Gli autori desiderano ringraziare Stefano per Crews dysfusion cDNA, anticorpi Dys e w le mosche 1118.

1. Raccolta degli embrioni <ol><li> Impostare gabbie a 25 ° C con 2-4 giorni di età w 1118 piastre succo flies.Grape vengono cambiati ogni ora durante il giorno per sincronizzare la raccolta delle uova in 1-2 giorni prima del periodo di raccolta </li><li> Raccogliere embrioni per 1 ora a 25 ° C </li><li> Tagliare un pezzo rettangolare di agar succo d&#39;uva, tagliate leggermente al centro con una lama di rasoio, lasciare una riga nel agar </li><li> Utilizzare una sonda di metallo per il trasferimento degli embrioni da piastra succo d&#39;uva al vostro pezzo di agar succo d&#39;uva, li allineano in linea retta con l&#39;asse più dell&#39;embrione a 45 gradi con la linea in mezzo l&#39;agar. Ottenere una retta di circa 50 embrioni. Assicurarsi che tutti gli embrioni punto nella stessa direzione, con estremità posteriore che punta lontano dalla linea. </li><li> Tagliare un pezzo rettangolare di nastro doppio bastone, e posizionarlo di una scivolata copertura 18x18mm. </li><li> Pick up embrioni con nastro doppio bastone sul vetrino </li><li> Mettere il vetrino di un vetrino, asciugare l&#39;embrione in aria per circa 10 min. </li><li> Coprire l&#39;embrione con un sottile strato di 700 Halocarbon, ora è pronto per l&#39;iniezione. </li></ol> 2. Tirare Needle Fai aghi microiniezione tirando tubi di vetro capillari. Noi utilizziamo un estrattore ago dal Instrument mondiale di precisione (modello PUL-1). Le specifiche estrattore programma aghi sono: calore: 1, ritardo di 4. 3. Riempimento del Needles Back-carico aghi utilizzando la pipetta Eppendorf p20 dotato di Eppendorf punte Microloader, normalmente carico 1,5-2 dsRNA microlitri 4. Break the Needles <ol><li> Prima di rompere l&#39;ago, inserire un vetrino in una diapositiva. </li><li> Preparare un vetrino con una goccia di olio al centro della diapositiva </li><li> Accendere il III Picospritzer picopump per regolare la pressione dell&#39;aria </li><li> Rompere l&#39;ago riempito contro il bordo di un vetrino, la creazione di una punta aguzza. </li><li> Quando la punta è rotto, passo sul pedale del Picospritzer III picopump, alcuni dsRNA sarà fuoriuscire dalla punta dell&#39;ago. </li><li> Estrarre il vetrino con il coprioggetto. </li><li> Inserire l&#39;ago sotto la goccia di olio al centro della diapositiva preparato prima. </li><li> Regolare l&#39;impostazione del III Picospritzer picopump per ottenere 100-200PL dsRNA quando fate un passo sul pedale. dsRNA può essere visto come una piccola goccia. </li></ol> 5. Iniezione <ol><li> Portare la punta dell&#39;ago alla parte posteriore dell &#39;embrione Blastoderm prima nello stesso piano focale e iniettare l&#39;embrione fuori centro del 30-50% lunghezza d&#39;uovo. </li><li> Dopo passo sul pedale del III Picospritzer picopump, una piccola quantità di dsRNA apparirà come un puntino nel sito di iniezione. </li></ol> 6. Analisi fenotipica <ol><li> Dopo l&#39;iniezione, collocare il vetrino in una camera coperta umida (plastica Petri) a 18 ° C fino a quando gli embrioni sviluppano allo stadio embrionale desiderato. </li><li> Utilizzare la sonda per rimuovere gli embrioni dal nastro biadesivo e