نشكر جورج ريو لتقديم المشورة بشأن التصوير موقفنا المبدئي انشاء ، Z. غيتاي لاقتراح استخدام ImageJ 13 إلى العد والديدان ، وجيه اشرف للحصول على مساعدة باستخدام Google SketchUp. CTM هو باحث بيو في العلوم الطبية الحيوية ، وهو باحث ماكنايت ، والباحث العلمي كيك.

<ol>
	<li>Bargmann, C. I., Hartwieg, E., Horvitz, H. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Odorant-selective+genes+and+neurons+mediate+olfaction+in+C.+elegans.">Odorant-selective genes and neurons mediate olfaction in C. elegans.</a> Cell. 74, 515-515 (1993).</li><li>Ward, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chemotaxis+by+the+nematode+Caenorhabditis+elegans:+identification+of+attractants+and+analysis+of+the+response+by+use+of+mutants.">Chemotaxis by the nematode Caenorhabditis elegans: identification of attractants and analysis of the response by use of mutants.</a> Proc Natl Acad Sci U S A. 70, 817-817 (1973).</li><li>Bono, M. d. e., Maricq, A. V. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neuronal+substrates+of+complex+behaviors+in+C.+elegans.">Neuronal substrates of complex behaviors in C. elegans.</a> Annu Rev Neurosci. 28, 451-451 (2005).</li><li>Mori, I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Genetics+of+chemotaxis+and+thermotaxis+in+the+nematode+Caenorhabditis+elegans.">Genetics of chemotaxis and thermotaxis in the nematode Caenorhabditis elegans.</a> Annu Rev Genet. 33, 399-399 (1999).</li><li>Zhang, Y., Lu, H., Bargmann, C. I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Pathogenic+bacteria+induce+aversive+olfactory+learning+in+Caenorhabditis+elegans.">Pathogenic bacteria induce aversive olfactory learning in Caenorhabditis elegans.</a> Nature. 438, 179-179 (2005).</li><li>Kauffman, A. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Insulin+signaling+and+dietary+restriction+differentially+influence+the+decline+of+learning+and+memory+with+age.">Insulin signaling and dietary restriction differentially influence the decline of learning and memory with age.</a> PLoS Biol. 8, e1000372-e1000372 (2010).</li><li>Torayama, I., Ishihara, T., Katsura, I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Caenorhabditis+elegans+integrates+the+signals+of+butanone+and+food+to+enhance+chemotaxis+to+butanone.">Caenorhabditis elegans integrates the signals of butanone and food to enhance chemotaxis to butanone.</a> J Neurosci. 27, 741-741 (2007).</li><li>Silva, A. J., Kogan, J. H., Frankland, P. W., Kida, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CREB+and+memory.">CREB and memory.</a> Annu Rev Neurosci. 21, 127-127 (1998).</li><li>Meyer, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Iterative+image+transformations+for+an+automatic+screening+of+cervical+smears.">Iterative image transformations for an automatic screening of cervical smears.</a> J Histochem Cytochem. 27, 128-128 (1979).</li><li>Otsu, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+Threshold+Selection+Method+from+Gray-Level+Histograms.">A Threshold Selection Method from Gray-Level Histograms.</a> IEEE Transactions on Systems, Man, and Cybernetics. 9, 62-62 (1979).</li><li>Brenner, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+genetics+of+Caenorhabditis+elegans.">The genetics of Caenorhabditis elegans.</a> Genetics. 77, 71-71 (1974).</li><li>Stephens, G. J., Johnson-Kerner, B., Bialek, W., Ryu, W. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dimensionality+and+dynamics+in+the+behavior+of+C.+elegans.">Dimensionality and dynamics in the behavior of C. elegans.</a> PLoS Comput Biol. 4, e1000028-e1000028 (2008).</li><li>Abramoff, M. a. g. e. l. h. a. e. s., Ram, P. J., J, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Image+Processing+with+ImageJ.">Image Processing with ImageJ.</a> Biophotonics International. 11, 36-36 (2004).</li></ol>

الإعلان عن أي تضارب في المصالح.

