ويؤيد الأمين العام بأموال من جامعة ولاية نيويورك في بوفالو من مؤسسة جون وOishei ر. وأيد عضو الكنيست من قبل الطلاب جائزة البحوث التي CURCA في UB.

1. إعداد الكواشف <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> إعداد إعداد العازلة تشريح بإضافة مركبات التالية : 128 مم كلوريد الصوديوم ، 1MM EGTA ، 4 مم MgCl 2 ، 2mm وبوكل ، HEPES 5mm ، و السكروز و 36 ملم في 1000 PH ، إلى 7.2 مل وتصفية تعقيم. </li></ol> 2. التحضير للتشريح <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> Siligard المكعب : هو قطع الجل إلى حوالي بوصة واحدة واسعة ، 1 بوصة طويلة وحوالي 1cm عالية. يتم وضع المكعب الجل على شريحة زجاجية أثناء تشريح. ويمكن استخدام مكعبات أكثر من مرة. </li><li style=";text-align:right;direction:rtl"> دبابيس : دبابيس تستخدم لتشريح يلزم اضافية قصيرة. في الجزء السفلي من المسامير الحادة minutien يعمل بشكل أفضل في تشريح. </li><li style=";text-align:right;direction:rtl"> حاجة واحدة في الربيع microdissection حادة المقص. </li><li style=";text-align:right;direction:rtl"> تحتاج اثنين ملقط يميل بشكل جيد. </li></ol> 3. جمع اليرقات <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> 3 تجول اليرقات طور مرحلي الثالثة التي تعبر عن البروتين GFP حويصلة الموسومة يتم جمعها على طبق بتري. </li><li style=";text-align:right;direction:rtl"> تغسل في ماء منزوع الأيونات اليرقات للتخلص من جميع المواد الغذائية. </li></ol> 4. تعيش تشريح اليرقات <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> يتم نقل يرقة إلى تشريح مكعب الجل على شريحة زجاجية. غير منغمسين في اليرقة العازلة تشريح. </li><li style=";text-align:right;direction:rtl"> وموهون يرقة في الأمامي والخلفي باستخدام اثنين من الدبابيس بشكل جيد مع الجانب الظهري تصل. </li><li style=";text-align:right;direction:rtl"> باستخدام مقص microdissection ، يتم إجراء قطع صغير في المنتصف قرب نهاية الخلفي. من هذا يتم إجراء شق طريق إلى قطع الأمامية. باستخدام اثنين من دبابيس ، دبوس إهاب قطع على الحواف الجانبية. </li><li style=";text-align:right;direction:rtl"> إضافة قطرة من تشريح العازلة. إزالة بعناية القناة الهضمية والأمعاء والهيئات الدهون بالملقط. معظم هذه الأنسجة طين عادة من خلال القطع الظهرية. </li><li style=";text-align:right;direction:rtl"> استبدال العازلة مع الطازجة العازلة تشريح. يجب أن تكون جافة اليرقة أبدا ، وينبغي أن يكون دائما في تشريح العازلة. </li><li style=";text-align:right;direction:rtl"> تتم حضانات تستخدم في الجسم الحي أو علامات MitoTracker LysoTracker في هذا الوقت ، من خلال تمييع في علامة حية في تشريح العازلة. بعد حضانة في علامة فيفو غسل اليرقة تشريح عدة مرات (5 يغسل سريع) باستخدام الطازجة العازلة تشريح. </li><li style=";text-align:right;direction:rtl"> بعد استبدال غسل الماضي دفع المسامير في syligard ساترة وعلى الفور. اليرقات جاهز الآن للمراقبة. </li></ol> 5. تعيش اليرقات التصوير تشريح <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> ضع ساترة والجل على خشبة المسرح والصورة باستخدام مجهر مجهر مقلوب. </li><li style=";text-align:right;direction:rtl"> نستخدم عدسة 100X إلى الحويصلات صورة الموسومة الأعصاب داخل القطعة اليرقات. هو أولا تقييم GFP التعبير في الهيئات خلية من خلايا العقدة البطنية قبل أن يتم تصوير الأعصاب قطعي. إذا لوحظ قوية تلطيخ GFP في الهيئات خلية في بطني العقدة ، ثم يتم تصوير الأعصاب واستخدامها في التقييم. </li><li style=";text-align:right;direction:rtl"> باستخدام نظام عرض ثنائي مع المرشحات لCFP / YFP أو YFP RFP / وتقسيم البرنامج عرض في وقت واحد يمكننا صورة اثنين من البروتين المفتاحية في الجسم الحي. </li></ol> 6. ممثل النتائج <img src="/files/ftp_upload/2151/2151fig1.jpg" alt="الشكل 1" /> الشكل 1 : صورة تظهر حويصلات ممثل محواري محواري كثيرة على مسارات عديدة في عصب قطعي اليرقات لاحظ النقط GFP ، تمثل تراكمات محواري. <img src="/files/ftp_upload/2151/2151fig2.jpg" alt="الشكل 2" /> الشكل 2 : صورة ممثل يظهر مسار واحد مع محواري محواري حويصلات عديدة داخل عصب قطعي اليرقات.

