نشكر برنار Foucart للحصول على المساعدة الفنية. وأيد هذا العمل من قبل الصندوق البلجيكي للبحوث العلمية (FRS-FNRS) وصندوق الملكة إليزابيث للبحوث الطبية. أنياس فيير هو زميل باحث في الصندوق البلجيكي للبحوث العلمية.

الإعلان عن أي تضارب في المصالح.

وقد وضعنا في المختبر لدينا بروتوكول الناجمة عن مزيج من الأساليب المتقدمة والمستخدمة من قبل مختبرات أخرى وجود خبرة كبيرة في الكمونية التسجيلات 11،17. ويتم تكييف هذا البروتوكول لالحصين الماوس الكبار، ويمكن استخدامها في الحيوانات في أي عمر ولأي الوراثي الخلفية. ك?...

في الوقت الحاضر، هناك فهم محدود من كيفية تخزين الذكريات معقدة وأشار على مستوى الدوائر العصبية. ومع ذلك، فإن فرضية توحيد تخزين الذاكرة متاحة ومقبولة على نطاق واسع: يتم تخزين ذكريات عن التغيرات في قوة الاتصالات المشبكية بين الخلايا العصبية في الجهاز العصبي المركزي. من تلقاء نفسها، وقد استفاد البحث عن اللدونة متشابك إلى حد كبير من اثنين من الاكتشافات. (1) وجدت تجربة المنوية، النعيم وومو 1، وذلك باستخدام أرنب تخدير سليمة، وفي هذا تسليم قصيرة عالية التردد (1 ثانية، 100 هرتز) التحفيز على مسار الثاقب من الحصين تسبب طويل الأمد (عدة ساعات) زيادة في اتصالات متشابك ذات الصلة. كان يطلق على هذه الظاهرة الرائعة &quot;الكمونية طويلة الأمد&quot; أو الكمونية من قبل دوغلاس وغودارد في عام 1975 2. (2) في وقت لاحق، تبين أن ظاهرة مماثلة يمكن أن تسبب في شرائح الدماغ (0.4 ملم) الحفاظ بشكل مصطنع على قيد الحياة في المختبر </eم&gt;. وقد لوحظ الكمونية الأكثر دراسة على نطاق واسع في المختبر من خلال تقديم واحدة أو عدة الكزازية إلى مجموعة من المحاور (ما يسمى الضمانات شيفر) أثناء تسجيل الناتجة حقل إمكانات متشابك مثير أثار في الخلايا العصبية الهرمية من ما يسمى المنطقة CA1. إلى حد كبير وكشفت آليات الكمونية الاستقراء. أساسا، كا 2 + تدفق من خلال المستقبلات NMDA ينشط الإنزيمات مع نتيجتان: أ الفسفرة من مستقبلات أمبا (والتي تزيد كفاءتها)، وإدماج مستقبلات أمبا اضافية في الغشاء بعد المشبكي 3. على النقيض من ذلك، فإن آليات للمرحلة صيانة الكمونية غير معروفة إلى حد كبير، وخاصة لأنه أكثر صعوبة بكثير تجريبيا للحفاظ على شريحة صحية لعدة ساعات من لمدة 30 إلى 60 دقيقة. وقد تم تخصيص الكثير من الدراسات لفهم آليات الكمونية ونظريات مثيرة للاهتمام قد وضعت على مدى السنوات 4-11. ولكن الأمم المتحدةسمسم الآن، لم يتم توضيح الآليات الجزيئية الكامنة وراء زيادة دقيقة مستقرة في قوة متشابك. هذا قد يكون عائدا جزئيا إلى صعوبة استخراج النتائج السابقة في مختبرات مختلفة باستخدام تقنيات مختلفة لإعداد والحفاظ على شرائح الحصين. في ورقة منهجيتها، Sajikumar وآخرون. 12 وشدد على أهمية الظروف التجريبية لإعداد شرائح قرن آمون الفئران وتسجيل الكمونية مستقرة. في هذا الفيديو نقدم جميع الخطوات الأمثل وضعت في المختبر لدينا على مر السنين لتكون قادرة على تسجيل الكمونية مستقرة جدا في شرائح الحصين الماوس. وقد أحرز هذا التحسين من البروتوكولات التي وضعت واستخدمت بنجاح من قبل مختبرات أخرى التي تدرس آليات الكمونية في الفئران والجرذان 13 11. فإنه يسمح للباحثين من ذوي الخبرة للحث وتسجيل الكمونية طويلة الأمد جدا في الفئران البالغة مع نسبة عالية من النجاح. عتم فحص أساس hysiological من صنع الكمونية بعناية وأظهرت 14. في هذه الورقة منهجية، وتبين لنا أن أي تعديلات من الظروف التجريبية، مثل درجة الحرارة أو الأوكسجين يمكن أن يكون لها تأثير عميق على صيانة الكمونية في حين يمكن إجراء تشريح تعديل عميق شرائح استثارة. ولا بد أيضا من التأكيد على أن مراقبة دقيقة من كل هذه المعايير يتطلب تدريب عدة أشهر للطلاب المبتدئين.

