ويؤيد هذا العمل من قبل صندوق بدء التشغيل من قسم العلوم البيولوجية في جامعة بوردو.

الجزء 1 : التحضيرات قبل microdissection <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> الحلول <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> E3 المتوسطة 4 (5 ملي مول كلوريد الصوديوم ، 0.17 ملي بوكل ، 0.33 ملي CaCl 2 و 0.33 ملي MgSO 4). </li><li style=";text-align:right;direction:rtl"> حل رينغر 1 ، 5 (116 ملي مول كلوريد الصوديوم ، و 2.9 ملي بوكل ، 1.8 ملي CaCl 2 ، 5 HEPES مم ، pH7.2) ، تصفية تعقيمها. </li><li style=";text-align:right;direction:rtl"> 5N هيدروكسيد الصوديوم. </li></ol></li><li style=";text-align:right;direction:rtl"> النقش الكيماوية من الإبر التنغستن <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> آمن كوب صغير يحتوي 5N هيدروكسيد الصوديوم على طبق بيتري بواسطة الطين. </li><li style=";text-align:right;direction:rtl"> إرفاق مشبك الورق إلى جانب الكأس ، بحيث يأتي في اتصال مع محلول هيدروكسيد الصوديوم. </li><li style=";text-align:right;direction:rtl"> توصيل القطب السالب من العاصمة امدادات الطاقة الى مشبك الورق والقطب الموجب إلى واحدة من نهاية قطعة قصيرة (~ 2cm) من سلك التنجستن. </li><li style=";text-align:right;direction:rtl"> التفاف على الطرف الآخر من سلك التنغستن مع كرة صغيرة من الطين وتراجع هذه الغاية في محلول هيدروكسيد الصوديوم. </li><li style=";text-align:right;direction:rtl"> زيادة الجهد ل3V تقريبا وتراجع السلك صعودا وهبوطا في محلول هيدروكسيد الصوديوم حتى يتم التوصل إلى سعر النقش جيدة. يمكن عادة إبرة في نوعية جيدة يكون محفورا في 10 دقيقة. </li><li style=";text-align:right;direction:rtl"> وسلك التنغستن عرضة لتصبح أرق حل تدريجيا. عندما يسقط الكرة من الطين ، فإن الجانب الآخر من الأسلاك التي لا تزال تعلق على القطب الموجب لها شكل إبرة حادة. </li><li style=";text-align:right;direction:rtl"> شطف إبرة حادة مع حل رينغر E3 أو لإزالة رواسب الملح. </li><li style=";text-align:right;direction:rtl"> إرفاق الإبرة إلى قضيب خشبي بواسطة الشريط أو حامل إبرة لسهولة التعامل. </li></ol></li><li style=";text-align:right;direction:rtl"> الثقافة لوحات <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> وفالكون 60 مم X البوليسترين لوحات ثقافة 15 جاهزة للاستخدام لmicrodissection الشبكية. </li><li style=";text-align:right;direction:rtl"> لتشريح RPE المرفقة شبكية العين ، سحق two أجنة تماما في لوحة الثقافة التي تحتوي على حل رينغر للتخلص من صوقية من السطح قبل 30 دقيقة من تشريح. قبل وقت قصير من التشريح ، وغسل لوحة على نطاق واسع مع الحل رينغر الطازج. </li></ol></li><li style=";text-align:right;direction:rtl"> أجنة جمع والتدريج <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> تمسك الزرد الكبار كما هو موضح 4 ، 5. </li><li style=";text-align:right;direction:rtl"> فصل الأسماك في أحواض تربية الوالدين ثابتة البشرى بواسطة مقسم ليلة قبل التزاوج. </li><li style=";text-align:right;direction:rtl"> إزالة الفاصل بعد تشغيل الضوء على غرفة في صباح اليوم التالي. تسمح للوالدين لعبور 10 دقيقة في فترات كل نصف ساعة. فصل الأسماك بعد كل معبر. </li><li style=";text-align:right;direction:rtl"> الحفاظ على الأجنة التي تم جمعها من كل عبور في E3 المتوسطة بشكل منفصل في 28 درجة مئوية. </li><li style=";text-align:right;direction:rtl"> الأجنة في مرحلة 10-12 التسميد آخر ساعة (HPF) وعلى الفور restage قبل التشريح في نقطة زمنية محددة ، وفقا للمعايير المقررة 1 ، 6. </li></ol></li></ol> الجزء 2 : تشريح -- إزالة المخ والتعرض العين 1 <ul style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> الإجراءات المذكورة في هذا المقطع هي مشتركة لتشريح شبكية العين (الجزء 3A) وRPE المرفقة شبكية العين (الجزء 3B). </li><li style=";text-align:right;direction:rtl"> تتم جميع تشريح غرامة من قبل غيض من ملقط دومون ويعاونه زوج آخر من ملقط دومون لتحديد المواقع الأنسجة. ويمكن استخدام إبرة التنجستن كيميائيا محفورا عن التلاعب أدق إذا لزم الأمر. </li><li style=";text-align:right;direction:rtl"> يتم تنفيذ كافة تشريح غرامة على التكبير ~ 5 - 8X تحت المجهر SZX16 أوليمبوس مجهزة هدفا 1X أو ما يعادلها. </li><li style=";text-align:right;direction:rtl"> الحفاظ على الأجنة في E3 المتوسطة في مقعد الحاضنة الأولى في 28 درجة مئوية بجانب المجهر للوصول السهل الجنين أثناء تشريح. </li><li style=";text-align:right;direction:rtl"> وتحسنت المرحلة المجهر إلى 28 درجة مئوية بحلول لوحة الحرارية للحد من تأثير تقلبات درجة الحرارة على التعبير الجيني. </li></ul><ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> أعد نقل الجنين في مرحلة تطويرية معينة إلى حل رينغر في 60 X 15 مم فالكون لوحة الثقافة كما هو موضح في الجزء 1 # 3. </li><li style=";text-align:right;direction:rtl"> قطع الرأس مع جزء من الجذع الأمامي بسرعة من الجسم. </li><li