وجيم قدم ايليجانس التعلم النقابي الشمية والمقايسات الذاكرة هنا التمييز بين عمليات التعلم حشدت والتعلم متباعدة ، والذاكرة على المدى القصير ، والذاكرة على المدى الطويل. هذه المقايسات الاعتماد على قدرات الديدان الى الحس الغذائية والكيميائية الروائح 1،2 في محيطهم وتكوين الجمعيات إيجابية بين البلدين. 6 ولذلك ، فإن فحوصات حساسة جدا لتجويع السكان في البدء من الحيوانات ، ويجب الحذر الشديد يجب اتخاذها لضمان تغذية جيدة الديدان قبل وبعد التدريب. تدريب واحد حشدت غلة الذاكرة على المدى القصير النقابي. زيادة عدد فترات متباعدة وتكييف نموذج التدريب عامل حاسم لتحقيق الذاكرة طويلة المدى الجمعياتي في C. ايليجانس كما هو الحال في الكائنات الحية الأخرى. 6،8 وربما يمكن تعديل هذا الاختبار لإنتاج ذكريات طويلة الأجل بين مختلف الجمعيات ومحفزات مشروطة دون شروط. ويمكن استخدام معارفنا النقابي والمقايسات الذاكرة لمقارنة قدرات التعلم والذاكرة من النوع البري للحيوانات متحولة أو الشيخوخة الجينية. على سبيل المثال ، يتم الاحتفاظ حين أن كلا من التعلم النقابي والجمعياتي على المدى الطويل انخفاض قدرات الذاكرة في الشيخوخة البرية من نوع الديدان ، ويتم الاحتفاظ يعد التعلم مع التقدم في العمر لدى الحيوانات مع اشارة الانسولين مخفضة ، والتعلم والذاكرة مع التقدم في السن يعد في الحيوانات مقيدة السعرات الحرارية. 6 هذه المقايسات هي أيضا قابلة للعلاج الدوائي أو التلاعب رني جيم. ايليجانس. على سبيل المثال ، والعلاج من الديدان مع DAF - 2 رني يحسن قصيرة الأجل وطويلة الأجل الذاكرة الجمعوية ، وعلى العكس ، انسداد نسخ الجين والبروتين مع المخدرات (أكتينوميسين التطوير وسيكلوهيكسيميد ، على التوالي) خلال التدريب متباعدة يعطل على المدى الطويل تكوين الذاكرة. 6 الذاكرة طويلة المدى هي عملية بالغة الأهمية للبقاء في جميع الحيوانات ، ويبدو أن الكثير من الآلات الجزيئية المشاركة في ذكرى رابطة Pavlovian يتم حفظها من الديدان إلى الثدييات. 6 والقدرة على التمييز واختبار التعلم النقابي ، قصيرة المدى والذاكرة طويلة الأمد باستخدام هذه المقايسات الشمية يجعل C. ايليجانس نظام ممتازة لمزيد من الدراسة من الذاكرة ، ويمكن أن توفر نظرة ثاقبة العمليات العصبية التي تؤدي إلى فقدان الذاكرة والتعلم في البشر.

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c. elegans positive butanone learning, short-term, and long-term associative memory assays

