The authors wish to thank Dr. Boris Reizis from the Department of Microbiology and Immunology at Columbia University for helpful discussions. We also wish to thank Dr. Margaret Bynoe, Dr. Rodman Getchell and Deequa Mahamed from the Department of Microbiology and Immunology at the College of Veterinary Medicine, Cornell University for technical assistance with flow cytometry and Lu Huang for assistance with video editing. The authors also wish to thank the members of Duhamel and Weiss laboratories for their critical review of the manuscript and video production, and Stephanie Yazinski from the Weiss laboratory for breeding and genotyping p53-/- mice. Experiments on animals were performed in accordance with the guidelines and regulations set forth by Cornell University Institutional Animal Care and Use Committee. This research was supported in part by funds provided by the US Department of Agriculture, Cooperative State Research, Education, and Extension Service, Animal Health and Disease Research Program (to G.E.D. and R.S.W.) and NIH grants R03 HD058220 and R01CA108773 (to R.S.W). The video was produced using in-house facilities by the personnel from the Duhamel &amp; Weiss laboratories.

1. تشريح الأورام <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> لتشريح الورم ، يتم وضع منشفة ورقية نظيفة أو ثنى الجراحية المتاح على لوحة التشريح ورشها مع الايثانول 70 ٪. </li><li style=";text-align:right;direction:rtl"> يصرح باستخدامها بشكل روتيني الفئران لهذا البروتوكول مع CO 2. ضع الماوس الموت الرحيم على منصة التشريح ورذاذ جانبي الحيوان مع الايثانول. يقام الماوس في مكان على منصة التشريح باستخدام دبابيس دفع أربعة أو أكثر من خلال إدراج الساقين ورشها جيدا مع الايثانول 70 ٪. </li><li style=";text-align:right;direction:rtl"> يتم قطع الجلد فوق العانة من خط الوسط الى قاعدة الرأس باستخدام مقص العقيمة ، مع تجنب عضلات الكامنة واختراق في تجاويف الجسم. </li><li style=";text-align:right;direction:rtl"> فتح التجويف البطني مع زوج جديد من مقص وملقط معقم والحرص على عدم الاضرار الأعضاء الداخلية. </li><li style=";text-align:right;direction:rtl"> فتح التجويف الصدري عن طريق تشريح وتنحرف القفص الصدري للكشف عن الورم ، دون الأوعية الدموية المدمرة. </li><li style=";text-align:right;direction:rtl"> تبقى منفصلة الورم من الأجهزة الأخرى ، ونقل قطعة حوالي 40-50 ٪ من الورم الكلي (تقريبا ما يصل الى 1.5 X 0.8 X 0.8 سم) في برنامج تلفزيوني الباردة على الجليد. </li><li style=";text-align:right;direction:rtl"> يمكن حفظ الجزء المتبقي من الورم لفحوصات أخرى ، ويمكن إجراء التشريح الكامل في هذا الوقت. </li></ol> 2. زراعة خلايا الغدد اللمفاوية <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> رذاذ الأنبوب الذي يحتوي على الورم مع تشريح الإيثانول 70 ٪ ونقلها إلى مجلس الوزراء للسلامة الأحيائية. </li><li style=";text-align:right;direction:rtl"> إضافة 10 مل من المتوسط ​​لثقافة عقيمة طبق بيتري 150 مم 2. </li><li style=";text-align:right;direction:rtl"> نقل قطعة من ورم في طبق بتري عن طريق الشفط لطيف مع ماصة. </li><li style=";text-align:right;direction:rtl"> منحنى اثنين العقيمة إبرة قياس 18 التي تواجه الجانب مشطوف بها. </li><li style=";text-align:right;direction:rtl"> فصل الورم باستخدام الإبر عازمة. </li><li style=";text-align:right;direction:rtl"> دوامة الطبق ، اضغط برفق ومكان في زاوية لجمع تعليق خلية إلى جنب ، مع تجنب القطع الكبيرة من الورم. </li><li style=";text-align:right;direction:rtl"> نضح تعليق الخلية ونقل إلى أنبوب مخروطي 50 مل مع تجنب القطع الكبيرة من الورم. </li><li style=";text-align:right;direction:rtl"> غسل لوحة مع 10 مل من متوسطة ونقل في أنبوب نفس الوقت تجنب القطع الكبيرة من الورم. </li><li style=";text-align:right;direction:rtl"> مزيج تعليق خلية مكونة من الخلايا الليمفاوية وخلايا انسجة بلطف ونقل 5 مل في دورق نسيج الثقافة T - 25 و 10 مل إلى T - 75 قارورة نسيج الثقافة. دوامة القوارير بلطف. </li><li style=";text-align:right;direction:rtl"> تعليق استخدام الخلايا المتبقية لجعل 2 و 4 و 10100 و 1000 التخفيفات أضعاف في حجم 2.5 مل النهائي (خلايا زراعة بكثافات مختلفة باستخدام عدة أنواع من السفن الثقافة يزيد من احتمال إنشاء خط T - الخلية). </li><li style=";text-align:right;direction:rtl"> الصفيحة 2.0 مل من كل تخفيف في الآبار الفردية لوحة 6 - جيدا. دوامة بلطف لوحة. </li><li style=";text-align:right;direction:rtl"> احتضان الخلايا لمدة 48 ساعة في ترطيب الاجواء 2 أكسيد الكربون في الهواء. </li></ol> 3. تغذية الخلايا الليمفاوية <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> بعد 48 ساعة من الحضانة ، إضافة 5 مل من المتوسط ​​إلى القارورة T - 25 و 10 مل من المتوسط ​​إلى القارورة T - 75 على طول الجدار مع الحد الأدنى من اضطراب في الخلايا. </li><li style=";text-align:right;direction:rtl"> إضافة 2 مل من المتوسط ​​إلى كل بئر من لوحة 6 - جيدا على طول الجدار مع الحد الأدنى من اضطراب في الخلايا. </li><li style=";text-align:right;direction:rtl"> احتضان خلايا لحاء 72 إضافية </li></ol> 4. الركض خلايا الغدد اللمفاوية <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> الأولي مرور <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> في