شكرا جزيلا لPranski الين وكارولين Suwyn للحصول على المساعدة التقنية الممتازة وهاري ليفين إلى الثالث ، M. بول ميرفي ، ومارلا التسخير لإجراء محادثات هامة. وقدم التمويل RR - 00165 ، PO1AG026423 ، P50AG025688 ، AG030539 ، ومؤسسة وودروف وجامعة إيموري جنة البحوث.

الجزء 1 : إعداد الخليط الأنسجة توضيح <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> Dounce التجانس الأنسجة القشرية غير المثبتة في حجم 4 مرات من الجليد الباردة العازلة (0.1M الفوسفات مخزنة المالحة [كا + + -- والمغنيسيوم + + خالية] زائد مثبط البروتياز 2X الكوكتيل [سانتا كروز]) مع ما يقرب من 30 جلدة مدقة حتى (العازلة إضافة أي 400μl ل100mg الأنسجة). </li><li style=";text-align:right;direction:rtl"> تدور الخليط لمدة 5 دقائق على 3000 غرام (4 درجات مئوية). إزالة بعناية وأوضح supernatants aliquots تخزين هذه الخلاصات في -80 درجة مئوية حتى استخدام. </li><li style=";text-align:right;direction:rtl"> تحديد تركيز البروتين الكلي (ميكروغرام / ميكرولتر) لتوضيح الخليط باستخدام حمض bicinchoninic (BCA) مقايسة ، وفقا لتعليمات الشركة الصانعة (ThermoFisher). </li></ol> الجزء 2 : SDS - PAGE إعداد نموذج <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> مع 10 أيضا ، 10-20 ٪ Tricine هلام (Invitrogen) ، وحجم الحد الأقصى الذي يمكن تحميله في البئر 25μl ~. ويشمل اجمالي حجم العينة SDS 2X العازلة و 10x وكيل الحد ، وبالتالي فإن الحد الأقصى لحجم جناسة أوضح أن يمكن تحميلها في البئر 10μl. أوضح 20 ٪ (ث / ت) ينبغي أن يكون الخليط القشرية تركيز البروتين الكلي أكبر من 5 ميكروغرام / ميكرولتر ، والسماح ل50μg البروتين الكلي لكل بئر. سوف عينات مع أقل من البروتين 5mg/ml تستلزم تحميل البروتين أقل مجموع لكل بئر. ومع ذلك ، ومستويات عالية من البروتين هي المثلى للكشف عن Aβ موحودي وتجميعها (50 60μg البروتين الكلي هو الأمثل). تحميل دائما نفس الكمية من البروتين الكلي لكل بئر. </li><li style=";text-align:right;direction:rtl"> لكل جيل ، وتحميل واحد على الأقل بشكل جيد مع 10μl من علامة الوزن الجزيئي مثل Plus2 SeeBlue (Invitrogen). كعنصر تحكم إيجابية ، تشغيل 10 - 100ng الاصطناعية أو Aβ40 Aβ42 الببتيد (مخفف في 1xPBS) في مكان آخر أيضا. </li><li style=";text-align:right;direction:rtl"> تحضير مخاليط رد فعل على الجليد ، وذلك باستخدام إذابة الطازجة ، أوضح الخليط. أنابيب لدوامة ثانية 50-10 ، والحرارة في حوض جاف على 100 درجة مئوية لمدة 5 دقائق ، ثم تدور بسرعة لإزالة جميع العينات التكثيف في الحد الأقصى. </li></ol> الجزء 3 : SDS - PAGE الكهربائي جل <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> تحميل عينات vortexed على جل Tricine 10-20 ٪ في Gelbox XCell قفل البسيطة سيل من المؤكد ، وذلك باستخدام Tricine SDS العازلة على التوالي ، وفقا لتعليمات الشركة الصانعة (Invitrogen) </li><li style=";text-align:right;direction:rtl"> تشغيل هلام في الجهد المستمر من 125V لمدة 90 دقيقة. اسمحوا عينات تستمر حتى الفرقة علامة 4KDa حوالي 1 سم من الجزء السفلي من هلام. </li></ol> الجزء 4 : نقل البروتينات من الهلام إلى الأغشية <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> إزالة المواد الهلامية بعناية من حالة من البلاستيك وتجميع ساندويتش نقل داخل وحدة لطخة XCell الثاني ، وفقا لتعليمات الشركة الصانعة (Invitrogen). قبل النشاف الرطب منصات والأغشية العازلة مع النيتروسليلوز 0.2μm نقل تريس ، جليكاين (20 ٪ الميثانول) ، وإزالة أي فقاعات من منصات النشاف أو تصفية شطيرة الورق / الغشاء. </li><li style=";text-align:right;direction:rtl"> في Gelbox XCell ، وملء الغرفة الداخلية العازلة مع نقل وملء الغرفة الخارجي مع DIH 2 O (التعرض الميثانول يمكن ارتداء أسفل gelbox البلاستيكية على مر الزمن). </li><li style=";text-align:right;direction:rtl"> تشغيل ونقل لمدة 2-3 ساعات في التيار المستمر 25mA. </li><li style=";text-align:right;direction:rtl"> عند اكتمال عملية النقل ، وتفكيك شطيرة وضع المواد الهلامية في DIH 2 O والأغشية في 1xPBS ، سواء في ساحة أطباق بتري بلاستيكية (أو حاوية أخرى مناسبة). </li><li style=";text-align:right;direction:rtl"> لتصور كفاءة نقل البروتين ، يمكن ملطخة المواد الهلامية مع SafeStain الازرق ببساطة (Invitrogen) ، والأغشية مع الشقائقية S الأحمر وصمة عار (الدريتش سيغما) ، وكلاهما وفقا لتعليمات الشركة الصانعة وهذا لا يتعارض مع تلوين immunoblotting. إذا تلطيخ يكشف عدم كفاءة نقل البروتين ، وتعديل مدة نقل في الخطوة 3. </li></ol> الجزء 5. مستضد حاتمة واسترجاع Immunoblotting <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> استرجاع المستضد هو خطوة هامة في الكشف عن الحواتم Aβ على الغشاء للربط الأضداد خلال immunoblotting. أي باخرة ، الميكروويف ، أو ماء الاستحمام تحافظ على درجة حرارة ثابتة تبلغ 100 درجة مئوية وسوف يكون كافيا. لاسترجاع مستضد في باخرة ، والحرارة ختم الغشاء في الحقيبة الثقيلة من البلاستيك مملوءة Kapak 1xPBS ، في درجة حرارة الغرفة. وضع الحقيبة في شقة باخرة قبل ساخنة ، وبمجرد الحقيبة تبدأ في التوسع ، واحتضان لمدة 15 دقيقة إضافية. السماح لتبرد ببطء الغشاء قبل إزالته من الحقيبة ، لمنع التجاعيد المفرطة. </li><li style=";text-align:right;direction:rtl"> في درجة حرارة الغرفة ، وإزالة الغشاء بعناية من الحقيبة تبخير وشطف الغشاء لمدة 5 دقائق في 1xPBS ، تليها شطف 5 دقائق في TBS - T (تريس مخزنة المالحة ، ودرجة الحموضة 8.0 مع 0.05 ٪ توين - 20 [سيغما] ) ، على شاكر المداري. احتضان الغشاء في محلول حظر (2.5 ٪ دهن الحليب في TBS - T) لمدة ساعة ، والهز. دون الشطف ، ونقل إلى غشاء صحن أو الحقيبة البلاستيكية التي تحتوي على الأجسام المضادة الأولية مخففة في حل حظر (6E10 في 1:1،000 [1μg/ml] 1:5،000 التخفيف [0.2μg/ml] ، كوفانس) ، فقاعة تجنبس. على احتضان شاكر المداري في درجة حرارة الغرفة لمدة ساعة ثم 24-48 ساعة تهتز عند 4 درجات مئوية (أطول الحضانة قد يعطي إشارة أفضل). </li><li style=";text-align:right;direction:rtl"> شطف الغشاء لمدة 30 دقيقة في TBS - T (واحد سريع شطف تليها 3 دقيقة يشطف X 10). </li><li style=";text-align:right;direction:rtl"> احتضان الغشاء في HRP - مترافق الضد الثانوية (أمرشام ECL الأغنام المناهضة للماوس ، وجنرال الكتريك للرعاية الصحية) ، مخففة في 1:10،000 في حل حظر لمدة 90 دقيقة على شاكر في درجة حرارة الغرفة. </li><li style=";text-align:right;direction:rtl"> شطف الغشاء لمدة 30 دقيقة في TBS - T (واحد سريع شطف تليها 3 دقيقة يشطف X 10). </li><li style=";text-align:right;direction:rtl"> على شاكر ، في احتضان الغشاء طازجة من صنع كاشف الغربية SuperSignal Electrochemiluminescence بيكو (ThermoFisher) لمدة 5 دقائق ، وصمة عار قبالة كاشف الزائدة على الورق الخالي من الوبر ومكان تصفية الغشاء في شريط الفيلم ، وبين حماة ورقة من البلاستيك. وصمة عار قبالة إضافية SuperSignal كاشف مع الغبار خالية Kimwipes إذا لزم الأمر. </li><li style=";text-align:right;direction:rtl"> يعرض الفيلم لكوداك MR Biomax لفترات من 30 ثانية تصل الى 30 دقيقة والتطور في تطوير الفيلم. بعد 5 دقائق ، على الأرجح أن عصابات مونومر Aβ تكون مشبعة. </li><li style=";text-align:right;direction:rtl"> يمكن تجريد أغشية (بعد الشطف في TBS - T) التي تهتز في استعادة بلس تجريد العازلة لمدة 30 دقيقة في درجة حرارة الغرفة وreprobed مع الأضداد إضافية إذا لزم الأمر. </li></ol> الجزء 6 : الممثل طخة مناعية : <img src="/files/ftp_upload/1916/1916fig1a.jpg" alt="الشكل 1A" /> <img src="/files/ftp_upload/1916/1916fig1b.jpg" alt="الرقم 1B" /> <img src="/files/ftp_upload/1916/1916fig1c.jpg" alt="الرقم 1C" /> ويتم تحليل الأرقام 1A - C. الخليط تحتوي على توضيح كيفية 50μg البروتين الكلي في الفترة من 7 بالكائن البشري لوجود Aβ multimeric وAPP. Immunoblotting مع 6E10 الضد يكشف مونومرات Aβ ، dimers ، trimers ، tetramers وAPP (عصابة أعلى) في جميع الحالات الزهايمر ، فضلا عن ارتفاع الوزن الجزيئي وفيرة Aβ multimers في حالات م 2. Aβ40 الاصطناعية تؤكد هوية الفرق انخفاض الوزن الجزيئي. م : مرض الزهايمر ، DLB : الخرف مع الهيئات ليوي ، ND : Nondemented الإنسان (أ) تعرض الفيلم لمدة 30 دقيقة ، و (ب) تعرض الفيلم 5 دقائق ، و (ج) 30 تعرض الفيلم الثاني.

