Name: murine model of allergen induced asthma
Uploaded: 2012-05-14T12:00:00
Description: Watch this Scientific Journal Video about Murine Model of Allergen Induced Asthma at JoVE.com

इस काम के एनआईएच अनुदान (RCR) के HL093196 और अटलांटा अनुसंधान और शिक्षा फाउंडेशन (Aref) के द्वारा समर्थित किया गया.

मैं Allergen संवेदनशील और चैलेंज (चित्रा 1 देखें) ए Intratracheal चैलेंज के लिए <ol><li> प्रारंभिक संवेदीकरण के लिए, 0 दिन और फिर 7 दिन पर ovalbumin के 20 μg (, सिग्मा Aldrich, सेंट लुइस, MO OVA) के साथ पुरुष या महिला C57BL / 6 या / BALB सी (6-8 ?...

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Physiol. 64, 2318-2323 (1988).</li><li>Hamelmann, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Noninvasive+measurement+of+airway+responsiveness+in+allergic+mice+using+barometric+plethysmography.">Noninvasive measurement of airway responsiveness in allergic mice using barometric plethysmography.</a> Am. J. Respir. Crit. Care Med. 156, 766-775 (1997).</li><li>Gelfand, E. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Pro:+mice+are+a+good+model+of+human+airway+disease.">Pro: mice are a good model of human airway disease.</a> Am. J. Respir. Crit. Care Med. 166, 5-8 (2002).</li><li>Shapiro, S. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Animal+models+of+asthma:+Pro:+Allergic+avoidance+of+animal+(model[s])+is+not+an+option.">Animal models of asthma: Pro: Allergic avoidance of animal (model[s]) is not an option.</a> Am. J. Respir. Crit. Care Med. 174, 1171-1173 (2006).</li><li>Zosky, G. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ovalbumin-sensitized+mice+are+good+models+for+airway+hyperresponsiveness+but+not+acute+physiological+responses+to+allergen+inhalation.">Ovalbumin-sensitized mice are good models for airway hyperresponsiveness but not acute physiological responses to allergen inhalation.</a> Clin. Exp. Allergy. 38, 829-838 (2008).</li><li>Nials, A. T., Uddin, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mouse+models+of+allergic+asthma:+acute+and+chronic+allergen+challenge.">Mouse models of allergic asthma: acute and chronic allergen challenge.</a> Dis. Model. Mech. 1, 213-220 (2008).</li><li>Wenzel, S., Holgate, S. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+mouse+trap:+It+still+yields+few+answers+in+asthma.">The mouse trap: It still yields few answers in asthma.</a> Am. J. Respir. Crit. Care Med. 174, 1173-1178 (2006).</li><li>Rayamajhi, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Non-surgical+Intratracheal+Instillation+of+Mice+with+Analysis+of+Lungs+and+Lung+Draining+Lymph+Nodes+by+Flow+Cytometry.">Non-surgical Intratracheal Instillation of Mice with Analysis of Lungs and Lung Draining Lymph Nodes by Flow Cytometry.</a> J. Vis. Exp. (51), e2702 (2011).</li><li>Swedin, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Comparison+of+aerosol+and+intranasal+challenge+in+a+mouse+model+of+allergic+airway+inflammation+and+hyperresponsiveness.">Comparison of aerosol and intranasal challenge in a mouse model of allergic airway inflammation and hyperresponsiveness.</a> Int. Arch. Allergy Immunol. 153, 249-258 (2010).</li><li>Gueders, M. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mouse+models+of+asthma:+a+comparison+between+C57BL/6+and+BALB/c+strains+regarding+bronchial+responsiveness,+inflammation,+and+cytokine+production.">Mouse models of asthma: a comparison between C57BL/6 and BALB/c strains regarding bronchial responsiveness, inflammation, and cytokine production.</a> Inflamm. Res. 58, 845-854 (2009).</li><li>Zhu, W., Gilmour, M. I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Comparison+of+allergic+lung+disease+in+three+mouse+strains+after+systemic+or+mucosal+sensitization+with+ovalbumin+antigen.">Comparison of allergic lung disease in three mouse strains after systemic or mucosal sensitization with ovalbumin antigen.</a> Immunogenetics. 61, 199-207 (2009).</li><li>Flandre, T. D., Leroy, P. L., Desmecht, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effect+of+somatic+growth,+strain,+and+sex+on+double-chamber+plethysmographic+respiratory+function+values+in+healthy+mice.">Effect of somatic growth, strain, and sex on double-chamber plethysmographic respiratory function values in healthy mice.</a> J. Appl. Physiol. 94, 1129-1136 (2003).</li><li>Hoymann, H. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Invasive+and+noninvasive+lung+function+measurements+in+rodents.">Invasive and noninvasive lung function measurements in rodents.</a> J. Pharmacol. Toxicol. Methods. 55, 16-26 (2007).</li><li>Chong, B. T., Agrawal, D. K., Romero, F. A., Townley, R. G. <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+bronchoconstriction+using+whole-body+plethysmograph:+comparison+of+freely+moving+versus+restrained+guinea+pigs.">Measurement of bronchoconstriction using whole-body plethysmograph: comparison of freely moving versus restrained guinea pigs.</a> J. Pharmacol. Toxicol. Methods. 39, 163-168 (1998).</li></ol>