نهاية اليوم الخامس من الحضانة ، وpassaged الخلايا في نسبة 1:1 ، مع الحفاظ على القوارير واللوحات الأصلية (الحفاظ على كثافة خلايا بتركيز حوالي مل / 3x106 خلال الممرات first يعزز النجاح في إنشاء استمرار خط الخلية). <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> للقارورة T - 25 ، ونقل 5 مل تعليق خلية في قارورة جديدة تحتوي على 5 مل من المتوسط. إضافة 5 مل من المتوسط ​​في قارورة الأصلي. </li><li style=";text-align:right;direction:rtl"> للقارورة T - 75 ، ونقل 10 مل من تعليق خلية في قارورة جديدة تحتوي على 10 مل من المتوسط. إضافة 10 مل من المتوسط ​​في قارورة الأصلي. </li><li style=";text-align:right;direction:rtl"> لوحة 6 - جيدا ، ونقل 2 مل من تعليق خلية من كل بئر في الآبار المماثلة من لوحة جديدة تحتوي على 2 مل من المتوسط ​​في كل بئر. إضافة 2 مل من المتوسط ​​في كل بئر من آبار الأصلي. </li></ol></li><li style=";text-align:right;direction:rtl"> احتضان جميع القوارير واللوحات ل72 ساعة إضافية في تجربتنا وضعت معظم خطوط الخلية من هذه إحدى الفقرات الثقافات (وجود مجاميع فضفاضة ملتصقة الخلية تعليق على خلايا انسجة المرفقة مؤشرا مبكرا على خط خلايا المنشأ). </li><li style=";text-align:right;direction:rtl"> لثقافات مع أقل أو لا تعليق خلية المجاميع ملتصقة فضفاضة ، وإطعام قوارير أو من خلال استبدال اللوحات بعناية ما يقرب من 50 ٪ من المتوسط ​​في كل ساعة 72 لتجنب إزالة الخلايا من الثقافة الأصلية ، ويتم ترك السفن ثقافة دائمة ودون عائق ما لا يقل عن 5 دقائق للسماح للخلايا الرواسب في قاع بواسطة الجاذبية قبل التطلع لطيف لطاف المتوسطة. </li></ol></li><li style=";text-align:right;direction:rtl"> الحفاظ على خطوط الخلايا المنشأ <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> وpassaged خطوط الخلايا أنشئت في قوارير جديدة والصفائح. لT - 25 و T - 75 قوارير ، إضافة 5 مل من النسخة الأصلية أوتعليق إحدى الفقرات في 5 مل من المتوسط. لمدة 6 - جيدا لوحات ، أضف 3 مل من التعليق الأصلي أو مرور خلية واحدة إلى 7 مل من المتوسط ​​في قارورة T - 25. الأعلاف والاحتفاظ الأصلي أو المرور من خلال استبدال ثقافة واحدة حجم إزالة مع مستنبت الطازجة. </li><li style=";text-align:right;direction:rtl"> أنشئ ممر خطوط الخلايا في قوارير T - 25 الجديدة. خطوط الخلية وقتا مضاعفة 18-24 ساعة. يتم الاحتفاظ بصورة روتينية الثقافات في كثافة مل / 1 - 3x106 وpassaged كل 3 أيام. إضافة الحجم المطلوب من الثقافة السابقة لمرور متوسطة جديدة لجعل ما يصل الى 10 مل. الأعلاف والإبقاء على الثقافة الأصلية. </li><li style=";text-align:right;direction:rtl"> بعد بضع فقرات ، فإن الخلايا غير ملتصقة مصيره دون دعم خلايا انسجة ملتصقة وتنفذ عددا أقل من الخلايا الملتصقة مع بعضها عبر الممر. بعد هذه النقطة ، يمكن الحفاظ على الثقافات في نسيج الثقافة غير المعالجة T - 25 قوارير. </li></ol></li></ol> 5. تجميد واستعادة خطوط خلية ورم الغدد اللمفاوية <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> يتم تجميد خطوط الخلية الطازجة في المتوسط ​​1640 RPMI تحتوي على 20 ٪ و DMSO FBS 10 ٪. </li><li style=";text-align:right;direction:rtl"> وطرد الخلايا من ثقافة قديمة في 48 ساعة T - 25 قارورة (حوالي 1.5x10 6 خلية / مل) في 1500 دورة في الدقيقة لمدة 5 دقائق في درجة حرارة الغرفة. بعد التخلص من طاف ، هي الخلايا إعادة علقت في 2 مل من المتوسط ​​تجميد الباردة. يتم وضع اثنين من 1.0 مل من حجم الخلية تعليق من كل قارورة في قنينات تجميد وتجميدها على الفور عند -80 درجة مئوية ، ونقل إلى النيتروجين السائل في اليوم التالي. </li><li style=";text-align:right;direction:rtl"> وتسترد الخلايا من تخزين النيتروجين السائل بواسطة ذوبان سريع ، وإعادة التعليق على محتويات في 10 مل من المتوسط ​​ثقافة جديدة. بدلا من ذلك ، يتم غسل الخلايا إذابة طازجة مرة واحدة في مستنبت دافئ لإزالة DMSO قبل إعادة التعليق في 10 مل من المتوسط ​​ثقافة جديدة. يتم استزراع الخلايا على الأقل قبل مرور 72 ساعة لاحقة. </li></ol> 6. ممثل النتائج جهاز الصراف الآلي -- / -- تي خلية الخط تطويرها باستخدام هذا البروتوكول ، وعينت DWJ - ATM - 1 تميزت تلطيخ المضادة للCD3 - FITC ، APC - المضادة والمعادية للCD4 CD8 PE وتحليل تدفق الخلوي (Figure1). وكان أكثر من 90 ٪ من الخلايا T - CD3 ، CD4 و CD8 الثلاثي إيجابية. <img src="/files/ftp_upload/2598/2598fig1.jpg" alt="الشكل 1" /> الشكل 1. توصيف خط تي خلية تم تطويرها باستخدام هذا البروتوكول. علامات سطح الخلية من جهاز الصراف الآلي المنشأة -- / -- خط الخلية المعينة تميزت DWJ - ATM - 1 بواسطة تلطيخ المضادة للCD3 - FITC ومعاداة CD4 - APC ، ومكافحة CD8 - PE وتدفق تحليل الخلوي. لفترة وجيزة ، تم غسلها 1X10 6 خلايا جديدة مرة واحدة في برنامج تلفزيوني الباردة (1500 دورة في الدقيقة / 5 دقائق) ، وحضنت في 4 درجات مئوية لمدة 10 دقيقة مع 200 ميكرولتر من الكوكتيل الأضداد (الأجسام المضادة في كل 1:200 التخفيف في برنامج تلفزيوني مع جيش صرب البوسنة 1 ٪. يمكن فحص الخلايا على الفور في حين تعد الخلايا الثابتة طازجة أو ثابتة لتحليلها لاحقا. بواسطة الفورمالين محايدة مضيفا مخزنة في نهائي تركيز 4 ٪ (المجلد / المجلد) وحضنت في 4 درجة مئوية لمدة 30 دقيقة ، تحصد بواسطة الطرد المركزي (1500 دورة في الدقيقة / 5 دقائق) ومعلق في 200 ميليلتر من برنامج تلفزيوني مع جيش صرب البوسنة 1 ٪. تم تحليل ما مجموعه 1 4 10 X الخلايا باستخدام FACS Calibur دينار بحريني ومحلل البرمجيات CellQuest دينار بحريني (العلوم البيولوجية ، وسان خوسيه ، كاليفورنيا).