style=";text-align:right;direction:rtl"> دبوس نهاية الخلفي من هذا النسيج على لوحة الثقافة مع ملقط مساعدة. </li><li style=";text-align:right;direction:rtl"> فتح الرأس على الجانب الظهري بدءا من الجبهة الأمامية. </li><li style=";text-align:right;direction:rtl"> إزالة المخ بحيث يتعرض الجانب الإنسي للعيون وتواجه التصاعدي لمزيد من التلاعب. </li></ol> 3A الجزء : 1 تشريح الشبكية <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> تحضير الجنين كما هو موضح في الجزء 2. </li><li style=";text-align:right;direction:rtl"> فرشاة بعناية RPE تعرض على الجانب الإنسي للكرة العين التي تواجه صعودا من قبل غيض من الملقط حتى ينظر إلى فتحة صغيرة في شبكية العين. </li><li style=";text-align:right;direction:rtl"> الاستمرار في تنظيف وتقشير العمل حتى في الجانب الإنسي للشبكية يكاد يتعرض جميع. تجنب خدش واللكم على شبكية العين تتعرض لها. </li><li style=";text-align:right;direction:rtl"> لإزالة RPE الوحشي على الشبكية التي تواجه الآن نحو الانخفاض ، والنهج الذي الفرشاة بزاوية 45 درجة تقريبا من سطح لوحة الثقافة. </li><li style=";text-align:right;direction:rtl"> إزالة RPE التي ترتبط بقوة نسبيا في مشرشر ORA التي تعلق جزء من فصل إلى RPE جلوحة ulture التشريح ، ومن ثم رفع شبكية العين برفق. </li><li style=";text-align:right;direction:rtl"> لفة الشبكية في الجزء السفلي من الطبق الثقافة لتنظيف RPE المتبقية. <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> لاحظنا أن هذا البوليسترين فالكون لوحة خاصة لديه ثقافة الالتزام التفضيلية للRPE لحوالي 20 دقيقة مرة واحدة سحقت جنين. وتستخدم هذه الخاصية لإزالة مخلفات RPE. ومع ذلك ، فإن خلايا الشبكية لا عصا على السطح إلى حد أقل ، والتي يمكن تفتيشها بشكل وثيق تحت التكبير عالية. على المرء أن توازن بين اكتمال إزالة RPE والنزاهة في شبكية العين. </li><li style=";text-align:right;direction:rtl"> العدسة تتمسك كثير من الأحيان إلى لوحة الثقافة ويفصل من شبكية العين خلال عملية المتداول. أحيانا ، فمن الضروري فصل العدسة عن طريق إبرة التنغستن محفورا مع دوامات العمل على سطح العدسة. </li></ol></li><li style=";text-align:right;direction:rtl"> ويمكن إزالة هذه الإجراءات بنجاح RPE من الشبكية دون المساومة على سلامة الأنسجة. ويدل على هذا التشكل شامل جيدة (الشكل 1B و &quot;B) والأنسجة (الشكل 1B&quot;) ، السهم وعلى وجه الخصوص ، والحفاظ على المصفوفة خارج الخلية في مبصرة بين طبقة وRPE هو جيد بشكل استثنائي (1B الشكل &quot;؛ مقارنة مع الأنسجة من الجنين كله (الشكل 1A &quot;)). </li></ol> 3B الجزء : RPE المرفقة تشريح الشبكية 3 <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> تحضير الجنين كما هو موضح في الجزء 2. </li><li style=";text-align:right;direction:rtl"> رأس دبوس إلى لوحة الثقافة التي ملقط مساعد. رفع العين بلطف من الجانب الخلفي والجانبي لفة على الجانب الأمامي. <ol class="lalpha" style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> ويعلق المشيمية الظنية والأنسجة الصلبة على السطح الخارجي للطبقة RPE نسبيا بإحكام على الجلد ، ويمكن مقشر معظمها من قبل المتداول خارج العين بعناية إلى الجانب الأمامي. </li></ol></li><li style=";text-align:right;direction:rtl"> إزالة العدسة بإبرة التنغستن بعد تعرض الجانب الوحشي من العين ، وعندما لا تزال تعلق على العين على الجلد. </li><li style=";text-align:right;direction:rtl"> يمكن لهذه الإجراءات المحافظة على طبقة RPE بنجاح كامل مع شبكية العين. يمكن choroids الافتراضي وإزالة الأنسجة الصلبة إلى حد كبير (الشكل 1C ، &#39;C و C&quot;). </li></ol> الجزء 4 : الأنسجة جمع العينات لعمل الحمض النووي الريبي <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> ويمكن جمع عينات تشريح في TRIzol في أنبوب microfuge ريبونوكلياز خالية من الحمض النووي الريبي لتوصيف المصب صفه قبل 1. </li></ol> ممثل النتائج <img src="/files/ftp_upload/2028/2028fig1.jpg" alt="الشكل 1" /> الشكل 1 (أ) والجانبي (A &#39;) عرض الظهرية من رأس اليرقات الزرد في 52 HPF قبل تشريح. (A &quot;) والفرع المقابل النسيجي للرئيس اليرقات في الفقرة (أ) و (A&#39;) ، (ب) والجانبي (B &#39;) عرض الظهرية لتشريح شبكية العين في 54 HPF. سطح الشبكية كان سليما من كل الاطراف وجهات النظر الظهرية (B &quot;) والفرع المقابل النسيجي للتشريح في شبكية العين (ب) و (B&#39;). وكان هيكل في شبكية العين وتصفيح الشبكية سليمة. على وجه الخصوص ، &quot;كانت محفوظة بشكل جيد (والسهام في شبكية العين تشريح (B المصفوفة خارج الخلية بين طبقة مبصرة وRPE A)&quot; والسهام). (C) والجانبي (C &#39;) عرض الإنسية لشبكية العين RPE المرفقة تشريح في 52 HPF. وكان RPE طبقة سليمة ومستمرة ، وهو ما تدل أيضا المقطع النسيجي للتشريح الأنسجة (C &quot;). وتبلغ مساحة بيضاء في&#39; C هو العصب البصري (السهم) للحصول على الأنسجة ، تم جمع عينات من الأنسجة وإصلاحها في 4 ٪ أجريت بارافورمالدهيد. بلاستيك وsectioning تضمين هذه العينات كما هو موضح 3. شريط مقياس = 50 ميكرومتر.