<table border="1">
	<tbody>
		<tr>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>Reagent/Material</td>
		</tr>
		<tr>
			<td>NaCl</td>
			<td>Sigma - Aldrich</td>
			<td>S7653</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>NaHCO3</td>
			<td>Sigma - Aldrich</td>
			<td>S8875</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>KCl</td>
			<td>Sigma - Aldrich</td>
			<td>P9333</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>D-glucose</td>
			<td>Sigma - Aldrich</td>
			<td>G7528</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>NaH2PO4</td>
			<td>Sigma - Aldrich</td>
			<td>S9638</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>MgSO4 1M</td>
			<td>Sigma - Aldrich</td>
			<td>63126</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>CaCl2</td>
			<td>Sigma - Aldrich</td>
			<td>C4901</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Carbogen</td>
			<td>Air Liquide (Belgium)</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Capillaries</td>
			<td>WPI, Inc. (UK)</td>
			<td>TW150-4</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Stimulating Electrodes</td>
			<td>FHC (USA)</td>
			<td>CE2B30</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Surgical tools</td>
			<td>FST (Germany)</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Filter paper 84 g/m2</td>
			<td>Sartorius</td>
			<td>FT-3-105-110</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Mesh</td>
			<td>Lycra</td>
			<td>15 den</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Glue</td>
			<td>UHU</td>
			<td>plus endfest300</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>Instrument</td>
		</tr>
		<tr>
			<td>Amplifier</td>
			<td>WPI, Inc. (UK)</td>
			<td>ISO-80</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Interface recording chamber</td>
			<td>FST (Germany)</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Peristaltic pumps</td>
			<td>Gilson (USA)</td>
			<td>Minipuls 3</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Temperature controller</td>
			<td>University of Edinburgh</td>
			<td><a href="http://www.etcsystem.com" target="_blank">www.etcsystem.com</a></td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Tissue Chopper</td>
			<td>Mcllwain</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Stimulators</td>
			<td>Grass (USA)</td>
			<td>S88X + SIU-V</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Program analysis</td>
			<td>WinLTP</td>
			<td><a href="http://www.winltp.com" target="_blank">www.winltp.com</a></td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Micromanipulators</td>
			<td>Narishige</td>
			<td>MM-3 and MMO-220A</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Surgical microscope</td>
			<td>Leica Microsystem</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>A/D converter</td>
			<td>National Instruments</td>
			<td>NIPCI-6229 M-series</td>
			<td>&nbsp;</td>
		</tr>
	</tbody>
</table>

improved preparation and preservation of hippocampal mouse slices for a very stable and reproducible recording of long-term potentiation

التقوية الطويلة الأمد (الكمونية) هو نوع من اللدونة متشابك يتميز بزيادة في قوة متشابك ويعتقد أن تشارك في ترميز الذاكرة. أثارت الكمونية في المنطقة CA1 من شرائح الحصين الحادة وقد درس على نطاق واسع. ولكن الآليات الجزيئية الكامنة وراء مرحلة الصيانة لهذه الظاهرة لا تزال غير مفهومة تماما. هذا قد يكون عائدا جزئيا إلى مختلف الظروف التجريبية المستخدمة من قبل مختبرات مختلفة. والواقع أن مرحلة الصيانة من الكمونية وتعتمد بشدة على معايير خارجية مثل الأوكسجين ودرجة الحرارة والرطوبة. بل هو أيضا تعتمد على المعلمات الداخلية مثل التوجه للطائرة تشريح والجدوى شريحة بعد تشريح. الاستفادة المثلى من كل هذه المعايير تمكن من تحريض على التقوية استنساخه جدا ومستقرة جدا على المدى الطويل. هذه المنهجية توفر إمكانية مواصلة استكشاف الآليات الجزيئية المشاركة في زيادة مستقرةفي قوة متشابك في شرائح قرن آمون. كما يسلط الضوء على أهمية الظروف التجريبية في المختبر التحقيق في الظواهر العصبية.