ذاكرة الخبرات والمعلومات المستخلصة أمر حاسم بالنسبة للكائنات لجعل الخيارات التي تساعد بقائهم على قيد الحياة. جيم ايليجانس يتنقل البيئة من خلال الكشف عن خلية عصبية محددة من الطعام والروائح الكيماوية 1 ، 2 ، ويمكن ربط الدول المغذية مع الروائح الكيماوية 3 ، 4 درجات الحرارة ، وتسببها مصدر الغذاء 5. هنا ، نحن تصف المقايسات من ايليجانس جيم النقابي التعلم والذاكرة الترابطية القصيرة الأجل والطويلة الأجل. تعديل النموذج لدينا خبير الشمية مكره التعلم بدلا من 6 إلى إنتاج رد فعل إيجابي ، ويشمل الفحص ~ 400 تجويع الديدان ، ثم تغذية الديدان في وجود الخلايا العصبية المستشعرة - AWC مماثلة متقلبة butanone جاذب كيميائي بتركيز الذي يتسبب انخفاض مؤشر الكيميائي ( لToroyama آخرون 7). عدد السكان معيار الكيميائي assay1 اختبارات جاذبية الديدان إلى الرائحة على الفور أو دقائق إلى ساعات بعد تكييف. بعد تكييف الكيميائي والبرية من نوع الحيوانات على زيادات butanone ~ مؤشر الانجذاب الكيميائي 0.6 وحدة ، في &quot;فهرس التعلم&quot;. التعلم النقابي يعتمد على وجود كل من المواد الغذائية وbutanone أثناء التدريب. الغذاء الإقران وbutanone لفترة تكييف واحد (&quot;تدريب حشدت&quot;) تنتج الذاكرة على المدى القصير النقابي الذي يستمر ~ 2 ساعة. تكييف فترات متعددة مع فترات الراحة بين (&quot;تدريب متباعدة&quot;) غلات الذاكرة طويلة المدى النقابي (&lt;40 ساعة) ، وتعتمد على عنصر البروتين cAMP في الاستجابة تجليد (CREB) ، 6 عامل النسخ المطلوبة على المدى الطويل عبر الذاكرة الأنواع 8 كما يتضمن البروتوكول لدينا طرق تحليل الصور من أجل تقرير سريع ودقيق للمؤشرات الكيميائي. يتم التقاط صور عالية التباين من الحيوانات على لوحات فحص الكيميائي وتحليلها بواسطة برنامج دودة الفرز في MATLAB. البرنامج بتصحيح لخلفية تفاوت باستخدام التحول tophat المورفولوجية. الأسلوب 9 أوتسو لثم يستخدم لتحديد عتبة للديدان منفصلة عن الخلفية. 10 جزيئات صغيرة جدا يتم إزالتها تلقائيا وأكبر المنظمات غير دودة المناطق (حواف الصفيحة أو اللكمات آغار) هي إزالة بالاختيار اليدوي. البرنامج ثم تقديرات حجم دودة واحدة من خلال تجاهل المناطق التي هي فوق حجم الأقصى المحدد وأخذ حجم متوسط ​​من المناطق المتبقية. ويقدر ثم عدد الديدان بقسمة مجموع المساحة التي تحتلها على النحو المحدد الديدان التي يقدر حجم دودة واحدة. لقد وجدنا أن يمكن تمييزها التعلم والذاكرة القصيرة الأجل والطويلة الأجل ، وأن هذه العمليات حصة مماثلة مع جزيئات مفتاح العالي الكائنات الحية. 6،8 لدينا المقايسات يمكن اختبار الجينات بسرعة مرشح رواية أو الجزيئات التي تؤثر على التعلم وقصيرة الأمد أو طويلة في الذاكرة على المدى C. ايليجانس ذات الصلة عبر الأنواع.

Watch this Scientific Journal Video about C. elegans Positive Butanone Learning, Short-term, and Long-term Associative Memory Assays at JoVE.com

C. elegans Positive Butanone Learning, Short-term, and Long-term Associative Memory Assays

نحن هنا وصف لاختبار أساليب جيم ايليجانس التعلم والذاكرة الترابطية الجمعياتي قصيرة الأجل وطويلة الأجل. هذه المقايسات السكان توظيف قدرات الديدان chemotax نحو odorants المتقلبة ، وتكوين الجمعيات إيجابية على الاقتران الغذاء مع butanone جاذب كيميائي. زيادة عدد فترات تكييف يحرض الذاكرة طويلة المدى.

جيم ايليجانس Butanone التعلم الإيجابي ، قصيرة الأجل وطويلة الأجل فحوصات الذاكرة الترابطية

The memory of experiences and learned information is critical for organisms to make choices that aid their survival. C. elegans navigates its environment ...

c-elegans-positive-butanone-learning-short-term-long-term-associative

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Neuroscience

C. elegans Positive Butanone Learning, Short-term, and Long-term Associative Memory Assays

29.2K Views.  Princeton University. نحن هنا وصف لاختبار أساليب جيم ايليجانس التعلم والذاكرة الترابطية الجمعياتي قصيرة الأجل وطويلة الأجل. هذه المقايسات السكان توظيف قدرات الديدان chemotax نحو odorants المتقلبة ، وتكوين الجمعيات إيجابية على الاقتران الغذاء مع butanone جاذب كيميائي. زيادة عدد فترات تكييف يحر...