<ol>
	<li>Barlow, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Atm-deficient+mice:+a+paradigm+of+ataxia+telangiectasia.">Atm-deficient mice: a paradigm of ataxia telangiectasia.</a> Cell. 86, 159-171 (1996).</li><li>Elson, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Pleiotropic+defects+in+ataxia-telangiectasia+protein-deficient+mice.">Pleiotropic defects in ataxia-telangiectasia protein-deficient mice.</a> Proc Natl Acad Sci U S A. 93, 13084-13089 (1996).</li><li>Kuang, X. <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+Atm-/-+thymic+lymphoma+cell+proliferation+in+vitro+and+in+vivo+by+dexamethasone.">Control of Atm-/- thymic lymphoma cell proliferation in vitro and in vivo by dexamethasone.</a> Cancer Chemother Pharmacol. 55, 203-212 (2005).</li><li>Browne, S. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Treatment+with+a+catalytic+antioxidant+corrects+the+neurobehavioral+defect+in+ataxia-telangiectasia+mice.">Treatment with a catalytic antioxidant corrects the neurobehavioral defect in ataxia-telangiectasia mice.</a> Free Radic Biol Med. 36, 938-942 (2004).</li><li>Jacks, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tumor+spectrum+analysis+in+p53-mutant+mice.">Tumor spectrum analysis in p53-mutant mice.</a> Curr Biol. 4, 1-7 (1994).</li><li>Chervinsky, D. S., Lam, D. H., Zhao, X. F., Melman, M. P., Aplan, P. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Development+and+characterization+of+T+cell+leukemia+cell+lines+established+from+SCL/LMO1+double+transgenic+mice.">Development and characterization of T cell leukemia cell lines established from SCL/LMO1 double transgenic mice.</a> Leukemia. 15, 141-147 (2001).</li><li>Sharma, V. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Notch1+contributes+to+mouse+T-cell+leukemia+by+directly+inducing+the+expression+of+c-myc.">Notch1 contributes to mouse T-cell leukemia by directly inducing the expression of c-myc.</a> Mol Cell Biol. 26, 8022-8031 (2006).</li><li>Maser, R. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chromosomally+unstable+mouse+tumours+have+genomic+alterations+similar+to+diverse+human+cancers.">Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers.</a> Nature. 447, 966-971 (2007).</li></ol>

No conflicts of interest declared.

