우리는 벌레를 계산하기 위해 ImageJ 13 사용하는 제안에 대한 Z. Gitai, 및 Google SketchUp에 도움을 위해 J. Ashraf, 설정의 초기 영상에 대한 조언 W. 류 감사합니다. CTM은 의생명 과학의 퓨 학술, 맥나이트 학술 및 켁 학자이다.

<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>

관심 없음 충돌 선언하지 않습니다.

C. 엘레간스 후각 연관 학습과 기억 assays 여기 massed 학습, 간격 학습, 단기 기억과 장기 기억의 과정을 구별을 제시. 이러한 assays들이 환경 1,2 음식과 화학 냄새를 감지하고 둘 사이에 긍정적인 연관 관계를 형성하는 웜 &#39;능력에 의존하고 있습니다. 6 따라서 assays 동물의 시작 인구 기아에 민감하고, 큰 관심이 있어야합니다 벌레가 잘 훈련 전후에 공급되는 것을 보장하기 위해 이동합니다. 싱글 massed 훈련은 단기 연관 메모리를 산출. 컨디셔닝 기간과 간격 훈련 패러다임의 증가 숫자는 C로 장기적인 연관 메모리 달성을위한 중요 엘레간스는 다른 유기체에 있기 때문입니다. 6,8 아마도이 분석은 다양한 시설과 무조건 자극 사이 협회의 장기 기억을 생산하기 위해 수정이 될 수 있습니다. 우리 연관 학습과 기억 assays은 노화 또는 유전 돌연변이 동물로 야생 유형의 학습과 기억 능력을 비교하는 데 사용할 수 있습니다. 예를 들어, 연관 학습과 야생 타입 벌레를 노화의 장기 연관 기억 능력의 저하 모두, 학습이 감소 인슐린 신호 전달, 그리고 학습 및 기억과 동물의 나이가 오래 유지되는 동안은 calorically 제한 동물의 나이가 오래 유지됩니다. 6 이러한 assays는 RNAi 치료 또는 C의 약리 조작 의무 아르 엘레간스. 예를 들어, DAF - 2 RNAi와 웜의 치료 향상 단기 및 장기 연관 메모리, 반대로 간격 훈련 동안 유전자 전사와 마약으로 단백질 합성 (actinomycin D와 cycloheximide, 각각)의 막힘은 장기 기억 형성을 방해. 6 짧은 연관 학습을 구분하고 테스트하는 능력 장기 기억은 모든 동물의 생존에 중요 프로세스이며, 그것은 파블로프의 조건 반사 협회의 메모리에 관련된 분자 기계의 많은 나타나는 포유류로 웜에서 보존됩니다. 6 이러한 후각 assays를 사용하여 장기와 장기 기억은 C.하게 메모리의 진학 훌륭한 시스템을 엘레간스, 그리고 학습과 인간의 메모리의 손실로 이어질 neurodegenerative 프로세스에 대한 통찰력을 제공할 수 있습니다.

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		<tr>
		<th>Material Name</th>
		<th>Type</th>
		<th>Company</th>
		<th>Catalogue Number</th>
		<th>Comment</th>
		</tr>
		</thead>
		<tbody>
		