Video: C. elegans Positive Butanone Learning, Short-term, and Long-term Associative Memory Assays

Assaying Locomotor, Learning, and Memory Deficits in Drosophila Models of Neurodegeneration

Advances in genetic methods have enabled the study of genes involved in human neurodegenerative diseases using Drosophila as a model system1. Most of these diseases, including Alzheimer's, Parkinson's and Huntington's disease are characterized by age-dependent deterioration in learning and memory functions and movement coordination2. Here we use behavioral assays, including the negative geotaxis assay3 and the aversive phototaxic suppression assay (APS assay)4,5, to show that some of the behavior characteristics associated with human neurodegeneration can be recapitulated in flies. In the negative geotaxis assay, the natural tendency of flies to move against gravity when agitated is utilized to study genes or conditions that may hinder locomotor capacities. In the APS assay, the learning and memory functions are tested in positively-phototactic flies trained to associate light with aversive bitter taste and hence avoid this otherwise natural tendency to move toward light. Testing these trained flies 6 hours post-training is used to assess memory functions. Using these assays, the contribution of any genetic or environmental factors toward developing neurodegeneration can be easily studied in flies.

Assaying Locomotor, Learning, and Memory Deficits in Drosophila Models of Neurodegeneration

Behavior assays for measuring locomotor functions, learning, and memory abilities in Drosophila.

يعاير الحركي ، والتعلم ، والذاكرة في العجز ذبابة الفاكهة نماذج من تنكس عصبي

Advances in genetic methods have enabled the study of genes involved in human neurodegenerative diseases using Drosophila as a model system1. Most of ...

In vivo Laser Axotomy in C. elegans

Neurons communicate with other cells via axons and dendrites, slender membrane extensions that contain pre- or post-synaptic specializations. If a neuron is damaged by injury or disease, it may regenerate. Cell-intrinsic and extrinsic factors influence the ability of a neuron to regenerate and restore function. Recently, the nematode C. elegans has emerged as an excellent model organism to identify genes and signaling pathways that influence the regeneration of neurons1-6. The main way to initiate neuronal regeneration in C. elegans is laser-mediated cutting, or axotomy. During axotomy, a fluorescently-labeled neuronal process is severed using high-energy pulses. Initially, neuronal regeneration in C. elegans was examined using an amplified femtosecond laser5. However, subsequent regeneration studies have shown that a conventional pulsed laser can be used to accurately sever neurons in vivo and elicit a similar regenerative response1,3,7.
We present a protocol for performing in vivo laser axotomy in the worm using a MicroPoint pulsed laser, a turnkey system that is readily available and that has been widely used for targeted cell ablation. We describe aligning the laser, mounting the worms, cutting specific neurons, and assessing subsequent regeneration. The system provides the ability to cut large numbers of neurons in multiple worms during one experiment. Thus, laser axotomy as described herein is an efficient system for initiating and analyzing the process of regeneration.

In vivo Laser Axotomy in C. elegans

A protocol to cut neurons in C. elegans with a MicroPoint pulsed laser is presented. We describe setting up the system, immobilizing worms, and severing labeled neurons. Advantages include a relatively low-cost system and the ability to sever neuronal processes or ablate cells in vivo.

في Axotomy الليزر المجراة في C. ايليجانس

Neurons communicate with other cells via axons and dendrites, slender membrane extensions that contain pre- or post-synaptic specializations. If a neuron ...

Optical Recording of Suprathreshold Neural Activity with Single-cell and Single-spike Resolution

Signaling of information in the vertebrate central nervous system is often carried by populations of neurons rather than individual neurons. Also propagation of suprathreshold spiking activity involves populations of neurons. Empirical studies addressing cortical function directly thus require recordings from populations of neurons with high resolution. Here we describe an optical method and a deconvolution algorithm to record neural activity from up to 100 neurons with single-cell and single-spike resolution. This method relies on detection of the transient increases in intracellular somatic calcium concentration associated with suprathreshold electrical spikes (action potentials) in cortical neurons. High temporal resolution of the optical recordings is achieved by a fast random-access scanning technique using acousto-optical deflectors (AODs)1. Two-photon excitation of the calcium-sensitive dye results in high spatial resolution in opaque brain tissue2. Reconstruction of spikes from the fluorescence calcium recordings is achieved by a maximum-likelihood method. Simultaneous electrophysiological and optical recordings indicate that our method reliably detects spikes (&gt;97% spike detection efficiency), has a low rate of false positive spike detection (&lt; 0.003 spikes/sec), and a high temporal precision (about 3 msec) 3. This optical method of spike detection can be used to record neural activity in vitro and in anesthetized animals in vivo3,4.