<ol>
	<li>Hardy, J., Selkoe, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+amyloid+hypothesis+of+Alzheimer's+disease:+progress+and+problems+on+the+road+to+therapeutics.">The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics.</a> Science. 297, 353-356 (2002).</li><li>Haass, C., Selkoe, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Soluble+protein+oligomers+in+neurodegeneration:+lessons+from+the+Alzheimer's+amyloid+beta-peptide.">Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid beta-peptide.</a> Nat. Rev. Mol. Cell. Biol. 8, 101-112 (2007).</li><li>Walker, L. C., LeVine, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+cerebral+proteopathies.">The cerebral proteopathies.</a> Neurobiol. Aging. 21, 559-561 (2000).</li><li>Selkoe, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Aging,+amyloid,+and+Alzheimer's+disease:+a+perspective+in+honor.">Aging, amyloid, and Alzheimer's disease: a perspective in honor.</a> of Carl Cotman. Neurochem. Res. 28, 1705-1713 (2003).</li><li>Walsh, D. M., Selkoe, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Abeta+oligomers+-+a+decade+of+discovery.">Abeta oligomers - a decade of discovery.</a> J. Neurochem. 101, 1172-1184 (2007).</li><li>Swerdlow, P. S., Finley, D., Varshavsky, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enhancement+of+immunoblot+sensitivity+by+heating+of+hydrated+filters.">Enhancement of immunoblot sensitivity by heating of hydrated filters.</a> Anal. Biochem. 156, 147-153 (1986).</li><li>Ida, N., Hartmann, T., Pantel, J., Schr&#246;der, J., Zerfass, R., F&#246;rstl, H., Sandbrink, R., Masters, C. L., Beyreuther, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Analysis+of+hetergeneous+A4+peptides+in+human+cerebrospinal+fuid+and+blood+by+a+newly+developed+sensitive+Western+blot+assay.">Analysis of hetergeneous A4 peptides in human cerebrospinal fuid and blood by a newly developed sensitive Western blot assay.</a> J. Biol. Chem. 271, 22908-22914 (1996).</li></ol>