spingerli verso il bordo dello slip di copertura. Lavare gli embrioni fuori dalla diapositiva in un flaconcino di raccolta con rete di nylon sul fondo utilizzando eptano, lavare 3 volte con PBT. Embrioni Dechorionate nel 50% di candeggina per 5 minuti, e lavare 3 volte con PBT. Trasferimento degli embrioni dal flacone collezione ad un pezzo di rete di nylon, e poi immergere la rete di nylon nella soluzione di fissativo (5 ml eptano, 4,5 ml di PBS, 0,5 ml di formaldeide 37%) per rilasciare embrioni. Fissare gli embrioni nella soluzione fissante per 30min. Devitellinize embrioni con metanolo, il trasferimento di embrioni per una provetta Eppendorf, e immunostain gli embrioni utilizzando protocolli standard. </li><li> Gli embrioni possono anche sviluppare appropriarsi stadio larvale. </li><li> Preparare un vetrino con una goccia di olio Halocarbon 700 nel mezzo </li><li> Trasferire una larve alla diapositiva, mettere un vetrino in cima </li><li> Osservare le larve al microscopio in campo chiaro. </li></ol> 7. Rappresentante dei risultati: Un esempio di dsRNA abbattere dysfusion (dis) gene in embrione Drosophlia è mostrato in Fig. 1. GFP-dsRNA embrioni iniettati sono il controllo negativo. Disfunzione è un fattore di trascrizione bHLH PAS espressi nelle cellule fusione tracheale. GFP-dsRNA embrioni iniettati mostrano normale fusione tracheale, e proteine ​​Dys è presente nelle cellule di fusione (Figura 1A). D&#39;altra parte, disfunzioni dsRNA embrioni iniettati mostrano fusione ramo fallito, e le proteine ​​Dys non sono presenti nelle cellule di fusione (Figura 1B). Quando dsRNA iniettato embrioni si sviluppano allo stadio larvale, la disfunzione dsRNA larve iniettate hanno mostrato la fusione ramo fallito (Fig.1D) rispetto al GFP-dsRNA controllo iniettato negativo (Figura 1C). Questi risultati hanno dimostrato efficace abbattere di espressione genica endogena disfunzioni da dsRNA iniezione in embrioni di Drosophila <img src="/files/ftp_upload/2477/2477fig1.jpg" alt="Figura 1" /> Figura 1. Rimozione della funzione di disfunzioni da disfunzione RNAi rivela tracheale fusione defects. Embrioni Blastoderm (w 1118) sono stati iniettati sia con GFP-dsRNA (controllo negativo) o disfunzioni dsRNA e analizzati per difetti tracheale. (A) Fase 16 embrioni iniettati con GFP-dsRNA e colorati con α-Dys e MAb 2A12 che macchia il lume tracheale. Prominente mostrata è il tronco laterale, che ha fuso. Le frecce indicano laterale tronco Dys cellule positive fusione. (B) Fase 16 embrioni iniettati con disfunzione dsRNA e colorati con α-Dys e MAb 2A12. L&#39;embrione ha mostrato una mancanza di fusione tronco laterale (l&#39;asterisco indica la posizione normale di un tronco di fusione laterale in embrioni di controllo). Nessun Dys cellule positive sono state osservate, indicando che la disfunzione RNA effettivamente abolito proteina Dys. (Da C a D) di secondo instar larve sia con GFP-dsRNA o disfunzione dsRNA sono stati esaminati dal campo chiaro microscopia per difetti tracheale. (C) Siti di fusione sono contrassegnati da un asterisco GFP-dsRNA larve controllo iniettato. (D) Il tronco laterale non è riuscito a fondere nel dys-RNA larve iniettate, (*) indica la posizione normale di una fusione tronco laterale.

