ويتم تمويل هذا العمل من قبل برنامج محقق بحوث الشباب، من مركز أبحاث الأمراض المعدية (ZINF) من جامعة فورتسبورغ. C-خوان غارسيا بيتانكور، وهو زميل الدكتوراه من كلية الدراسات العليا في علوم الحياة (GSLS) من جامعة فورتسبورغ.

<ol>
	<li>Costerton, J. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Overview+of+microbial+biofilms.">Overview of microbial biofilms.</a> J. Ind. Microbiol. 15, 137-140 (1995).</li><li>Davey, M. E., O'Toole, G. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microbial+biofilms:+from+ecology+to+molecular+genetics.">Microbial biofilms: from ecology to molecular genetics.</a> Microbiol. Mol. Biol. Rev. 64, 847-867 (2000).</li><li>Kolenbrander, P. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Oral+microbial+communities:+biofilms,+interactions,+and+genetic+systems.">Oral microbial communities: biofilms, interactions, and genetic systems.</a> Annu. Rev. 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Bacteriol. 188, 3099-3109 (2006).</li><li>Vlamakis, H., Aguilar, C., Losick, R., Kolter, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Control+of+cell+fate+by+the+formation+of+an+architecturally+complex+bacterial+community.">Control of cell fate by the formation of an architecturally complex bacterial community.</a> Genes Dev. 22, 945-953 (2008).</li><li>Stewart, P. S., Franklin, M. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Physiological+heterogeneity+in+biofilms.">Physiological heterogeneity in biofilms.</a> Nat. Rev. Microbiol. 6, 199-210 (2008).</li><li>Veening, J. W., Smits, W. K., Kuipers, O. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Bistability,+epigenetics,+and+bet-hedging+in+bacteria.">Bistability, epigenetics, and bet-hedging in bacteria.</a> Annu. Rev. Microbiol. 62, 193-210 (2008).</li><li>Aguilar, C., Vlamakis, H., Guzman, A., Losick, R., Kolter, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=KinD+is+a+checkpoint+protein+linking+spore+formation+to+extracellular-matrix+production+in+Bacillus+subtilis+biofilms.">KinD is a checkpoint protein linking spore formation to extracellular-matrix production in Bacillus subtilis biofilms.</a> MBio. 1, (2010).</li><li>Lopez, D., Fischbach, M. A., Chu, F., Losick, R., Kolter, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Structurally+diverse+natural+products+that+cause+potassium+leakage+trigger+multicellularity+in+Bacillus+subtilis.">Structurally diverse natural products that cause potassium leakage trigger multicellularity in Bacillus subtilis.</a> Proc. Natl. Acad. Sci. U.S.A. 106, 280-285 (2009).</li><li>Lopez, D., Vlamakis, H., Losick, R., Kolter, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cannibalism+enhances+biofilm+development+in+Bacillus+subtilis.">Cannibalism enhances biofilm development in Bacillus subtilis.</a> Mol. Microbiol. 74, 609-618 (2009).</li><li>Arima, K., Kakinuma, A., Tamura, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Surfactin,+a+crystalline+peptidelipid+surfactant+produced+by+Bacillus+subtilis:+isolation,+characterization+and+its+inhibition+of+fibrin+clot+formation.">Surfactin, a crystalline peptidelipid surfactant produced by Bacillus subtilis: isolation, characterization and its inhibition of fibrin clot formation.</a> Biochem. Biophys. Res. Commun. 31, 488-494 (1968).</li><li>Romero, D., Vlamakis, H., Losick, R., Kolter, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+accessory+protein+required+for+anchoring+and+assembly+of+amyloid+fibres+in+B.+subtilis+biofilms.">An accessory protein required for anchoring and assembly of amyloid fibres in B. subtilis biofilms.</a> Mol. Microbiol. 80, 1155-1168 (2011).</li><li>Hardwood, C. R., Cutting, S. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Molecular Biological Methods for Bacillus. , (1990).</li><li>Novick, R. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Genetic+systems+in+staphylococci.">Genetic systems in staphylococci.</a> Methods Enzymol. 204, 587-636 (1991).</li><li>Yasbin, R. E., Young, F. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transduction+in+Bacillus+subtilis+by+bacteriophage+SPP1.">Transduction in Bacillus subtilis by bacteriophage SPP1.</a> J. Virol. 14, 1343-1348 (1974).</li><li>Branda, S. S., Gonzalez-Pastor, J. E., Ben-Yehuda, S., Losick, R., Kolter, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fruiting+body+formation+by+Bacillus+subtilis.">Fruiting body formation by Bacillus subtilis.</a> Proc. Natl. Acad. Sci. U.S.A. 98, 11621-11626 (2001).</li><li>Nakano, 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=srfA+is+an+operon+required+for+surfactin+production,+competence+development,+and+efficient+sporulation+in+Bacillus+subtilis.">srfA is an operon required for surfactin production, competence development, and efficient sporulation in Bacillus subtilis.</a> J. Bacteriol. 173, 1770-1778 (1991).</li><li>Gonzalez-Pastor, J. E., Hobbs, E. C., Losick, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cannibalism+by+sporulating+bacteria.">Cannibalism by sporulating bacteria.</a> Science. 301, 510-513 (2003).</li><li>Aguilar, C., Vlamakis, H., Losick, R., Kolter, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Thinking+about+Bacillus+subtilis+as+a+multicellular+organism.">Thinking about Bacillus subtilis as a multicellular organism.</a> Curr. Opin. Microbiol. 10, 638-643 (2007).</li><li>Shapiro, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Thinking+about+bacterial+populations+as+multicellular+organisms.">Thinking about bacterial populations as multicellular organisms.</a> Annu. Rev. Microbiol. 52, 81-104 (1998).</li></ol>