على الرغم من أهمية تجميع Aβ في التسبب في مرض الزهايمر 1،4،5 ، وقد وصفت دراسات قليلة كميا أو توزيع multimers Aβ متنوعة في عينات الأنسجة البشرية القشرية 2. المناعى التقنيات استخداما لا تسمح للتمييز من الأنواع المتميزة Aβ multimeric في الأنسجة القشرية الثابتة. الخليط غير...

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		<div>
		<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>Complete Protease Inhibitor Cocktail Tablets</td>
<td>&nbsp;</td>
<td>Santa Cruz Biotechnology</td>
<td>Sc-29130</td>
<td>1 tablet in 25ml buffer</td>
</tr>
<tr>
<td>BCA Protein Assay kit</td>
<td>&nbsp;</td>
<td>ThermoFisher Scientific</td>
<td>23225</td>
<td>&nbsp;</td>
<tr>
<td>XCell SureLock Mini-Cell and XCell II Blot Module Kit CE Mark</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>EI0002</td>
<td>&nbsp;</td>
<tr>
<td>Novex Tricine SDS Sample Buffer (2X)</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>LC1676</td>
<td>&nbsp;</td>
<tr>
<td>NuPAGE Sample Reducing Agent (10X)</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>NP0004</td>
<td>&nbsp;</td>
<tr>
<td>SeeBlue Plus2 Pre-Stained Standard</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>LC5925</td>
<td>&nbsp;</td>
<tr>
<td>Novex 10-20% Tricine Gel 1.0 mm, 10 well</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>EC6625BOX</td>
<td>&nbsp;</td>
<tr>
<td>Nitrocellulose membranes, 0.2 &mu;m pore size</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>LC2000</td>
<td>&nbsp;</td>
<tr>
<td>Novex Tricine SDS Running Buffer (10X)</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>LC1675</td>
<td>&nbsp;</td>
<tr>
<td>Novex Tris-Glycine Transfer Buffer (25X)</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>LC3675</td>
<td>&nbsp;</td>
<tr>
<td>SimplyBlue SafeStain</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>LC6060</td>
<td>Will not interfere with immunostaining</td>
</tr>
<tr>
<td>ATX Ponceau S Red staining solution</td>
<td>&nbsp;</td>
<td>Sigma Aldrich</td>
<td>09276</td>
<td>Will not interfere with immunostaining</td>
</tr>
<tr>
<td>Kapak heat sealable plastic sample pouches</td>
<td>&nbsp;</td>
<td>Fisher Scientific</td>
<td>0181225AA</td>
<td>&nbsp;</td>
<tr>
<td>6E10 mouse monoclonal antibody to A&beta;(1-16)</td>
<td>&nbsp;</td>
<td>Covance</td>
<td>SIG-39320</td>
<td>Dilute 1:1,000 up to 1:5,000 for WB</td>
</tr>
<tr>
<td>Tween 20</td>
<td>&nbsp;</td>
<td>Sigma Aldrich</td>
<td>P2287</td>
<td>&nbsp;</td>
<tr>
<td>ECL Mouse IgG, HRP-Linked Whole A&beta; (from sheep)</td>
<td>&nbsp;</td>
<td>GE Healthcare Life Sciences</td>
<td>NA931-1ML</td>
<td>Dilute at 1:10,000</td>
</tr>
<tr>
<td>SuperSignal West Pico Chemiluminescent Substrate</td>
<td>&nbsp;</td>
<td>ThermoFisher</td>
<td>34077</td>
<td>&nbsp;</td>
<tr>
<td>Kodak Biomax MR Film</td>
<td>&nbsp;</td>
<td>Carestream Health</td>
<td>870 1302</td>
<td>&nbsp;</td>		</tbody>
		</table>
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sds-page/immunoblot detection of a&beta; multimers in human cortical tissue homogenates using antigen-epitope retrieval

للطي الشاذ والبلمرة من اميلويد β (Aβ) يعتقد الببتيد للشروع في تعاقب الاعصاب في التسبب بمرض الزهايمر<sup&gt; 1</sup&gt;. Aβ هي في الغالب ما بين 40 -- الببتيد حمض أميني أو 42 ، وهذا هو عرضة للتجميع الذاتي في β ورقة الغنية ييفات اميلويد التي تم العثور عليها في عينات من لويحات خرف الدماغ في مرض الزهايمر. أدلة متزايدة تشير إلى أن انخفاض الوزن الجزيئي ، multimers Aβ ذوبان أكثر سمية من اميلويد Aβ ييفي<sup&gt; 2</sup&gt;. تحديد وتقدير حجم الأنواع الوزن Aβ multimeric المنخفضة والعالية الجزيئية في أنسجة الدماغ هو هدف أساسي في مجال أمراض الزهايمر ، ويمكن تطبيق الأساليب المستخدمة أيضا إلى تحديد وتوصيف multimers السامة في proteopathies أخرى<sup&gt; 3</sup&gt;. ويمكن الكشف عن multimers Aβ طبيعيا بواسطة SDS - الكهربائي للهلام بولي أكريلاميد تليها immunoblotting مع Aβ محددة الأجسام المضادة. ومع ذلك ، فإن الانفصال وكشف Aβ multimeric يتطلب استخدام الخليط القشرية عالية التركيز واسترجاع صغيرة في الأغشية مستضد النيتروسليلوز مسام الحجم. نحن هنا وصف الأسلوب لإعداد الخليط أوضح القشرية الإنسان ، والفصل بين البروتينات التي SDS - PAGE ، ومستضد حاتمة استرجاع / النشاف الغربية مع 6E10 الضد إلى المنطقة N - محطة من الببتيد Aβ. باستخدام هذا البروتوكول ، ونحن باستمرار اكتشاف مونومرات Aβ ، dimers ، trimers ، tetramers ، وارتفاع الوزن الجزيئي multimers في الأنسجة القشرية من البشر مع أمراض الزهايمر.