<ol>
	<li>St Johnston, D., Nusslein-Volhard, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+origin+of+pattern+and+polarity+in+the+Drosophila+embryo.">The origin of pattern and polarity in the Drosophila embryo.</a> Cell. 68, 201-219 (1992).</li><li>Venken, K. J., Bellen, H. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Emerging+technologies+for+gene+manipulation+in+Drosophila+melanogaster.">Emerging technologies for gene manipulation in Drosophila melanogaster.</a> Nat. Rev. Genet. 6, 167-178 (2005).</li><li>Fire, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Potent+and+specific+genetic+interference+by+double-stranded+RNA+in+Caenorhabditis+elegans.">Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans.</a> Nature. 391, 806-811 (1998).</li><li>Kennerdell, J. R., Carthew, R. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Use+of+dsRNA-mediated+genetic+interference+to+demonstrate+that+frizzled+and+frizzled+2+act+in+the+wingless+pathway.">Use of dsRNA-mediated genetic interference to demonstrate that frizzled and frizzled 2 act in the wingless pathway.</a> Cell. 95, 1017-1026 (1998).</li><li>Misquitta, L., Paterson, B. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Targeted+disruption+of+gene+function+in+Drosophila+by+RNA+interference+(RNA-i):+a+role+for+nautilus+in+embryonic+somatic+muscle+formation.">Targeted disruption of gene function in Drosophila by RNA interference (RNA-i): a role for nautilus in embryonic somatic muscle formation.</a> Proc. Natl. Acad. Sci. U. S. A. 96, 1451-1456 (1999).</li><li>Horowitz, A., Simons, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Branching+morphogenesis.">Branching morphogenesis.</a> Circ. Res. 103, 784-795 (2008).</li><li>Hogan, B. L., Kolodziej, P. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Organogenesis:+molecular+mechanisms+of+tubulogenesis.">Organogenesis: molecular mechanisms of tubulogenesis.</a> Nat. Rev. Genet. 3, 513-523 (2002).</li><li>Ghabrial, A., Luschnig, S., Metzstein, M. M., Krasnow, M. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Branching+morphogenesis+of+the+Drosophila+tracheal+system.">Branching morphogenesis of the Drosophila tracheal system.</a> Annu. Rev. Cell Dev. Biol. 19, 623-647 (2003).</li><li>Jiang, L., Crews, S. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dysfusion+transcriptional+control+of+Drosophila+tracheal+migration,+adhesion,+and+fusion.">Dysfusion transcriptional control of Drosophila tracheal migration, adhesion, and fusion.</a> Mol. Cell. Biol. 26, 6547-6556 (2006).</li><li>Jiang, L., Crews, S. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Drosophila+dysfusion+basic+helix-loop-helix+(bHLH)-PAS+gene+controls+tracheal+fusion+and+levels+of+the+trachealess+bHLH-PAS+protein.">The Drosophila dysfusion basic helix-loop-helix (bHLH)-PAS gene controls tracheal fusion and levels of the trachealess bHLH-PAS protein.</a> Mol. Cell. Biol. 23, 5625-5637 (2003).</li></ol>