In this protocol, we provide detailed procedures to establish murine T-cell lines from two different mouse genotypes; Atm-/- [FVB/N-Atmtm1Led/J] and p53-/- [129/S6-Trp53tm1Tyj/J]. By using this protocol, a total of 6 (out of 7 attempts) Atm-/- and three (out of 5 attempts) p53-/- murine T-cell lines have been established in our laboratory. Representative data demonstrating that cell line DWJ-Atm-1, an<e...

<ul>
<li>Ice bucket</li>
<li>70% ethanol</li>
<li>Dissection pad consisting of foam block covered with aluminum foil and pins</li>
<li>Two sets of small sterile scissors and forceps</li>
<li>Sterile 150 mm2 Petri dish (Thermo Fisher Scientific, Waltham, MA; cat. #08-757-13)</li>
<li>Sterile 18 gauge needles</li>
<li>50 mL conical tubes (Corning Inc., Corning NY; cat # 430829)</li>
<li>10% buffered formalin</li>
<li>Tissue culture flasks 
<ul>
<li>T-25 (TPP, Trasadingen, Switzerland; cat # 90025)</li>
<li>T-75 (TPP, Trasadingen, Switzerland; cat # 90075)</li>
</ul>
</li>
<li>6-well plates (Corning Inc., Corning NY; cat # 3506)</li>
<li>Sterile phosphate buffered saline pH 7.2 (PBS)</li>
<li>Culture medium 
<ul>
<li>RPMI 1640 with 25 mM HEPES, 200 mM L-glutamine (Lonza, Walkersville, MD; cat#12-115F) supplemented with the following:
<ul>
<li>10% heat inactivated (56&deg;C, 30 min) fetal bovine serum (FBS; Hyclone, Logan, UT; cat# SH30088.03)</li>
<li>1% penicillin and streptomycin (Mediatech, Manassas,VA; cat# 30-002-CI)</li>
<li>1% nonessential amino acids (Mediatech; cat#25-025-CI)</li>
<li>55 mM 2&beta;-mercaptoethanol (Sigma, St Louis, MO; cat#M752)</li>
</ul>
</li></ul>
</li>
<li>Dimethyl sulfoxide (DMSO; Calbiochem, La Jolla, CA; cat # 317275)</li>
<li>Antibodies (eBioScience, San Diego, CA)
<ul>
<li>anti-CD3-FITC (cat. #11-0031-85)</li>
<li>anti-CD4-APC (cat. #17-0041-83)</li>
<li>anti-CD8-PE (cat.#12-081-85)</li>
</ul>
</li>
<li>Bovine serum albumin (BSA; Life Technologies, Grand Island, NY; cat #. 11018-017)</li>
<li>Concanavalin A (Sigma cat# C5275)</li>
<li>1.8 mL freezing vials (Nunc, Roskilde, Denmark; cat# 368632)</li>
</ul>

derivation of thymic lymphoma t-cell lines from atm-/- and p53-/- mice

Established cell lines are a critical research tool that can reduce the use of laboratory animals in research. Certain strains of genetically modified mice, such as Atm-/- and p53-/- consistently develop thymic lymphoma early in life 1,2, and thus, can serve as a reliable source for derivation of murine T-cell lines. Here we present a detailed protocol for the development of established murine thymic lymphoma T-cell lines without the need to add interleukins as described in previous protocols 1,3. Tumors were harvested from mice aged three to six months, at the earliest indication of visible tumors based on the observation of hunched posture, labored breathing, poor grooming and wasting in a susceptible strain 1,4. We have successfully established several T-cell lines using this protocol and inbred strains ofAtm-/- [FVB/N-Atmtm1Led/J] 2 and p53-/- [129/S6-Trp53tm1Tyj/J] 5 mice. We further demonstrate that more than 90% of the established T-cell population expresses CD3, CD4 and CD8. Consistent with stably established cell lines, the T-cells generated by using the present protocol have been passaged for over a year.

Watch this Scientific Journal Video about Derivation of Thymic Lymphoma T-cell Lines from Atm-/- and p53-/- Mice at JoVE.com

Derivation of Thymic Lymphoma T-cell Lines from Atm-/- and p53-/- Mice

In this video we demonstrate a protocol to establish mouse thymic lymphoma cell lines. By following this protocol, we have successfully established several T-cell lines from Atm-/- and p53-/- mice with thymic lymphoma.