ليس لدينا ما يكشف.

حقيقة أن المجتمعات البكتيرية تظهر مجموعات سكانية فرعية من الخلايا معربا عن مجموعة محددة من الأدلة الجينات تعقيد المجتمعات الميكروبية 33،34. يجب أن هذا البروتوكول يساعد على تحديد ما إذا كان يقتصر على التعبير عن أي الجينات التي تهم جزء من السكان خاصة من خلايا متخص...

<table border="1" style=";text-align:right;direction:rtl"><tbody><tr><td> تقنية </td><td> اسم كاشف </td><td> شركة </td><td> فهرس العدد </td></tr><tr><td rowspan="11"> MSgg التكوين </td><td> فوسفات البوتاسيوم 5mM </td><td> روث </td><td> 6878 </td></tr><tr><td> 100mM اجتماعات الأطراف </td><td> سيغما الدريخ </td><td> M1254 </td></tr><tr><td> المغنيسيوم كلوريد 2MM </td><td> روث </td><td> 2189.1 </td></tr><tr><td> 700μM كلوريد الكالسيوم </td><td> روث </td><td> A119.1 </td></tr><tr><td> 50μM كلوريد الحديديك </td><td> سيغما الدريخ </td><td> 157740 </td></tr><tr><td> الزنك كلوريد 1μM </td><td> Applichem </td><td> A2076 </td></tr><tr><td> الثيامين 2μM </td><td> سيغما الدريخ </td><td> 74625 </td></tr><tr><td> الجلسرين بنسبة 0.5٪ </td><td> روث </td><td> 7533 </td></tr><tr><td> Glutaلم 0.5٪ </td><td> سيغما الدريخ </td><td> 49621 </td></tr><tr><td> التربتوفان 50μg/ml </td><td> سيغما الدريخ </td><td> T0254 </td></tr><tr><td> فينيلالاناين 50μg/ml </td><td> سيغما الدريخ </td><td> P2126 </td></tr><tr><td> خلية تثبيت </td><td> بارافورمالدهيد </td><td> روث </td><td> 0335 </td></tr><tr><td></td><td> اسم المعدات </td><td> شركة </td><td> فهرس العدد </td></tr><tr><td> صوتنة </td><td> خلية Sonicator </td><td> Bandelin </td><td> D-1000 </td></tr><tr><td> مضان المجهر </td><td> مضان المجهر </td><td> لايكا </td><td> DMI6000B </td></tr><tr><td></td><td> اسم البرنامج </td><td> شركة </td><td> فهرس العدد </td></tr><tr><td> مضان المجهر </td> &lt;TD&gt; عساف </td><td> لايكا </td><td></td></tr><tr><td> تدفق الخلوي </td><td> FCASDiva </td><td> دينار بحريني </td><td></td></tr><tr><td> تدفق الخلوي </td><td> FlowJo </td><td> Treestar </td><td></td></tr></tbody></table>

single-cell analysis of bacillus subtilis biofilms using fluorescence microscopy and flow cytometry

