فإن الكتاب أود أن أشكر الدكتور كلاوس Kaestner لهبة Ngn3 - الفئران الجذعية الجنينية EGFP خط الخلية ، والسيدة لوسي براون وجوهر الخلوي التحليلية للمساعدة في فرز الخلايا. وقد تم تمويل هذا العمل في جزء من المنح والمعاهد الوطنية للصحة R21DK069997 R01DK081587 ومنحت لHTK من معهد كاليفورنيا للطب التجديدي (CIRM) المنح التدريبية التي تمنح للميغاواط وLS

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ليس لدينا شيء في الكشف عنها.

واقتصرت مستعمرة المقايسات التي تسمح التقييمات الكمية والفنية للأسلاف البنكرياس الفردية حتى الآن ، مما أعاق كثيرا من التقدم في دراسات الجذعية البنكرياس والسلف بيولوجيا الخلية. جوهر مقايسة مستعمرة هو أنه يقيس القدرة الذاتية للخلايا الاصلية ، بدلا من النمط الظاهري فقط ، مما يسمح لوحظ أن وظائف وإمكانات نسب من الخلايا الاصلية. بل هو أيضا أداة الكمية التي يمكن تحديد عدد الأسلاف في عدد معين من السكان. في مجال الخلايا الجذعية المكونة للدم ، لعبت أدوارا مهمة المقايسات مستعمرة في تحديد الهوية ، فضلا عن فك رموز متطلبات عامل النمو ، والتفاعلات ، والآليات التي تحكم التزام نسب هذه الخلايا. 6 وفي مجال السلف البنكرياس بيولوجيا الخلية وجهاز البنكرياس 7 (8) ، أو الجزء الأكبر الثقافات 9-13 وقد وضعت ولكن هذه المقايسات لا تعالج questi البيولوجيةإضافات على مستوى خلية واحدة. دون تحليلات خلية واحدة ، لا يمكن وجود البنكرياس الجذعية المتعددة المحتملة / أسلاف يثبت بشكل لا لبس فيه (14). هنا نظهر أن الانسولين معربا عن تشكيل مستعمرة الأسلاف يمكن يعاير باستخدام ثلاثي الأبعاد ، والتي تحتوي على Matrigel ، ثقافة النظام شبه صلبة. على الرغم من أنه تم تطوير نظام تعليق 15،16 الثقافة الذي يسمح احد الأسلاف البنكرياس البالغين لتتكاثر وتتمايز إلى &quot;pancreatospheres&quot; ، مقايسة لدينا مستعمرة يوفر مزايا إضافية. أولا ، لدينا شبه صلبة وسائل الاعلام نظام يسمح الثقافة الطلاء لمدة تصل إلى 25،000 الخلايا فرز لكل 500 ميكرولتر الثقافة وسائل الإعلام لكل بئر - 24 مع الحفاظ على تشكيل مستعمرة مما أدى إلى مجموعة خطية. 2 وفي المقابل ، فإن مقايسة pancreatosphere تعليق يتطلب استخدام واحد طريقة ترسب الخلايا من الخلية فارز للسماح بتحليل خلية واحدة ، وبالتالي حجم أكبر من وسائل الإعلام والثقافة ، وحاضنة الفضاءمطلوبة. لذلك ، لدينا تجربة مستعمرة من السهل نسبيا وفعالة من حيث التكلفة لإجراء عندما بدأت أعداد كبيرة من خلايا مختلفة تحتاج إلى وقت واحد مقابل لأنشطة السلف. الثانية ، لدينا شبه صلبة وسائل الإعلام يسمح التوزيع الموحد لمكونات المصفوفة خارج الخلية ، وعوامل النمو ، والذي يسمح كل من انتشار الأسلحة النووية وتمايز تحدث في نفس البئر. في المقابل ، فإنه من الصعب توفير هذه البيئة ، ولا سيما مصفوفة ، إلى الخلايا في الثقافة الايقاف. نحن ندرك أنه مع اسلوبنا لا يمكن أن تثبت بشكل قاطع أن يتم اشتقاق كل مستعمرة من خلية واحدة ، كما يمكن ان اثنين من أسلاف المتمركزة بالقرب من كل مستعمرة عشوائيا الآخر والشكل. ومع ذلك ، يمكن التغلب على هذه المشكلة عن طريق تحليل ثانوي التلاعب به واحد الخلية. ويمكن مباشرة انتقاء واحد من الخلايا فرز تثبت بشكل قاطع الأصل خلية واحدة في كل مستعمرة. باختصار ، للانسولين والتعبير عن تشكيل مستعمرة نشاط المواليةوصف genitors في شبه صلبة وسائل الاعلام هنا يوفر فرصا فريدة للدراسات الميكانيكية للأسلاف البنكرياس على مستوى خلية واحدة. على سبيل المثال ، في تقرير سابق وجدنا أن إضافة Matrigel ، وهي مزيج النفط الخام من البروتينات المصفوفة خارج الخلية ، في الثقافة هو مطلوب وسائل الاعلام عن تشكيل الانسولين معربا عن مستعمرات من خلايا + Ngn3 - EGFP (2) ، مما يدل على المصفوفة خارج الخلية هو المهم بالنسبة لأولئك الأسلاف. باستخدام هذا الاختبار مستعمرة ، سيكون من الممكن الآن لمزيد من تشريح وتحديد الاحتياجات مصفوفة محددة لمثل هذا النشاط. بالإضافة إلى دراسة الأسلاف المستمدة من الخلايا الجذعية الجنينية ، ونحن حاليا بالتحقيق في ما إذا كان هذا الفحص المختبري في النظام كما يدعم تشكيل المستعمرات المميزة الأخرى المستمدة من البنكرياس والكبد من الفئران قبل الولادة والكبار ، وكذلك من الأنسجة البشرية البنكرياس جثي خالية من الجزر.