اشتقاق خطوط التوتة تي خلية سرطان الغدد الليمفاوية من أجهزة الصراف الآلي -- / --</sup و البروتين p53 -- / --</sup الفئران

Established cell lines are a critical research tool that can reduce the use of laboratory animals in research. Certain strains of genetically modified ...

derivation-of-thymic-lymphoma-t-cell-lines-from-atm-and-p53-mice

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Immunology and Infection

Derivation of Thymic Lymphoma T-cell Lines from Atm-/- and p53-/- Mice

12.2K Views.  Cornell University. In this video we demonstrate a protocol to establish mouse thymic lymphoma cell lines. By following this protocol, we have successfully established several T-cell lines from Atm-/- and p53-/- mice with thymic lymphoma.

Video: Derivation of Thymic Lymphoma T-cell Lines from Atm-/- and p53-/- Mice

Transnuclear Mice with Pre-defined T Cell Receptor Specificities Against Toxoplasma gondii Obtained Via SCNT

Lymphocytes, such as T cells, undergo genetic V(D)J recombination, to generate a receptor with a certain specificity1. Mice transgenic for a rearranged antigen-specific T cell receptor (TCR) have been an indispensable tool to study T cell development and function. However, such TCRs are usually isolated from the relevant T cells after long-term culture often following repeated antigen stimulation, which unavoidably selects for T cells with high affinity. Random genomic integration of the TCR &alpha;- and &beta;-chain and expression from non-endogenous promoters can lead to variations in expression level and kinetics.
Epigenetic reprogramming via somatic cell nuclear transfer provides a tool to generate embryonic stem cells and mice from any cell of interest. Consequently, when SCNT is applied to T cells of known specificity, these genetic V(D)J rearrangements are transferred to the SCNT-embryonic stem cells (ESCs) and the mice derived from them, while epigenetic marks are reset. We have demonstrated that T cells with pre-defined specificities against Toxoplasma gondii can be used to generate mouse models that express the specific TCR from their endogenous loci, without experimentally introduced genetic modification. The relative ease and speed with which such transnuclear models can be obtained holds promise for the construction of other disease models.

Transnuclear Mice with Pre-defined T Cell Receptor Specificities Against Toxoplasma gondii Obtained Via SCNT

We demonstrate here that epigenetic reprogramming via Somatic Cell Nuclear Transfer (SCNT) can be used as a tool to generate mouse models with pre-defined T cell receptor (TCR) specificities. These transnuclear mice express the corresponding TCR from their endogenous locus under the control of the endogenous promoter.

Transnuclear الفئران مع الخصوصيات المحددة مسبقا ضد مستقبلات الخلايا T المقوسة الغوندية الحصول عليها عن طريق SCNT

Lymphocytes, such as T cells, undergo genetic V(D)J recombination, to generate a receptor with a certain specificity1. Mice transgenic for a rearranged ...

Retroviral Transduction of T-cell Receptors in Mouse T-cells

T-cell receptors (TCRs) play a central role in the immune system. TCRs on T-cell surfaces can specifically recognize peptide antigens presented by antigen presenting cells (APCs)1. This recognition leads to the activation of T-cells and a series of functional outcomes (e.g. cytokine production, killing of the target cells). Understanding the functional role of TCRs is critical to harness the power of the immune system to treat a variety of immunology related diseases (e.g. cancer or autoimmunity).
It is convenient to study TCRs in mouse models, which can be accomplished in several ways. Making TCR transgenic mouse models is costly and time-consuming and currently there are only a limited number of them available2-4. Alternatively, mice with antigen-specific T-cells can be generated by bone marrow chimera. This method also takes several weeks and requires expertise5. Retroviral transduction of TCRs into in vitro activated mouse T-cells is a quick and relatively easy method to obtain T-cells of desired peptide-MHC specificity. Antigen-specific T-cells can be generated in one week and used in any downstream applications. Studying transduced T-cells also has direct application to human immunotherapy, as adoptive transfer of human T-cells transduced with antigen-specific TCRs is an emerging strategy for cancer treatment6.
Here we present a protocol to retrovirally transduce TCRs into in vitro activated mouse T-cells. Both human and mouse TCR genes can be used. Retroviruses carrying specific TCR genes are generated and used to infect mouse T-cells activated with anti-CD3 and anti-CD28 antibodies. After in vitro expansion, transduced T-cells are analyzed by flow cytometry.

We present a protocol to produce antigen-specific mouse T-cells using retroviral transduction

تنبيغ من فيروسات تي خلية المستقبلات في الخلايا التائية ماوس

T-cell receptors (TCRs) play a central role in the immune system. TCRs on T-cell surfaces can specifically recognize peptide antigens presented by antigen ...