एलर्जी airway रोग के पशु मॉडल नैदानिक ​​अस्थमा के लिए प्रासंगिक अध्ययन के लिए महत्वपूर्ण उपकरण प्रदान करते हैं. अलग अलग मॉडल, अलग प्रजातियों और प्रतिजनों को रोजगार का एक संख्या में विकसित किया गया है. माउस...

<table border="1"><tbody><tr><td> सामग्री नाम </td><td> कंपनी </td><td> सूचीपत्र संख्या </td><td> टिप्पणियाँ </td></tr><tr><td> Ovalbumin </td><td> सिग्मा Aldrich सेंट लुइस, MO </td><td> A5503 </td><td></td></tr><tr><td> एल्यूमिनियम हीड्राकसीड </td><td> सिग्मा Aldrich </td><td> 239,186 </td><td></td></tr><tr><td> Acetyl-बीटा methylcholine क्लोराइड </td><td> सिग्मा Aldrich </td><td> A2251 </td><td></td></tr><tr><td> Pentobarbital सोडियम नमक </td><td> सिग्मा Aldrich </td><td> P3761 </td><td></td></tr><tr><td> पूरे शरीर plethysmography प्रणाली (WBP) </td><td> Buxco रिसर्च सिस्टम्स Wilmington, नेकां </td><td></td><td> <a href="http://www.buxco.com" target="_blank">http://www.buxco.com</a> </td></tr><tr><td> FlexiVent </td><td>SCIREQ इंक, मॉन्ट्रियल, कनाडा </td><td></td><td> <a href="http://www.scireq.com" target="_blank">http://www.scireq.com</a> </td></tr><tr><td> प्रकाश माइक्रोस्कोप </td><td> Leica माइक्रोसिस्टम्स इंक, भैंस ग्रोव, आईएल </td><td></td><td></td></tr><tr><td> 4 cytospin </td><td> थर्मो वैज्ञानिक Asheville, नेकां </td><td></td><td></td></tr><tr><td> दाग डिफ - त्वरित </td><td> सीमेंस Newark, DE </td><td> B4132-1a </td><td></td></tr><tr><td> दोहराए विंदुक </td><td> Tridak टोरिंगटन, सीटी </td><td> STP4001 - 0025 </td><td></td></tr></tbody></table>