<ol>
	<li>Leung, Y. F., Dowling, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Gene+expression+profiling+of+zebrafish+embryonic+retina.">Gene expression profiling of zebrafish embryonic retina.</a> Zebrafish. 2, 269-283 (2005).</li><li>Leung, Y. F., Ma, P., Link, B. A., Dowling, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Factorial+microarray+analysis+of+zebrafish+retinal+development.">Factorial microarray analysis of zebrafish retinal development.</a> Proc Natl Acad Sci U S A. 105, 12909-12914 (2008).</li><li>Leung, Y. F., Ma, P., Dowling, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Gene+expression+profiling+of+zebrafish+embryonic+retinal+pigment+epithelium+in+vivo.">Gene expression profiling of zebrafish embryonic retinal pigment epithelium in vivo.</a> Invest Ophthalmol Vis Sci. 48, 881-890 (2007).</li><li>Nusslein-Volhard, C., Dahm, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Zebrafish : a practical approach. , (2002).</li><li>Westerfield, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+zebrafish+book+:+a+guide+for+the+laboratory+use+of+zebrafish+(Danio+rerio).">The zebrafish book : a guide for the laboratory use of zebrafish (Danio rerio).</a> , (2000).</li><li>Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B., Schilling, T. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Stages+of+embryonic+development+of+the+zebrafish.">Stages of embryonic development of the zebrafish.</a> Dev Dyn. 203, 253-310 (1995).</li><li>Fadool, J. M., Dowling, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Zebrafish:+a+model+system+for+the+study+of+eye+genetics.">Zebrafish: a model system for the study of eye genetics.</a> Prog Retin Eye Res. 27, 89-110 (2008).</li></ol>

وقد أجريت تجارب على الحيوانات وفقا للمبادئ التوجيهية واللوائح التي وضعتها رعاية الحيوان بوردو واللجنة الاستخدام.

ويمكن للأنسجة العين Microdissection الزرد الحصول على شبكية العين سليمة وفعالة شبكية العين RPE المرفقة. هذا يساعد كثيرا الدراسات المتعلقة التعبير نسيج العين محددة (شبكية العين أو أي RPE). في الواقع ، لقد نجحنا في استغلال هذه الإجراءات للحصول على الحمض النووي الريبي ملامح التعبي...

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		<table border="1">
		<thead>
		<tr>
		<th>Material Name</th>
		<th>Type</th>
		<th>Company</th>
		<th>Catalogue Number</th>
		<th>Comment</th>
		</tr>
		</thead>
		<tbody>
		