Watch this Scientific Journal Video about SDS-PAGE/Immunoblot Detection of AÎ² Multimers in Human Cortical Tissue Homogenates using Antigen-Epitope Retrieval at JoVE.com

SDS-PAGE/Immunoblot Detection of A&amp;#946; Multimers in Human Cortical Tissue Homogenates using Antigen-Epitope Retrieval

وصفنا تقنية لإعداد الخليط أوضح القشرية الإنسان ، وفصل البروتين SDS - PAGE ، واسترجاع مستضد immunoblotting مع الضد إلى الببتيد Aβ. باستخدام هذا البروتوكول ، ونحن باستمرار اكتشاف Aβ موحودي multimeric في الأنسجة والقشرية من البشر مع أمراض الزهايمر.

SDS-PAGE/Immunoblot الكشف عن Multimers Aβ في الأنسجة البشرية القشرية الخليط باستخدام مستضد استرجاع حاتمة

The anomalous folding and polymerization of the &beta;-amyloid (A&beta;) peptide is thought to initiate the neurodegenerative cascade in Alzheimer's ...

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Neuroscience

SDS-PAGE/Immunoblot Detection of A&beta; Multimers in Human Cortical Tissue Homogenates using Antigen-Epitope Retrieval

23.9K Views.  Emory University. وصفنا تقنية لإعداد الخليط أوضح القشرية الإنسان ، وفصل البروتين SDS - PAGE ، واسترجاع مستضد immunoblotting مع الضد إلى الببتيد Aβ. باستخدام هذا البروتوكول ، ونحن باستمرار اكتشاف Aβ موحودي multimeric في الأنسجة والقشرية من البشر مع أمراض الزهايمر.

Video: SDS-PAGE/Immunoblot Detection of A&#946; Multimers in Human Cortical Tissue Homogenates using Antigen-Epitope Retrieval

Cryopreservation of Cortical Tissue Blocks for the Generation of Highly Enriched Neuronal Cultures

In this study, we outline a standardized protocol for the successful cryopreservation and thawing of cortical brain tissue blocks to generate highly enriched neuronal cultures. For this protocol the freezing medium used is 10% dimethyl sulfoxide (DMSO) diluted in Hank's Buffered Salt Solution (HBSS). Blocks of cortical tissue are transferred to cryovials containing the freezing medium and slowly frozen at -1&deg;C/min in a rate-controlled freezing container. Post-thaw processing and dissociation of frozen tissue blocks consistently produced neuronal-enriched cultures which exhibited rapid neuritic growth during the first 5 days in culture and significant expansion of the neuronal network within 10 days. Immunocytochemical staining with the astrocytic marker glial fibrillary acidic protein (GFAP) and the neuronal marker beta-tubulin class III, revealed high numbers of neurons and astrocytes in the cultures. Generation of neural precursor cell cultures after tissue block dissociation resulted in rapidly expanding neurospheres, which produced large numbers of neurons and astrocytes under differentiating conditions. This simple cryopreservation protocol allows for the rapid, efficient, and inexpensive preservation of cortical brain tissue blocks, which grants increased flexibility for later generation of neuronal, astrocyte, and neuronal precursor cell cultures.

Here, we describe a method for efficient cryopreservation and thawing of cortical brain tissue blocks to generate highly enriched neuronal cultures. This simple protocol provides flexibility for later generation of neuronal, astrocyte, and neuronal precursor cell cultures.

الحفظ بالتبريد من كتل الأنسجة القشرية للجيل الثقافات متعلق بالخلايا العصبية التخصيب

In this study, we outline a standardized protocol for the successful cryopreservation and thawing of cortical brain tissue blocks to generate highly ...

Time-lapse Live Imaging of Clonally Related Neural Progenitor Cells in the Developing Zebrafish Forebrain

Precise patterns of division, migration and differentiation of neural progenitor cells are crucial for proper brain development and function1,2. To understand the behavior of neural progenitor cells in the complex in vivo environment, time-lapse live imaging of neural progenitor cells in an intact brain is critically required. In this video, we exploit the unique features of zebrafish embryos to visualize the development of forebrain neural progenitor cells in vivo. We use electroporation to genetically and sparsely label individual neural progenitor cells. Briefly, DNA constructs coding for fluorescent markers were injected into the forebrain ventricle of 22 hours post fertilization (hpf) zebrafish embryos and electric pulses were delivered immediately. Six hours later, the electroporated zebrafish embryos were mounted with low melting point agarose in glass bottom culture dishes. Fluorescently labeled neural progenitor cells were then imaged for 36hours with fixed intervals under a confocal microscope using water dipping objective lens. The present method provides a way to gain insights into the in vivo development of forebrain neural progenitor cells and can be applied to other parts of the central nervous system of the zebrafish embryo.

The present video demonstrates a method which takes advantage of the combination of electroporation and confocal microscopy to perform live imaging on individual neural progenitor cells in the developing zebrafish forebrain. In vivo analysis of the development of forebrain neural progenitor cells at a clonal level can be achieved in this way.

الوقت الفاصل بين التصوير حية من خلايا ذات صلة Clonally السلف العصبية في الدماغ المقدم اسماك الزرد النامية

Precise patterns of division, migration and differentiation of neural progenitor cells are crucial for proper brain development and function1,2. To ...