تشكيل بيوفيلم هو سمة عامة للجميع تقريبا 1-6 البكتيريا. عندما البكتيريا تشكل الأغشية الحيوية، وخلايا المغطى في المصفوفة خارج الخلية التي شكلت في معظمها من البروتينات وexopolysaccharides، من بين عوامل أخرى 7-10. المغطى المجتمع الميكروبية داخل بيوفيلم يظهر في كثير من الأحيان التمييز بين subpopulation متميزة من الخلايا المتخصصة 11-17. هذه القطعان تتعايش وغالبا ما تظهر التنظيم المكاني والزماني في بيوفيلم 18-21. تشكيل بيوفيلم في نموذج العصوية الرقيقة الحي يتطلب التفريق بين مجموعات سكانية فرعية متميزة من الخلايا المتخصصة. فيما بينها، وsubpopulation من المنتجين مصفوفة، المسؤولة عن انتاج وإفراز المصفوفة خارج الخلية من بيوفيلم أمر ضروري لتشكيل بيوفيلم 11،19. وبالتالي، التفريق بين المنتجين المصفوفة هو السمة المميزة لتشكيل بيوفيلم في B. الرقيقة. وقد استخدمنا للصحفيين فلوري لتصور وتحديد subpopulation من المنتجين مصفوفة في الأغشية الحيوية من B. 15،19،22-24 الرقيقة. بشكل ملموس، لاحظنا أن subpopulation من المنتجين مصفوفة يفرق ردا على وجود الذات المنتجة خارج الخلية إشارة surfactin 25. ومن المثير للاهتمام، ويتم إنتاج surfactin بواسطة جزء من السكان من خلايا متخصصة تختلف عن subpopulation من المنتجين مصفوفة 15. وقد فصلنا في هذا التقرير على نهج الفنية اللازمة لتصور وتحديد subpopulation من المنتجين والمنتجين surfactin مصفوفة داخل الأغشية الرقيقة من B.. للقيام بذلك، يتم إدراج صحفيين فلوري من الجينات اللازمة لإنتاج مصفوفة والإنتاج surfactin في كروموسوم من B. الرقيقة. يتم التعبير للصحفيين فقط في جزء من السكان من الخلايا المتخصصة. ثم، يمكن أن تكون القطعانرصدها باستخدام المجهر مضان والتدفق الخلوي (انظر الشكل 1). حقيقة أن مجموعات سكانية فرعية مختلفة من الخلايا المتخصصة التعايش داخل المجتمعات المتعددة الخلايا من البكتيريا يعطينا وجهة نظر مختلفة حول تنظيم التعبير الجيني في بدائيات النوى. هذا البروتوكول لا يتناول هذه الظاهرة بشكل تجريبي، ويمكن أن تتكيف بسهولة مع أي نموذج العمل الأخرى، لإلقاء الضوء على الآليات الجزيئية الكامنة وراء عدم التجانس المظهري داخل المجتمع الميكروبية.

Watch this Scientific Journal Video about Single-cell Analysis of Bacillus subtilis Biofilms Using Fluorescence Microscopy and Flow Cytometry at JoVE.com

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

وعموما الأغشية الحيوية الميكروبية التي تشكلها مجموعات سكانية فرعية متميزة من الخلايا المتخصصة. وحيد الخلية تحليل هذه القطعان يتطلب استخدام للصحفيين فلوري. نحن هنا وصف بروتوكول لتصور ورصد عدة subpopulationswithin<em&gt; ب. الرقيقة</em&gt; الأغشية الحيوية باستخدام المجهر مضان والتدفق الخلوي.

وحيد الخلية تحليل<emالعصوية الرقيقة> الأغشية الحيوية باستخدام المجهر الإسفار والتدفق الخلوي

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 ...