<tr>
<td>Cordless pestle motor</td>
<td>&nbsp;</td>
<td>VWR</td>
<td>47747-370</td>
<td>&nbsp;</td>
<tr>
<td>DC power supply</td>
<td>&nbsp;</td>
<td>Lascar</td>
<td>PSU130</td>
<td>Any DC supply would work. The specific voltage of a different machine will need further optimization.</td>
</tr>
<tr>
<td>Disposable pestle &amp; microtube, 1.5 mL (DNase, RNase and pyrogen-free)</td>
<td>&nbsp;</td>
<td>VWR</td>
<td>47747-366</td>
<td>These are used for tissue collection in TRIzol for expression analysis.</td>
</tr>
<tr>
<td>Dumont #5 forceps, Tips: 0.05 x 0.01mm, Inox</td>
<td>&nbsp;</td>
<td>World Precision Instruments</td>
<td>500341</td>
<td>Fine tip dimension is desirable but is not inflexible, as one may need to sharpen the tip from time to time.</td>
</tr>
<tr>
<td>Dumont #5SF forceps, Tips: 0.025 x 0.005mm, Inox</td>
<td>&nbsp;</td>
<td>Fine Science Tools</td>
<td>11252-00</td>
<td>Fine tip dimension is desirable but is not inflexible, as one may need to sharpen the tip from time to time.</td>
</tr>
<tr>
<td>Falcon polystyrene culture plates, 60 X 15 mm</td>
<td>&nbsp;</td>
<td>BD Biosciences</td>
<td>351007</td>
<td>These plates are used as dissection plates.</td>
</tr>
<tr>
<td>Olympus SZX16 Stereomicroscope</td>
<td>&nbsp;</td>
<td>Olympus</td>
<td>SZX16</td>
<td>Any stereomicroscope would work. We used Leica stereomicroscope in previous studies1-3 without any issues. We also use the 1X objective exclusively for the dissection even though we have a 2X objective installed. </td>
</tr>
<tr>
<td>Sharpening stone</td>
<td>&nbsp;</td>
<td>Fine Science Tools</td>
<td>29008-01</td>
<td>Use this to sharpen the tip of the forceps if necessary</td>
</tr>
<tr>
<td>Thermo plate</td>
<td>&nbsp;</td>
<td>Tokai Hit</td>
<td>MATS-U55SZX2B</td>
<td>This is used to maintain the temperature of the tissue throughout dissection and minimize the influence of temperature fluctuation on gene expression. We also put the whole microscope in an environmentally controlled room at 28&deg;C during dissection in previous studies1-3 with good success.</td>
</tr>
<tr>
<td>Trizol, 100 mL</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>15596-026</td>
<td>&nbsp;</td>
<tr>
<td>tungsten wire, 0.015 inch diameter</td>
<td>&nbsp;</td>
<td>World Precision Instruments</td>
<td>TGW1510</td>
<td>&nbsp;</td>
<tr>
<td>Wooden Applicator</td>
<td>&nbsp;</td>
<td>Puritan</td>
<td>807</td>
<td>This is used for holding the chemically-etched tungsten needle.</td>
</tr>		</tbody>
		</table>
		</div>

microdissection of zebrafish embryonic eye tissues

الزرد هو نموذج حيواني شعبية للبحث حول التنمية بسبب العين السريعة لها<em&gt; السابقين الرحم</em&gt; التنمية والخصوبة جيدة. قبل 3 أيام الإخصاب آخر (DPF) ، سوف تظهر اليرقات أول استجابة بصرية. وقد تم تحديد العديد من الجينات لمراقبة تطور العين سليمة ، ولكن ما زلنا بعيدين عن فهم كامل للبنية الوراثية الكامنة. كامل التعبير الجيني التنميط الجينوم هو أداة مفيدة لتوضيح الشبكة التنظيمية الجينية للتنمية العين. ومع ذلك ، فإن صغر حجم العين الجنينية في الزرد يجعلها صعبة للحصول على أنسجة العين سليمة ونقية للتحليل التعبير. على سبيل المثال ، وطول الأمامي الخلفي للعين بين 2 و 3 ايام فقط ما يقرب من 200-300 ميكرون ، في حين أن قطر العدسة أقل ميكرومتر 100. أيضا ، والظهارة الصبغية الشبكية (RPE) الكامنة وراء شبكية العين هو مجرد الظهارة طبقة واحدة. في حين يمكن الحصول على ملامح التعبير الجيني من الجنين كله ، فهي لا تمثل بدقة التعبير عن هذه الأنسجة. بالتالي لا بد من الحصول على نسيج النقي عن التنميط الجيني التعبير ناجحا للتنمية العين. لمعالجة هذه المسألة ، وقد طورنا نهجا لmicrodissect الشبكية سليمة وشبكية العين مع RPE المرفق من DPF 1-3 ، والتي تغطي المراحل الرئيسية التشكل العين. يمكن أن تتم جميع الإجراءات مع ملقط غرامة ولوازم المختبرات العامة في إطار stereomicroscopes القياسية. لتشريح الشبكية ، تتم إزالة RPE طبقة واحدة ، وخلع من قبل التنظيف العمل والتقيد تفضيلية من مخلفات RPE على سطح لوحة الثقافة لتشريح. لRPE المرفقة تشريح الشبكية ، تتم إزالة RPE انضمام إلى لوحة تشريح قبل تشريح بحيث يمكن للRPE تماما مع الحفاظ على شبكية العين. ويمكن لعمل دقيق لرفع هذا النسيج منفصلة بكفاءة المشيمية الظنية والصلبة. ويمكن إزالة العدسة في كلتا الحالتين بواسطة إبرة التنغستن محفورا كيميائيا. باختصار ، يمكن الحصول على نهجنا أنسجة العين سليمة ، واستخدمت بنجاح لدراسة ملامح الأنسجة محددة التعبير الشبكية الزرد<sup&gt; 1 ، 2</sup&gt; والشبكية الصباغ الظهارة<sup&gt; 3</sup&gt;.