<table border="1" style=";text-align:right;direction:rtl"><tbody><tr><td> المادة / الكاشف </td><td> شركة </td><td> كتالوج عدد </td><td> تعليقات </td></tr><tr><td> 1X DMEM / F - 12 (1:1) </td><td> Mediatech </td><td> 15-090 - CV </td><td></td></tr><tr><td> الجنين مصل العجل </td><td> نسيج الثقافة البيولوجية </td><td> 201 </td><td> الرجوع إلى القسم 1.1 </td></tr><tr><td> L - الجلوتامين </td><td> Gibco </td><td> 25030-081 </td><td></td></tr><tr><td> 1X Dulbecco في برنامج تلفزيوني </td><td> Mediatech </td><td> 21-031 - CV </td><td></td></tr><tr><td> المصل البقري ألبومين </td><td> سيغما </td><td> A8412 </td><td> 7.5 ٪ </td></tr><tr><td> Matrigel </td><td> بيكتون ديكنسون </td><td> 356231 </td><td> انخفاض النمو عامل </td></tr><tr><td> Methylcellulose </td><td> Sinetsu الكيميائية ، طوكيو ، اليابان </td><td></td><td> 1500 سنتي بواز (عالية السادسscosity) </td></tr><tr><td> نيكوتيناميد </td><td> سيغما </td><td> N0636 </td><td></td></tr><tr><td> الإنسان المؤتلف Activin βB </td><td> R &amp; D أنظمة </td><td> AB - 659 - 025 </td><td></td></tr><tr><td> Exendin - 4 </td><td> سيغما </td><td> E7144 </td><td></td></tr><tr><td> الإنسان المؤتلف VEGF - A </td><td> R &amp; D أنظمة </td><td> 293 VE - 010 </td><td></td></tr><tr><td> 24 كذلك لوحات </td><td> Costar </td><td> 3473 </td><td> منخفضة جدا التعلق </td></tr><tr><td> 60mm طبق بتري مع الشبكة </td><td> نونك </td><td> 169558 </td><td></td></tr></tbody></table>