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Immunology and Infection

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

20.3K Views.  University of Würzburg. وعموما الأغشية الحيوية الميكروبية التي تشكلها مجموعات سكانية فرعية متميزة من الخلايا المتخصصة. وحيد الخلية تحليل هذه القطعان يتطلب استخدام للصحفيين فلوري. نحن هنا وصف بروتوكول لتصور ورصد عدة subpopulationswithin ب. الرقيقة الأغشية الحيوية باستخدام المجهر مضان ?...

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

Flow Cytometry Analysis of Immune Cells Within Murine Aortas

Atherosclerosis is a chronic inflammatory process of medium and large size vessels that is characterized by the formation of plaques consisting of foam cells, immune cells, vascular endothelial and smooth muscle cells, platelets, extracellular matrix, and a lipid-rich core with extensive necrosis and fibrosis of surrounding tissues.1 The innate and adaptive arms of the immune response are involved in the initiation, development and persistence of atherosclerosis.2, 3 There is a significant body of evidence that different subsets of the immune cells, such as macrophages, dendritic cells, T and B lymphocytes, are present within the aortas of healthy and atherosclerosis-prone mice4. Additionally, immune cells are found in the surrounding aortic adventitia which suggests an important role of this tissue in atherogenesis.2
For some time, the quantitative detection of different types of immune cells, their activation status, and the cellular composition within the aortic wall was limited by RT-PCR and immunohistochemical methods for the study of atherosclerosis. Few attempts were made to perform flow cytometry using human aortas, and a number of problems, such as a high autofluorescence, have been reported5,6. Human atherosclerotic plaques were digested with collagenase 1, and free cells were collected and stained for CD14+/CD11c+ to highlight macrophage-derived foam cells. In this study, a "mock" channel was used to avoid false-positive staining.6 Necrotic materials accumulating during the digestion process give rise in a large amount of debris that generates a high autofluorescence in aortic samples. To resolve this problem, a panel of negative and positive controls has been proposed, but only double staining could be applied in these samples. We have developed a new flow cytometry-based method7 to analyze the immune cell composition and characterize the activation, proliferation, differentiation of immune cells in healthy and atherosclerosis-prone aorta. This method allows the investigation of the immune cell composition of the aortic wall and opens possibilities to use a broad spectrum of immunological methods for investigations of immune aspects of this disease.

This paper presents a flow cytometry-based method to investigate the immune composition of aortas. The paper also illustrates an additional technique that allows examining surrounding adventitia and vessel wall separately. This method opens possibilities to perform phenotypical analyses of aortic leukocytes and apply several immunological assays for atherosclerosis studies.

تحليل التدفق الخلوي للخلايا المناعية وفي الفئران Aortas

Atherosclerosis is a chronic inflammatory process of medium and large size vessels that is characterized by the formation of plaques consisting of foam ...

Live Cell Imaging of Bacillus subtilis and Streptococcus pneumoniae using Automated Time-lapse Microscopy

During the last few years scientists became increasingly aware that average data obtained from microbial population based experiments are not representative of the behavior, status or phenotype of single cells. Due to this new insight the number of single cell studies rises continuously (for recent reviews see 1,2,3). However, many of the single cell techniques applied do not allow monitoring the development and behavior of one specific single cell in time (e.g. flow cytometry or standard microscopy).
Here, we provide a detailed description of a microscopy method used in several recent studies 4, 5, 6, 7, which allows following and recording (fluorescence of) individual bacterial cells of Bacillus subtilis and Streptococcus pneumoniae through growth and division for many generations. The resulting movies can be used to construct phylogenetic lineage trees by tracing back the history of a single cell within a population that originated from one common ancestor. This time-lapse fluorescence microscopy method cannot only be used to investigate growth, division and differentiation of individual cells, but also to analyze the effect of cell history and ancestry on specific cellular behavior. Furthermore, time-lapse microscopy is ideally suited to examine gene expression dynamics and protein localization during the bacterial cell cycle. The method explains how to prepare the bacterial cells and construct the microscope slide to enable the outgrowth of single cells into a microcolony. In short, single cells are spotted on a semi-solid surface consisting of growth medium supplemented with agarose on which they grow and divide under a fluorescence microscope within a temperature controlled environmental chamber. Images are captured at specific intervals and are later analyzed using the open source software ImageJ.