Watch this Scientific Journal Video about Microdissection of Zebrafish Embryonic Eye Tissues at JoVE.com

Microdissection of Zebrafish Embryonic Eye Tissues

توضح هذه المقالة نهج لشبكية العين microdissect الزرد مع وبدون صباغ الشبكية ظهارة المرفقة ، 1-3 أجنة postfertilization يوما.

Microdissection من الأنسجة الجنينية العين اسماك الزرد

Zebrafish is a popular animal model for research on eye development because of its rapid ex utero development and good fecundity. By 3 days post ...

microdissection-of-zebrafish-embryonic-eye-tissues

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Biology

16.1K Views.  Purdue University. توضح هذه المقالة نهج لشبكية العين microdissect الزرد مع وبدون صباغ الشبكية ظهارة المرفقة ، 1-3 أجنة postfertilization يوما.

Video: Microdissection of Zebrafish Embryonic Eye Tissues

Laser Capture Microdissection of Mammalian Tissue

Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or formalin-fixed, paraffin-embedded tissue sections. LMD techniques rely on a thermo labile membrane placed either on top of, or underneath, the tissue section. In one method, focused laser energy is used to melt the membrane onto the underlying cells, which can then be lifted out of the tissue section. In the other, the laser energy vaporizes the foil along a path "drawn" on the tissue, allowing the selected cells to fall into a collection device. Each technique allows the selection of cells with a minimum resolution of several microns. DNA, RNA, protein, and lipid samples may be isolated and analyzed from micro-dissected samples. In this video, we demonstrate the use of the Leica AS-LMD laser microdissection instrument in seven segments, including an introduction to the principles of LMD, initializing the instrument for use, general considerations for sample preparation, mounting the specimen and setting up capture tubes, aligning the microscope, adjusting the capture controls, and capturing tissue specimens. Laser-capture micro-dissection enables the investigator to isolate samples of pure cell populations as small as a few cell-equivalents. This allows the analysis of cells of interest that are free of neighboring contaminants, which may confound experimental results.

الليزر Microdissection القبض على أنسجة الثدييات

Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or ...

Live Imaging of the Zebrafish Embryonic Brain by Confocal Microscopy

In this video, we demonstrate the method our lab has developed to analyze the cell shape changes and rearrangements required to bend and fold the developing zebrafish brain (Gutzman et al, 2008). Such analysis affords a new understanding of the underlying cell biology required for development of the 3D structure of the vertebrate brain, and significantly increases our ability to study neural tube morphogenesis. The embryonic zebrafish brain is shaped beginning at 18 hours post fertilization (hpf) as the ventricles within the neuroepithelium inflate. By 24 hpf, the initial steps of neural tube morphogenesis are complete. Using the method described here, embryos at the one cell stage are injected with mRNA encoding membrane-targeted green fluorescent protein (memGFP). After injection and incubation, the embryo, now between 18 and 24 hpf, is mounted, inverted, in agarose and imaged by confocal microscopy. Notably, the zebrafish embryo is transparent making it an ideal system for fluorescent imaging. While our analyses have focused on the midbrain-hindbrain boundary and the hindbrain, this method could be extended for analysis of any region in the zebrafish to a depth of 
80-100 &mu;m.

In this video, we demonstrate a method by which to analyze the developing vertebrate brain in live zebrafish embryos at single cell resolution by confocal microscopy. This includes the method by which we inject the single-cell zebrafish embryo and subsequently mount and image the developing brain.

يعيش تصوير الدماغ الجنينية اسماك الزرد بواسطة الميكروسكوب متحد البؤر

In this video, we demonstrate the method our lab has developed to analyze the cell shape changes and rearrangements required to bend and fold the ...

Lens Transplantation in Zebrafish and its Application in the Analysis of Eye Mutants

The lens plays an important role in the development of the optic cup[1,2]. Using the zebrafish as a model organism, questions regarding lens development can be addressed. The zebrafish is useful for genetic studies due to several advantageous characteristics, including small size, high fecundity, short lifecycle, and ease of care. Lens development occurs rapidly in zebrafish. By 72 hpf, the zebrafish lens is functionally mature [3]. Abundant genetic and molecular resources are available to support research in zebrafish. In addition, the similarity of the zebrafish eye to those of other vertebrates provides basis for its use as an excellent animal model of human defects[4-7]. Several zebrafish mutants exhibit lens abnormalities, including high levels of cell death, which in some cases leads to a complete degeneration of lens tissues [8]. To determine whether lens abnormalities are due to intrinsic causes or to defective interactions with the surrounding tissues, transplantation of a mutant lens into a wild-type eye is performed. Using fire-polished metal needles, mutant or wild-type lenses are carefully dissected from the donor animal, and transferred into the host. To distinguish wild-type and mutant tissues, a transgenic line is used as the donor. This line expresses membrane-bound GFP in all tissues, including the lens. This transplantation technique is an essential tool in the studies of zebrafish lens mutants.

Lens development involves interactions with other tissues. Several zebrafish eye mutants are characterized by an abnormally small lens size. Here we demonstrate a lens transplantation experiment to determine whether this phenotype is due to intrinsic causes or defective interactions with tissues that surround the lens.