Nessun conflitto di interessi dichiarati.

L&#39;attuale metodo di iniezione di dsRNA consente qui una analisi molto sensibile e rapida della funzione del gene nello sviluppo di Drosophila tracheale. Questo metodo può potenzialmente essere applicato per analizzare la funzione del gene per altri tessuti e lo sviluppo degli organi.

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<td>Halocarbon oil 700</td>
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rnai interference by dsrna injection into drosophila embryos

Screening genetico è uno dei metodi più potenti disponibili per ottenere intuizioni complesso processo biologico 1. Nel corso degli anni molti miglioramenti e strumenti per la manipolazione genetica si sono resi disponibili in Drosophila 2. Subito dopo la scoperta iniziale Frie e Mello 3 che doppio filamento di RNA possono essere utilizzate per knockdown l&#39;attività di singoli geni in Caenorhabditis elegans, è stato mostrato interferenza dell&#39;RNA (RNAi) per fornire un potente approccio inverso genetico di analizzare le funzioni del gene nello sviluppo di Drosophila organo 4, 5. Molti organi, compreso il polmone, rene, fegato e sistema vascolare, sono composti da tubolari ramificate reti di trasporto che i fluidi vitali o gas 6, 7. L&#39;analisi della formazione di Drosophila tracheale fornisce un ottimo sistema modello per studiare la morfogenesi degli altri organi tubolari 8. The Berkeley Drosophila Genome Project ha rivelato centinaia di geni che si esprimono nel sistema tracheale. Per studiare i meccanismi molecolari e cellulari della formazione del tubo, la sfida è comprendere il ruolo di questi geni nello sviluppo tracheale. Qui, abbiamo descritto un metodo dettagliato di dsRNA iniezione in embrione di Drosophila espressione genica knockdown individuali. Siamo riusciti abbattuto endogeno dysfusion (dis) espressione genica mediante iniezione dsRNA. Disfunzione è un bHLH-PAS proteina espressa nelle cellule fusione tracheali, ed è necessario per la fusione ramo tracheale 9, 10. disfunzione RNAi completamente eliminato espressione disfunzioni e ha portato in difetto di fusione tracheale. Questo metodo relativamente semplice fornisce uno strumento per identificare i geni requried per tissure e lo sviluppo degli organi in Drosophila.

Watch this Scientific Journal Video about RNAi Interference by dsRNA Injection into Drosophila Embryos at JoVE.com

RNAi Interference by dsRNA Injection into Drosophila Embryos

RNA interference è stato dimostrato molto efficace per analizzare la funzione del gene in<em&gt; Drosophila</emSviluppo&gt; tracheale. Un protocollo dettagliato utilizzato da Jiang laboratorio di iniettare dsRNA in embrioni di volare a knockdown espressione genica è illustrato. Questa tecnica ha il potenziale per lo screening dei geni necessari per lo sviluppo di tessuti e organi in<em&gt; Drosophila</em&gt;.

L&#39;interferenza di RNAi per iniezione in dsRNA Drosophila Embrioni

Genetic screening is one of the most powerful methods available for gaining insights into complex biological process 1. Over the years many improvements ...

rnai-interference-by-dsrna-injection-into-drosophila-embryos

Universidad de Cartagena UDEC

Research

JoVE Journal

Biology

RNAi Interference by dsRNA Injection into Drosophila Embryos

16.1K Views.  Oakland University. RNA interference è stato dimostrato molto efficace per analizzare la funzione del gene in Drosophila tracheale. Un protocollo dettagliato utilizzato da Jiang laboratorio di iniettare dsRNA in embrioni di volare a knockdown espressione genica è illustrato. Questa tecnica ha il potenziale per lo screening dei geni necessari per lo sviluppo di tessuti e organi in Drosophila.

Video: RNAi Interference by dsRNA Injection into Drosophila Embryos

Injection of dsRNA into Female A. aegypti Mosquitos

Reverse genetic approaches have proven extremely useful for determining  which genes underly resistance to vector pathogens in mosquitoes.  This video protocol illustrates a method used by the James lab to inject dsRNA into female A. aegypti mosquitoes, which harbor the dengue virus.  The technique for calibrating injection needles, manipulating the injection setup, and injecting dsRNA into the thorax is illustrated.

Reverse genetic approaches have proven extremely useful for determining which genes underly resistance to vector pathogens in mosquitoes. This video protocol illustrates a method used by the James lab to inject dsRNA into female A. aegypti mosquitoes, which harbor the dengue virus. The technique for calibrating injection needles, manipulating the injection setup, and injecting dsRNA into the thorax is illustrated.

Iniezione di dsRNA in femmine di A. aegypti Zanzare

Reverse genetic approaches have proven extremely useful for determining  which genes underly resistance to vector pathogens in mosquitoes.  This video ...

Ricerca

Biologia

Injection of An. stephensi Embryos to Generate Malaria-resistant Mosquitoes

The introduction of exogenous genes into the genomes of mosquitoes requires microinjection techniques tailored to the specific species of interest. This video protocol demonstrates a method used by the James laboratory to microinject DNA constructs into Anopheles stephensi embryos for the generation of transformed mosquitoes. Techniques for preparing microinjection needles, collecting and preparing embryos and performing the microinjection are illustrated.