Examination of Thymic Positive and Negative Selection by Flow Cytometry

A healthy immune system requires that T cells respond to foreign antigens while remaining tolerant to self-antigens. Random rearrangement of the T cell receptor (TCR) &alpha; and &beta; loci generates a T cell repertoire with vast diversity in antigen specificity, both to self and foreign. Selection of the repertoire during development in the thymus is critical for generating safe and useful T cells. Defects in thymic selection contribute to the development of autoimmune and immunodeficiency disorders1-4. 
T cell progenitors enter the thymus as double negative (DN) thymocytes that do not express CD4 or CD8 co-receptors. Expression of the &alpha;&beta;TCR and both co-receptors occurs at the double positive (DP) stage. Interaction of the &alpha;&beta;TCR with self-peptide-MHC (pMHC) presented by thymic cells determines the fate of the DP thymocyte. High affinity interactions lead to negative selection and elimination of self-reactive thymocytes. Low affinity interactions result in positive selection and development of CD4 or CD8 single positive (SP) T cells capable of recognizing foreign antigens presented by self-MHC5.
Positive selection can be studied in mice with a polyclonal (wildtype) TCR repertoire by observing the generation of mature T cells. However, they are not ideal for the study of negative selection, which involves deletion of small antigen-specific populations. Many model systems have been used to study negative selection but vary in their ability to recapitulate physiological events6. For example, in vitro stimulation of thymocytes lacks the thymic environment that is intimately involved in selection, while administration of exogenous antigen can lead to non-specific deletion of thymocytes7-9. Currently, the best tools for studying in vivo negative selection are mice that express a transgenic TCR specific for endogenous self-antigen. However, many classical TCR transgenic models are characterized by premature expression of the transgenic TCR&alpha; chain at the DN stage, resulting in premature negative selection. Our lab has developed the HYcd4 model, in which the transgenic HY TCR&alpha; is conditionally expressed at the DP stage, allowing negative selection to occur during the DP to SP transition as occurs in wildtype mice10.
Here, we describe a flow cytometry-based protocol to examine thymic positive and negative selection in the HYcd4 mouse model. While negative selection in HYcd4 mice is highly physiological, these methods can also be applied to other TCR transgenic models. We will also present general strategies for analyzing positive selection in a polyclonal repertoire applicable to any genetically manipulated mice.

We present a flow cytometry-based method to examine T cell development in vivo using genetically manipulated mice on a wildtype or T cell receptor transgenic background.

دراسة التوتة اختيار الإيجابية والسلبية من قياس التدفق الخلوي

A healthy immune system requires that T cells respond to foreign  antigens while remaining tolerant to self-antigens. Random rearrangement of the  T cell ...

Real-time Live Imaging of T-cell Signaling Complex Formation

Protection against infectious diseases is mediated by the immune system 1,2. T lymphocytes are the master coordinators of the immune system, regulating the activation and responses of multiple immune cells 3,4. T-cell activation is dependent on the recognition of specific antigens displayed by antigen presenting cells (APCs). The T-cell antigen receptor (TCR) is specific to each T-cell clone and determines antigen specificity 5. The binding of the TCR to the antigen induces the phosphorylation of components of the TCR complex. In order to promote T-cell activation, this signal must be transduced from the membrane to the cytoplasm and the nucleus, initiating various crucial responses such as recruitment of signaling proteins to the TCR;APC site (the immune synapse), their molecular activation, cytoskeletal rearrangement, elevation of intracellular calcium concentration, and changes in gene expression 6,7. The correct initiation and termination of activating signals is crucial for appropriate T-cell responses. The activity of signaling proteins is dependent on the formation and termination of protein-protein interactions, post translational modifications such as protein phosphorylation, formation of protein complexes, protein ubiquitylation and the recruitment of proteins to various cellular sites 8. Understanding the inner workings of the T-cell activation process is crucial for both immunological research and clinical applications.
Various assays have been developed in order to investigate protein-protein interactions; however, biochemical assays, such as the widely used co-immunoprecipitation method, do not allow protein location to be discerned, thus precluding the observation of valuable insights into the dynamics of cellular mechanisms. Additionally, these bulk assays usually combine proteins from many different cells that might be at different stages of the investigated cellular process. This can have a detrimental effect on temporal resolution. The use of real-time imaging of live cells allows both the spatial tracking of proteins and the ability to temporally distinguish between signaling events, thus shedding light on the dynamics of the process 9,10. We present a method of real-time imaging of signaling-complex formation during T-cell activation. Primary T-cells or T-cell lines, such as Jurkat, are transfected with plasmids encoding for proteins of interest fused to monomeric fluorescent proteins, preventing non-physiological oligomerization 11. Live T cells are dropped over a coverslip pre-coated with T-cell activating antibody 8,9, which binds to the CD3/TCR complex, inducing T-cell activation while overcoming the need for specific activating antigens. Activated cells are constantly imaged with the use of confocal microscopy. Imaging data are analyzed to yield quantitative results, such as the colocalization coefficient of the signaling proteins.

We describe a live-cell imaging method that provides insight into protein dynamics during the T-cell activation process. We demonstrate the combined usage of the T-cell spreading assay, confocal microscopy and imaging analysis to yield quantitative results to follow signaling complex formation throughout T-cell activation.

في الوقت الحقيقي تصوير لايف تي خلية اشارة تشكيل مجمع

Protection against infectious diseases is mediated by the immune system 1,2. T lymphocytes are the master coordinators of the immune system, regulating ...