a quantitative assay for insulin-expressing colony-forming progenitors

وقد أعاق مجال الجذعية البنكرياس والسلف بيولوجيا الخلية بسبب نقص في المختبر المقايسات الفنية والكمية التي تسمح للتحليل خلية واحدة. تحليلات الأسلاف واحدة هي ذات أهمية حاسمة لأنها توفر سبل نهائي لإثبات بشكل قاطع احتمال نسب أسلاف الفردية. على الرغم من أن وضعت وسائل لتوليد &quot;pancreatospheres&quot; في الثقافة تعليق من الخلايا واحدة ، وجود عدة قيود. الأول ، هو تستغرق وقتا طويلا لتنفيذ واحد ترسب الخلايا لعدد كبير من الخلايا ، والتي بدورها الأوامر كميات كبيرة من وسائل الإعلام والثقافة ، والفضاء. الثانية ، ترقيم pancreatospheres الناتج كثيفة العمالة ، وخصوصا عندما تردد الأسلاف pancreatosphere - الشروع منخفضة. الثالث ، ومقايسة pancreatosphere ليس وسيلة فعالة للسماح كلا من الانتشار والتفريق بين الأسلاف البنكرياس في الثقافة نفسها بشكل جيد ، وإعادةstricting فائدة الفحص. للتغلب على هذه القيود ، وقد تم وضع شبه صلبة وسائل الاعلام القائمة على مقايسة مستعمرة الأسلاف البنكرياس ويرد في هذا التقرير. هذا الأسلوب يستفيد من مفهوم موجود من مقايسة مستعمرة المكونة للدم ، والذي يستخدم لتوفير methylcellulose اللزوجة إلى وسائل الإعلام ، والسماح للخلايا الاصلية في البقاء في الفضاء الثلاثي الأبعاد كما أنها تخضع الانتشار فضلا عن التمايز. لإثراء الانسولين معربا عن تشكيل مستعمرة الأسلاف من السكان غير متجانسة ، ونحن نعرب عن الخلايا التي استخدمت neurogenin (NGN) 3 ، والسلف البنكرياس الصماء علامة الخلية. الفئران الجذعية الجنينية (ES) الخلايا المشتقة من الخلايا معربا عن Ngn3 المفتاحية المعززة الأخضر مراسل بروتين فلوري تم فرزها وما يصل الى 25000 في الخلايا وكذلك في المرفق مطلية منخفضة 24 الأطباق الثقافة أيضا. اجتمع : كل الواردة من 500 ميكرولتر من شبه صلبة وسائل الاعلام مع المكونات الرئيسية التاليةhylcellulose ، Matrigel ، نيكوتيناميد ، exendin - 4 ، βB activin ، ووسائل الإعلام المكيفة التي تم جمعها من الفئران الخلايا المشتقة من خلية البنكرياس مثل وفاق. بعد 8 إلى 12 يوما للثقافة ، معربا عن الانسولين مع المستعمرات مميزة تشكلت مورفولوجيا ويمكن لمزيد من التحليل للتعبير الجين البنكرياس باستخدام كمية RT - PCR وتلطيخ immunoflourescent لتحديد تكوين نسب كل مستعمرة. باختصار ، لدينا تجربة مستعمرة يسمح السهل الكشف النوعي والكمي لأسلاف ظيفية ضمن مجموعة من السكان غير متجانسة من الخلايا. بالإضافة إلى ذلك ، شكل وسائل الاعلام شبه صلبة تتيح عرض موحد لمكونات المصفوفة خارج الخلية ، وعوامل نمو الخلايا ، مما الأسلاف لتتكاثر والتفريق في المختبر. هذا الاختبار مستعمرة يوفر فرصا فريدة للدراسات الميكانيكية للخلايا البنكرياس السلف على مستوى خلية واحدة.