وقد استخدمت هذه المنهجية لتحليل خصائص التقوية طويلة الأمد طويل الأجل يتسبب في شرائح الحصين الحادة من الكبار الفئران C57BL/6J (JANVIER SAS، فرنسا) 14. والمثير للدهشة، وقد أدى تحسين الظروف التجريبية إلى طريقة جديدة للنظر إلى الكمونية. نحن أظهرت أن زيادة طويلة الأمد في قوة ?...

Watch this Scientific Journal Video about Improved Preparation and Preservation of Hippocampal Mouse Slices for a Very Stable and Reproducible Recording of Long-term Potentiation at JoVE.com

Improved Preparation and Preservation of Hippocampal Mouse Slices for a Very Stable and Reproducible Recording of Long-term Potentiation

وتعرض هذه الورقة منهجية كاملة لإعداد والحفاظ على<em&gt; في المختبر</em&gt; شرائح الحصين الحادة من فئران بالغة. هذا البروتوكول يسمح للتسجيل من التقوية طويلة الأجل طويلة الأمد مستقرة جدا (الكمونية) لأكثر من 8 ساعات مع نسبة نجاح 95٪.

تحسين إعداد والحفاظ على شرائح الحصين ماوس لتسجيل مستقرة جدا وقابلة للتكرار من التقوية بعيدة المدى

Long-term potentiation (LTP) is a type of synaptic plasticity characterized by an increase in synaptic strength and believed to be involved in memory ...

improved-preparation-preservation-hippocampal-mouse-slices-for-very

Research

JoVE Journal

Neuroscience

26.6K Views.  University of Mons. وتعرض هذه الورقة منهجية كاملة لإعداد والحفاظ على في المختبر شرائح الحصين الحادة من فئران بالغة. هذا البروتوكول يسمح للتسجيل من التقوية طويلة الأجل طويلة الأمد مستقرة جدا (الكمونية) لأكثر من 8 ساعات مع نسبة نجاح 95٪.

Video: Improved Preparation and Preservation of Hippocampal Mouse Slices for a Very Stable and Reproducible Recording of Long-term Potentiation

Preparation of Oligomeric &beta;-amyloid1-42 and Induction of Synaptic Plasticity Impairment on Hippocampal Slices

Impairment of synaptic connections is likely to underlie the subtle amnesic changes occurring at the early stages of Alzheimer s Disease (AD). &beta;-amyloid (A&beta;), a peptide produced in high amounts in AD, is known to reduce Long-Term Potentiation (LTP), a cellular correlate of learning and memory. Indeed, LTP impairment caused by A&beta; is a useful experimental paradigm for studying synaptic dysfunctions in AD models and for screening drugs capable of mitigating or reverting such synaptic impairments. Studies have shown that A&beta; produces the LTP disruption preferentially via its oligomeric form. Here we provide a detailed protocol for impairing LTP by perfusion of oligomerized synthetic A&beta;1-42 peptide onto acute hippocampal slices. In this video, we outline a step-by-step procedure for the preparation of oligomeric A&beta;1-42. Then, we follow an individual experiment in which LTP is reduced in hippocampal slices exposed to oligomerized A&beta;1-42 compared to slices in a control experiment where no A&beta;1-42 exposure had occurred.

Preparation of Oligomeric &amp;#946;-amyloid1-42 and Induction of Synaptic Plasticity Impairment on Hippocampal Slices

One feature of Alzheimer's Disease is the elevation of A&beta;1-42 peptide. Here we provide a protocol for preparing synthetic A&beta;1-42 oligomers, which impairs hippocampal Long-Term Potentiation, a cellular correlate of memory. This procedure is useful for investigating mechanisms of A&beta;-induced pathology and drug screening.

إعداد Oligomeric β اميلويد 1-42 والتعريفي للعاهة اللدونة متشابك على شرائح الحصين

Impairment of synaptic connections is likely to underlie the subtle amnesic changes occurring at the early stages of Alzheimer s Disease (AD). ...