Live Cell Imaging of Bacillus subtilis and Streptococcus pneumoniae using Automated Time-lapse Microscopy

This protocol provides a step-by-step procedure to monitor single cell behavior of different bacteria in time using automated fluorescence time-lapse microscopy. Furthermore, we provide guidelines how to analyze the microscopy images.

تعيش خلية من التصوير<emالعصوية الرقيقة> و العقدية الرئوية الآلي باستخدام الميكروسكوب مرور الزمن

During the last few years scientists became increasingly aware that average data obtained from microbial population based experiments are not ...

A Simple and Rapid Protocol to Non-enzymatically Dissociate Fresh Human Tissues for the Analysis of Infiltrating Lymphocytes

The ability of malignant cells to evade the immune system, characterized by tumor escape from both innate and adaptive immune responses, is now accepted as an important hallmark of cancer. Our research on breast cancer focuses on the active role that tumor infiltrating lymphocytes play in tumor progression and patient outcome. Toward this goal, we developed a methodology for the rapid isolation of intact lymphoid cells from normal and abnormal tissues in an effort to evaluate them proximate to their native state. Homogenates prepared using a mechanical dissociator show both increased viability and cell recovery while preserving surface receptor expression compared to enzyme-digested tissues. Furthermore, enzymatic digestion of the remaining insoluble material did not recover additional CD45+ cells indicating that quantitative and qualitative measurements in the primary homogenate likely genuinely reflect infiltrating subpopulations in the tissue fragment. The lymphoid cells in these homogenates can be easily characterized using immunological (phenotype, proliferation, etc.) or molecular (DNA, RNA and/or protein) approaches. CD45+ cells can also be used for subpopulation purification, in vitro expansion or cryopreservation. An additional benefit of this approach is that the primary tissue supernatant from the homogenates can be used to characterize and compare cytokines, chemokines, immunoglobulins and antigens present in normal and malignant tissues. This protocol functions extremely well for human breast tissues and should be applicable to a wide variety of normal and abnormal tissues.

This protocol describes the rapid non-enzymatic dissociation of fresh human tissue fragments for qualitative and quantitative assessment of CD45+ cells (lymphocytes/leukocytes) present in various normal and malignant human tissues. Additionally, the supernatant obtained from the primary tissue homogenate can be collected and stored for further analysis or experimentation.

بروتوكول بسيطة وسريعة لغير إنزيمي فصل الطازجة الأنسجة البشرية لتحليل التسلل اللمفاويات

The ability of malignant cells to evade the immune system, characterized by tumor escape from both innate and adaptive immune responses, is now accepted ...

Prevention of Heat Stress Adverse Effects in Rats by Bacillus subtilis Strain

This study was designed to evaluate the protective effect of the Bacillus subtilis strain against complications related to heat stress. Thirty-two Sprague-Dawley rats were used in this study. Animals were orally treated twice a day for two days with B. subtilis BSB3 strain or PBS. The next day after the last treatment, each group was divided and two experimental groups (one treated with PBS and one treated with B. subtilis) were placed at 45 oC for 25 min. Two control groups stayed for 25 min at room temperature. All rats were euthanized and different parameters were analyzed in all groups. Adverse effects of heat stress are registered by the decrease of villi height and total mucosal thickness in the intestinal epithelium; translocation of bacteria from the lumen; increased vesiculation of erythrocytes and elevation of the lipopolysaccharides (LPS) level in the blood. The protective efficacy of treatment is evaluated by prevention of these side effects. The protocol was set up for the oral treatment of rats with bacteria for prevention of heat stress complications, but this protocol can be modified and used for other routes of administration and for analysis of different compounds.

Prevention of Heat Stress Adverse Effects in Rats by Bacillus subtilis Strain

We described a protocol for prevention of heat stress effects in rats by oral pre-treatment with beneficial bacteria. This protocol can be modified and used for various routes of administration and for analysis of different compounds.

الوقاية من الإجهاد الحراري الآثار السلبية في الجرذان التي كتبها<emالعصوية الرقيقة&gt;</em&gt; الانفعال

This study was designed to evaluate the protective effect of the Bacillus subtilis strain against complications related to heat stress. Thirty-two ...