Watch this Scientific Journal Video about A Quantitative Assay for Insulin-expressing Colony-forming Progenitors at JoVE.com

A Quantitative Assay for Insulin-expressing Colony-forming Progenitors

تم وصف مولد الرمع مقايسة ثلاثية الأبعاد التي تسمح البنكرياس مثل الأسلاف على التمايز إلى المستعمرات معربا عن الانسولين. هذا الأسلوب يستفيد من شبه صلبة تحتوي على وسائل الاعلام methylcellulose ، Matrigel وعوامل النمو ، والتي تتكاثر والأسلاف واحد يفرق<em&gt; في المختبر</em&gt; ، والسماح الكمي لعدد من الأسلاف وظيفية في عدد السكان.

والفحص الكمية للأنسولين ، معربا عن الأسلاف لتشكيل مستعمرة

The field of pancreatic stem and progenitor cell biology has been hampered by a lack of in vitro functional and quantitative assays that allow for the ...

a-quantitative-assay-for-insulin-expressing-colony-forming-progenitors

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13.4K Views.  California State University Channel Islands. تم وصف مولد الرمع مقايسة ثلاثية الأبعاد التي تسمح البنكرياس مثل الأسلاف على التمايز إلى المستعمرات معربا عن الانسولين. هذا الأسلوب يستفيد من شبه صلبة تحتوي على وسائل الاعلام methylcellulose ، Matrigel وعوامل النمو ، والتي تتكاثر والأسلاف واحد يفرق في المختبر ، وال...

Video: A Quantitative Assay for Insulin-expressing Colony-forming Progenitors

Quantitative Phosphoproteomics in Fatty Acid Stimulated Saccharomyces cerevisiae

This protocol describes the growth and stimulation, with the fatty acid oleate, of isotopically heavy and light S. cerevisiae cells. Cells are ground using a cryolysis procedure in a ball mill grinder and the resulting grindate brought into solution by urea solubilization. This procedure allows for the lysis of the cells in a metabolically inactive state, preserving phosphorylation and preventing reorientation of the phosphoproteome during cell lysis.  Following reduction, alkylation, trypsin digestion of the proteins, the samples are desalted on C18 columns and the sample complexity reduced by fractionation using hydrophilic interaction chromatography (HILIC). HILIC columns preferentially retain hydrophilic molecules which is well suited for phosphoproteomics.  Phosphorylated peptides tend to elute later in the chromatographic profile than the non phosphorylated counterparts. After fractionation, phosphopeptides are enriched using immobilized metal chromatography, which relies on charge-based affinities for phosphopeptide enrichment. At the end of this procedure the samples are ready to be quantitatively analyzed by mass spectrometry.

Quantitative Phosphoproteomics in Fatty Acid Stimulated Saccharomyces cerevisiae

Description of a quantitative phosphorylation procedure using cryolysis, urea solubilziation, HILIC fractionation and IMAC enrichment of phosphorylated peptides.

حفز Phosphoproteomics الكمية في الأحماض الدهنية السكيراء الجعوية</em

This protocol describes the growth and stimulation, with the fatty acid oleate, of isotopically heavy and light S. cerevisiae cells. Cells are ground ...

Isolation and Large Scale Expansion of Adult Human Endothelial Colony Forming Progenitor Cells

This paper introduces a novel recovery strategy for endothelial colony forming progenitor cells (ECFCs) from heparinized but otherwise unmanipulated adult human peripheral blood within a mean of 12 days. After large scale expansion &gt;1x108 ECFCs can be obtained for further tests. Advantageously by using pHPL the contact of human cells with bovine serum antigens can be excluded. By flow cytometry and immunohistochemistry the isolated cells can be characterized as ECFC and their in vitro functionality to form vascular like structures can be tested in a matrigel assay. Further these cells can be subcutaneously injected in a mouse model to form functional, perfused vessels in vivo. After long term expansion and cryopreservation proliferation, function and genomic stability appear to be preserved. 3,4
This animal-protein free isolation and expansion method is easily applicable to generate a large quantity of ECFCs.