<ol>
	<li>Brand, A. H., Perrimon, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Targeted+gene+expression+as+a+means+of+altering+cell+fates+and+generating+dominant+phenotypes.">Targeted gene expression as a means of altering cell fates and generating dominant phenotypes.</a> Development. 118, 401-415 (1993).</li><li>Hurd, D. D., Saxton, W. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Kinesin+mutations+cause+motor+neuron+disease+phenotypes+by+disrupting+fast+axonal+transport+in+Drosophila.">Kinesin mutations cause motor neuron disease phenotypes by disrupting fast axonal transport in Drosophila.</a> Genetics. 144, 1075-1085 (1996).</li><li>Gunawardena, S., Her, L. S., Brusch, R. G., Laymon, R. A., Niesman, I. R., Gordesky-Gold, B., Sintasath, L., Bonini, N. M., Goldstein, L. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Disruption+of+axonal+transport+by+loss+of+huntingtin+or+expression+of+pathogenic+polyQ+proteins+in+Drosophila.">Disruption of axonal transport by loss of huntingtin or expression of pathogenic polyQ proteins in Drosophila.</a> Neuron. 40, 25-40 (2003).</li></ol>

الإعلان عن أي تضارب في المصالح.

في مجال التصوير فيفو النقل حويصلة متشابك داخل الأعصاب يرقات ذبابة الفاكهة قطعي هو أداة قوية لدراسة آليات النقل في محواري. لقد اعتدنا في السابق على هذا البروتوكول لتقييم ديناميات النقل داخل الأعصاب اليرقات يكرر الإعراب عن توسيع polyQ لتوضيح كيفية توسيع ي...

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<td>1 Pair Micro Dissection Scissors</td>
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<td>Fine Scientific </td>
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<td>Spring scissors &#x2013; 6mm blade. 0.125 mm tip diameter</td>
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<td>2 Pair Forceps</td>
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<td>Fischer Scientific</td>
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<td>Fisherbrand Dissecting Micro-Adson serrated tip forceps</td>
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<td>Box of Dissection Pins</td>
<td>&nbsp;</td>
<td>Fine Scientific </td>
<td>&nbsp;</td>
<td>Minutien Pins 0.1mm diameter</td>
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in vivo visualization of synaptic vesicles within drosophila larval segmental axons

توضيح آليات النقل محواري أثبتت أنها مهمة جدا في تحديد كيفية العيوب في وسائل النقل لمسافات طويلة تؤثر أمراض عصبية مختلفة. يمكن عيوب أساسية في هذه العملية لها آثار ضارة على أداء الخلايا العصبية والتنمية. قمنا بتطوير بروتوكول التشريح الذي تم تصميمه لفضح<em&gt; ذبابة الفاكهة</em&gt; الأعصاب قطعي اليرقات لعرض المحاور النقل في الوقت الحقيقي. وقد تكيفت على هذا البروتوكول لأننا نعيش من تصوير واحد نشرته هيرد وساكستون (1996) تستخدم لimmunolocalizatin الأعصاب قطعي اليرقات. تشريح دقيق والظروف المناسبة العازلة ذات أهمية حاسمة لتحقيق أقصى قدر من عمر اليرقات تشريح. عندما يوظف بشكل صحيح ، وقد أظهرت يرقات تشريح قوية حويصلة النقل لمدة 2-3 ساعات في ظل الظروف الفسيولوجية. نستخدم أسلوب UAS - GAL4<sup&gt; 1</sup&gt; للتعبير عن GFP الموسومة APP أو حويصلات synaptotagmin ضمن محور عصبي واحد أو العديد من المحاور في الأعصاب قطعي اليرقات باستخدام مختلف الخلايا العصبية GAL4 السائقين. علامات أخرى الموسومة fluorescently ، على سبيل المثال mitochrondria (MitoTracker) أو lysosomes (LysoTracker) ، يمكن أن ينطبق أيضا على اليرقات قبل المشاهدين. ويمكن الاطلاع GFP - حويصلة الحركة وحركة الجسيمات في وقت واحد باستخدام موجات منفصلة.