Methodologies for Studying B. subtilis Biofilms as a Model for Characterizing Small Molecule Biofilm Inhibitors

This work assesses different methodologies to study the impact of small molecule biofilm inhibitors, such as D-amino acids, on the development and resilience of Bacillus subtilis biofilms. First, methods are presented that select for small molecule inhibitors with biofilm-specific targets in order to separate the effect of the small molecule inhibitors on planktonic growth from their effect on biofilm formation. Next, we focus on how inoculation conditions affect the sensitivity of multicellular, floating B. subtilis cultures to small molecule inhibitors. The results suggest that discrepancies in the reported effects of such inhibitors such as D-amino acids are due to inconsistent pre-culture conditions. Furthermore, a recently developed protocol is described for evaluating the contribution of small molecule treatments towards biofilm resistance to antibacterial substances. Lastly, scanning electron microscopy (SEM) techniques are presented to analyze the three-dimensional spatial arrangement of cells and their surrounding extracellular matrix in a B. subtilis biofilm. SEM facilitates insight into the three-dimensional biofilm architecture and the matrix texture. A combination of the methods described here can greatly assist the study of biofilm development in the presence and absence of biofilm inhibitors, and shed light on the mechanism of action of these inhibitors.

Methodologies for Studying B. subtilis Biofilms as a Model for Characterizing Small Molecule Biofilm Inhibitors

This study presents the development of reproducible methodologies to study biofilm inhibitors and their effects on Bacillus subtilis multicellularity.

منهجيات لدراسة<em&gt; B. الرقيقة</em&gt; الأغشية الحيوية نموذجا للتميز الصغيرة جزيء بيوفيلم المانعون

This work assesses different methodologies to study the impact of small molecule biofilm inhibitors, such as D-amino acids, on the development and ...

Fluorescence-activated Cell Sorting for Purification of Plasmacytoid Dendritic Cells from the Mouse Bone Marrow

Fluorescence-activated cell sorting (FACS) is a technique to purify specific cell populations based on phenotypes detected by flow cytometry. This method enables researchers to better understand the characteristics of a single cell population without the influence of other cells. Compared to other methods of cell enrichment, such as magnetic-activated cell sorting (MCS), FACS is more flexible and accurate for cell separation due to the ability of phenotype detection by flow cytometry. In addition, FACS is usually capable of separating multiple cell populations simultaneously, which improves the efficiency and diversity of experiments. Although FACS has some limitations, it has been broadly used to purify cells for functional studies in both in vitro and in vivo settings. Here we report a protocol using fluorescence-activated cell sorting to isolate a very rare population of immune cells, plasmacytoid dendritic cells (pDC), with high purity from the bone marrow of lupus-prone mice for in vitro functional studies of pDC.

We report a protocol using fluorescence-activated cell sorting to isolate plasmacytoid dendritic cells (pDC) with high purity from the bone marrow of lupus-prone mice for functional studies of pDC.

مضان تنشيط الفرز الخليوي لتنقية الخلايا الجذعية بلازماوية الشكل من الفأر نخاع العظم

Fluorescence-activated cell sorting (FACS) is a technique to purify specific cell populations based on phenotypes detected by flow cytometry. This method ...

Isolation and In Vitro Culture of Murine and Human Alveolar Macrophages

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

Isolation and In Vitro Culture of Murine and Human Alveolar Macrophages

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

العزلة والثقافة في المختبر من البلاعم السنخية مورين والبشرية

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

Characterization of Human Monocyte Subsets by Whole Blood Flow Cytometry Analysis

Monocytes are key contributors in various inflammatory disorders and alterations to these cells, including their subset proportions and functions, can have pathological significance. An ideal method for examining alterations to monocytes is whole blood flow cytometry as the minimal handling of samples by this method limits artifactual cell activation. However, many different approaches are taken to gate the monocyte subsets leading to inconsistent identification of the subsets between studies. Here we demonstrate a method using whole blood flow cytometry to identify and characterize human monocyte subsets (classical, intermediate, and non-classical). We outline how to prepare the blood samples for flow cytometry, gate the subsets (ensure contaminating cells have been removed), and determine monocyte subset expression of surface markers &#8212; in this example M1 and M2 markers. This protocol can be extended to other studies that require a standard gating method for assessing monocyte subset proportions and monocyte subset expression of other functional markers.

