Este trabalho é apoiado por fundos de inicialização da Universidade de Louisville e CA135123 dos Institutos Nacionais de Saúde (para CH).

1. Cultura de Células e Transfecção <ol><li> Células COS-7 foram cultivadas em Meio de Dulbecco Modificado de Eagle (DMEM), suplementado com 4,5 g / l de glucose e 10% de soro fetal bovino (FBS). </li><li> Transfecção de plasmídeo foi feito com Lipofectamina de acordo com as instruções do fabricante (Invitrogen). </li></ol> 2. Análise microscópica de fluorescência de células de expressão de superfície SNARE <ol><li> Um dia antes da transfecção, 3 × 10 4 células COS-7 foram semeadas em lamelas estéreis de 12 milímetros de vidro (Fisher Scientific), contidos em placas de 24 poços. </li><li> Para v-células em cada cavidade, 0,25 ug do plasmídeo que codifica tTA (BRST-Off, CLONTECH) é co-transfectadas com 0,25 ng dos plasmídeos que expressam invertidas VAMPS. </li><li> Para t-células em cada cavidade, 0,25 ug do plasmídeo que codifica TRE-LacZ (pBI-G, CLONTECH) é co-transfectadas com 0,25 ug de cada um dos plasmídeos que expressam invertidas SNAP-25 e syntaxins 1 ou 4. </li><li> 24 horas após transfection, as células são fixadas com paraformaldeído a 4% em PBS + + (PBS suplementado com 0,1 g / l de CaCl2 e 0,1 g / l de MgCl 2), durante 10 min e, em seguida, bloqueadas em FBS a 10% em PBS + +, durante 30 minutos. </li><li> As células são incubadas durante 1,5 horas com os anti-Myc 9E10 anticorpos monoclonais (sobrenadante da cultura de hibridoma pura). </li><li> Depois de quatro lavagens com PBS + +, as células são incubadas durante 1 hora com FITC-anticorpos secundários conjugados (Jackson ImmunoResearch Laboratories) a uma diluição de 1:500. </li><li> Depois de quatro lavagens com PBS + +, as células marcadas são montados em Prolongar reagente Antifade Gold (Invitrogen). </li><li> Imagens confocal são coletados em um microscópio de varredura a laser confocal Olympus. As imagens são processadas com o software Adobe Photoshop. </li></ol> 3. Análise FACS de células de expressão de superfície SNARE <ol><li> Um dia antes da transfecção, 2 × 10 5 células COS-7 foram semeadas em cada poço de placas de 6 poços. </li><li> 24 hr após transfection com o virado SNARE, BRST-Off e pBI-G plasmídeos, as células são fixadas com paraformaldeído a 1% em PBS + +, durante 15 minutos, e, em seguida, bloqueadas em FBS a 10% em PBS + +, durante 15 minutos. </li><li> As células são incubadas com o anti-Myc 9E10 anticorpos monoclonais durante 60 min. </li><li> Após três lavagens com PBS + +, as células são marcadas com FITC-conjugado de anticorpos secundários (diluição a 1:200) durante 45 min. </li><li> Após três lavagens com PBS + +, as células são raspadas das placas com um raspador de células. </li><li> 15.000 células são analisadas utilizando um citómetro de fluxo FACSCalibur (BD Biosciences). A intensidade média de fluorescência de cada amostra é obtido utilizando o software CellQuest Pro. </li></ol> 4. Ensaio de Fusão celular enzimática <ol><li> Um dia antes da transfecção, 1,2 x 10 6 células COS-7 foram semeadas em cada placa de cultura de tecidos de 100 mm e 2 x 10 5 células COS-7 foram semeadas em cada poço de placas de 6 poços. </li><li> Para v-células, 0,5 - 5 mg cada de Flipped VAMP plasmídeo é co-transf ectadas com 5 ug de BRST-Off para dentro das células em cada placa de cultura de 100 mm. As células de controlo são co-transfectadas com o vector vazio pcDNA3.1 (+) e BRST-Off. Para impedir que o N-glicosilação de gáspeas 1, 4, 5, 7 e 8, tunicamicina (10 ug / ml) é incluída no meio de cultura celular durante a transfecção. </li><li> Para t-células em cada poço das placas de 6 poços, 1 ug do virado SNAP-25 e plasmídeo pBI-G são co-transfectadas com 0,5 ug de plasmídeo ou invertida syntaxin1 0,05 ug de plasmídeo syntaxin4 invertida. </li><li> 24 horas após a transfecção, o V-células são separadas de pratos de cultura com a enzima livre de dissociação celular Buffer (Invitrogen). As células destacadas são contadas com um hemocitómetro e novamente suspensas em HEPES-tampão DMEM suplementado com FBS a 10%, 6,7 ug / ml de tunicamicina e 0,67 mM de DTT. </li><li> 4,8 x 10 5 ressuspenso v-As células são adicionadas a cada poço já contendo as células-T. </li><li> Depois de 6, 12 ou 24 horas de ratos de 37 ° C em CO2 a 5% </sub&gt;, a expressão de β-galactosidase é medida utilizando o β-Galactosidase Sistema de Ensaio Enzimático com Tampão de Lise Repórter de acordo com as instruções do fabricante (Promega). Resumidamente, as células são lavadas duas vezes com PBS, e depois foram lisadas em tampão de lise repórter. Os lisados ​​de células são misturadas com um volume igual de Tampão de Ensaio x 2. Como um controlo em branco, o Tampão de Lise Repórter é misturado com o tampão de Ensaio 2 ×. </li><li> Após 90 min, a reacção colorimétrica é parada pela adição de carbonato de sódio 1 M. </li><li> Absorvância a 420 nm é medida utilizando um espectrofotómetro de HITACHI 100-40. </li></ol>