Anopheles stephensi mosquitoes are vectors for malaria inhabiting India and throughout Asia. This video demonstrates the technique for performing microinjections of this species with transgenes that will confer resistance to the malaria to the mosquito. Much of the methodology demonstrated in this video is applicable to microinjection techniques of other mosquito species.

Iniezione di An. Gli embrioni stephensi per generare la malaria resistenti zanzare

The introduction of exogenous genes into the genomes of mosquitoes requires microinjection techniques tailored to the specific species of interest. This ...

In Utero Intraventricular Injection and Electroporation of E16 Rat Embryos

In-utero in-vivo injection and electroporation of the embryonic rat neocortex provides a powerful tool for the manipulation of individual progenitors lining the walls of the lateral ventricle. This technique is now widely used to study the processes involved in corticogenesis by over-expressing or knocking down genes and observing the effects on cellular proliferation, migration, and differentiation. In comparison to traditional knockout strategies, in-utero electroporation provides a rapid means to manipulate a population of cells during a specific temporal window. In this video protocol, we outline the experimental methodology for preparing rats for surgery, exposing the uterine horns through laporatomy, injecting DNA into the lateral ventricles of the developing embryo, electroporating DNA into the progenitors lining the lateral wall, and caring for animals post-surgery. Our laboratory uses this protocol for surgeries on E15-E21 rats, however it is most commonly performed at E16 as shown in this video.

In Utero iniezione intraventricolare e Elettroporazione di embrioni di ratto E16

In-utero in-vivo injection and electroporation of the embryonic rat neocortex provides a powerful tool for the manipulation of individual progenitors ...

Live Dissection of Drosophila Embryos: Streamlined Methods for Screening Mutant Collections by Antibody Staining

Drosophila embryos between stages 14 and 17 of embryonic development can be readily dissected to generate "fillet" preparations. In these preparations, the central nervous system runs down the middle, and is flanked by the body walls. Many different phenotypes have been examined using such preparations. In most cases, the fillets were generated by dissection of antibody-stained fixed whole-mount embryos. These "fixed dissections" have some disadvantages, however. They are time-consuming to execute, and it is difficult to sort mutant (GFP-negative) embryos from stocks in which mutations are maintained over GFP balancer chromosomes. Since 2002, our group has been conducting deficiency and ectopic expression screens to identify ligands for orphan receptors. In order to do this, we developed streamlined protocols for live embryo dissection and antibody staining of collections containing hundreds of balanced lines. We have concluded that it is considerably more efficient to examine phenotypes in large collections of stocks by live dissection than by fixed dissection. Using the protocol described here, a single trained individual can screen up to 10 lines per day for phenotypes, examining 4-7 mutant embryos from each line under a compound microscope. This allows the identification of mutations conferring subtle, low-penetrance phenotypes, since up to 70 hemisegments per line are scored at high magnification with a 40X water-immersion lens.

Live Dissection of Drosophila Embryos: Streamlined Methods for Screening Mutant Collections by Antibody Staining

We describe a streamlined protocol for generating "fillet" preparations of Drosophila embryos of specific genotypes. This protocol allows efficient execution of a variety of genetic screens. It also allows excellent visualization of structures in the late embryo.

Dissezione di vivere Drosophila Embrioni: Metodi semplificati per lo screening Collezioni Mutant dalla colorazione anticorpale

Drosophila embryos between stages 14 and 17 of embryonic development can be readily dissected to generate "fillet" preparations.  In these preparations, ...