Watch this Scientific Journal Video about In vivo Visualization of Synaptic Vesicles Within Drosophila Larval Segmental Axons at JoVE.com

In vivo Visualization of Synaptic Vesicles Within Drosophila Larval Segmental Axons

يناقش هذا البروتوكول تشريح حية<em&gt; ذبابة الفاكهة</em&gt; اليرقات لغرض التصوير حركة الحويصلات GFP محواري الموسومة على المسارات أنيبيب.

في التصور المجراة من الحويصلات متشابك ضمن محاور عصبية ذبابة الفاكهة القطاعي اليرقات

Elucidating the mechanisms of axonal transport has shown to be very important in determining how defects in long distance transport affect different ...

in-vivo-visualization-synaptic-vesicles-within-drosophila-larval

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Neuroscience

In vivo Visualization of Synaptic Vesicles Within Drosophila Larval Segmental Axons

9.4K Views.  SUNY-University at Buffalo. يناقش هذا البروتوكول تشريح حية ذبابة الفاكهة اليرقات لغرض التصوير حركة الحويصلات GFP محواري الموسومة على المسارات أنيبيب.

Video: In vivo Visualization of Synaptic Vesicles Within Drosophila Larval Segmental Axons

Visualization of Larval Segmental Nerves in 3rd Instar Drosophila Larval Preparations

Drosophila melanogaster is emerging as a powerful model system for studying the development and function of the nervous system, particularly because of its convenient genetics and fully sequenced genome. Additionally, the larval nervous system is an ideal model system to study mechanisms of axonal transport as the larval segmental nerves contain bundles of axons with their cell bodies located within the brain and their nerve terminals ending along the length of the body. Here we describe the procedure for visualization of synaptic vesicle proteins within larval segmental nerves. If done correctly, all components of the nervous system, along with associated tissues such as muscles and NMJs, remain intact, undamaged, and ready to be visualized. 3rd instar larvae carrying various mutations are dissected, fixed, incubated with synaptic vesicle antibodies, visualized and compared to wild type larvae. This procedure can be adapted for several different synaptic or neuronal antibodies and changes in the distribution of a variety of proteins can be easily observed within larval segmental nerves.

Visualization of Larval Segmental Nerves in 3rd Instar Drosophila Larval Preparations

Drosophila melanogaster larvae provide an ideal model system to investigate the mechanisms of axonal transport within larval segmental nerves. Using this procedure, 3rd instar larvae carrying various mutations can be compared to wild type larvae.

تصور الأعصاب القطاعي اليرقات في 3 الثالثة طور مرحلي ذبابة الفاكهة التحضيرات اليرقات

Drosophila melanogaster is emerging as a powerful model system for studying the development and function of the nervous system, particularly because of ...