High Sensitivity 5-hydroxymethylcytosine Detection in Balb/C Brain Tissue

DNA hydroxymethylation is a long known modification of DNA, but has recently become a focus in epigenetic research. Mammalian DNA is enzymatically modified at the 5th carbon position of cytosine (C) residues to 5-mC, predominately in the context of CpG dinucleotides. 5-mC is amenable to enzymatic oxidation to 5-hmC by the Tet family of enzymes, which are believed to be involved in development and disease. Currently, the biological role of 5-hmC is not fully understood, but is generating a lot of interest due to its potential as a biomarker. This is due to several groundbreaking studies identifying 5-hydroxymethylcytosine in mouse embryonic stem (ES) and neuronal cells. Research techniques, including bisulfite sequencing methods, are unable to easily distinguish between 5-mC and 5-hmC . A few protocols exist that can measure global amounts of 5-hydroxymethylcytosine in the genome, including liquid chromatography coupled with mass spectrometry analysis or thin layer chromatography of single nucleosides digested from genomic DNA. Antibodies that target 5-hydroxymethylcytosine also exist, which can be used for dot blot analysis, immunofluorescence, or precipitation of hydroxymethylated DNA, but these antibodies do not have single base resolution.In addition, resolution depends on the size of the immunoprecipitated DNA and for microarray experiments, depends on probe design. Since it is unknown exactly where 5-hydroxymethylcytosine exists in the genome or its role in epigenetic regulation, new techniques are required that can identify locus specific hydroxymethylation. The EpiMark 5-hmC and 5-mC Analysis Kit provides a solution for distinguishing between these two modifications at specific loci. The EpiMark 5-hmC and 5-mC Analysis Kit is a simple and robust method for the identification and quantitation of 5-methylcytosine and 5-hydroxymethylcytosine within a specific DNA locus. This enzymatic approach utilizes the differential methylation sensitivity of the isoschizomers MspI and HpaII in a simple 3-step protocol. Genomic DNA of interest is treated with T4-BGT, adding a glucose moeity to 5-hydroxymethylcytosine. This reaction is sequence-independent, therefore all 5-hmC will be glucosylated; unmodified or 5-mC containing DNA will not be affected. This glucosylation is then followed by restriction endonuclease digestion. MspI and HpaII recognize the same sequence (CCGG) but are sensitive to different methylation states. HpaII cleaves only a completely unmodified site: any modification (5-mC, 5-hmC or 5-ghmC) at either cytosine blocks cleavage. MspI recognizes and cleaves 5-mC and 5-hmC, but not 5-ghmC. The third part of the protocol is interrogation of the locus by PCR. As little as 20 ng of input DNA can be used. Amplification of the experimental (glucosylated and digested) and control (mock glucosylated and digested) target DNA with primers flanking a CCGG site of interest (100-200 bp) is performed. If the CpG site contains 5-hydroxymethylcytosine, a band is detected after glucosylation and digestion, but not in the non-glucosylated control reaction. Real time PCR will give an approximation of how much hydroxymethylcytosine is in this particular site. In this experiment, we will analyze the 5-hydroxymethylcytosine amount in a mouse Babl/C brain sample by end point PCR.

The EpiMark 5-hmC and 5-mC Analysis Kit can be used to analyze and quantitate 5-methylcytosine and 5-hydroxymethylcytosine within a spe cific locus. The kit distinguishes 5-mC from 5-hmC by the addition of glucose to the hydroxyl group of 5-hmC via an enzymatic reaction utilizing &beta;-glucosyltransferase (T4-BGT). When 5-hmC occurs In the context of CCGG, this modification converts a cleavable MspI site to a non-cleavable site.

الحساسية العالية 5 - hydroxymethylcytosine كشفها في أنسجة المخ BALB / C

DNA hydroxymethylation is a long known modification of DNA, but has recently become a focus in epigenetic research.   Mammalian DNA is enzymatically ...

Coherence between Brain Cortical Function and Neurocognitive Performance during Changed Gravity Conditions

Previous studies of cognitive, mental and/or motor processes during short-, medium- and long-term weightlessness have only been descriptive in nature, and focused on psychological aspects. Until now, objective observation of neurophysiological parameters has not been carried out - undoubtedly because the technical and methodological means have not been available -, investigations into the neurophysiological effects of weightlessness are in their infancy (Schneider et al. 2008).
While imaging techniques such as positron emission tomography (PET) and magnetic resonance imaging (MRI) would be hardly applicable in space, the non-invasive near-infrared spectroscopy (NIRS) technique represents a method of mapping hemodynamic processes in the brain in real time that is both relatively inexpensive and that can be employed even under extreme conditions. The combination with electroencephalography (EEG) opens up the possibility of following the electrocortical processes under changing gravity conditions with a finer temporal resolution as well as with deeper localization, for instance with electrotomography (LORETA).
Previous studies showed an increase of beta frequency activity under normal gravity conditions and a decrease under weightlessness conditions during a parabolic flight (Schneider et al. 2008a+b). Tilt studies revealed different changes in brain function, which let suggest, that changes in parabolic flight might reflect emotional processes rather than hemodynamic changes. However, it is still unclear whether these are effects of changed gravity or hemodynamic changes within the brain. Combining EEG/LORETA and NIRS should for the first time make it possible to map the effect of weightlessness and reduced gravity on both hemodynamic and electrophysiological processes in the brain. Initially, this is to be done as part of a feasibility study during a parabolic flight. Afterwards, it is also planned to use both techniques during medium- and long-term space flight.
It can be assumed that the long-term redistribution of the blood volume and the associated increase in the supply of oxygen to the brain will lead to changes in the central nervous system that are also responsible for anaemic processes, and which can in turn reduce performance (De Santo et al. 2005), which means that they could be crucial for the success and safety of a mission (Genik et al. 2005, Ellis 2000).
Depending on these results, it will be necessary to develop and employ extensive countermeasures. Initial results for the MARS500 study suggest that, in addition to their significance in the context of the cardiovascular and locomotor systems, sport and physical activity can play a part in improving neurocognitive parameters. Before this can be fully established, however, it seems necessary to learn more about the influence of changing gravity conditions on neurophysiological processes and associated neurocognitive impairment.