murine model of allergen induced asthma

अस्थमा रुग्णता और मृत्यु दर का एक प्रमुख कारण है, दुनिया भर में कुछ 300 मिलियन लोगों को प्रभावित 8 अमेरिका की आबादी का 1% से अधिक अस्थमा है, अन्य बीमारियों, एलर्जी airway रोग के पशु मॉडल की सुविधा बहुत साथ के रूप में प्रसार में वृद्धि के साथ 2. अंतर्निहित pathophysiology की समझ में मदद करने के लिए, संभावित चिकित्सात्मक लक्ष्यों की पहचान, और संभव नए उपचारों के preclinical परीक्षण की अनुमति है. कई पशु प्रजातियों में एलर्जी airway रोग का मॉडल विकसित किया गया है, लेकिन murine मॉडल विशेष रूप से आकर्षक कम लागत, तैयार की उपलब्धता है, और इन जानवरों की अच्छी तरह से विशेषता प्रतिरक्षा प्रणाली के कारण हैं. ट्रांसजेनिक उपभेदों के एक किस्म के 3 उपलब्धि आगे आकर्षण बढ़ जाती है इन मॉडलों के 4 यहाँ हम एलर्जी airway रोग के दो murine मॉडल का वर्णन, दोनों प्रतिजन के रूप में रोजगार ovalbumin. Intraperitoneal इंजेक्शन, एक मॉडल deliv द्वारा प्रारंभिक संवेदीकरण के बादnebulization, intratracheal वितरण द्वारा अन्य द्वारा प्रतिजन चुनौती ERS. इन दो मॉडल पूरक लाभ प्रदान करते हैं, प्रत्येक मानव अस्थमा के प्रमुख विशेषताओं में नकल उतार के साथ 5. और eosinophil अमीर airway सूजन, तीव्र अस्थमा के प्रमुख विशेषताएं एक अतिरंजित airway के (Ahr airway के hyperresponsiveness) methacholine जैसे उत्तेजनाओं के जवाब शामिल हैं. ये भी हमारे murine मॉडल, 5,6 में allergen चुनौती का प्रमुख प्रभाव और हम उन्हें मापने के लिए तकनीक का वर्णन है और इस प्रकार प्रयोगात्मक हेरफेर के प्रभाव का मूल्यांकन. विशेष रूप से, हम दोनों की airway hyperresponsiveness को मापने के रूप में के रूप में अच्छी तरह से वायुमार्ग और फेफड़ों में सूजन कोशिकाओं की घुसपैठ का आकलन करने के लिए तरीकों के लिए 7 आक्रामक और गैर इनवेसिव 8 तकनीक का वर्णन. Airway सूजन कोशिकाओं ब्रोन्कोएल्वियोलर पानी से धोना द्वारा एकत्र कर रहे हैं जबकि फेफड़ों के ऊतकविकृतिविज्ञानी अंग भर में सूजन के मार्कर का आकलन करने के लिए प्रयोग किया जाता है. इनतकनीक तरीके कि मानव में संभव नहीं होगा में अस्थमा के अध्ययन के लिए शक्तिशाली उपकरण प्रदान करते हैं.

Watch this Scientific Journal Video about Murine Model of Allergen Induced Asthma at JoVE.com

Murine Model of Allergen Induced Asthma

एलर्जी अस्थमा के प्रयोगात्मक माउस मॉडल रोग रोगजनन का अध्ययन करने और नई चिकित्सा विज्ञान के विकास के लिए नई संभावनाओं की पेशकश करते हैं. इन मॉडलों को अच्छी तरह से मापने एलर्जी प्रतिरक्षा प्रतिक्रिया, airway सूजन, और फेफड़े के pathophysiology शासी कारक के लिए अनुकूल हैं.

Allergen प्रेरित अस्थमा की murine मॉडल

Asthma is a major cause of morbidity and mortality, affecting some 300 million people throughout the world.1 More than 8% of the US population has asthma, ...

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Murine Model of CD40-activation of B cells