Endothelial colony forming progenitor cells (ECFCs) are a promising tool to study vascular homeostasis and repair.1,2 This paper introduces a novel animal-serum free method for isolation and expansion of ECFC from heparinised adult human peripheral blood with pooled human platelet lysate (pHPL) diminishing the risk of anti-bovine immunisation.

العزلة وتوقعات بنمو كبير من الكبار الإنسان خلايا غشائي السلف تشكيل مستعمرة

This paper introduces a novel recovery strategy for endothelial colony forming progenitor cells (ECFCs) from heparinized but otherwise unmanipulated adult ...

Isolation and Animal Serum Free Expansion of Human Umbilical Cord Derived Mesenchymal Stromal Cells (MSCs) and Endothelial Colony Forming Progenitor Cells (ECFCs)

The umbilical cord is a rich source for progenitor cells with high proliferative potential including mesenchymal stromal cells (also termed mesenchymal stem cells, MSCs) and endothelial colony forming progenitor cells (ECFCs). Both cell types are key players in maintaining the integrity of tissue and are probably also involved in regenerative processes and tumor formation.
To study their biology and function in a comparative manner it is important to have both cells types available from the same donor. It may also be beneficial for regenerative purposes to derive MSCs and ECFCs from the same tissue.
Because cellular therapeutics should eventually find their way from bench to bedside we established a new method to isolate and further expand progenitor cells without the use of animal protein. Pooled human platelet lysate (pHPL) replaced fetal bovine serum in all steps of our protocol to completely avoid contact of the cells to xenogeneic proteins.
This video demonstrates a methodology for the isolation and expansion of progenitor cells from one umbilical cord.
All materials and procedures will be described.

Isolation and Animal Serum Free Expansion of Human Umbilical Cord Derived Mesenchymal Stromal Cells MSCs and Endothelial Colony Forming Progenitor Cells ECFCs

This protocol describes the isolation and subsequent expansion of mesenchymal stromal cells and endothelial colony forming cells without the use of animal serum to generate autologous pairs for experimental transplantation purposes.

العزلة والحيوان التوسع الحرة المصل الحبل السري الإنسان المستمدة الخلايا اللحمية الوسيطة (MSCS) وغشائي خلايا مستعمرة السلف التشكيل (ECFCs)

The umbilical cord is a rich source for progenitor cells with high proliferative potential including mesenchymal stromal cells (also termed mesenchymal ...

Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay

The study of erythropoiesis aims to understand how red cells are formed from earlier hematopoietic and erythroid progenitors. Specifically, the rate of red cell formation is regulated by the hormone erythropoietin (Epo), whose synthesis is triggered by tissue hypoxia. A threat to adequate tissue oxygenation results in a rapid increase in Epo, driving an increase in erythropoietic rate, a process known as the erythropoietic stress response. The resulting increase in the number of circulating red cells improves tissue oxygen delivery. An efficient erythropoietic stress response is therefore critical to the survival and recovery from physiological and pathological conditions such as high altitude, anemia, hemorrhage, chemotherapy or stem cell transplantation. 
The mouse is a key model for the study of erythropoiesis and its stress response. Mouse definitive (adult-type) erythropoiesis takes place in the fetal liver between embryonic days 12.5 and 15.5, in the neonatal spleen, and in adult spleen and bone marrow. Classical methods of identifying erythroid progenitors in tissue rely on the ability of these cells to give rise to red cell colonies when plated in Epo-containing semi-solid media. Their erythroid precursor progeny are identified based on morphological criteria. Neither of these classical methods allow access to large numbers of differentiation-stage-specific erythroid cells for molecular study. Here we present a flow-cytometric method of identifying and studying differentiation-stage-specific erythroid progenitors and precursors, directly in the context of freshly isolated mouse tissue. The assay relies on the cell-surface markers CD71, Ter119, and on the flow-cytometric 'forward-scatter' parameter, which is a function of cell size. The CD71/Ter119 assay can be used to study erythroid progenitors during their response to erythropoietic stress in vivo, for example, in anemic mice or mice housed in low oxygen conditions. It may also be used to study erythroid progenitors directly in the tissues of genetically modified adult mice or embryos, in order to assess the specific role of the modified molecular pathway in erythropoiesis.