The effect of weightlessness and hypergravity on both hemodynamic and electrophysiological processes in the brain is going to be followed during parabolic flight by EEG and NIRS techniques. 
A feasibility study of a more complex experiment, which is planned to carry out during medium- and long-term space flight.

الترابط بين وظائف الدماغ القشرية وأداء عصبي خلال تغيير شروط الجاذبية

Previous studies of cognitive, mental and/or motor processes during short-, medium- and long-term weightlessness have only been descriptive in nature, and ...

Generation of Neural Stem Cells from Discarded Human Fetal Cortical Tissue

Neural stem cells (NSCs) reside along the ventricular zone neuroepithelium during the development of the cortical plate. These early progenitors ultimately give rise to intermediate progenitors and later, the various neuronal and glial cell subtypes that form the cerebral cortex. The capacity to generate and expand human NSCs (so called neurospheres) from discarded normal fetal tissue provides a means with which to directly study the functional aspects of normal human NSC development 1-5. This approach can also be directed toward the generation of NSCs from known neurological disorders, thereby affording the opportunity to identify disease processes that alter progenitor proliferation, migration and differentiation 6-9. We have focused on identifying pathological mechanisms in human Down syndrome NSCs that might contribute to the accelerated Alzheimer's disease phenotype 10,11. Neither in vivo nor in vitro mouse models can replicate the identical repertoire of genes located on human chromosome 21. 
Here we use a simple and reliable method to isolate Down syndrome NSCs from aborted human fetal cortices and grow them in culture. The methodology provides specific aspects of harvesting the tissue, dissection with limited anatomical landmarks, cell sorting, plating and passaging of human NSCs. We also provide some basic protocols for inducing differentiation of human NSCs into more selective cell subtypes.

A simple and reliable method on isolation and culture of neural stem cells from discarded human fetal cortical tissue is described. Cultures derived from known human neurological disorders can be used for characterization of pathological cellular and molecular processes, as well as provide a platform to assess pharmacological efficacy.

جيل من الخلايا الجذعية العصبية من الأنسجة الجنينية البشرية المهملة القشرية

Neural stem cells (NSCs) reside along the ventricular zone neuroepithelium during the development of the cortical plate. These early progenitors ...

Functional Calcium Imaging in Developing Cortical Networks

A hallmark pattern of activity in developing nervous systems is spontaneous, synchronized network activity. Synchronized activity has been observed in intact spinal cord, brainstem, retina, cortex and dissociated neuronal culture preparations. During periods of spontaneous activity, neurons depolarize to fire single or bursts of action potentials, activating many ion channels. Depolarization activates voltage-gated calcium channels on dendrites and spines that mediate calcium influx. Highly synchronized electrical activity has been measured from local neuronal networks using field electrodes. This technique enables high temporal sampling rates but lower spatial resolution due to integrated read-out of multiple neurons at one electrode. Single cell resolution of neuronal activity is possible using patch-clamp electrophysiology on single neurons to measure firing activity. However, the ability to measure from a network is limited to the number of neurons patched simultaneously, and typically is only one or two neurons. The use of calcium-dependent fluorescent indicator dyes has enabled the measurement of synchronized activity across a network of cells. This technique gives both high spatial resolution and sufficient temporal sampling to record spontaneous activity of the developing network.
A key feature of newly-forming cortical and hippocampal networks during pre- and early postnatal development is spontaneous, synchronized neuronal activity (Katz &amp; Shatz, 1996; Khaziphov &amp; Luhmann, 2006). This correlated network activity is believed to be essential for the generation of functional circuits in the developing nervous system (Spitzer, 2006). In both primate and rodent brain, early electrical and calcium network waves are observed pre- and postnatally in vivo and in vitro (Adelsberger et al., 2005; Garaschuk et al., 2000; Lamblin et al., 1999). These early activity patterns, which are known to control several developmental processes including neuronal differentiation, synaptogenesis and plasticity (Rakic &amp; Komuro, 1995; Spitzer et al., 2004) are of critical importance for the correct development and maturation of the cortical circuitry.
In this JoVE video, we demonstrate the methods used to image spontaneous activity in developing cortical networks. Calcium-sensitive indicators, such as Fura 2-AM ester diffuse across the cell membrane where intracellular esterase activity cleaves the AM esters to leave the cell-impermeant form of indicator dye. The impermeant form of indicator has carboxylic acid groups which are able to then detect and bind calcium ions intracellularly.. The fluorescence of the calcium-sensitive dye is transiently altered upon binding to calcium. Single or multi-photon imaging techniques are used to measure the change in photons being emitted from the dye, and thus indicate an alteration in intracellular calcium. Furthermore, these calcium-dependent indicators can be combined with other fluorescent markers to investigate cell types within the active network.

Spontaneous activity of developing neuronal networks can be measured using AM-ester forms of calcium-sensitive indicator dyes. Changes in intracellular calcium, indicating neuronal activation, are detected as transient changes in indicator fluorescence with one- or two-photon imaging. This protocol can be adapted for a range of developmentally-dependent neuronal networks in vitro.

أسلوب التصوير الكالسيوم في تطوير شبكات القشرية

A hallmark pattern of activity in developing nervous systems is spontaneous, synchronized network activity. Synchronized activity has been observed in ...