Research on B cells has shown that CD40 activation improves their antigen presentation capacity. When stimulated with interleukin-4 and CD40 ligand (CD40L), human B cells can be expanded without difficulties from small amounts of peripheral blood within 14 days to very large amounts of highly-pure CD40-B cells (&gt;109 cells per patient) from healthy donors as well as cancer patients1-4. CD40-B cells express important lymph node homing molecules and can attract T cells in vitro5. Furthermore they efficiently take up, process and present antigens to T cells6,7. CD40-B cells were shown to not only prime na&iacute;ve, but also expand memory T cells8,9. Therefore CD40-activated B cells (CD40-B cells) have been studied as an alternative source of immuno-stimulatory antigen-presenting cells (APC) for cell-based immunotherapy1,5,10. In order to further study whether CD40-B cells induce effective T cell responses in vivo and to study the underlying mechanism we established a cell culture system for the generation of murine CD40-activated B cells. Using splenocytes or purified B cells from C57BL/6 mice for CD40-activation, optimal conditions were identified as follows: Starting from splenocytes of C57BL/6 mice (haplotype H-2b) lymphocytes are purified by density gradient centrifugation and co-cultured with HeLa cells expressing recombinant murine CD40 ligand (tmuCD40L HeLa)11. Cells are recultured every 3-4 days and key components such as CD40L, interleukin-4, -Mercaptoethanol and cyclosporin A are replenished. In this protocol we demonstrate how to obtain fully activated murine CD40-B cells (mCD40B) with similar APC-phenotype to human CD40-B cells (Fig 1a,b). CD40-stimulation leads to a rapid outgrowth and expansion of highly pure (&gt;90%) CD19+ B cells within 14 days of cell culture (Fig 1c,d). To avoid contamination with non-transfected cells, expression of the murine CD40 ligand on the transfectants has to be controlled regularly (Fig 2). Murine CD40-activated B cells can be used to study B-cell activation and differentiation as well as to investigate their potential to function as APC in vitro and in vivo. Moreover, they represent a promising tool for establishing therapeutic or preventive vaccination against tumors and will help to answer questions regarding safety and immunogenicity of this approach12.

In this video, we demonstrate the procedure of CD40-activation and expansion of murine B cells from splenocytes of C57BL/6 mice, which can be used as a model antigen-presenting cell (APC) to study induction of immunity.

बी कोशिकाओं की CD40 सक्रियण के murine मॉडल

Research on B cells has shown that CD40 activation improves their antigen presentation capacity. When stimulated with interleukin-4 and CD40 ligand ...

Pseudomonas aeruginosa Induced Lung Injury Model

In order to study human acute lung injury and pneumonia, it is important to develop animal models to mimic various pathological features of this disease. Here we have developed a mouse lung injury model by intra-tracheal injection of bacteria Pseudomonas aeruginosa (P. aeruginosa or PA). Using this model, we were able to show lung inflammation at the early phase of injury. In addition, alveolar epithelial barrier leakiness was observed by analyzing bronchoalveolar lavage (BAL); and alveolar cell death was observed by Tunel assay using tissue prepared from injured lungs. At a later phase following injury, we observed cell proliferation required for the repair process. The injury was resolved 7 days from the initiation of P. aeruginosa injection. This model mimics the sequential course of lung inflammation, injury and repair during pneumonia. This clinically relevant animal model is suitable for studying pathology, mechanism of repair, following acute lung injury, and also can be used to test potential therapeutic agents for this disease.

Pseudomonas aeruginosa Induced Lung Injury Model

We have developed a mouse lung injury model by intra-tracheal injection of bacteria Pseudomonas aeruginosa. This model mimics lung injury during pneumonia and is clinically relevant.

Pseudomonas aeruginosa प्रेरित फेफड़ों की चोट मॉडल

In order to study human acute lung injury and pneumonia, it is important to develop animal models to mimic various pathological features of this disease. ...

A Murine Model of Group B Streptococcus Vaginal Colonization

Streptococcus agalactiae (group B Streptococcus, GBS), is a Gram-positive, asymptomatic colonizer of the human gastrointestinal tract and vaginal tract of 10 - 30% of adults. In immune-compromised individuals, including neonates, pregnant women, and the elderly, GBS may switch to an invasive pathogen causing sepsis, arthritis, pneumonia, and meningitis. Because GBS is a leading bacterial pathogen of neonates, current prophylaxis is comprised of late gestation screening for GBS vaginal colonization and subsequent peripartum antibiotic treatment of GBS-positive mothers. Heavy GBS vaginal burden is a risk factor for both neonatal disease and colonization. Unfortunately, little is known about the host and bacterial factors that promote or permit GBS vaginal colonization. This protocol describes a technique for establishing persistent GBS vaginal colonization using a single &#946;-estradiol pre-treatment and daily sampling to determine bacterial load. It further details methods to administer additional therapies or reagents of interest and to collect vaginal lavage fluid and reproductive tract tissues. This mouse model will further the understanding of the GBS-host interaction within the vaginal environment, which will lead to potential therapeutic targets to control maternal vaginal colonization during pregnancy and to prevent transmission to the vulnerable newborn. It will also be of interest to increase our understanding of general bacterial-host interactions in the female vaginal tract.