In-vivo Centrifugation of Drosophila Embryos

A major strategy for purifying and isolating different types of intracellular organelles is to separate them from each other based on differences in buoyant density. However, when cells are disrupted prior to centrifugation, proteins and organelles in this non-native environment often inappropriately stick to each other. Here we describe a method to separate organelles by density in intact, living Drosophila embryos. Early embryos before cellularization are harvested from population cages, and their outer egg shells are removed by treatment with 50% bleach. Embryos are then transferred to a small agar plate and inserted, posterior end first, into small vertical holes in the agar. The plates containing embedded embryos are centrifuged for 30 min at 3000g. The agar supports the embryos and keeps them in a defined orientation. Afterwards, the embryos are dug out of the agar with a blunt needle. Centrifugation separates major organelles into distinct layers, a stratification easily visible by bright-field microscopy. A number of fluorescent markers are available to confirm successful stratification in living embryos. Proteins associated with certain organelles will be enriched in a particular layer, demonstrating colocalization. Individual layers can be recovered for biochemical analysis or transplantation into donor eggs. This technique is applicable for organelle separation in other large cells, including the eggs and oocytes of diverse species.

In-vivo Centrifugation of Drosophila Embryos

We describe a method to separate organelles by density in living Drosophila embryos. Embryos are embedded in agar and centrifuged. This technique yields reproducible separation of major organelles along the anterior-posterior embryo axis. This method facilitates colocalization experiments and yields organelle fractions for biochemical analysis and transplantation experiments.

In vivo centrifugazione di embrioni di Drosophila

A major strategy for purifying and isolating different types of intracellular organelles is to separate them from each other based on differences in ...

Bacterial Delivery of RNAi Effectors: Transkingdom RNAi

RNA interference (RNAi) represents a high effective mechanism for specific inhibition of mRNA expression. Besides its potential as a powerful laboratory tool, the RNAi pathway appears to be promising for therapeutic utilization. For development of RNA interference (RNAi)-based therapies, delivery of RNAi-mediating agents to target cells is one of the major obstacles. A novel strategy to overcome this hurdle is transkingdom RNAi (tkRNAi). This technology uses non-pathogenic bacteria, e.g. Escherichia coli, to produce and deliver therapeutic short hairpin RNA (shRNA) into target cells to induce RNAi. A first-generation tkRNAi-mediating vector, TRIP, contains the bacteriophage T7 promoter for expression regulation of a therapeutic shRNA of interest. Furthermore, TRIP has the Inv locus from Yersinia pseudotuberculosis that encodes invasin, which permits natural noninvasive bacteria to enter &beta;1-integrin-positive mammalian cells and the HlyA gene from Listeria monocytogenes, which produces listeriolysin O. This enzyme allows the therapeutic shRNA to escape from entry vesicles within the cytoplasm of the target cell. TRIP constructs are introduced into a competent non-pathogenic Escherichia coli strain, which encodes T7 RNA polymerase necessary for the T7 promoter-driven synthesis of shRNAs. A well-characterized cancer-associated target molecule for different RNAi strategies is ABCB1 (MDR1/P-glycoprotein, MDR1/P-gp). This ABC-transporter acts as a drug extrusion pump and mediates the "classical" ABCB1-mediated multidrug resistance (MDR) phenotype of human cancer cells which is characterized by a specific cross resistance pattern. Different ABCB1-expressing MDR cancer cells were treated with anti-ABCB1 shRNA expression vector bearing E. coli. This procedure resulted in activation of the RNAi pathways within the cancer cells and a considerable down regulation of the ABCB1 encoding mRNA as well as the corresponding drug extrusion pump. Accordingly, drug accumulation was enhanced in the pristine drug-resistant cancer cells and the MDR phenotype was reversed. By means of this model the data provide the proof-of-concept that tkRNAi is suitable for modulation of cancer-associated factors, e.g. ABCB1, in human cancer cells.

For development of RNA interference (RNAi)-based therapies, a novel strategy was developed, transkingdom RNAi (tkRNAi). This technology uses non-pathogenic bacteria to produce and deliver therapeutic short hairpin RNA (shRNA) into target cells. Here, tkRNAi was successfully applied for reversal of classical ABCB1-mediated multidrug resistance (MDR) of cancer cells.