<tr>
<td>Sodium Azide</td>
<td>&nbsp;</td>
<td>Fisher Scientific</td>
<td>S227</td>
<td>Prepare 1 M concentration in distilled water</td>
</tr>
<tr>
<td>Ethyl Alcohol 190 Proof</td>
<td>&nbsp;</td>
<td>Pharmco-Aaper</td>
<td>DSP-CT-18</td>
<td>&gt;95% Ethanol may have impurities that interfere with chemotaxis assays</td>
</tr>
<tr>
<td>2-Butanone 99+%</td>
<td>&nbsp;</td>
<td>Acros</td>
<td>14967-0010</td>
<td>&nbsp;</td>
<tr>
<td>Basler IEEE-1394/FireWire Area Scan CMOS Camera</td>
<td>&nbsp;</td>
<td>Edmund Optics</td>
<td>NT56-683</td>
<td>&nbsp;</td>
<tr>
<td>InfiniMite Video Lens &#x2013; Alpha Industrial</td>
<td>&nbsp;</td>
<td>Edmund Optics</td>
<td>NT56-202</td>
<td>&nbsp;</td>
<tr>
<td>Dolan-Jenner MI-150 Fiber Optic Illuminator</td>
<td>&nbsp;</td>
<td>Edmund Optics</td>
<td>NT55-718</td>
<td>&nbsp;</td>
<tr>
<td>8&#x201D; x 8&#x201D; Backlight</td>
<td>&nbsp;</td>
<td>Schott Fostec</td>
<td>A08927</td>
<td>&nbsp;</td>
<tr>
<td>Standard Boom Stand</td>
<td>&nbsp;</td>
<td>Edmund Optics</td>
<td>NT54-120</td>
<td>&nbsp;</td>
<tr>
<td>3/4&#x201D; Post Adaptor for Boom Stands</td>
<td>&nbsp;</td>
<td>Edmund Optics</td>
<td>NT54-124</td>
<td>&nbsp;</td>
<tr>
<td>Standard Fixed 1/4-20 Mounting Plate</td>
<td>&nbsp;</td>
<td>Edmund Optics</td>
<td>NT54-122</td>
<td>&nbsp;</td>		</tbody>
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c. elegans positive butanone learning, short-term, and long-term associative memory assays

경험과 배운 정보의 기억은 그들의 생존을 지원 결정을 내려야하는 생물에 대해 중요합니다. C.가 엘레간스 음식과 화학 냄새 1, 2의 신경 세포 특정 감지를 통해 환경을 이동하고, 화학 냄새 3, 온도 4 및 음식 소스 5 pathogenicity과 영양 상태를 연결할 수 있습니다. 여기, 우리는 C. 엘레간스 연관 학습과 단기 및 장기 연관 메모리 assays을 설명합니다. 우리는 대신에 긍정적인 반응을 생산하는 aversive 후각 학습 패러다임 6 수정, 분석은 다음 AWC 신경 세포 - 감지 (낮은 chemotactic 인덱스를 elicits 농도에서 휘발성 chemoattractant의 butanone을 유사한 존재에있는 벌레를 먹이 ~ 400 벌레를 굶주리고 포함 Toroyama 외. 7). 표준 인구 assay1 테스트 즉시 odorant 또는 조절 후 시간 분 웜 &#39;매력 chemotaxis. butanone 증가 에어컨, 야생 형 동물 &#39;chemotaxis 후 ~ 0.6 Chemotaxis 지수 단위는 &quot;학습 색인&quot;. 연관 학습은 훈련 기간 동안 음식과 butanone 모두의 존재에 따라 좌우됩니다. 단일 에어컨 기간 ( &quot;massed 교육&quot;)에 대한 페어링 음식과 butanone는 ~ 2 시간 정도 단기 연관 메모리를 생산하고 있습니다. ( &quot;간격 훈련&quot;) 사이의 휴식 기간으로 여러 컨디셔닝 기간이 장기적인 연관 메모리 (&lt;40 시간) 수율, 그리고 캠프 반응 요소 바인딩 단백질 (CREB), 6에 걸쳐 장기 기억에 필요한 전사 인자에 따라 좌우됩니다 종 8. 우리 프로토콜은 또한 chemotaxis 인덱스의 신속하고 정확한 결정을위한 영상 분석 방법을 포함하고 있습니다. chemotaxis 분석 플레이트에 동물의 하이 콘트라스트 이미지는 MatLab에서 벌레 계산 소프트웨어로 캡처하고 분석합니다. 소프트웨어는 형태학의 tophat 변환을 사용하여 고르지 배경 수정 9. 오오 츠의 방법은 다음 배경에서 별도로 벌레로 임계값을 결정하는 데 사용됩니다. 10 아주 작은 입자가 아닌 웜 영역을 (플레이트 가장자리 또는 한천 펀치) 자동으로 제거하고 큰 있습니다 수동 선택에 의해 삭제되었습니다. 소프트웨어는 다음 지정된 최대 크기 이상의 아르 영역을 무시하고 나머지 지역의 평균 크기를 복용하여 단일 벌레의 크기를 추정하고있다. 벌레의 수는 다음 하나의 벌레의 예상 크기에 의해 벌레에 의해 점유로 식별 전체 지역을 나누어 추정된다. 우리는 학습과 단기 및 장기 기억을 구분할 수 것으로 나타났습니다, 이러한 프로세스가 높은 생물과 유사한 핵심 분자를 공유. 6,8 우리 assays 신속하게 새로운 후보 유전자 또는 학습 및 단기 또는 장기에 영향을 분자를 테스트할 수 있습니다 C.에서 장기 기억 수종에 걸쳐 관련성이 엘레간스.