Morphological Analysis of Drosophila Larval Peripheral Sensory Neuron Dendrites and Axons Using Genetic Mosaics

Nervous system development requires the correct specification of neuron position and identity, followed by accurate neuron class-specific dendritic development and axonal wiring. Recently the dendritic arborization (DA) sensory neurons of the Drosophila larval peripheral nervous system (PNS) have become powerful genetic models in which to elucidate both general and class-specific mechanisms of neuron differentiation.
There are four main DA neuron classes (I-IV)1. They are named in order of increasing dendrite arbor complexity, and have class-specific differences in the genetic control of their differentiation2-10. The DA sensory system is a practical model to investigate the molecular mechanisms behind the control of dendritic morphology11-13 because: 1) it can take advantage of the powerful genetic tools available in the fruit fly, 2) the DA neuron dendrite arbor spreads out in only 2 dimensions beneath an optically clear larval cuticle making it easy to visualize with high resolution in vivo, 3) the class-specific diversity in dendritic morphology facilitates a comparative analysis to find key elements controlling the formation of simple vs. highly branched dendritic trees, and 4) dendritic arbor stereotypical shapes of different DA neurons facilitate morphometric statistical analyses.
DA neuron activity modifies the output of a larval locomotion central pattern generator14-16. The different DA neuron classes have distinct sensory modalities, and their activation elicits different behavioral responses14,16-20. Furthermore different classes send axonal projections stereotypically into the Drosophila larval central nervous system in the ventral nerve cord (VNC)21. These projections terminate with topographic representations of both DA neuron sensory modality and the position in the body wall of the dendritic field7,22,23. Hence examination of DA axonal projections can be used to elucidate mechanisms underlying topographic mapping7,22,23, as well as the wiring of a simple circuit modulating larval locomotion14-17.
We present here a practical guide to generate and analyze genetic mosaics24 marking DA neurons via MARCM (Mosaic Analysis with a Repressible Cell Marker)1,10,25 and Flp-out22,26,27 techniques (summarized in Fig. 1).

Morphological Analysis of Drosophila Larval Peripheral Sensory Neuron Dendrites and Axons Using Genetic Mosaics

The dendritic arborization sensory neurons of the Drosophila larval peripheral nervous system are useful models to elucidate both general and neuron class-specific mechanisms of neuron differentiation. We present a practical guide to generate and analyze dendritic arborization neuron genetic mosaics.

تحليل الصرفي ذبابة الفاكهة اليرقات المحيطية الانشعابيات عصبون حسي والمحاوير استخدام الفسيفساء الوراثية

Nervous system development requires the correct specification of neuron position and identity, followed by accurate neuron class-specific dendritic ...

Visualization of Proprioceptors in Drosophila Larvae and Pupae

Proprioception is the ability to sense the motion, or position, of body parts by responding to stimuli arising within the body. In fruitflies and other insects proprioception is provided by specialized sensory organs termed chordotonal organs (ChOs) 2. Like many other organs in Drosophila, ChOs develop twice during the life cycle of the fly. First, the larval ChOs develop during embryogenesis. Then, the adult ChOs start to develop in the larval imaginal discs and continue to differentiate during metamorphosis.
The development of larval ChOs during embryogenesis has been studied extensively 10,11,13,15,16. The centerpiece of each ChO is a sensory unit composed of a neuron and a scolopale cell. The sensory unit is stretched between two types of accessory cells that attach to the cuticle via specialized epidermal attachment cells 1,9,14. When a fly larva moves, the relative displacement of the epidermal attachment cells leads to stretching of the sensory unit and consequent opening of specific transient receptor potential vanilloid (TRPV) channels at the outer segment of the dendrite 8,12. The elicited signal is then transferred to the locomotor central pattern generator circuit in the central nervous system.
Multiple ChOs have been described in the adult fly 7. These are located near the joints of the adult fly appendages (legs, wings and halters) and in the thorax and abdomen. In addition, several hundreds of ChOs collectively form the Johnston's organ in the adult antenna that transduce acoustic to mechanical energy 3,5,17,4.
In contrast to the extensive knowledge about the development of ChOs in embryonic stages, very little is known about the morphology of these organs during larval stages. Moreover, with the exception of femoral ChOs 18 and Johnston's organ, our knowledge about the development and structure of ChOs in the adult fly is very fragmentary.
Here we describe a method for staining and visualizing ChOs in third instar larvae and pupae. This method can be applied together with genetic tools to better characterize the morphology and understand the development of the various ChOs in the fly.

Visualization of Proprioceptors in Drosophila Larvae and Pupae

A method to immunostain and visualize chordotonal organs in larvae and pupae of Drosophila melanogaster is described.