Consegna batterica di RNAi per DJ: Transkingdom RNAi

RNA interference (RNAi) represents a high effective mechanism for specific inhibition of mRNA expression. Besides its potential as a powerful laboratory ...

Intraperitoneal Injection into Adult Zebrafish

A convenient method for chemically treating zebrafish is to introduce the reagent into the tank water, where it will be taken up by the fish. However, this method makes it difficult to know how much reagent is absorbed or taken up per fish. Some experimental questions, particularly those related to metabolic studies, may be better addressed by delivering a defined quantity to each fish, based on weight. Here we present a method for intraperitoneal (IP) injection into adult zebrafish. Injection is into the abdominal cavity, posterior to the pelvic girdle. This procedure is adapted from veterinary methods used for larger fish. It is safe, as we have observed zero mortality. Additionally, we have seen bleeding at the injection site in only 5 out of 127 injections, and in each of those cases the bleeding was brief, lasting several seconds, and the quantity of blood lost was small. Success with this procedure requires gentle handling of the fish through several steps including fasting, weighing, anesthetizing, injection, and recovery. Precautions are required to minimize stress throughout the procedure. Our precautions include using a small injection volume and a 35G needle. We use Cortland salt solution as the vehicle, which is osmotically balanced for freshwater fish. Aeration of the gills is maintained during the injection procedure by first bringing the fish into a surgical plane of anesthesia, which allows slow operculum movements, and second, by holding the fish in a trough within a water-saturated sponge during the injection itself. We demonstrate the utility of IP injection by injecting glucose and monitoring the rise in blood glucose level and its subsequent return to normal. As stress is known to increase blood glucose in teleost fish, we compare blood glucose levels in vehicle-injected and non-injected adults and show that the procedure does not cause a significant rise in blood glucose.

We demonstrate intraperitoneal injection into adult zebrafish. We use a 10 &mu;l NanoFil microsyringe controlled by a Micro4 controller and UltraMicroPump III. This demonstration includes the use of cold water as an anesthetic.

Iniezione intraperitoneale in Zebrafish adulti

A convenient method for chemically treating zebrafish is to introduce the reagent into the tank water, where it will be taken up by the fish. However, ...

Upright Imaging of Drosophila Embryos

Several well-known morphogenetic gradients and cellular movements occur along the dorsal/ventral axis of the Drosophila embryo. However, the current techniques used to view such processes are somewhat limited. The following protocol describes a new technique for mounting fixed and labeled Drosophila embryos for coronal viewing with confocal imaging. This method consists of embedding embryos between two layers of glycerin jelly mounting media, and imaging jelly strips positioned upright. The first step for sandwiching the embryos is to make a thin bedding of glycerin jelly on a slide. Next, embryos are carefully aligned on this surface and covered with a second layer of jelly. After the second layer is solidified, strips of jelly are cut and flipped upright for imaging. Alternatives are described for visualizing the embryos depending upon the type of microscope stand to be used. Since all cells along the dorsal-ventral axis are imaged within a single confocal Z-plane, our method allows precise measurement and comparison of fluorescent signals without photobleaching or light scattering common to 3D reconstructions of longitudinally mounted embryos.

Upright Imaging of Drosophila Embryos

Here we present a mounting protocol for stained Drosophila embryos in an upright position that allows imaging of cross-sections using Confocal microscopy.

Imaging verticale di Drosophila Embrioni

Several well-known morphogenetic gradients and cellular movements occur along the dorsal/ventral axis of the Drosophila embryo. However, the current ...