A Murine Model of Group B Streptococcus Vaginal Colonization

The purpose of this protocol is to imitate human group B Streptococcus (GBS) vaginal colonization in a murine model. This method may be used to investigate host immune responses and bacterial factors contributing to GBS vaginal persistence, as well as to test therapeutic strategies.

ग्रुप &#39;बी&#39; के एक murine मॉडल<em&gt; स्ट्रेप्टोकोकस</em&gt; योनि औपनिवेशीकरण

Streptococcus agalactiae (group B Streptococcus, GBS), is a Gram-positive, asymptomatic colonizer of the human gastrointestinal tract and vaginal tract of ...

Flow Cytometric Analysis of Particle-bound Bet v 1 Allergen in PM10

Flow cytometry is a method widely used to quantify suspended solids such as cells or bacteria in a size range from 0.5 to several tens of micrometers in diameter. In addition to a characterization of forward and sideward scatter properties, it enables the use of fluorescent labeled markers like antibodies to detect respective structures. Using indirect antibody staining, flow cytometry is employed here to quantify birch pollen allergen (precisely Bet v 1)-loaded particles of 0.5 to 10 &#181;m in diameter in inhalable particulate matter (PM10, particle size &#8804;10 &#181;m in diameter). PM10 particles may act as carriers of adsorbed allergens possibly transporting them to the lower respiratory tract, where they could trigger allergic reactions.
So far the allergen content of PM10 has been studied by means of enzyme linked immunosorbent assays (ELISAs) and scanning electron microscopy. ELISA measures the dissolved and not the particle-bound allergen. Compared to scanning electron microscopy, which can visualize allergen-loaded particles, flow cytometry may additionally quantify them. As allergen content of ambient air can deviate from birch pollen count, allergic symptoms might perhaps correlate better with allergen exposure than with pollen count. In conjunction with clinical data, the presented method offers the opportunity to test in future experiments whether allergic reactions to birch pollen antigens are associated with the Bet v 1 allergen content of PM10 particles &#62;0.5 &#181;m.

Here, we present a protocol to quantify allergen-loaded particles by flow cytometry. Ambient particulate matter particles may act as carriers of adsorbed allergens. We show here that flow cytometry, a method widely used to characterize suspended solids &#62;0.5 &#181;m in diameter, can be used to measure these allergen-loaded particles.

कण-बाउंड बेट वी PM10 में 1 allergen के प्रवाह cytometric विश्लेषण

Flow cytometry is a method widely used to quantify suspended solids such as cells or bacteria in a size range from 0.5 to several tens of micrometers in ...

Small RNA Transfection in Primary Human Th17 Cells by Next Generation Electroporation

CD4+ T cells can differentiate into several subsets of effector T helper cells depending on the surrounding cytokine milieu. Th17 cells can be generated from na&#239;ve CD4+ T cells in vitro by activating them in the presence of the polarizing cytokines IL-1&#946;, IL-6, IL-23, and TGF&#946;. Th17 cells orchestrate immunity against extracellular bacteria and fungi, but their aberrant activity has also been associated with several autoimmune and inflammatory diseases. Th17 cells are identified by the chemokine receptor CCR6 and defined by their master transcription factor, ROR&#947;t, and characteristic effector cytokine, IL-17A. Optimized culture conditions for Th17 cell differentiation facilitate mechanistic studies of human T cell biology in a controlled environment. They also provide a setting for studying the importance of specific genes and gene expression programs through RNA interference or the introduction of microRNA (miRNA) mimics or inhibitors. This protocol provides an easy to use, reproducible, and highly efficient method for transient transfection of differentiating primary human Th17 cells with small RNAs using a next generation electroporation device.

Next generation electroporation is an efficient method for transfecting human Th17 cells with small RNAs to alter gene expression and cell behavior.

अगली पीढ़ी Electroporation द्वारा प्राथमिक मानव Th17 कोशिकाओं में छोटे आरएनए अभिकर्मक

CD4+ T cells can differentiate into several subsets of effector T helper cells depending on the surrounding cytokine milieu. Th17 cells can be generated ...