زرع عدسة في اسماك الزرد وتطبيقاتها في تحليل المسوخ العين

The lens plays an important role in the development of the optic cup[1,2]. Using the zebrafish as a model organism, questions regarding lens development ...

Tissue Targeted Embryonic Chimeras: Zebrafish Gastrula Cell Transplantation

Certain fundamental questions in the field of developmental biology can only be answered when cells are placed in novel environments or when small groups of cells in a larger context are altered.  Watching how one cell interacts with and behaves in a unique environment is essential to characterizing cell functions.  Determining how the localized misexpression of a specific protein influences surrounding cells provides insightful information on the roles that protein plays in a variety of developmental processes.  Our lab uses the zebrafish model system to uniquely combine genetic approaches with classical transplantation techniques to generate genotypic or phenotypic chimeras.  We study neuron-glial cell interactions during the formation of forebrain commissures in zebrafish. This video describes a method that allows our lab to investigate the role of astroglial populations in the diencephalon and the roles of specific guidance cues that influence projecting axons as they cross the midline. Due to their transparency zebrafish embryos are ideal models for this type of ectopic cell placement or localized gene misexpression. Tracking transplanted cells can be accomplished using a vital dye or a transgenic fish line expressing a fluorescent protein. We demonstrate here how to prepare donor embryos with a vital dye tracer for transplantation, as well as how to extract and transplant cells from one gastrula staged embryo to another.  We present data showing ectopic GFP+ transgenic cells within the forebrain of zebrafish embryos and characterize the location of these cells with respect to forebrain commissures.  In addition, we show laser scanning confocal timelapse microscopy of Alexa 594 labeled cells transplanted into a GFP+ transgenic host embryo.  These data provide evidence that gastrula staged transplantation enables the targeted positioning of ectopic cells to address a variety of questions in Developmental Biology.

Zebrafish cell transplantation enables the combination of genetics and embryology to generate tissue specific chimeras. This video demonstrates gastrula staged cell transplantations that have allowed our lab to investigate the roles of astroglial populations and specific guidance cues during commissure formation in the forebrain.

الأنسجة الجنينية الوهم المستهدفة : اسماك الزرد المعيدة زرع الخلايا

Certain fundamental questions in the field of developmental biology can only be answered when cells are placed in novel environments or when small groups ...

RNA Isolation from Embryonic Zebrafish and cDNA Synthesis for Gene Expression Analysis

Many important and complex laboratory procedures require an input of high quality, intact RNA.  A degraded sample or the presence of impurities can lead to disastrous results in downstream experimental applications.  It is therefore, of utmost importance to use solid techniques with numerous safeguards and quality control checks to ensure a superior sample.  Herein, we detail a protocol to isolate total RNA from whole zebrafish embryos using a commercially available chemical denaturant and subsequent cleanup to remove traces of DNA and impurities using a commercial RNA isolation kit. As RNA is relatively unstable and easily prone to cleavage by RNAses, most protocols assay gene expression using a cDNA product that is directly synthesized from an RNA template. We detail a procedure to convert RNA into the more stable cDNA product using a commercially available kit. Throughout these procedures there are numerous quality control checks to ensure that the sample is not degraded or contaminated.  The end product of these protocols is cDNA that is suitable for microarray analysis, RT-PCR or long-term storage.    

The isolation of high quality, intact RNA is an essential step in many laboratory protocols. Here, we demonstrate RNA extraction from whole zebrafish embryos and cDNA synthesis for subsequent application in various experimental procedures including gene expression microarray analysis.

عزل الحمض النووي الريبي من الجنينية التجميعي واسماك الزرد [كدنا] لتحليل الجينات

Many important and complex laboratory procedures require an input of high quality, intact RNA.  A degraded sample or the presence of impurities can lead ...

Immunostaining of Dissected Zebrafish Embryonic Heart

Zebrafish embryo becomes a popular in vivo vertebrate model for studying cardiac development and human heart diseases due to its advantageous embryology and genetics 1,2. About 100-200 embryos are readily available every week from a single pair of adult fish. The transparent embryos that develop ex utero make them ideal for assessing cardiac defects 3. The expression of any gene can be manipulated via morpholino technology or RNA injection 4. Moreover, forward genetic screens have already generated a list of mutants that affect different perspectives of cardiogenesis 5. 
Whole mount immunostaining is an important technique in this animal model to reveal the expression pattern of the targeted protein to a particular tissue 6. However, high resolution images that can reveal cellular or subcellular structures have been difficult, mainly due to the physical location of the heart and the poor penetration of the antibodies. 
 Here, we present a method to address these bottlenecks by dissecting heart first and then conducting the staining process on the surface of a microscope slide. To prevent the loss of small heart samples and to facilitate solution handling, we restricted the heart samples within a circle on the surface of the microscope slides drawn by an immEdge pen. After the staining, the fluorescence signals can be directly observed by a compound microscope. 
Our new method significantly improves the penetration for antibodies, since a heart from an embryonic fish only consists of few cell layers. High quality images from intact hearts can be obtained within a much reduced procession time for zebrafish embryos aged from day 2 to day 6. Our method can be potentially extended to stain other organs dissected from either zebrafish or other small animals.