Preparation of Acute Hippocampal Slices from Rats and Transgenic Mice for the Study of Synaptic Alterations during Aging and Amyloid Pathology

The rodent hippocampal slice preparation is perhaps the most broadly used tool for investigating mammalian synaptic function and plasticity. The hippocampus can be extracted quickly and easily from rats and mice and slices remain viable for hours in oxygenated artificial cerebrospinal fluid. Moreover, basic electrophysisologic techniques are easily applied to the investigation of synaptic function in hippocampal slices and have provided some of the best biomarkers for cognitive impairments. The hippocampal slice is especially popular for the study of synaptic plasticity mechanisms involved in learning and memory. Changes in the induction of long-term potentiation and depression (LTP and LTD) of synaptic efficacy in hippocampal slices (or lack thereof) are frequently used to describe the neurologic phenotype of cognitively-impaired animals and/or to evaluate the mechanism of action of nootropic compounds. This article outlines the procedures we use for preparing hippocampal slices from rats and transgenic mice for the study of synaptic alterations associated with brain aging and Alzheimer's disease (AD)1-3. Use of aged rats and AD model mice can present a unique set of challenges to researchers accustomed to using younger rats and/or mice in their research. Aged rats have thicker skulls and tougher connective tissue than younger rats and mice, which can delay brain extraction and/or dissection and consequently negate or exaggerate real age-differences in synaptic function and plasticity. Aging and amyloid pathology may also exacerbate hippocampal damage sustained during the dissection procedure, again complicating any inferences drawn from physiologic assessment. Here, we discuss the steps taken during the dissection procedure to minimize these problems. Examples of synaptic responses acquired in "healthy" and "unhealthy" slices from rats and mice are provided, as well as representative synaptic plasticity experiments. The possible impact of other methodological factors on synaptic function in these animal models (e.g. recording solution components, stimulation parameters) are also discussed. While the focus of this article is on the use of aged rats and transgenic mice, novices to slice physiology should find enough detail here to get started on their own studies, using a variety of rodent models.

This article outlines procedures for preparing hippocampal slices from rats and transgenic mice for the study of synaptic alterations associated with brain aging and age-related neurodegenerative diseases, such as Alzheimer&#x2019;s disease.

إعداد شرائح الحصين الحادة من الجرذان والفئران المعدلة وراثيا لدراسة التعديلات متشابك وامراض الشيخوخة خلال اميلويد

The rodent hippocampal slice preparation is perhaps the most broadly used tool for investigating mammalian synaptic function and plasticity. The ...

Reproducible Mouse Sciatic Nerve Crush and Subsequent Assessment of Regeneration by Whole Mount Muscle Analysis

Regeneration in the peripheral nervous system (PNS) is widely studied both for its relevance to human disease and to understand the robust regenerative response mounted by PNS neurons thereby possibly illuminating the failures of CNS regeneration1. Sciatic nerve crush (axonotmesis) is one of the most common models of peripheral nerve injury in rodents2. Crushing interrupts all axons but Schwann cell basal laminae are preserved so that regeneration is optimal3,4. This allows the investigator to study precisely the ability of a growing axon to interact with both the Schwann cell and basal laminae4. Rats have generally been the preferred animal models for experimental nerve crush. They are widely available and their lesioned sciatic nerve provides a reasonable approximation of human nerve lesions5,4. Though smaller in size than rat nerve, the mouse nerve has many similar qualities. Most importantly though, mouse models are increasingly valuable because of the wide availability of transgenic lines now allows for a detailed dissection of the individual molecules critical for nerve regeneration6, 7. Prior investigators have used multiple methods to produce a nerve crush or injury including simple angled forceps, chilled forceps, hemostatic forceps, vascular clamps, and investigator-designed clamps8,9,10,11,12. Investigators have also used various methods of marking the injury site including suture, carbon particles and fluorescent beads13,14,1. We describe our method to obtain a reproducibly complete sciatic nerve crush with accurate and persistent marking of the crush-site using a fine hemostatic forceps and subsequent carbon crush-site marking. As part of our description of the sciatic nerve crush procedure we have also included a relatively simple method of muscle whole mount we use to subsequently quantify regeneration.

In this report we describe a method to crush mouse sciatic nerve. This method uses readily available hemostatic forceps and easily and reproducibly produces complete sciatic nerve crush. In addition, we describe a method to prepare muscle whole mounts suitable for analysis of nerve regeneration after sciatic nerve crush.