Understanding the function of the vertebrate central nervous system requires recordings from many neurons because cortical function arises on the level of populations of neurons. Here we describe an optical method to record suprathreshold neural activity with single-cell and single-spike resolution, dithered random-access scanning. This method records somatic fluorescence calcium signals from up to 100 neurons with high temporal resolution. A maximum-likelihood algorithm deconvolves the underlying suprathreshold neural activity from the somatic fluorescence calcium signals. This method reliably detects spikes with high detection efficiency and a low rate of false positives and can be used to study neural populations in vitro and in vivo.

بصري تسجيل النشاط العصبي للقرار suprathreshold وحيدة الخلية واحد مسمار-

Signaling of information in the vertebrate central nervous system is often carried by populations of neurons rather than individual neurons. Also ...

C. elegans Tracking and Behavioral Measurement

We have developed instrumentation, image processing, and data analysis techniques to quantify the locomotory behavior of C. elegans as it crawls on the surface of an agar plate. For the study of the genetic, biochemical, and neuronal basis of behavior, C. elegans is an ideal organism because it is genetically tractable, amenable to microscopy, and shows a number of complex behaviors, including taxis, learning, and social interaction1,2. Behavioral analysis based on tracking the movements of worms as they crawl on agar plates have been particularly useful in the study of sensory behavior3, locomotion4, and general mutational phenotyping5. Our system works by moving the camera and illumination system as the worms crawls on a stationary agar plate, which ensures no mechanical stimulus is transmitted to the worm. Our tracking system is easy to use and includes a semi-automatic calibration feature. A challenge of all video tracking systems is that it generates an enormous amount of data that is intrinsically high dimensional. Our image processing and data analysis programs deal with this challenge by reducing the worms shape into a set of independent components, which comprehensively reconstruct the worms behavior as a function of only 3-4 dimensions6,7. As an example of the process we show that the worm enters and exits its reversal state in a phase specific manner.

C. elegans Tracking and Behavioral Measurement

We have developed a video-rate tracking microscope system that can record and quantify C. elegans behavior at high resolution and high speeds. We have also developed computational methods to reduce the dimensionality of the worm images to a fundamental set of measurements that completely describe the shape of the worm.

C. ايليجانس تتبع وقياس السلوكية

We have developed instrumentation, image processing, and data analysis techniques to quantify the locomotory behavior of C. elegans as it crawls on the ...

Appetitive Associative Olfactory Learning in Drosophila Larvae

In the following we describe the methodological details of appetitive associative olfactory learning in Drosophila larvae. The setup, in combination with genetic interference, provides a handle to analyze the neuronal and molecular fundamentals of specifically associative learning in a simple larval brain.
Organisms can use past experience to adjust present behavior. Such acquisition of behavioral potential can be defined as learning, and the physical bases of these potentials as memory traces1-4. Neuroscientists try to understand how these processes are organized in terms of molecular and neuronal changes in the brain by using a variety of methods in model organisms ranging from insects to vertebrates5,6. For such endeavors it is helpful to use model systems that are simple and experimentally accessible. The Drosophila larva has turned out to satisfy these demands based on the availability of robust behavioral assays, the existence of a variety of transgenic techniques and the elementary organization of the nervous system comprising only about 10,000 neurons (albeit with some concessions: cognitive limitations, few behavioral options, and richness of experience questionable)7-10.
Drosophila larvae can form associations between odors and appetitive gustatory reinforcement like sugar11-14. In a standard assay, established in the lab of B. Gerber, animals receive a two-odor reciprocal training: A first group of larvae is exposed to an odor A together with a gustatory reinforcer (sugar reward) and is subsequently exposed to an odor B without reinforcement 9. Meanwhile a second group of larvae receives reciprocal training while experiencing odor A without reinforcement and subsequently being exposed to odor B with reinforcement (sugar reward). In the following both groups are tested for their preference between the two odors. Relatively higher preferences for the rewarded odor reflect associative learning - presented as a performance index (PI). The conclusion regarding the associative nature of the performance index is compelling, because apart from the contingency between odors and tastants, other parameters, such as odor and reward exposure, passage of time and handling do not differ between the two groups9.