Recording Human Electrocorticographic (ECoG) Signals for Neuroscientific Research and Real-time Functional Cortical Mapping

Neuroimaging studies of human cognitive, sensory, and motor processes are usually based on noninvasive techniques such as electroencephalography (EEG), magnetoencephalography or functional magnetic-resonance imaging. These techniques have either inherently low temporal or low spatial resolution, and suffer from low signal-to-noise ratio and/or poor high-frequency sensitivity. Thus, they are suboptimal for exploring the short-lived spatio-temporal dynamics of many of the underlying brain processes. In contrast, the invasive technique of electrocorticography (ECoG) provides brain signals that have an exceptionally high signal-to-noise ratio, less susceptibility to artifacts than EEG, and a high spatial and temporal resolution (i.e., &lt;1 cm/&lt;1 millisecond, respectively). ECoG involves measurement of electrical brain signals using electrodes that are implanted subdurally on the surface of the brain. Recent studies have shown that ECoG amplitudes in certain frequency bands carry substantial information about task-related activity, such as motor execution and planning1, auditory processing2 and visual-spatial attention3. Most of this information is captured in the high gamma range (around 70-110 Hz). Thus, gamma activity has been proposed as a robust and general indicator of local cortical function1-5. ECoG can also reveal functional connectivity and resolve finer task-related spatial-temporal dynamics, thereby advancing our understanding of large-scale cortical processes. It has especially proven useful for advancing brain-computer interfacing (BCI) technology for decoding a user's intentions to enhance or improve communication6 and control7. Nevertheless, human ECoG data are often hard to obtain because of the risks and limitations of the invasive procedures involved, and the need to record within the constraints of clinical settings. Still, clinical monitoring to localize epileptic foci offers a unique and valuable opportunity to collect human ECoG data. We describe our methods for collecting recording ECoG, and demonstrate how to use these signals for important real-time applications such as clinical mapping and brain-computer interfacing. Our example uses the BCI2000 software platform8,9 and the SIGFRIED10 method, an application for real-time mapping of brain functions. This procedure yields information that clinicians can subsequently use to guide the complex and laborious process of functional mapping by electrical stimulation.
Prerequisites and Planning:
Patients with drug-resistant partial epilepsy may be candidates for resective surgery of an epileptic focus to minimize the frequency of seizures. Prior to resection, the patients undergo monitoring using subdural electrodes for two purposes: first, to localize the epileptic focus, and second, to identify nearby critical brain areas (i.e., eloquent cortex) where resection could result in long-term functional deficits. To implant electrodes, a craniotomy is performed to open the skull. Then, electrode grids and/or strips are placed on the cortex, usually beneath the dura. A typical grid has a set of 8 x 8 platinum-iridium electrodes of 4 mm diameter (2.3 mm exposed surface) embedded in silicon with an inter-electrode distance of 1cm. A strip typically contains 4 or 6 such electrodes in a single line. The locations for these grids/strips are planned by a team of neurologists and neurosurgeons, and are based on previous EEG monitoring, on a structural MRI of the patient's brain, and on relevant factors of the patient's history. Continuous recording over a period of 5-12 days serves to localize epileptic foci, and electrical stimulation via the implanted electrodes allows clinicians to map eloquent cortex. At the end of the monitoring period, explantation of the electrodes and therapeutic resection are performed together in one procedure.
In addition to its primary clinical purpose, invasive monitoring also provides a unique opportunity to acquire human ECoG data for neuroscientific research. The decision to include a prospective patient in the research is based on the planned location of their electrodes, on the patient's performance scores on neuropsychological assessments, and on their informed consent, which is predicated on their understanding that participation in research is optional and is not related to their treatment. As with all research involving human subjects, the research protocol must be approved by the hospital's institutional review board. The decision to perform individual experimental tasks is made day-by-day, and is contingent on the patient's endurance and willingness to participate. Some or all of the experiments may be prevented by problems with the clinical state of the patient, such as post-operative facial swelling, temporary aphasia, frequent seizures, post-ictal fatigue and confusion, and more general pain or discomfort.
At the Epilepsy Monitoring Unit at Albany Medical Center in Albany, New York, clinical monitoring is implemented around the clock using a 192-channel Nihon-Kohden Neurofax monitoring system. Research recordings are made in collaboration with the Wadsworth Center of the New York State Department of Health in Albany. Signals from the ECoG electrodes are fed simultaneously to the research and the clinical systems via splitter connectors. To ensure that the clinical and research systems do not interfere with each other, the two systems typically use separate grounds. In fact, an epidural strip of electrodes is sometimes implanted to provide a ground for the clinical system. Whether research or clinical recording system, the grounding electrode is chosen to be distant from the predicted epileptic focus and from cortical areas of interest for the research. Our research system consists of eight synchronized 16-channel g.USBamp amplifier/digitizer units (g.tec, Graz, Austria). These were chosen because they are safety-rated and FDA-approved for invasive recordings, they have a very low noise-floor in the high-frequency range in which the signals of interest are found, and they come with an SDK that allows them to be integrated with custom-written research software. In order to capture the high-gamma signal accurately, we acquire signals at 1200Hz sampling rate-considerably higher than that of the typical EEG experiment or that of many clinical monitoring systems. A built-in low-pass filter automatically prevents aliasing of signals higher than the digitizer can capture. The patient's eye gaze is tracked using a monitor with a built-in Tobii T-60 eye-tracking system (Tobii Tech., Stockholm, Sweden). Additional accessories such as joystick, bluetooth Wiimote (Nintendo Co.), data-glove (5th Dimension Technologies), keyboard, microphone, headphones, or video camera are connected depending on the requirements of the particular experiment.
Data collection, stimulus presentation, synchronization with the different input/output accessories, and real-time analysis and visualization are accomplished using our BCI2000 software8,9. BCI2000 is a freely available general-purpose software system for real-time biosignal data acquisition, processing and feedback. It includes an array of pre-built modules that can be flexibly configured for many different purposes, and that can be extended by researchers' own code in C++, MATLAB or Python. BCI2000 consists of four modules that communicate with each other via a network-capable protocol: a Source module that handles the acquisition of brain signals from one of 19 different hardware systems from different manufacturers; a Signal Processing module that extracts relevant ECoG features and translates them into output signals; an Application module that delivers stimuli and feedback to the subject; and the Operator module that provides a graphical interface to the investigator.
A number of different experiments may be conducted with any given patient. The priority of experiments will be determined by the location of the particular patient's electrodes. However, we usually begin our experimentation using the SIGFRIED (SIGnal modeling For Realtime Identification and Event Detection) mapping method, which detects and displays significant task-related activity in real time. The resulting functional map allows us to further tailor subsequent experimental protocols and may also prove as a useful starting point for traditional mapping by electrocortical stimulation (ECS).
Although ECS mapping remains the gold standard for predicting the clinical outcome of resection, the process of ECS mapping is time consuming and also has other problems, such as after-discharges or seizures. Thus, a passive functional mapping technique may prove valuable in providing an initial estimate of the locus of eloquent cortex, which may then be confirmed and refined by ECS. The results from our passive SIGFRIED mapping technique have been shown to exhibit substantial concurrence with the results derived using ECS mapping10.
The protocol described in this paper establishes a general methodology for gathering human ECoG data, before proceeding to illustrate how experiments can be initiated using the BCI2000 software platform. Finally, as a specific example, we describe how to perform passive functional mapping using the BCI2000-based SIGFRIED system.