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Não há conflitos de interesse declarados.

O ensaio de fusão de células original, 6 determina SNARE mediadas por eventos de fusão de células por microscopia de fluorescência. Descrevemos aqui um ensaio que quantifica inovador SNARE mediadas por eventos de fusão de células activado por expressão de β-galactosidase e medição espectrométrica. Utilizando este ensaio, que rotineiramente analisar 15-20 v-e t-SNARE combinações em uma única experiência. Utilizando citometria de fluxo para medir a expressão SNARE na superfície da célula, é ...

<table border="1"><tbody><tr><td> Nome do reagente e equipamento </td><td> Companhia </td><td> Número de catálogo </td></tr><tr><td> DMEM </td><td> Invitrogen </td><td> 12800-017 </td></tr><tr><td> Células COS-7 </td><td> ATCC </td><td> CRL-1651 </td></tr><tr><td> tunicamicina </td><td> Sigma-Aldrich </td><td> T7765-5mg </td></tr><tr><td> BRST-Off </td><td> Clontech </td><td> K1620-A </td></tr><tr><td> pBI-G </td><td> Clontech </td><td> 6150-1 </td></tr><tr><td> lipofectamina </td><td> Invitrogen </td><td> 18324-012 </td></tr><tr><td> Enzima livre de célula de solução de dissociação </td><td> Invitrogen </td><td> 13151-014 </td></tr><tr><td> Coelho anti-TET anticorpo policlonal Repressor </td><td> Millipore </td><td> AB3541 </td></tr><tr><td> FITC-conjugado de burro anti-IgG de ratinho (H + L) </td><td> JacImmunoResearch KSON </td><td> 715-095-150 </td></tr><tr><td> Microscópio de varredura a laser confocal </td><td> Olimpo </td><td> FV1000 </td></tr><tr><td> FACSCalibur citômetro de fluxo </td><td> BD Biosciences </td><td></td></tr><tr><td> β-Galactosidase Sistema de Ensaio Enzima com Tampão de Lise Repórter </td><td> Promega </td><td> E2000 </td></tr><tr><td> Modelo 100-40 espectrofotómetro de UV-VIS </td><td> Hitachi </td><td> C740843 </td></tr></tbody></table>

analysis of snare-mediated membrane fusion using an enzymatic cell fusion assay

As interacções dos SNARE (s factor de N-etilmaleimida sensível oluble ttachment um re ceptor de proteína) de proteínas em vesículas (v-SNAREs) e sobre as membranas-alvo (t-SNAREs) catalisam fusão das vesículas intracelulares 1-4. Os ensaios de reconstituição são essenciais para dissecar o mecanismo e regulação de SNARE mediada por fusão de membrana 5. Num ensaio de células de fusão 6,7, proteínas SNARE são expressos ectopicamente na superfície da célula. Estes &quot;invertida&quot; SNARE proteínas unidade de fusão célula-célula, demonstrando que SNAREs são suficientes para fundir as membranas celulares. Uma vez que o ensaio de fusão de células é baseada na análise microscópica, é menos eficaz quando utilizado para a análise múltipla v-e t-SNARE interacções quantitativamente. Descrevemos aqui um novo ensaio que quantifica 8 SNARE mediadas por eventos de fusão de células activado por expressão de β-galactosidase. Doiscomponentes do sistema de expressão do gene Tet-Off 9 são utilizados como um sistema de leitura: o transactivador tetraciclina controlada (tTA) e um plasmídeo repórter que codifica para o gene LacZ sob o controlo do elemento de resposta a tetraciclina (TRE-LacZ). Nós tTA em transfectar células COS-7 que expressam invertidas v-SNARE proteínas na superfície da célula (V-células) e transfectam TRE-LacZ em células COS-7 que expressam invertida t-SNARE proteínas na superfície celular (células T) . SNARE dependente da fusão dos v-e t-células resulta na ligação de tTA a TRE, a activação da transcrição do LacZ e da expressão de β-galactosidase. A actividade de β-galactosidase é quantificado utilizando um método colorimétrico por absorvância a 420 nm. As proteínas de vesículas associadas a membranas (Vamps) são v-SNAREs que residem em várias pós-Golgi compartimentos vesiculares 10-15. Ao expressar Vamps 1, 3, 4, 5, 7 e 8 no mesmo nível, compara-se a sua fusão de membranaactividades utilizando o ensaio enzimático de fusão celular. Com base em medições de espectrometria, este ensaio proporciona uma abordagem para a análise quantitativa SNARE mediada por fusão de membrana e de alto rendimento estudos.