تصور في Proprioceptors<em&gt; ذبابة الفاكهة</em&gt; يرقات وشرانق

Proprioception is the ability to sense the motion, or position, of body parts by responding to stimuli arising within the body. In fruitflies and other ...

Dissection and Immunohistochemistry of Larval, Pupal and Adult Drosophila Retinas

The compound eye of Drosophila melanogaster consists of about 750 ommatidia (unit eyes). Each ommatidium is composed of about 20 cells, including lens-secreting cone cells, pigment cells, a bristle cell and eight photoreceptors (PRs) R1-R8 2. The PRs have specialized microvillar structures, the rhabdomeres, which contain light-sensitive pigments, the Rhodopsins (Rhs). The rhabdomeres of six PRs (R1-R6) form a trapezoid and contain Rh1 3 4. The rhabdomeres of R7 and R8 are positioned in tandem in the center of the trapezoid and share the same path of light. R7 and R8 PRs stochastically express different combinations of Rhs in two main subtypes5: In the 'p' subtype, Rh3 in pR7s is coupled with Rh5 in pR8s, whereas in the 'y' subtype, Rh4 in yR7s is associated with Rh6 in yR8s 6 7 8.
Early specification of PRs and development of ommatidia begins in the larval eye-antennal imaginal disc, a monolayer of epithelial cells. A wave of differentiation sweeps across the disc9 and initiates the assembly of undifferentiated cells into ommatidia10-11. The 'founder cell' R8 is specified first and recruits R1-6 and then R7 12-14. Subsequently, during pupal development, PR differentiation leads to extensive morphological changes 15, including rhabdomere formation, synaptogenesis and eventually rh expression.
In this protocol, we describe methods for retinal dissections and immunohistochemistry at three defined periods of retina development, which can be applied to address a variety of questions concerning retinal formation and developmental pathways. Here, we use these methods to visualize the stepwise PR differentiation at the single-cell level in whole mount larval, midpupal and adult retinas (Figure 1).

Dissection and Immunohistochemistry of Larval, Pupal and Adult Drosophila Retinas

The Drosophila retina is a crystal-like lattice composed of a small number of cell types that are generated in a stereotyped manner 1. Its amenability to sophisticated genetic analysis allows the study of complex developmental programs. This protocol describes dissections and immunohistochemistry of retinas at three discrete developmental stages, with a focus on photoreceptor differentiation.

تشريح والمناعية من اليرقات، العذراء وتعليم الكبار<em&gt; ذبابة الفاكهة</em&gt; شبكية العين

The compound eye of Drosophila melanogaster consists of about 750 ommatidia (unit eyes). Each ommatidium is composed of about 20 cells, including ...

Functional Analysis of the Larval Feeding Circuit in Drosophila

The serotonergic feeding circuit in Drosophila melanogaster larvae can be used to investigate neuronal substrates of critical importance during the development of the circuit. Using the functional output of the circuit, feeding, changes in the neuronal architecture of the stomatogastric system can be visualized. Feeding behavior can be recorded by observing the rate of retraction of the mouth hooks, which receive innervation from the brain. Locomotor behavior is used as a physiological control for feeding, since larvae use their mouth hooks to traverse across an agar substrate. Changes in feeding behavior can be correlated with the axonal architecture of the neurites innervating the gut. Using immunohistochemistry it is possible to visualize and quantitate these changes. Improper handling of the larvae during behavior paradigms can alter data as they are very sensitive to manipulations. Proper imaging of the neurite architecture innervating the gut is critical for precise quantitation of number and size of varicosities as well as the extent of branch nodes. Analysis of most circuits allow only for visualization of neurite architecture or behavioral effects; however, this model allows one to correlate the functional output of the circuit with the impairments in neuronal architecture.

Functional Analysis of the Larval Feeding Circuit in Drosophila

The feeding circuit in Drosophila melanogaster larvae serves a simple yet powerful model that allows changes in feeding rate to be correlated with alterations in the stomatogastric neural circuitry. This circuit is composed of central serotonergic neurons that send projections to the mouth hooks as well as the foregut.

التحليل الوظيفي للتغذية اليرقات الدائرة في ذبابة الفاكهة</i

The serotonergic  feeding circuit in Drosophila  melanogaster larvae can be used to investigate neuronal substrates of  critical importance during the ...