Appetitive Associative Olfactory Learning in Drosophila Larvae

Drosophila larvae are able to associate odor stimuli with gustatory reward. Here we describe a simple behavioral paradigm that allows the analysis of appetitive associative olfactory learning.

مشهي التعلم النقابي في الشم<em&gt; ذبابة الفاكهة</em&gt; اليرقات

In the following we describe the methodological  details of appetitive associative olfactory learning in Drosophila larvae. The setup, in combination with ...

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 ...

Agarose Microchambers for Long-term Calcium Imaging of Caenorhabditis elegans

Behavior is controlled by the nervous system. Calcium imaging is a straightforward method in the transparent nematode Caenorhabditis elegans to measure the activity of neurons during various behaviors. To correlate neural activity with behavior, the animal should not be immobilized but should be able to move. Many behavioral changes occur during long time scales and require recording over many hours of behavior. This also makes it necessary to culture the worms in the presence of food. How can worms be cultured and their neural activity imaged over long time scales? Agarose Microchamber Imaging (AMI) was previously developed to culture and observe small larvae and has now been adapted to study all life stages from early L1 until the adult stage of C. elegans. AMI can be performed on various life stages of C. elegans. Long-term calcium imaging is achieved without immobilizing the animals by using short externally triggered exposures combined with an electron multiplying charge-coupled device (EMCCD) camera recording. Zooming out or scanning can scale up this method to image up to 40 worms in parallel. Thus, a method is described to image behavior and neural activity over long time scales in all life stages of C. elegans.

Agarose Microchambers for Long-term Calcium Imaging of Caenorhabditis elegans

Imaging behavior and neural activity over long time scales without immobilization of the animal is a prerequisite to understand behavior. Agarose microfluidic chambers imaging (AMI) can be used to image neural activity and behavior for all life stages of Caenorhabditis elegans.

Microchambers الاغاروز لفترة طويلة التصوير الكالسيوم من<em&gt; انواع معينة ايليجانس</em

Behavior is controlled by the nervous system. Calcium imaging is a straightforward method in the transparent nematode Caenorhabditis elegans to measure ...

Assessing Spatial Learning and Memory in Small Squamate Reptiles

Clinical research has leveraged a variety of paradigms to assess cognitive decline, commonly targeting spatial learning and memory abilities. However, interest in the cognitive processes of nonmodel species, typically within an ecological context, has also become an emerging field of study. In particular, interest in the cognitive processes in reptiles is growing although experimental studies on reptilian cognition are sparse. The few reptilian studies that have experimentally tested for spatial learning and memory have used rodent paradigms modified for use in reptiles. However, ecologically important aspects of the physiology and behavior of this taxonomic group must be taken into account when testing for spatially based cognition. Here, we describe modifications of the dry land Barnes maze and associated testing protocol that can improve performance when probing for spatial learning and memory ability in small squamate reptiles. The described paradigm and procedures were successfully used with male side-blotched lizards (Uta stansburiana), demonstrating that spatial learning and memory can be assessed in this taxonomic group with an ecologically relevant apparatus and protocol.

This paper describes a modification of the Barnes maze, a standard rodent paradigm used to assess spatial memory and learning, for use in small squamate reptiles.

تقييم التعلم المكاني والذاكرة في Squamate الزواحف الصغيرة

Clinical research has leveraged a variety of paradigms to assess cognitive decline, commonly targeting spatial learning and memory abilities. However, ...