استنساخه سحق الفأر العصب الوركي وتقييم لاحق للتجديد من قبل الجامعة جبل تحليل العضلات

Regeneration in the peripheral nervous system (PNS) is widely studied both for its relevance to human disease and to understand the robust regenerative ...

A Polished and Reinforced Thinned-skull Window for Long-term Imaging of the Mouse Brain

In vivo imaging of cortical function requires optical access to the brain without disruption of the intracranial environment. We present a method to form a polished and reinforced thinned skull (PoRTS) window in the mouse skull that spans several millimeters in diameter and is stable for months. The skull is thinned to 10 to 15 &mu;m in thickness with a hand held drill to achieve optical clarity, and is then overlaid with cyanoacrylate glue and a cover glass to: 1) provide rigidity, 2) inhibit bone regrowth and 3) reduce light scattering from irregularities on the bone surface. Since the skull is not breached, any inflammation that could affect the process being studied is greatly reduced. Imaging depths of up to 250 &mu;m below the cortical surface can be achieved using two-photon laser scanning microscopy. This window is well suited to study cerebral blood flow and cellular function in both anesthetized and awake preparations. It further offers the opportunity to manipulate cell activity using optogenetics or to disrupt blood flow in targeted vessels by irradiation of circulating photosensitizers.

We present a method to form an imaging window in the mouse skull that spans millimeters and is stable for months without inflammation of the brain. This method is well suited for longitudinal studies of blood flow, cellular dynamics, and cell/vascular structure using two-photon microscopy.

مصقول وعززت ضعيفة، جمجمة نافذة على المدى الطويل التصوير من مخ الفأر

In vivo imaging of cortical function requires optical access to the brain without disruption of the intracranial environment. We present a method to form ...

Preparation of an Awake Mouse for Recording Neural Responses and Injecting Tracers

It is well known that anesthesia alters neural response properties in various regions of the brain.13. In the auditory system, fundamental response properties of brainstem neurons including threshold, frequency specificity, and inhibitory sidebands are altered in significant ways under anesthesia1-2. These observations prompted physiologists to seek ways to record from single neurons without the contaminating effects of anesthesia. One result was a decerebrate preparation, where the brainstem was completely transected at the level of the midbrain4. The drawbacks of this preparation are a formidable surgery, the elimination of descending projections from the forebrain, and an inability to use sensory stimulation to examine structures above the midbrain. A different strategy has been to implant electrode arrays chronically to record from single neurons and multiunit clusters while the animal is awake and/or behaving5,6. These techniques however are not compatible with injecting tracer dyes after first electrophysiologically characterizing a brain structure. To avoid altering neural response properties with anesthetics while recording electrophysiological response properties from single neurons, we have adapted a head restraint technique long used in bats7-9 to mouse10-12. Using this method, we are able to conduct electrophysiological recordings over several days in the unanesthetized mouse. At the end of the recording sessions, we can then inject a dye to reconstruct electrode positions and recording sites or inject a tracer so that pathways to and from the recording loci can be determined. This method allows for well isolated single neuron recordings over multiple days without the use anesthetics.

Electrophysiological characterization of neuronal responses is important for understanding brain function and for guiding the placement of dyes for pathway tracing. However, many studies are performed in anesthetized animals. To understand brain function without anesthetics, we developed a method to record neuronal response properties and inject dyes in awake mouse.

إعداد الفأر استيقظ لتسجيل الردود العصبية وحقن الراسمات

It is well known that anesthesia alters neural response properties in various regions of the brain.13.  In the auditory system, fundamental response ...