A flow-cytometric method for identification and molecular analysis of differentiation-stage-specific murine erythroid progenitors and precursors, directly in freshly &#x2013;harvested mouse bone marrow, spleen or fetal liver. The assay relies on cell-surface markers CD71, Ter119, and cell size.

تحديد وتحليل الأسلاف محمر ماوس باستخدام CD71/TER119 التدفق cytometric الفحص

The study of erythropoiesis aims to understand how red cells are formed from earlier hematopoietic and erythroid progenitors. Specifically, the rate of ...

Phenotypic and Functional Characterization of Endothelial Colony Forming Cells Derived from Human Umbilical Cord Blood

Longstanding views of new blood vessel formation via angiogenesis, vasculogenesis, and arteriogenesis have been recently reviewed1. The presence of circulating endothelial progenitor cells (EPCs) were first identified in adult human peripheral blood by Asahara et al. in 1997 2 bringing an infusion of new hypotheses and strategies for vascular regeneration and repair. EPCs are rare but normal components of circulating blood that home to sites of blood vessel formation or vascular remodeling, and facilitate either postnatal vasculogenesis, angiogenesis, or arteriogenesis largely via paracrine stimulation of existing vessel wall derived cells3. No specific marker to identify an EPC has been identified, and at present the state of the field is to understand that numerous cell types including proangiogenic hematopoietic stem and progenitor cells, circulating angiogenic cells, Tie2+ monocytes, myeloid progenitor cells, tumor associated macrophages, and M2 activated macrophages participate in stimulating the angiogenic process in a variety of preclinical animal model systems and in human subjects in numerous disease states4, 5. Endothelial colony forming cells (ECFCs) are rare circulating viable endothelial cells characterized by robust clonal proliferative potential, secondary and tertiary colony forming ability upon replating, and ability to form intrinsic in vivo vessels upon transplantation into immunodeficient mice6-8. While ECFCs have been successfully isolated from the peripheral blood of healthy adult subjects, umbilical cord blood (CB) of healthy newborn infants, and vessel wall of numerous human arterial and venous vessels 6-9, CB possesses the highest frequency of ECFCs7 that display the most robust clonal proliferative potential and form durable and functional blood vessels in vivo8, 10-13. While the derivation of ECFC from adult peripheral blood has been presented14, 15, here we describe the methodologies for the derivation, cloning, expansion, and in vitro as well as in vivo characterization of ECFCs from the human umbilical CB.

Endothelial colony forming cells (ECFCs) are circulating endothelial cells with robust clonal proliferative potential that display intrinsic in vivo vessel forming ability. Phenotypic and functional characterization of outgrowth endothelial cells derived from CB are important to identify and isolate bona fide ECFCs for potential clinical application in repairing damaged tissues.

توصيف المظهري والوظيفي للخلايا غشائي مستعمرة تشكيل المستمدة من الإنسان دم الحبل السري

Longstanding views of new blood vessel formation via angiogenesis, vasculogenesis, and arteriogenesis have been recently reviewed1. The presence of ...