Generation and Long-term Maintenance of Nerve-free Hydra

The interstitial cell lineage of Hydra includes multipotent stem cells, and their derivatives: gland cells, nematocytes, germ cells, and nerve cells. The interstitial cells can be eliminated through two consecutive treatments with colchicine, a plant-derived toxin that kills dividing cells, thus erasing the potential for renewal of the differentiated cells that are derived from the interstitial stem cells. This allows for the generation of Hydra that lack nerve cells. A nerve-free polyp cannot open its mouth to feed, egest, or regulate osmotic pressure. Such animals, however, can survive and be cultured indefinitely in the laboratory if regularly force-fed and burped. The lack of nerve cells allows for studies of the role of the nervous system in regulating animal behavior and regeneration. Previously published protocols for nerve-free Hydra maintenance involve outdated techniques such as mouth-pipetting with hand-pulled micropipette tips to feed and clean the Hydra. Here, an improved protocol for maintenance of nerve-free Hydra is introduced. Fine-tipped forceps are used to force open the mouth and insert freshly killed Artemia. Following force-feeding, the body cavity of the animal is flushed with fresh medium using a syringe and hypodermic needle to remove undigested material, referred to here as "burping". This new method of force-feeding and burping nerve-free Hydra through the use of forceps and syringes eliminates the need for mouth-pipetting using hand-pulled micropipette tips. It thus makes the process safer and significantly more time efficient. To ensure that the nerve cells in the hypostome have been eliminated, immunohistochemistry using anti-tyrosine-tubulin is conducted.

Generation and Long-term Maintenance of Nerve-free Hydra

Through a double treatment with colchicine, a plant-derived toxin that kills dividing cells, nerve-free Hydra vulgaris can be generated. These Hydra cannot feed or egest on their own. This paper describes an improved method for long-term maintenance of nerve free Hydra vulgaris in the laboratory.

توليد وصيانة طويلة الأجل خالية من الأعصاب<em&gt; حيدرة</em

The interstitial cell lineage of Hydra includes multipotent stem cells, and their derivatives: gland cells, nematocytes, germ cells, and nerve cells. The ...

Long-term Sensory Conflict in Freely Behaving Mice

Long-term sensory conflict protocols are a valuable means of studying motor learning. The presented protocol produces a persistent sensory conflict for experiments aimed at studying long-term learning in mice. By permanently wearing a device fixed on their heads, mice are continuously exposed to a sensory mismatch between visual and vestibular inputs while freely moving in home cages. Therefore, this protocol readily enables the study of the visual system and multisensory interactions over an extended timeframe that would not be accessible otherwise. In addition to lowering the experimental costs of long-term sensory learning in naturally behaving mice, this approach accommodates the combination of in vivo and in vitro experiments. In the reported example, video-oculography is performed to quantify the vestibulo-ocular reflex (VOR) and optokinetic reflex (OKR) before and after learning. Mice exposed to this long-term sensory conflict between visual and vestibular inputs presented a strong VOR gain decrease but exhibited few OKR changes. Detailed steps of device assembly, animal care, and reflex measurements are hereby reported.

The presented protocol produces a persistent sensory conflict for experiments aimed at studying long-term learning. By permanently wearing a fixed device on their heads, mice are continuously exposed to a sensory mismatch between visual and vestibular inputs while freely moving in home cages.

الصراع الحسي طويلة الأجل في التصرف بحرية الفئران

Long-term sensory conflict protocols are a valuable means of studying motor learning. The presented protocol produces a persistent sensory conflict for ...

جيم ايليجانس Butanone التعلم الإيجابي ، قصيرة الأجل وطويلة الأجل فحوصات الذاكرة الترابطية

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يعاير الحركي ، والتعلم ، والذاكرة في العجز ذبابة الفاكهة نماذج من تنكس عصبي

في Axotomy الليزر المجراة في C. ايليجانس

بصري تسجيل النشاط العصبي للقرار suprathreshold وحيدة الخلية واحد مسمار-

C. ايليجانس تتبع وقياس السلوكية

مشهي التعلم النقابي في الشم

A قراءات الجزيئية من التكيف على المدى الطويل في الشم

Microchambers الاغاروز لفترة طويلة التصوير الكالسيوم من

تقييم التعلم المكاني والذاكرة في Squamate الزواحف الصغيرة

توليد وصيانة طويلة الأجل خالية من الأعصاب

الصراع الحسي طويلة الأجل في التصرف بحرية الفئران