protocol to isolate mouse spleen-derived exosomes using a combination of digestion with collagenase type I and ultracentrifugation.

Fare Dalak Dokularından Elde Edilen Eksozomların İzolasyonu ve Karakterizasyonu

Exosomes (Exo) are lipid-bilayer structures secreted by various cells, including those of animals, plants, and prokaryotes. Previous studies have revealed ...

Fare Dalak gentleMACS Dissociator Tek Hücreli Cezalar hazırlanması

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Rat splenositlerin T Hücre Büyüme Faktörü hazırlanması

Standardize Hazırlık gentleMACS Dissociator kullanarak Fare Akciğer Doku Tek Hücre Cezalar

Fare Sinir Doku Hücre Tek Cezalar Üretimi

Akış Sitometrinin Kullanımı T Hücrelerinde Kromatin Devleti değerlendirmek için

Mor-Heyecanlı Hücre-Geçirgen DNA Bağlayıcı Boya Kullanılarak Murine Spermatojenik Hücrelerin İzolasyon

Murin Dalak Dokusu Oluşumunu Araştırmak için Bazal Membran Matris Kapsüllü Hücre Agregasyonu

Yalıtım ve yüksek tuz evlat edinen Transfer dendritik hücreler antijen sunan tedavi

Murine B Hücre Gelişiminin Akış Sitometrik Karakterizasyonu

Fare Dalak Dokularından Elde Edilen Eksozomların İzolasyonu ve Karakterizasyonu

Fare Dalak Dokularından Elde Edilen Eksozomların İzolasyonu ve Karakterizasyonu