A Quantitative Fitness Analysis Workflow

Quantitative Fitness Analysis (QFA) is an experimental and computational workflow for comparing fitnesses of microbial cultures grown in parallel1,2,3,4. QFA can be applied to focused observations of single cultures but is most useful for genome-wide genetic interaction or drug screens investigating up to thousands of independent cultures. The central experimental method is the inoculation of independent, dilute liquid microbial cultures onto solid agar plates which are incubated and regularly photographed. Photographs from each time-point are analyzed, producing quantitative cell density estimates, which are used to construct growth curves, allowing quantitative fitness measures to be derived. Culture fitnesses can be compared to quantify and rank genetic interaction strengths or drug sensitivities. The effect on culture fitness of any treatments added into substrate agar (e.g. small molecules, antibiotics or nutrients) or applied to plates externally (e.g. UV irradiation, temperature) can be quantified by QFA.
The QFA workflow produces growth rate estimates analogous to those obtained by spectrophotometric measurement of parallel liquid cultures in 96-well or 200-well plate readers. Importantly, QFA has significantly higher throughput compared with such methods. QFA cultures grow on a solid agar surface and are therefore well aerated during growth without the need for stirring or shaking.
QFA throughput is not as high as that of some Synthetic Genetic Array (SGA) screening methods5,6. However, since QFA cultures are heavily diluted before being inoculated onto agar, QFA can capture more complete growth curves, including exponential and saturation phases3. For example, growth curve observations allow culture doubling times to be estimated directly with high precision, as discussed previously1.
Here we present a specific QFA protocol applied to thousands of S. cerevisiae cultures which are automatically handled by robots during inoculation, incubation and imaging. Any of these automated steps can be replaced by an equivalent, manual procedure, with an associated reduction in throughput, and we also present a lower throughput manual protocol. The same QFA software tools can be applied to images captured in either workflow.
We have extensive experience applying QFA to cultures of the budding yeast S. cerevisiae but we expect that QFA will prove equally useful for examining cultures of the fission yeast S. pombe and bacterial cultures.

Quantitative Fitness Analysis (QFA) is a complementary series of experimental and computational methods for estimating microbial culture fitnesses. QFA estimates the effect of genetic mutations, drugs or other applied treatments on microbe growth. Experiments scaling from focussed analysis of single cultures to thousands of parallel cultures can be designed.

تحليل كمي لياقة سير العمل

Quantitative Fitness Analysis (QFA) is an experimental and computational workflow for comparing fitnesses of microbial cultures grown in parallel1,2,3,4. ...

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes

Biochemical assays with recombinant human MHC II molecules can provide rapid, quantitative insights into immunogenic epitope identification, deletion, or design1,2. Here, a peptide-MHC II binding assay is scaled to 384-well format. The scaled down protocol reduces reagent costs by 75% and is higher throughput than previously described 96-well protocols1,3-5. Specifically, the experimental design permits robust and reproducible analysis of up to 15 peptides against one MHC II allele per 384-well ELISA plate. Using a single liquid handling robot, this method allows one researcher to analyze approximately ninety test peptides in triplicate over a range of eight concentrations and four MHC II allele types in less than 48 hr. Others working in the fields of protein deimmunization or vaccine design and development may find the protocol to be useful in facilitating their own work. In particular, the step-by-step instructions and the visual format of JoVE should allow other users to quickly and easily establish this methodology in their own labs.

Biochemical assays with recombinant human MHC II molecules can provide rapid, quantitative insights into immunogenic epitope identification, deletion, or design. &#160;Here, a peptide-MHC II binding assay scaled to 384-well plates is described. This cost effective format should prove useful in the fields of protein deimmunization and vaccine design and development.

A تجليد الفحص إنتاجية عالية MHC II لتحليل الكمي لالببتيد الحواتم

Biochemical assays with recombinant human MHC II molecules can provide rapid, quantitative insights into immunogenic epitope identification, deletion, or ...

A Strategy for Sensitive, Large Scale Quantitative Metabolomics

Metabolite profiling has been a valuable asset in the study of metabolism in health and disease. However, current platforms have different limiting factors, such as labor intensive sample preparations, low detection limits, slow scan speeds, intensive method optimization for each metabolite, and the inability to measure both positively and negatively charged ions in single experiments. Therefore, a novel metabolomics protocol could advance metabolomics studies. Amide-based hydrophilic chromatography enables polar metabolite analysis without any chemical derivatization. High resolution MS using the Q-Exactive (QE-MS) has improved ion optics, increased scan speeds (256 msec at resolution 70,000), and has the capability of carrying out positive/negative switching. Using a cold methanol extraction strategy, and coupling an amide column with QE-MS enables robust detection of 168 targeted polar metabolites and thousands of additional features simultaneously.&#160; Data processing is carried out with commercially available software in a highly efficient way, and unknown features extracted from the mass spectra can be queried in databases.