A rapid way to conduct immunostaining of zebrafish embryonic heart is described. Compared to the whole mount immunostaining approach, this method dramatically increases the penetration of the antibodies, which allows obtaining high resolution images that reveal cellular/subcellular structures in the heart within a much reduced processing time.

Immunostaining تشريح القلب الجنينية اسماك الزرد

Zebrafish embryo becomes a popular in vivo vertebrate model for studying cardiac development and human heart diseases due to its advantageous embryology ...

In vivo Electroporation of Morpholinos into the Adult Zebrafish Retina

Many devastating inherited eye diseases result in progressive and irreversible blindness because humans cannot regenerate dying or diseased retinal neurons. In contrast, the adult zebrafish retina possesses the robust ability to spontaneously regenerate any neuronal class that is lost in a variety of different retinal damage models, including retinal puncture, chemical ablation, concentrated high temperature, and intense light treatment 1-8. Our lab extensively characterized regeneration of photoreceptors following constant intense light treatment and inner retinal neurons after intravitreal ouabain injection 2, 5, 9. In all cases, resident M&uuml;ller glia re-enter the cell cycle to produce neuronal progenitors, which continue to proliferate and migrate to the proper retinal layer, where they differentiate into the deficient neurons. 
	We characterized five different stages during regeneration of the light-damaged retina that were highlighted by specific cellular responses. We identified several differentially expressed genes at each stage of retinal regeneration by mRNA microarray analysis 10. Many of these genes are also critical for ocular development. To test the role of each candidate gene/protein during retinal regeneration, we needed to develop a method to conditionally limit the expression of a candidate protein only at times during regeneration of the adult retina. 
	Morpholino oligos are widely used to study loss of function of specific proteins during the development of zebrafish, Xenopus, chick, mouse, and tumors in human xenografts 11-14. These modified oligos basepair with complementary RNA sequence to either block the splicing or translation of the target RNA. Morpholinos are stable in the cell and can eliminate or "knockdown" protein expression for three to five days 12. 
	Here, we describe a method to efficiently knockdown target protein expression in the adult zebrafish retina. This method employs lissamine-tagged antisense morpholinos that are injected into the vitreous of the adult zebrafish eye. Using electrode forceps, the morpholino is then electroporated into all the cell types of the dorsal and central retina. Lissamine provides the charge on the morpholino for electroporation and can be visualized to assess the presence of the morpholino in the retinal cells. 
	Conditional knockdown in the retina can be used to examine the role of specific proteins at different times during regeneration. Additionally, this approach can be used to study the role of specific proteins in the undamaged retina, in such processes as visual transduction and visual processing in second order neurons.

In vivo Electroporation of Morpholinos into the Adult Zebrafish Retina

A method to conditionally knockdown a target protein&#x2019;s expression in the adult zebrafish retina is described, which involves intravitreally injecting antisense morpholinos and electroporating them into the retina. The resulting protein is knocked down for several days, which allows testing the protein&#x2019;s role in the regenerating or intact retina.

في الجسم الحي من Electroporation Morpholinos في شبكية العين اسماك الزرد الكبار

Many devastating inherited eye diseases result in progressive and irreversible blindness because humans cannot regenerate dying or diseased retinal ...

A System for ex vivo Culturing of Embryonic Pancreas

The pancreas controls vital functions of our body, including the production of digestive enzymes and regulation of blood sugar levels1. Although in the past decade many studies have contributed to a solid foundation for understanding pancreatic organogenesis, important gaps persist in our knowledge of early pancreas formation2. A complete understanding of these early events will provide insight into the development of this organ, but also into incurable diseases that target the pancreas, such as diabetes or pancreatic cancer. Finally, this information will generate a blueprint for developing cell-replacement therapies in the context of diabetes.
 During embryogenesis, the pancreas originates from distinct embryonic outgrowths of the dorsal and ventral foregut endoderm at embryonic day (E) 9.5 in the mouse embryo3,4. Both outgrowths evaginate into the surrounding mesenchyme as solid epithelial buds, which undergo proliferation, branching and differentiation to generate a fully mature organ2,5,6. Recent evidences have suggested that growth and differentiation of pancreatic cell lineages, including the insulin-producing &beta;-cells, depends on proper tissue-architecture, epithelial remodeling and cell positioning within the branching pancreatic epithelium7,8. However, how branching morphogenesis occurs and is coordinated with proliferation and differentiation in the pancreas is largely unknown. This is in part due to the fact that current knowledge about these developmental processes has relied almost exclusively on analysis of fixed specimens, while morphogenetic events are highly dynamic.
 Here, we report a method for dissecting and culturing mouse embryonic pancreatic buds ex vivo on glass bottom dishes, which allow direct visualization of the developing pancreas (Figure 1). This culture system is ideally devised for confocal laser scanning microscopy and, in particular, live-cell imaging. Pancreatic explants can be prepared not only from wild-type mouse embryos, but also from genetically engineered mouse strains (e.g. transgenic or knockout), allowing real-time studies of mutant phenotypes. Moreover, this ex vivo culture system is valuable to study the effects of chemical compounds on pancreatic development, enabling to obtain quantitative data about proliferation and growth, elongation, branching, tubulogenesis and differentiation. In conclusion, the development of an ex vivo pancreatic explant culture method combined with high-resolution imaging provides a strong platform for observing morphogenetic and differentiation events as they occur within the developing mouse embryo.