A Molecular Readout of Long-term Olfactory Adaptation in C. elegans

During sustained stimulation most sensory neurons will adapt their response by decreasing their sensitivity to the signal. The adaptation response helps shape attention and also protects cells from over-stimulation. Adaptation within the olfactory circuit of C. elegans was first described by Colbert and Bargmann1,2. Here, the authors defined parameters of the olfactory adaptation paradigm, which they used to design a genetic screen to isolate mutants defective in their ability to adapt to volatile odors sensed by the Amphid Wing cells type C (AWC) sensory neurons. When wildtype C. elegans animals are exposed to an attractive AWC-sensed odor3 for 30 min they will adapt their responsiveness to the odor and will then ignore the adapting odor in a chemotaxis behavioral assay for ~1 hr. When wildtype C. elegans animals are exposed to an attractive AWC-sensed odor for ~1 hr they will then ignore the adapting odor in a chemotaxis behavioral assay for ~3 hr. These two phases of olfactory adaptation in C. elegans were described as short-term olfactory adaptation (induced after 30 min odor exposure), and long-term olfactory adaptation (induced after 60 min odor exposure). Later work from L'Etoile et al.,4 uncovered a Protein Kinase G (PKG) called EGL-4 that is required for both the short-term and long-term olfactory adaptation in AWC neurons. The EGL-4 protein contains a nuclear localization sequence that is necessary for long-term olfactory adaptation responses but dispensable for short-term olfactory adaptation responses in the AWC4. By tagging EGL-4 with a green fluorescent protein, it was possible to visualize the localization of EGL-4 in the AWC during prolonged odor exposure. Using this fully functional GFP-tagged EGL-4 (GFP::EGL-4) molecule we have been able to develop a molecular readout of long-term olfactory adaptation in the AWC5. Using this molecular readout of olfactory adaptation we have been able to perform both forward and reverse genetic screens to identify mutant animals that exhibit defective subcellular localization patterns of GFP::EGL-4 in the AWC6,7. Here we describe: 1) the construction of GFP::EGL-4 expressing animals; 2) the protocol for cultivation of animals for long-term odor-induced nuclear translocation assays; and 3) the scoring of the long-term odor-induced nuclear translocation event and recovery (re-sensitization) from the nuclear GFP::EGL-4 state.

A Molecular Readout of Long-term Olfactory Adaptation in C. elegans

Here we describe a molecular readout of long-term olfactory adaptation in Caenorhabditis elegans. The Protein Kinase G, EGL-4, is necessary for stable adaptation responses in the primary sensory neuron pair called AWC. During prolonged odor exposure EGL-4 translocates from the cytosol to nucleus of the AWC.

A قراءات الجزيئية من التكيف على المدى الطويل في الشم<em&gt; C. ايليجانس</em

During sustained stimulation most sensory neurons will adapt their response by decreasing their sensitivity to the signal. The adaptation response helps ...

Paired Whole Cell Recordings in Organotypic Hippocampal Slices

Pair recordings involve simultaneous whole cell patch clamp recordings from two synaptically connected neurons, enabling not only direct electrophysiological characterization of the synaptic connections between individual neurons, but also pharmacological manipulation of either the presynaptic or the postsynaptic neuron. When carried out in organotypic hippocampal slice cultures, the probability that two neurons are synaptically connected is significantly increased. This preparation readily enables identification of cell types, and the neurons maintain their morphology and properties of synaptic function similar to that in native brain tissue. A major advantage of paired whole cell recordings is the highly precise information it can provide on the properties of synaptic transmission and plasticity that are not possible with other more crude techniques utilizing extracellular axonal stimulation. Paired whole cell recordings are often perceived as too challenging to perform. While there are challenging aspects to this technique, paired recordings can be performed by anyone trained in whole cell patch clamping provided specific hardware and methodological criteria are followed. The probability of attaining synaptically connected paired recordings significantly increases with healthy organotypic slices and stable micromanipulation allowing independent attainment of pre- and postsynaptic whole cell recordings. While CA3-CA3 pyramidal cell pairs are most widely used in the organotypic slice hippocampal preparation, this technique has also been successful in CA3-CA1 pairs and can be adapted to any neurons that are synaptically connected in the same slice preparation. In this manuscript we provide the detailed methodology and requirements for establishing this technique in any laboratory equipped for electrophysiology.

Pair recordings are simultaneous whole cell patch clamp recordings from two synaptically connected neurons, enabling precise electrophysiological and pharmacological characterization of the synapses between individual neurons. Here we describe the detailed methodology and requirements for establishing this technique in organotypic hippocampal slice cultures in any laboratory equipped for electrophysiology.

تقرن تسجيلات خلية كاملة في عضوي شرائح الحصين

Pair recordings involve simultaneous whole cell patch clamp recordings from two synaptically connected neurons, enabling not only direct ...