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels

This protocol describes noninvasive sampling of undisturbed upper airway mucosal lining fluid. It also details the extraction procedure used prior to the analysis of immune mediators in fluid eluates for the study of the airway topical immune signature, without the need for stimulation procedures (often used by other techniques). The mucosal lining fluid is sampled on a strip of filter paper placed at the anterior part of the inferior turbinate and left for 2 min of absorption. Analytes are eluted from the filter papers, and the extracted protein-based eluates are analyzed by an electrochemiluminescence-based immunoassay, allowing for the high-sensitivity quantification of low- and high-level analytes in the same sample. We measured the in vivo levels of 20 preselected immune mediators related to specific immune signaling pathways in the upper airway mucosa, but the technique is not limited to that specific panel or sampling site. The technique was first implemented in 7-year-old children from the Copenhagen Prospective Studies on Asthma in Childhood2000 (COPSAC2000) cohort with allergic rhinitis. It was thereafter used in the longitudinal COPSAC2010 birth cohort, sampled at 1 month, 2 years, and 6 years of age and at instances of acute respiratory symptoms. We successfully obtained and analyzed samples from 620 (89%) of 700 1-month-old children; a few samples were below the assay detection limit (reported as the median (Inter-Quartile Range (IQR)). The number of samples below the detection limit (i.e.&#160;from 0 to the set point for the lower limit of detection) for each mediator was 29 (7.25 - 119.5). This technique enables the quantification of the in vivo airway mucosal immune profile from birth, can be applied longitudinally, and can be applied to studies on the effect of genetics and early-life environmental exposures, pathophysiology, endotyping, and monitoring of respiratory diseases, and development and evaluation of novel therapeutics.

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels

This protocol describes a noninvasive technique for the sampling of undisturbed mucosal lining fluid from the upper airways. It can be used to perform the quantification of in vivo levels of protein mediators, such as cytokines and chemokines, in subjects of all ages.

Vivo में ऊपरी Airway प्रतिरक्षा-मध्यस्थ स्तर की मात्रा का ठहराव के लिए Mucosal अस्तर द्रव का noninvasive नमूना

This protocol describes noninvasive sampling of undisturbed upper airway mucosal lining fluid. It also details the extraction procedure used prior to the ...

Analysis of Shear Flow-induced Migration of Murine Marginal Zone B Cells In Vitro

Marginal zone B cells (MZBs) are a population of B cells that reside in the mouse splenic marginal zones that envelop follicles. To reach the follicles, MZBs must migrate up the shear force of blood flow. We present here a method for analyzing this flow-induced MZB migration in vitro. First, MZBs are isolated from the mouse spleen. Second, MZBs are settled on integrin ligands in flow chamber slides, exposed to shear flow, and imaged under a microscope while migrating. Third, images of the migrating MZBs are processed using the MTrack2 automatic cell tracking plugin for ImageJ, and the resulting cell tracks are quantified using the Ibidi chemotaxis tool. The migration data reveal how fast the cells move, how often they change direction, whether the shear flow vector affects their migration direction, and which integrin ligands are involved. Although we use MZBs, the method can easily be adapted for analyzing migration of any leukocyte that responds to the force of shear flow.

Marginal zone B cells (MZBs) respond to the force of shear flow by re-orienting their migration path up the flow. This protocol shows how to record and analyze the migration using a fluidics unit, pump, microscope imaging system, and free software.

Murine सीमांत क्षेत्र बी कोशिकाओं के कतरनी प्रवाह प्रेरित प्रवासन का विश्लेषण इन विट्रो में

Marginal zone B cells (MZBs) are a population of B cells that reside in the mouse splenic marginal zones that envelop follicles. To reach the follicles, ...

A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease

Dengue virus (DENV), an arthropod-borne virus transmitted by mosquitoes, may cause the severe disease known as dengue hemorrhagic fever, which is characterized by lethal complications due to plasma leakage, ascites, pleural effusion, respiratory distress, severe bleeding, and organ impairment. A few cases of DENV infection present neurological manifestations; however, studies have not explored DENV-induced neuropathogenesis further. In this study, we present a protocol to use an immunocompetent outbred ICR (Institute of Cancer Research) mouse for investigating the induction of central nervous system (CNS) infection with DENV, followed by the progression of acute viral encephalitis-like disease.