A System for ex vivo Culturing of Embryonic Pancreas

Here, we describe a method for isolation, culture and manipulation of mouse embryonic pancreas. This represents an excellent ex vivo system for studying various aspects of pancreatic development, including morphogenesis, differentiation and growth. Pancreatic bud explants can be cultured for several days and used in a range of different applications, including whole-mount immunofluorescence and live imaging.

نظام ل<em&gt; خارج الجسم</em&gt; التثقيف البنكرياس الجنينية

The pancreas controls vital functions of our body,  including the production of digestive enzymes and regulation of blood sugar  levels1. Although in the ...

Laser-inflicted Injury of Zebrafish Embryonic Skeletal Muscle

Various experimental approaches have been used in mouse to induce muscle injury with the aim to study muscle regeneration, including myotoxin injections (bupivacaine, cardiotoxin or notexin), muscle transplantations (denervation-devascularization induced regeneration), intensive exercise, but also murine muscular dystrophy models such as the mdx mouse (for a review of these approaches see 1). In zebrafish, genetic approaches include mutants that exhibit muscular dystrophy phenotypes (such as runzel2 or sapje3) and antisense oligonucleotide morpholinos that block the expression of dystrophy-associated genes4. Besides, chemical approaches are also possible, e.g. with Galanthamine, a chemical compound inhibiting acetylcholinesterase, thereby resulting in hypercontraction, which eventually leads to muscular dystrophy5. However, genetic and pharmacological approaches generally affect all muscles within an individual, whereas the extent of physically inflicted injuries are more easily controlled spatially and temporally1. Localized physical injury allows the assessment of contralateral muscle as an internal control. Indeed, we recently used laser-mediated cell ablation to study skeletal muscle regeneration in the zebrafish embryo6, while another group recently reported the use of a two-photon laser (822 nm) to damage very locally the plasma membrane of individual embryonic zebrafish muscle cells7.
Here, we report a method for using the micropoint laser (Andor Technology) for skeletal muscle cell injury in the zebrafish embryo. The micropoint laser is a high energy laser which is suitable for targeted cell ablation at a wavelength of 435 nm. The laser is connected to a microscope (in our setup, an optical microscope from Zeiss) in such a way that the microscope can be used at the same time for focusing the laser light onto the sample and for visualizing the effects of the wounding (brightfield or fluorescence). The parameters for controlling laser pulses include wavelength, intensity, and number of pulses.
Due to its transparency and external embryonic development, the zebrafish embryo is highly amenable for both laser-induced injury and for studying the subsequent recovery. Between 1 and 2 days post-fertilization, somitic skeletal muscle cells progressively undergo maturation from anterior to posterior due to the progression of somitogenesis from the trunk to the tail8, 9. At these stages, embryos spontaneously twitch and initiate swimming. The zebrafish has recently been recognized as an important vertebrate model organism for the study of tissue regeneration, as many types of tissues (cardiac, neuronal, vascular etc.) can be regenerated after injury in the adult zebrafish10, 11.

The method presented here comprises the precise injury of live zebrafish embryos with high-energy laser pulses and the subsequent analysis of these injuries and their recovery with time. We also show how genetically labeled single or groups of skeletal muscle cells can be tracked during and after laser light induced damage.

الليزر بإلحاق الضرر من العضلات الهيكلية اسماك الزرد الجنينية

Various experimental approaches have been used in mouse to induce muscle injury with the aim to study muscle regeneration, including myotoxin injections ...

Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations

The zebrafish has proven to be a valuable model system for exploring skeletal muscle function and for studying human muscle diseases. Despite the many advantages offered by in vivo analysis of skeletal muscle in the zebrafish, visualizing the complex and finely structured protein milieu responsible for muscle function, especially in whole embryos, can be problematic. This hindrance stems from the small size of zebrafish skeletal muscle (60 &mu;m) and the even smaller size of the sarcomere. Here we describe and demonstrate a simple and rapid method for isolating skeletal myofibers from zebrafish embryos and larvae. We also include protocols that illustrate post preparation techniques useful for analyzing muscle structure and function. Specifically, we detail the subsequent immunocytochemical localization of skeletal muscle proteins and the qualitative analysis of stimulated calcium release via live cell calcium imaging. Overall, this video article provides a straight-forward and efficient method for the isolation and characterization of zebrafish skeletal myofibers, a technique which provides a conduit for myriad subsequent studies of muscle structure and function.

Zebrafish are an emerging system for modeling human disorders of the skeletal muscle. We describe a fast and efficient method to isolate skeletal muscle myofibers from embryonic and larval zebrafish. This method yields a high-density myofiber preparation suitable for study of single skeletal muscle fiber morphology, protein subcellular localization, and muscle physiology.

تحليل الجنينية واليرقات الزرد الهيكل العظمي Myofibers من الاستعدادات فصلها

The zebrafish has  proven to be a valuable model system for exploring skeletal muscle function and  for studying human muscle diseases. Despite  the many ...