Para desenvolver um ensaio de fusão celular quantitativo, tiramos vantagem da activação transcricional forte pela ligação de tTA a TRE. Na ausência de tTA, a transcrição do gene LacZ em TRE-LacZ é silenciosa. Quando tTA estiver presente, liga-se ao TRE e activa a transcrição de LacZ. Figura 1 mostra um fluxograma do ensaio enzimático das células de fusão. tTA é transfectado em células que v-v-SNARE expressa proteínas na superfície celular, e TRE-LacZ...

Watch this Scientific Journal Video about Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay at JoVE.com

Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay

Nós desenvolvemos um ensaio de fusão de células que quantifica SNARE mediadas por eventos de fusão da membrana por expressão activada de β-galactosidase.

Análise de SNARE mediada por fusão de membrana usando um ensaio de fusão celular enzimática

The interactions of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor)  proteins on vesicles (v-SNAREs) and on target membranes ...

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Research

JoVE Journal

Biology

13.9K visualizações.  University of Louisville School of Medicine. Nós desenvolvemos um ensaio de fusão de células que quantifica SNARE mediadas por eventos de fusão da membrana por expressão activada de β-galactosidase.

Vídeo: Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay

Studying Membrane Biogenesis with a Luciferase-Based Reporter Gene Assay

To study the coordination of different lipid synthesis pathways during membrane biogenesis it is useful to work with an experimental system where membrane biogenesis occurs rapidly and in an inducible manner. We have found that phagocytosis of latex beads is practical for these purposes as cells rapidly synthesize membrane lipids to replenish membrane pools lost as  wrapping material  during particle engulfment. Here, we describe procedures for studying changes in phagocytosis-induced gene expression with a luciferase-based reporter gene approach using the Dual-Glo  Luciferase Assay System from Promega.

Here, we describe procedures for studying changes in phagocytosis-induced gene expression with a luciferase-based reporter gene approach using the Dual-GloTM Luciferase Assay System from Promega.

Estudando Biogenesis de membrana com um ensaio de luciferase Gene-Based Reporter

To study the coordination of different lipid synthesis pathways during membrane biogenesis it is useful to work with an experimental system where membrane ...

Biologia

Method for Measurement of Viral Fusion Kinetics at the Single Particle Level

Membrane fusion is an essential step during entry of enveloped viruses into cells. Conventional fusion assays typically report on a large number of fusion events, making it difficult to quantitatively analyze the sequence of the molecular steps involved. We have developed an in vitro, two-color fluorescence assay to monitor kinetics of single virus particles fusing with a target bilayer on an essentially fluid support.
Influenza viral particles are incubated with a green lipophilic fluorophore to stain the membrane and a red hydrophilic fluorophore to stain the viral interior. We deposit a ganglioside-containing lipid bilayer on the dextran-functionilized glass surface of a flow cell, incubate the viral particles on the planar bilayer and image the fluorescence of a 100 x 100 &mu;m2 area, containing several hundreds of particles, on a CCD camera. By imaging both the red and green fluorescence, we can simultaneously monitor the behavior of the membrane dye (green) and the aqueous content (red) of the particles.
Upon lowering the pH to a value below the fusion pH, the particles will fuse with the membrane. Hemifusion, the merging of the outer leaflet of the viral membrane with the outer leaflet of the target membrane, will be visible as a sudden change in the green fluorescence of a particle. Upon the subsequent fusion of the two remaining distal leaflets a pore will be formed and the red-emitting fluorophore in the viral particle will be released under the target membrane. This event will give rise to a decrease of the red fluorescence of individual particles. Finally, the integrated fluorescence from a pH-sensitive fluorophore that is embedded in the target membrane reports on the exact time of the pH drop.
From the three fluorescence-time traces, all the important events (pH drop, lipid mixing upon hemifusion, content mixing upon pore formation) can now be extracted in a straightforward manner and for every particle individually. By collecting the elapsed times for the various transitions for many individual particles in histograms, we can determine the lifetimes of the corresponding intermediates. Even hidden intermediates that do not have a direct fluorescent observable can be visualized directly from these histograms.