Here, we present a protocol for creating an immunocompetent ICR (Institute of Cancer Research) murine model of central nervous system infection to display the development of neuropathy. Monitoring acute viral encephalitic disorders by identical disease scores could be performed for showing dengue virus-induced neuropathy in vivo.

डेंगू वायरस प्रेरित तीव्र वायरल एन्सेफेलाइटिस जैसी बीमारी का एक Murine मॉडल

Dengue virus (DENV), an arthropod-borne virus transmitted by mosquitoes, may cause the severe disease known as dengue hemorrhagic fever, which is ...

Robust Ligature-Induced Model of Murine Periodontitis for the Evaluation of Oral Neutrophils

The main advantages of studying the pathophysiology of periodontal disease utilizing murine models are the reduced cost of animals, array of genetically modified strains, the vast number of analyses that can be performed on harvested soft and hard tissues. However, many of these systems are subject to procedural criticisms. As an alternative, the ligature-induced model of periodontal disease, driven by the localized development and retention of a dysbiotic oral microbiome, can be employed, which is rapidly induced and relatively reliable. Unfortunately, the variants of ligature-induced murine periodontitis protocol are isolated to focal regions of the periodontium and subject to premature avulsion of the installed ligature. This minimizes the amount of tissue available for subsequent analyses and increases the number of animals required for study. This protocol describes the precise manipulations required to place extended molar ligatures with improved retention and usage of a novel rinse technique to recover oral neutrophils in mice with an alternative approach that mitigates the aforementioned technical challenges.

This article presents a protocol for establishing a ligature-induced model of murine periodontitis involving multiple maxillary molars, resulting in larger areas of the involved gingival tissue and bone for subsequent analysis as well as reduced animal usage. A technique to assess oral neutrophils in a manner analogous to human subjects is also described.

ओरल न्यूट्रोफिल्स के मूल्यांकन के लिए मोनी पेरिन पीरियोडोंटाइटिस का मजबूत लिगेचर-प्रेरित मॉडल

The main advantages of studying the pathophysiology of periodontal disease utilizing murine models are the reduced cost of animals, array of genetically ...

Systematic Scoring Analysis for Intestinal Inflammation in a Murine Dextran Sodium Sulfate-Induced Colitis Model

Murine colitis models are tools that are extensively employed in studies focused on understanding the pathobiology of inflammatory intestinal disorders. However, robust standards for objective and reproducible quantification of disease severity remain to be defined. Most colitis analysis methods rely on limited histological scoring of small segments of intestine, leading to partial or biased analyses. Here, we combine high-resolution image acquisition and longitudinal analysis of the entire colon to quantify intestinal injury and ulceration in the dextran sodium sulfate (DSS) induced model of murine colitis. This protocol allows for the generation of objective and reproducible results without extensive user training. Here, we provide comprehensive details on sample preparation and image analysis using examples of data from DSS induced colitis. This method can be easily adapted to other models of murine colitis that have significant inflammation associated with mucosal injury. We demonstrate that the fraction of inflamed/injured and eroded/ulcerated mucosa relative to the complete length of the colon closely parallels clinical findings such as weight loss amid DSS-induced disease progression. This histological protocol provides a reliable time and cost-effective aid to standardize analyses of disease activity in an unbiased way in DSS colitis experiments.

Systematic scoring of intestinal inflammation using a free computer-assisted system is a powerful tool to quantitatively compare histopathological changes in colitis models characterized by the presence of ulcers and inflammatory changes. Histological colitis score evaluation strengthens clinical observations and facilitates data interpretation.

एक मुरीन डेक्सट्रान सोडियम सल्फेट-प्रेरित कोलाइटिस मॉडल में आंतों की सूजन के लिए व्यवस्थित स्कोरिंग विश्लेषण

Murine colitis models are tools that are extensively employed in studies focused on understanding the pathobiology of inflammatory intestinal disorders. ...