Here we present a protocol for characterizing monocyte subsets by whole blood flow cytometry. This includes outlining how to gate the subsets and assess their expression of surface markers and giving an example of the assessment of the expression of M1 (inflammatory) and M2 markers (anti-inflammatory).

وصف مجموعات فرعية الوحيدات البشرية بالدم كله يتدفق التحليل الخلوي

Monocytes are key contributors in various inflammatory disorders and alterations to these cells, including their subset proportions and functions, can ...

Quantification of Efferocytosis by Single-cell Fluorescence Microscopy

Studying the regulation of efferocytosis requires methods that are able to accurately quantify the uptake of apoptotic cells and to probe the signaling and cellular processes that control efferocytosis. This quantification can be difficult to perform as apoptotic cells are often efferocytosed piecemeal, thus necessitating methods which can accurately delineate between the efferocytosed portion of an apoptotic target versus residual unengulfed cellular fragments. The approach outlined herein utilizes dual-labeling approaches to accurately quantify the dynamics of efferocytosis and efferocytic capacity of efferocytes such as macrophages. The cytosol of the apoptotic cell is labeled with a cell-tracking dye to enable monitoring of all apoptotic cell-derived materials, while surface biotinylation of the apoptotic cell allows for differentiation between internalized and non-internalized apoptotic cell fractions. The efferocytic capacity of efferocytes is determined by taking fluorescent images of live or fixed cells and quantifying the amount of bound versus internalized targets, as differentiated by streptavidin staining. This approach offers several advantages over methods such as flow cytometry, namely the accurate delineation of non-efferocytosed versus efferocytosed apoptotic cell fractions, the ability to measure efferocytic dynamics by live-cell microscopy, and the capacity to perform studies of cellular signaling in cells expressing fluorescently-labeled transgenes. Combined, the methods outlined in this protocol serve as the basis for a flexible experimental approach that can be used to accurately quantify efferocytic activity and interrogate cellular signaling pathways active during efferocytosis.

Efferocytosis, the phagocytic removal of apoptotic cells, is required to maintain homeostasis and is facilitated by receptors and signaling pathways that allow for the recognition, engulfment, and internalization of apoptotic cells. Herein, we present a fluorescence microscopy protocol for the quantification of efferocytosis and the activity of efferocytic signaling pathways.

التحديد الكمي افيروسيتوسيس بالفحص المجهري Fluorescence خلية واحدة

Studying the regulation of efferocytosis requires methods that are able to accurately quantify the uptake of apoptotic cells and to probe the signaling ...

Preparation of Whole Bone Marrow for Mass Cytometry Analysis of Neutrophil-lineage Cells

In this article, we present a protocol that is optimized to preserve neutrophil-lineage cells in fresh BM for whole BM CyTOF analysis. We utilized a myeloid-biased 39-antibody CyTOF panel to evaluate the hematopoietic system with a focus on the neutrophil-lineage cells by using this protocol. The CyTOF result was analyzed with an open-resource dimensional reduction algorithm, viSNE, and the data was presented to demonstrate the outcome of this protocol. We have discovered new neutrophil-lineage cell populations based on this protocol. This protocol of fresh whole BM preparation may be used for 1), CyTOF analysis to discover unidentified cell populations from whole BM, 2), investigating whole BM defects for patients with blood disorders such as leukemia, 3), assisting optimization of fluorescence-activated flow cytometry protocols that utilize fresh whole BM.

Here, we present a protocol to process fresh bone marrow (BM) isolated from mouse or human for high-dimensional mass cytometry (Cytometry by Time-Of-Flight, CyTOF) analysis of neutrophil-lineage cells.

إعداد نخاع العظام كله لتحليل الكتلة الخلايا من الخلايا العدلية النسب

In this article, we present a protocol that is optimized to preserve neutrophil-lineage cells in fresh BM for whole BM CyTOF analysis. We utilized a ...

وحيد الخلية تحليل الأغشية الحيوية باستخدام المجهر الإسفار والتدفق الخلوي