Laser Nanosurgery of Cerebellar Axons In Vivo

Only a few neuronal populations in the central nervous system (CNS) of adult mammals show local regrowth upon dissection of their axon. In order to understand the mechanism that promotes neuronal regeneration, an in-depth analysis of the neuronal types that can remodel after injury is needed. Several studies showed that damaged climbing fibers are capable of regrowing also in adult animals1,2. The investigation of the time-lapse dynamics of degeneration and regeneration of these axons within their complex environment can be performed by time-lapse two-photon fluorescence (TPF) imaging in vivo3,4. This technique is here combined with laser surgery, which proved to be a highly selective tool to disrupt fluorescent structures in the intact mouse cortex5-9.
This protocol describes how to perform TPF time-lapse imaging and laser nanosurgery of single axonal branches in the cerebellum in vivo. Olivocerebellar neurons are labeled by anterograde tracing with a dextran-conjugated dye and then monitored by TPF imaging through a cranial window. The terminal portion of their axons are then dissected by irradiation with a Ti:Sapphire laser at high power. The degeneration and potential regrowth of the damaged neuron are monitored by TPF in vivo imaging during the days following the injury.

Laser Nanosurgery of Cerebellar Axons In Vivo

Two-photon imaging, coupled to laser nanodissection, are useful tools to study degenerative and regenerative processes in the central nervous system with subcellular resolution. This protocol shows how to label, image, and dissect single climbing fibers in the cerebellar cortex in vivo.

الليزر Nanosurgery من مخيخي محاور عصبية<em&gt; في فيفو</em

Only a few neuronal populations in the central nervous system (CNS) of adult mammals show local regrowth upon dissection of their axon. In order to ...

Live Imaging of Drosophila Larval Neuroblasts

Stem cells divide asymmetrically to generate two progeny cells with unequal fate potential: a self-renewing stem cell and a differentiating cell. Given their relevance to development and disease, understanding the mechanisms that govern asymmetric stem cell division has been a robust area of study. Because they are genetically tractable and undergo successive rounds of cell division about once every hour, the stem cells of the Drosophila central nervous system, or neuroblasts, are indispensable models for the study of stem cell division. About 100 neural stem cells are located near the surface of each of the two larval brain lobes, making this model system particularly useful for live imaging microscopy studies. In this work, we review several approaches widely used to visualize stem cell divisions, and we address the relative advantages and disadvantages of those techniques that employ dissociated versus intact brain tissues. We also detail our simplified protocol used to explant whole brains from third instar larvae for live cell imaging and fixed analysis applications.

Live Imaging of Drosophila Larval Neuroblasts

This protocol details a streamlined method used to conduct live cell imaging in the context of an intact larval brain. Live cell imaging approaches are invaluable for the study of asymmetric neural stem cell divisions as well as other neurogenic and developmental processes, consistently uncovering mechanisms that were previously overlooked.

التصوير المباشر ل<em&gt; ذبابة الفاكهة</em&gt; اليرقات Neuroblasts

Stem cells divide asymmetrically to generate two progeny cells with unequal fate potential: a self-renewing stem cell and a differentiating cell. Given ...

Culturing In Vivo-like Murine Astrocytes Using the Fast, Simple, and Inexpensive AWESAM Protocol

The AWESAM (a low-cost easy stellate astrocyte method) protocol entails a fast, simple, and inexpensive way to generate large quantities of in vivo-like mouse and rat astrocyte monocultures: Brain cells can be isolated from different brain regions, and after a week of cell culture, non-astrocytic cells are shaken off by placing the culture dishes on a shaker for 6 h in the incubator. The remaining astrocytes are then passaged into new plates with an astrocyte-specific medium (termed NB+H). NB+H contains low concentrations of heparin-binding EGF-like growth factor (HBEGF), which is used in place of serum in medium. After growing in NB+H, AWESAM astrocytes have a stellate morphology and feature fine processes. Moreover, these astrocytes have more in vivo-like gene expression than astrocytes generated by previously published methods. Ca2+ imaging, vesicle dynamics, and other events close to the membrane can thus be studied in the fine astrocytic processes in vitro, e.g., using live cell confocal or TIRF microscopy. Notably, AWESAM astrocytes also exhibit spontaneous Ca2+ signaling similar to astrocytes in vivo.