Metabolite profiling has been a valuable asset in the study of metabolism in health and disease. Utilizing normal-phased liquid chromatography coupled to high-resolution mass spectrometry with polarity switching and a rapid duty cycle, we describe a protocol to analyze the polar metabolic composition of biological material with high sensitivity, accuracy, and resolution.

استراتيجية للحساسية، مقياس كبيرة الكمية الايض

Metabolite profiling has been a valuable asset in the study of metabolism in health and disease. However, current platforms have different limiting ...

Quantitative Immunofluorescence Assay to Measure the Variation in Protein Levels at Centrosomes

Centrosomes are small but important organelles that serve as the poles of mitotic spindle to maintain genomic integrity or assemble primary cilia to facilitate sensory functions in cells. The level of a protein may be regulated differently at centrosomes than at other .cellular locations, and the variation in the centrosomal level of several proteins at different points of the cell cycle appears to be crucial for the proper regulation of centriole assembly. We developed a quantitative fluorescence microscopy assay that measures relative changes in the level of a protein at centrosomes in fixed cells from different samples, such as at different phases of the cell cycle or after treatment with various reagents. The principle of this assay lies in measuring the background corrected fluorescent intensity corresponding to a protein at a small region, and normalize that measurement against the same for another protein that does not vary under the chosen experimental condition. Utilizing this assay in combination with BrdU pulse and chase strategy to study unperturbed cell cycles, we have quantitatively validated our recent observation that the centrosomal pool of VDAC3 is regulated at centrosomes during the cell cycle, likely by proteasome-mediated degradation specifically at centrosomes.

Here, a novel quantitative fluorescence assay is developed to measure changes in the level of a protein specifically at centrosomes by normalizing that protein&#8217;s fluorescence intensity to that of an appropriate internal standard.

الكمية المناعي الفحص لقياس التفاوت في مستويات البروتين في Centrosomes

Centrosomes are small but important organelles that serve as the poles of mitotic spindle to maintain genomic integrity or assemble primary cilia to ...

Development of a Quantitative Recombinase Polymerase Amplification Assay with an Internal Positive Control

It was recently demonstrated that recombinase polymerase amplification (RPA), an isothermal amplification platform for pathogen detection, may be used to quantify DNA sample concentration using a standard curve. In this manuscript, a detailed protocol for developing and implementing a real-time quantitative recombinase polymerase amplification assay (qRPA assay) is provided. Using HIV-1 DNA quantification as an example, the assembly of real-time RPA reactions, the design of an internal positive control (IPC) sequence, and co-amplification of the IPC and target of interest are all described. Instructions and data processing scripts for the construction of a standard curve using data from multiple experiments are provided, which may be used to predict the concentration of unknown samples or assess the performance of the assay. Finally, an alternative method for collecting real-time fluorescence data with a microscope and a stage heater as a step towards developing a point-of-care qRPA assay is described. The protocol and scripts provided may be used for the development of a qRPA assay for any DNA target of interest.

Provided is a protocol for developing a real-time recombinase polymerase amplification assay to quantify initial concentration of DNA samples using either a thermal cycler or a microscope and stage heater. Also described is the development of an internal positive control. Scripts are provided for processing raw real-time fluorescence data.

تطوير الكمية Recombinase البلمرة التضخيم الفحص مع الرقابة الداخلية إيجابي

It was recently demonstrated that recombinase polymerase amplification (RPA), an isothermal amplification platform for pathogen detection, may be used to ...