Primary Cell Cultures from Drosophila Gastrula Embryos

Here we describe a method for preparing and culturing primary cells dissociated from Drosophila gastrula embryos. In brief, a large amount of staged embryos from young and healthy flies are collected, sterilized, and then physically dissociated into a single cell suspension using a glass homogenizer. After being plated on culture plates or chamber slides at an appropriate density in culture medium, these cells can further differentiate into several morphologically-distinct cell types, which can be identified by their specific cell markers. Furthermore, we present conditions for treating these cells with double stranded (ds) RNAs to elicit gene knockdown. Efficient RNAi in Drosophila primary cells is accomplished by simply bathing the cells in dsRNA-containing culture medium. The ability to carry out effective RNAi perturbation, together with other molecular, biochemical, cell imaging analyses, will allow a variety of questions to be answered in Drosophila primary cells, especially those related to differentiated muscle and neuronal cells.

Primary Cell Cultures from Drosophila Gastrula Embryos

We provide a detailed protocol for preparing primary cells dissociated from Drosophila embryos. The ability to carry out the effective RNAi perturbation, together with other molecular, biochemical and cell imaging methods will allow a variety of questions to be addressed in Drosophila primary cells.

Colture cellulari primarie da Drosophila Gastrula embrioni

Here we describe a method for preparing and culturing primary cells dissociated from Drosophila gastrula embryos.   In brief, a large amount of staged ...

Imaging Cell Shape Change in Living Drosophila Embryos

The developing Drosophila melanogaster embryo undergoes a number of cell shape changes that are highly amenable to live confocal imaging. Cell shape changes in the fly are analogous to those in higher organisms, and they drive tissue morphogenesis. So, in many cases, their study has direct implications for understanding human disease (Table 1)1-5. On the sub-cellular scale, these cell shape changes are the product of activities ranging from gene expression to signal transduction, cell polarity, cytoskeletal remodeling and membrane trafficking. Thus, the Drosophila embryo provides not only the context to evaluate cell shape changes as they relate to tissue morphogenesis, but also offers a completely physiological environment to study the sub-cellular activities that shape cells.
The protocol described here is designed to image a specific cell shape change called cellularization. Cellularization is a process of dramatic plasma membrane growth, and it ultimately converts the syncytial embryo into the cellular blastoderm. That is, at interphase of mitotic cycle 14, the plasma membrane simultaneously invaginates around each of ~6000 cortically anchored nuclei to generate a sheet of primary epithelial cells. Counter to previous suggestions, cellularization is not driven by Myosin-2 contractility6, but is instead fueled largely by exocytosis of membrane from internal stores7. Thus, cellularization is an excellent system for studying membrane trafficking during cell shape changes that require plasma membrane invagination or expansion, such as cytokinesis or transverse-tubule (T-tubule) morphogenesis in muscle.
Note that this protocol is easily applied to the imaging of other cell shape changes in the fly embryo, and only requires slight adaptations such as changing the stage of embryo collection, or using "embryo glue" to mount the embryo in a specific orientation (Table 1)8-19. In all cases, the workflow is basically the same (Figure 1). Standard methods for cloning and Drosophila transgenesis are used to prepare stable fly stocks that express a protein of interest, fused to Green Fluorescent Protein (GFP) or its variants, and these flies provide a renewable source of embryos. Alternatively, fluorescent proteins/probes are directly introduced into fly embryos via straightforward micro-injection techniques9-10. Then, depending on the developmental event and cell shape change to be imaged, embryos are collected and staged by morphology on a dissecting microscope, and finally positioned and mounted for time-lapse imaging on a confocal microscope.

Imaging Cell Shape Change in Living Drosophila Embryos

Early development of the fruit fly, Drosophila melanogaster, is characterized by a number of cell shape changes that are well suited for imaging approaches. This article will describe basic tools and methods required for live confocal imaging of Drosophila embryos, and will focus on a cell shape change called cellularization.

Imaging Forma Modifica cella in Living Drosophila Embrioni

The developing Drosophila melanogaster embryo undergoes a number of cell shape changes that are highly amenable to live confocal imaging.  Cell shape ...

L'interferenza di RNAi per iniezione in dsRNA Drosophila Embrioni

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