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

여기 방법 C. 엘레간스 연관 학습과 단기 및 장기 연관 메모리를 테스트하기 위해 설명합니다. 이러한 인구 assays은 휘발성 odorants 향해 chemotax에 웜 기능을 채용하고 chemoattractant butanone과 함께 음식을 페어링에 긍정적인 연관 관계를 형성하고 있습니다. 에어컨 기간의 수를 늘리면 장기 기억을 유도.

C. 엘레간스 긍정적인 Butanone 학습, 단기 및 장기 연관 메모리 Assays

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

Research

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Neuroscience

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

29.2K 조회수.  Princeton University. 여기 방법 C. 엘레간스 연관 학습과 단기 및 장기 연관 메모리를 테스트하기 위해 설명합니다. 이러한 인구 assays은 휘발성 odorants 향해 chemotax에 웜 기능을 채용하고 chemoattractant butanone과 함께 음식을 페어링에 긍정적인 연관 관계를 형성하고 있습니다. 에어컨 기간의 수를 늘리면 장기 기억을 유도.

비디오: 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.

에 시금 운동력이있는 사람, 학습, 및 메모리 적자 Drosophila</emNeurodegeneration의> 모델

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

연구

신경과학

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.

C로 생체내 레이저 Axotomy에서 엘레간스

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.

단일 셀 및 단일 스파이크 해상도 suprathreshold 신경 활동의 광 기록

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. elegans 추적 및 행동 측정

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.

에 Appetitive 연관 강한 학습<em&gt; Drosophila</em&gt; 애벌레

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.

의 장기 강한 적응의 분자 판독<em&gt; C. elegans</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.

의 장기 칼슘 이미징을위한 아가로 오스 Microchambers<em&gt; 예쁜 꼬마 선충</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.

작은 Squamate 파충류에서 공간 학습 및 메모리 평가

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.

신경이없는 세대의 장기간 유지 관리<em&gt; 히드라</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.

자유롭게 행동 하는 쥐에 장기 감각 충돌

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

C. 엘레간스 긍정적인 Butanone 학습, 단기 및 장기 연관 메모리 Assays

요약

더 많은 비디오 탐색

이 비디오의 챕터

에 시금 운동력이있는 사람, 학습, 및 메모리 적자 Drosophila 모델

C로 생체내 레이저 Axotomy에서 엘레간스

단일 셀 및 단일 스파이크 해상도 suprathreshold 신경 활동의 광 기록

C. elegans 추적 및 행동 측정

에 Appetitive 연관 강한 학습

의 장기 강한 적응의 분자 판독

의 장기 칼슘 이미징을위한 아가로 오스 Microchambers

작은 Squamate 파충류에서 공간 학습 및 메모리 평가

신경이없는 세대의 장기간 유지 관리

자유롭게 행동 하는 쥐에 장기 감각 충돌