Long-term Time Lapse Imaging of Mouse Cochlear Explants

Here we present a method for long-term time-lapse imaging of live embryonic mouse cochlear explants. The developmental program responsible for building the highly ordered, complex structure of the mammalian cochlea proceeds for around ten days. In order to study changes in gene expression over this period and their response to pharmaceutical or genetic manipulation, long-term imaging is necessary. Previously, live imaging has typically been limited by the viability of explanted tissue in a humidified chamber atop a standard microscope. Difficulty in maintaining optimal conditions for culture growth with regard to humidity and temperature has placed limits on the length of imaging experiments. A microscope integrated into a modified tissue culture incubator provides an excellent environment for long term-live imaging. In this method we demonstrate how to establish embryonic mouse cochlear explants and how to use an incubator microscope to conduct time lapse imaging using both bright field and fluorescent microscopy to examine the behavior of a typical embryonic day (E) 13 cochlear explant and Sox2, a marker of the prosensory cells of the cochlea, over 5 days.

Live imaging of the embryonic mammalian cochlea is challenging because the developmental processes at hand operate on a temporal gradient over ten days. Here we present a method for culturing and then imaging embryonic cochlear explant tissue taken from a fluorescent reporter mouse over five days.

على المدى الطويل الوقت الفاصل بين التصوير من الفأر القوقعة إإكسبلنتس

Here we present a method for long-term time-lapse imaging of live embryonic mouse cochlear explants. The developmental program responsible for building ...

A Simplified Method for Ultra-Low Density, Long-Term Primary Hippocampal Neuron Culture

Culturing primary hippocampal neurons in vitro facilitates mechanistic interrogation of many aspects of neuronal development. Dissociated embryonic hippocampal neurons can often grow successfully on glass coverslips at high density under serum-free conditions, but low density cultures typically require a supply of trophic factors by co-culturing them with a glia feeder layer, preparation of which can be time-consuming and laborious. In addition, the presence of glia may confound interpretation of results and preclude studies on neuron-specific mechanisms. Here, a simplified method is presented for ultra-low density (~2,000 neurons/cm2), long-term (&#62;3 months) primary hippocampal neuron culture that is under serum free conditions and without glia cell support. Low density neurons are grown on poly-D-lysine coated coverslips, and flipped on high density neurons grown in a 24-well plate. Instead of using paraffin dots to create a space between the two neuronal layers, the experimenters can simply etch the plastic bottom of the well, on which the high density neurons reside, to create a microspace conducive to low density neuron growth. The co-culture can be easily maintained for &#62;3 months without significant loss of low density neurons, thus facilitating the morphological and physiological study of these neurons. To illustrate this successful culture condition, data are provided to show profuse synapse formation in low density cells after prolonged culture. This co-culture system also facilitates the survival of sparse individual neurons grown in islands of poly-D-lysine substrates and thus the formation of autaptic connections.

Low density cultures of primary hippocampal neurons usually require glia feeder layer to supply neurotrophic factors and sustain longevity. We describe here a simplified method to culture ultra-low density neurons on glass coverslips in the presence of a high density neuronal feeder layer, which facilitates investigation of specific neuronal-autonomous mechanisms.

والطريقة المبسطة للفائقة منخفضة الكثافة، طويل الأجل الابتدائية الحصين العصبية الثقافة

Culturing primary hippocampal neurons in vitro facilitates mechanistic interrogation of many aspects of neuronal development. Dissociated embryonic ...

Recording Synaptic Plasticity in Acute Hippocampal Slices Maintained in a Small-volume Recycling-, Perfusion-, and Submersion-type Chamber System

Even though experiments on brain slices have been in use since 1951, problems remain that reduce the probability of achieving a stable and successful analysis of synaptic transmission modulation when performing field potential or intracellular recordings. This manuscript describes methodological aspects that might be helpful in improving experimental conditions for the maintenance of acute brain slices and for recording field excitatory postsynaptic potentials in a commercially available submersion chamber with an outflow-carbogenation unit. The outflow-carbogenation helps to stabilize the oxygen level in experiments that rely on the recycling of a small buffer reservoir to enhance the cost-efficiency of drug experiments. In addition, the manuscript presents representative experiments that examine the effects of different carbogenation modes and stimulation paradigms on the activity-dependent synaptic plasticity of synaptic transmission.

This protocol describes the stabilization of the oxygen level in a small volume of recycled buffer and methodological aspects of recording activity-dependent synaptic plasticity in submerged acute hippocampal slices.

تسجيل اللدونة متشابك في شرائح هيبوكامبال الحاد تحتفظ في صغيرة الحجم-إعادة التدوير، ونضح-، وغمر من نوع نظام الدائرة

Even though experiments on brain slices have been in use since 1951, problems remain that reduce the probability of achieving a stable and successful ...