Transplantation of Tail Skin to Study Allogeneic CD4 T Cell Responses in Mice

The study of T cell responses and their consequences during allo-antigen recognition requires a model that enables one to distinguish between donor and host T cells, to easily monitor the graft, and to adapt the system in order to answer different immunological questions. Medawar and colleagues established allogeneic tail-skin transplantation in mice in 1955. Since then, the skin transplantation model has been continuously modified and adapted to answer specific questions. The use of tail-skin renders this model easy to score for graft rejection, requires neither extensive preparation nor deep anesthesia, is applicable to animals of all genetic background, discourages ischemic necrosis, and permits chemical and biological intervention. 
In general, both CD4+ and CD8+ allogeneic T cells are responsible for the rejection of allografts since they recognize mismatched major histocompatibility antigens from different mouse strains. Several models have been described for activating allogeneic T cells in skin-transplanted mice. The identification of major histocompatibility complex (MHC) class I and II molecules in different mouse strains including C57BL/6 mice was an important step toward understanding and studying T cell-mediated alloresponses. In the tail-skin transplantation model described here, a three-point mutation (I-Abm12) in the antigen-presenting groove of the MHC-class II (I-Ab) molecule is sufficient to induce strong allogeneic CD4+ T cell activation in C57BL/6 mice. Skin grafts from I-Abm12 mice on C57BL/6 mice are rejected within 12-15 days, while syngeneic grafts are accepted for up to 100 days. The absence of T cells (CD3-/- and Rag2-/- mice) allows skin graft acceptance up to 100 days, which can be overcome by transferring 2 x 104 wild type or transgenic T cells. Adoptively transferred T cells proliferate and produce IFN-&#947; in I-Abm12-transplanted Rag2-/- mice.

Tail-skin transplantation is a powerful model for studying T cell-dependent rejection and tolerance induction during allogeneic immune responses in mice. The advantages of this protocol are minor invasive surgery, and ease of monitoring with no need to sacrifice the recipient mouse.

زرع الجلد الذيل لدراسة خيفي CD4 T الردود الخليوي في الفئران

The study of T cell responses and their consequences during allo-antigen recognition requires a model that enables one to distinguish between donor and ...

Derivation of T Cells In Vitro from Mouse Embryonic Stem Cells

The OP9/OP9-DL1 co-culture system has become a well-established method for deriving differentiated blood cell types from embryonic and hematopoietic progenitors of both mouse and human origin. It is now used to address a growing variety of complex genetic, cellular and molecular questions related to hematopoiesis, and is at the cutting edge of efforts to translate these basic findings to therapeutic applications. The procedures are straightforward and routinely yield robust results. However, achieving successful hematopoietic differentiation in vitro requires special attention to the details of reagent and cell culture maintenance. Furthermore, the protocol features technique sensitive steps that, while not difficult, take care and practice to master. Here we focus on the procedures for differentiation of T lymphocytes from mouse embryonic stem cells (mESC). We provide a detailed protocol with discussions of the critical steps and parameters that enable reproducibly robust cellular differentiation in vitro. It is in the interest of the field to consider wider adoption of this technology, as it has the potential to reduce animal use, lower the cost and shorten the timelines of both basic and translational experimentation.

Derivation of T Cells In Vitro from Mouse Embryonic Stem Cells

Mouse embryonic stem cells can be differentiated to T cells in vitro using the OP9-DL1 co-culture system. Success in this procedure requires careful attention to reagent/cell maintenance, and key technique sensitive steps. Here we discuss these critical parameters and provide a detailed protocol to encourage adoption of this technology.

اشتقاق خلايا T<em&gt; في المختبر</em&gt; من الفأر الجنينية الخلايا الجذعية

The OP9/OP9-DL1 co-culture system has become a well-established method for deriving differentiated blood cell types from embryonic and hematopoietic ...

Mouse Na&#239;ve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets

Antigen inexperienced (na&#239;ve) CD4+ T cells undergo expansion and differentiation to effector subsets at the time of T cell receptor (TCR) recognition of cognate antigen presented on MHC class II. The cytokine signals present in the environment at the time of TCR activation are a major factor in determining the effector fate of a na&#239;ve CD4+ T cell. Although the cytokine environment during na&#239;ve T cell activation may be complex and involve both redundant and opposing signals in vivo, the addition of various cytokine combinations during naive CD4+ T cell activation in vitro can readily promote the establishment of effector T helper lineages with hallmark cytokine and transcription factor expression. Such differentiation experiments are commonly used as a first step for the evaluation of targets believed to promote or inhibit the development of certain CD4+ T helper subsets. The addition of mediators, such as signaling agonists, antagonists, or other cytokines, during the differentiation process can also be used to study the influence of a particular target on T cell differentiation. Here, we describe a basic protocol for the isolation of na&#239;ve T cells from mouse and the subsequent steps necessary for polarizing na&#239;ve cells to various T helper effector lineages in vitro.

Mouse Na&#239;ve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets

Na&#239;ve CD4+ T cells polarize to various subsets depending on the environment at the time of activation. The differentiation of na&#239;ve CD4+ T cells to various effector subsets can be achieved in vitro through the addition of T cell receptor stimuli and specific cytokine signals.

الماوس السذاجة CD4<sup&gt; +</sup&gt; عزل T خلية و<em&gt; في المختبر</em&gt; التمايز إلى T مجموعات فرعية خلية

Antigen inexperienced (na&#239;ve) CD4+ T cells undergo expansion and differentiation to effector subsets at the time of T cell receptor (TCR) recognition ...