Recording Human Electrocorticographic ECoG Signals for Neuroscientific Research and Real-time Functional Cortical Mapping

We present a method for collecting electrocorticographic signals for research purposes from humans who are undergoing invasive epilepsy monitoring. We show how to use the BCI2000 software platform for data collection, signal processing and stimulus presentation. Specifically, we demonstrate SIGFRIED, a BCI2000-based tool for real-time functional brain mapping.

تسجيل الإنسان Electrocorticographic (ECOG) إشارات للبحوث العلمية العصبية في الوقت الحقيقي ورسم الخرائط القشرية وظيفي

Neuroimaging studies of human cognitive, sensory, and motor processes are usually based on noninvasive techniques such as electroencephalography (EEG), ...

Quantification of Filamentous Actin (F-actin) Puncta in Rat Cortical Neurons

Filamentous actin protein (F-actin) plays a major role in spinogenesis, synaptic plasticity, and synaptic stability. Changes in dendritic F-actin rich structures suggest alterations in synaptic integrity and connectivity. Here we provide a detailed protocol for culturing primary rat cortical neurons, Phalloidin staining for F-actin puncta, and subsequent quantification techniques. First, the frontal cortex of E18 rat embryos are dissociated into low-density cell culture, then the neurons grown in vitro for at least 12-14 days. Following experimental treatment, the cortical neurons are stained with AlexaFluor 488 Phalloidin (to label the dendritic F-actin puncta) and microtubule-associated protein 2 (MAP2; to validate the neuronal cells and dendritic integrity). Finally, specialized software is used to analyze and quantify randomly selected neuronal dendrites. F-actin rich structures are identified on second order dendritic branches (length range 25-75 &#181;m) with continuous MAP2 immunofluorescence. The protocol presented here will be a useful method for investigating changes in dendritic synapse structures subsequent to experimental treatments.

Quantification of Filamentous Actin F-actin Puncta in Rat Cortical Neurons

Filamentous actin (F-actin) plays an important role in spinogenesis, synaptic plasticity, and synaptic stability. Quantification of F-actin puncta is therefore a useful tool to study the integrity of synaptic structures. This protocol describes the procedures of quantifying F-actin puncta labeled with Phalloidin in low-density primary cortical neuronal cultures.

الكمي لشعيري أكتين (F-الأكتين) نقاط وفي الجرذ العصبونات القشرية

Filamentous actin protein (F-actin) plays a major role in spinogenesis, synaptic plasticity, and synaptic stability. Changes in dendritic F-actin rich ...

Quantification of Endosome and Lysosome Motilities in Cultured Neurons Using Fluorescent Probes

In the brain, membrane trafficking systems play important roles in regulating neuronal functions, such as neuronal morphology, synaptic plasticity, survival, and glial communications. To date, numerous studies have reported that defects in these systems cause various neuronal diseases. Thus, understanding the mechanisms underlying vesicle dynamics may provide influential clues that could aid in the treatment of several neuronal disorders. Here, we describe a method for quantifying vesicle motilities, such as motility distance and rate of movement, using a software plug-in for the ImageJ platform. To obtain images for quantification, we labeled neuronal endosome-lysosome structures with EGFP-tagged vesicle marker proteins and observed the movement of vesicles using a time-lapse microscopy. This method is highly useful and simplify measuring vesicle motility in neurites, such as axons and dendrites, as well as in the soma of both neurons and glial cells. Furthermore, this method can be applied to other cell lines, such as fibroblasts and endothelial cells. This approach could provide a valuable advancement of our understanding of membrane trafficking.

The investigation of membrane trafficking is crucial for understanding neuronal functions. Here, we introduce a method for quantifying vesicle motility in neurons. This is a convenient method that can be adapted to the quantification of membrane trafficking in the nervous system.

كمي من إندوسوم و ليسوسوم التحركات في الخلايا العصبية المستزرعة باستخدام تحقيقات الفلورسنت

In the brain, membrane trafficking systems play important roles in regulating neuronal functions, such as neuronal morphology, synaptic plasticity, ...

Visualization of Cortical Modules in Flattened Mammalian Cortices

The cortex of mammalian brains is parcellated into distinct substructures or modules. Cortical modules typically lie parallel to the cortical sheet, and can be delineated by certain histochemical and immunohistochemical methods. In this study, we highlight a method to isolate the cortex from mammalian brains and flatten them to obtain sections parallel to the cortical sheet. We further highlight selected histochemical and immunohistochemical methods to process these flattened tangential sections to visualize cortical modules. In the somatosensory cortex of various mammals, we perform cytochrome oxidase histochemistry to reveal body maps or cortical modules representing different parts of the body of the animal. In the medial entorhinal cortex, an area where grid cells are generated, we utilize immunohistochemical methods to highlight modules of genetically determined neurons which are arranged in a grid-pattern in the cortical sheet across several species. Overall, we provide a framework to isolate and prepare layer-wise flattened cortical sections, and visualize cortical modules using histochemical and immunohistochemical methods in a wide variety of mammalian brains.

This article describes a detailed methodology to obtain flattened tangential sections from mammalian cortices and visualize cortical modules using histochemical and immunohistochemical methods.

التصور للوحدات القشرية في الأرض كورتيسيس الثدييات

The cortex of mammalian brains is parcellated into distinct substructures or modules. Cortical modules typically lie parallel to the cortical sheet, and ...