Culturing In Vivo-like Murine Astrocytes Using the Fast, Simple, and Inexpensive AWESAM Protocol

The AWESAM protocol described here is optimal for culturing murine astrocytes in isolation from other brain cells in a fast, simple, and inexpensive manner. AWESAM astrocytes exhibit spontaneous Ca2+ signaling, morphology, and gene expression profiles similar to astrocytes in vivo.

استزراع في فيفو--مثل مورين Astrocytes استخدام بروتوكول أوسام سريعة وبسيطة وغير مكلفة

The AWESAM (a low-cost easy stellate astrocyte method) protocol entails a fast, simple, and inexpensive way to generate large quantities of in vivo-like ...

Focal Macropatch Recordings of Synaptic Currents from the Drosophila Larval Neuromuscular Junction

Drosophila neuromuscular junction (NMJ) is an excellent model system to study glutamatergic synaptic transmission. We describe the technique of focal macropatch recordings of synaptic currents from visualized boutons at the Drosophila larval NMJ. This technique requires customized fabrication of recording micropipettes, as well as a compound microscope equipped with a high magnification, long-distance water immersion objective, differential interference contrast (DIC) optics, and a fluorescent attachment. The recording electrode is positioned on the top of a selected synaptic bouton visualized with DIC optics, epi-fluorescence, or both. The advantage of this technique is that it allows monitoring the synaptic activity of a limited number of sites of release. The recording electrode has&#160;a diameter of several microns, and the release sites positioned outside of the electrode rim do&#160;not significantly affect the recorded currents. The recorded synaptic currents have fast kinetics and can be readily resolved. These advantages are especially important for the studies of mutant fly lines with enhanced spontaneous or asynchronous synaptic activity.

Focal Macropatch Recordings of Synaptic Currents from the Drosophila Larval Neuromuscular Junction

Synaptic currents can be recorded focally from visualized synaptic boutons at the Drosophila third instar larvae neuromuscular junction. This technique enables monitoring the activity of a single synaptic bouton.

تسجيلات ماكروباتش المحورية للتيارات متشابك من الوصلات العصبية العضلية اليرقات المورفولوجية

Drosophila neuromuscular junction (NMJ) is an excellent model system to study glutamatergic synaptic transmission. We describe the technique of focal ...

Combining Optogenetics with Artificial microRNAs to Characterize the Effects of Gene Knockdown on Presynaptic Function within Intact Neuronal Circuits

The purpose of this protocol is to characterize the effect of gene knockdown on presynaptic function within intact neuronal circuits. We describe a workflow on how to combine artificial microRNA (miR)-mediated RNA interference with optogenetics to achieve selective stimulation of manipulated presynaptic boutons in acute brain slices. The experimental approach involves the use of a single viral construct and a single neuron-specific promoter to drive the expression of both an optogenetic probe and artificial miR(s) against presynaptic gene(s). When stereotactically injected in the brain region of interest, the expressed construct makes it possible to stimulate with light exclusively the neurons with reduced expression of the gene(s) under investigation. This strategy does not require the development and maintenance of genetically modified mouse lines and can in principle be applied to other organisms and to any neuronal gene of choice. We have recently applied it to investigate how the knockdown of alternative splice isoforms of presynaptic P/Q-type voltage-gated calcium channels (VGCCs) regulates short-term synaptic plasticity at CA3 to CA1 excitatory synapses in acute hippocampal slices. A similar approach could also be used to manipulate and probe the neuronal circuitry in vivo.

This protocol provides a workflow on how to combine artificial microRNA-mediated RNA interference with optogenetics to stimulate specifically presynaptic boutons with reduced expression of selective gene(s) within intact neuronal circuits.

الجمع بين أوبتوجينيتيكس ميكرورناس الاصطناعية لتوصيف "تأثيرات الجينات ضربة قاضية" في وظيفة Presynaptic داخل "الدوائر العصبية سليمة"

The purpose of this protocol is to characterize the effect of gene knockdown on presynaptic function within intact neuronal circuits. We describe a ...