Retroviral Transduction of Bone Marrow Progenitor Cells to Generate T-cell Receptor Retrogenic Mice

T cell receptor (TCR) signaling is essential in the development and differentiation of T cells in the thymus and periphery, respectively. The vast array of TCRs proves studying a specific antigenic response difficult. Therefore, TCR transgenic mice were made to study positive and negative selection in the thymus as well as peripheral T cell activation, proliferation and tolerance. However, relatively few TCR transgenic mice have been generated specific to any given antigen. Thus, studies involving TCRs of varying affinities for the same antigenic peptide have been lacking. The generation of a new TCR transgenic line can take six or more months. Additionally, any specific backcrosses can take an additional six months. In order to allow faster generation and screening of multiple TCRs, a protocol for retroviral transduction of bone marrow was established with stoichiometric expression of the TCR&#945; and TCR&#946; chains and the generation of retrogenic mice. Each retrogenic mouse is essentially a founder, virtually negating a founder effect, while the length of time to generate a TCR retrogenic is cut from six months to approximately six weeks. Here we present a rapid and flexible alternative to TCR transgenic mice that can be expressed on any chosen background with any particular TCR.

We present a rapid and flexible protocol for a single T cell receptor (TCR) retroviral-based in vivo expression system. Retroviral vectors are used to transduce bone marrow progenitor cells to study T cell development and function of a single TCR in vivo as an alternative to TCR transgenic mice.

فيروسات تنبيغ من خلايا نخاع العظم السلف لتوليد خلايا T مستقبلات Retrogenic الفئران

T cell receptor (TCR) signaling is essential in the development and differentiation of T cells in the thymus and periphery, respectively.  The vast array ...

Preparation and Applications of Organotypic Thymic Slice Cultures

Thymic selection proceeds in a unique and highly organized thymic microenvironment resulting in the generation of a functional, self-tolerant T cell repertoire. In vitro models to study T lineage commitment and development have provided valuable insights into this process. However, these systems lack the complete three-dimensional thymic milieu necessary for T cell development and, therefore, are incomplete approximations of in vivo thymic selection. Some of the challenges related to modeling T cell development can be overcome by using in situ models that provide an intact thymic microenvironment that fully supports thymic selection of developing T cells. Thymic slice organotypic cultures complement existing in situ techniques. Thymic slices preserve the integrity of the thymic cortical and medullary regions and provide a platform to study development of overlaid thymocytes of a defined developmental stage or of endogenous T cells within a mature thymic microenvironment. Given the ability to generate ~20 slices per mouse, thymic slices present a unique advantage in terms of scalability for high throughput experiments. Further, the relative ease in generating thymic slices and potential to overlay different thymic subsets or other cell populations from diverse genetic backgrounds enhances the versatility of this method. Here we describe a protocol for the preparation of thymic slices, isolation and overlay of thymocytes, and dissociation of thymic slices for flow cytometric analysis. This system can also be adapted to study non-conventional T cell development as well as visualize thymocyte migration, thymocyte-stromal cell interactions, and TCR signals associated with thymic selection by two-photon microscopy.

We describe the preparation of thymic slices that, in combination with flow cytometry, can be used to model positive and negative selection of developing T cells. Thymic slices can also be adapted for the in situ analysis of thymocyte migration, localization, and signaling via immunofluorescence and two-photon microscopy.

إعداد وتطبيقات الثقافات عضوي التوتة شريحة

Thymic selection proceeds in a unique and highly organized thymic microenvironment resulting in the generation of a functional, self-tolerant T cell ...

An Efficient and Simple Method to Establish NK and T Cell Lines from Patients with Chronic Active Epstein-Barr Virus Infection

A number of methods have been described to establish NK/T cell lines from patients with lymphoma or lymphoproliferative syndrome. These methods employed feeder cells, purified NK or T cells with as much as 10 mL of blood, or a high-dose of IL-2. This study presents a new method with a powerful and simple strategy to establish NK and T cell lines by culturing the peripheral blood mononuclear cells (PBMC) with the addition of recombinant human IL-2 (rhIL-2), and uses as little as 2 mL of whole blood. The cells can proliferate quickly in two weeks and be maintained for more than 3 months. With this method, 7 NK or T cell lines have been established with a high success rate. This method is simple, reliable, and applicable to establishing cell lines from more cases of CAEBV or NK/T cell lymphoma.

A simple method for obtaining NK and T cell clones from CAEBV patients was developed with high efficiency, a small amount of peripheral blood, and a low-dose of IL-2.

طريقة فعالة وبسيطة وضع ناغورني كاراباخ وخطوط الخلايا T من المرضى المصابين بالعدوى المزمنة النشطة فيروس ابشتاين-بار

A number of methods have been described to establish NK/T cell lines from patients with lymphoma or lymphoproliferative syndrome. These methods employed ...

اشتقاق خطوط التوتة تي خلية سرطان الغدد الليمفاوية من أجهزة الصراف الآلي -- / -- و البروتين p53 -- / -- الفئران

اشتقاق خطوط التوتة تي خلية سرطان الغدد الليمفاوية من أجهزة الصراف الآلي^{-- / -- و البروتين p53^{-- / -- الفئران}}