We present an in vitro, two-color fluorescence assay to visualize the fusion of single virus particles with a fluid target bilayer. By labeling viral particles with fluorophores that differentially stain the viral membrane and its interior, we are able to monitor the kinetics of hemifusion and pore formation.

Método para Medição da Cinética de Fusão Viral no Nível única partícula

Membrane fusion is an essential step during entry of enveloped viruses into cells. Conventional fusion assays typically report on a large number of fusion ...

Anterior Cervical Discectomy and Fusion in the Ovine Model

Anterior cervical discectomy and fusion (ACDF) is the most common surgical operation for cervical radiculopathy and/or myelopathy in patients who have failed conservative treatment1,5. Since the operation was first described by Cloward2 and Smith and Robinson6 in 1958, a variety refinements in technique, graft material and implants have been made3. In particular, there is a need for safe osteoinductive agents that could benefit selected patients. The ovine model has been shown to have anatomical, biomechanical, bone density and radiological properties that are similar to the human counterpart, the most similar level being C3/44. It is therefore an ideal model in which preclinical studies can be performed. In particular this methodology may be useful to researchers interested in evaluating different devices and biologics, including stem cells, for potential application in human spinal surgery.

This video demonstrates the technique of anterior cervical discectomy and fusion in the ovine model.

Discectomia Cervical Anterior e Fusão no Modelo de Ovinos

Anterior cervical discectomy and fusion (ACDF) is the most common surgical operation for cervical radiculopathy and/or myelopathy in patients who have ...

Fluorescent Labeling of COS-7 Expressing SNAP-tag Fusion Proteins for Live Cell Imaging

SNAP-tag and CLIP-tag protein labeling systems enable the specific, covalent attachment of molecules, including fluorescent dyes, to a protein of interest in live cells. These systems offer a broad selection of fluorescent substrates optimized for a range of imaging instrumentation. Once cloned and expressed, the tagged protein can be used with a variety of substrates for numerous downstream applications without having to clone again. There are two steps to using this system: cloning and expression of the protein of interest as a SNAP-tag fusion, and labeling of the fusion with the SNAP-tag substrate of choice. The SNAP-tag is a small protein based on human O6-alkylguanine-DNA-alkyltransferase (hAGT), a DNA repair protein. SNAP-tag labels are dyes conjugated to guanine or chloropyrimidine leaving groups via a benzyl linker. In the labeling reaction, the substituted benzyl group of the substrate is covalently attached to the SNAP-tag. CLIP-tag is a modified version of SNAP-tag, engineered to react with benzylcytosine rather than benzylguanine derivatives. When used in conjunction with SNAP-tag, CLIP-tag enables the orthogonal and complementary labeling of two proteins simultaneously in the same cells.

SNAP-tag and CLIP-tag protein labeling systems enable the specific, covalent attachment of molecules, including fluorescent dyes, to a protein of interest in live cells. Once cloned and expressed, the tagged protein can be used with a variety of substrates for numerous downstream applications without having to clone again.

Labeling fluorescentes de COS-7 expressando as proteínas SNAP tag-Fusion para imagens de células vivas

SNAP-tag and CLIP-tag protein labeling systems enable the specific, covalent attachment of molecules, including fluorescent dyes, to a protein of interest ...

A Faster, High Resolution, mtPA-GFP-based Mitochondrial Fusion Assay Acquiring Kinetic Data of Multiple Cells in Parallel Using Confocal Microscopy

Mitochondrial fusion plays an essential role in mitochondrial calcium homeostasis, bioenergetics, autophagy and quality control. Fusion is quantified in living cells by photo-conversion of matrix targeted photoactivatable GFP (mtPAGFP) in a subset of mitochondria. The rate at which the photoconverted molecules equilibrate across the entire mitochondrial population is used as a measure of fusion activity. Thus far measurements were performed using a single cell time lapse approach, quantifying the equilibration in one cell over an hour. Here, we scale up and automate a previously published live cell method based on using mtPAGFP and a low concentration of TMRE (15 nm). This method involves photoactivating a small portion of the mitochondrial network, collecting highly resolved stacks of confocal sections every 15 min for 1 hour, and quantifying the change in signal intensity. Depending on several factors such as ease of finding PAGFP expressing cells, and the signal of the photoactivated regions, it is possible to collect around 10 cells within the 15 min intervals. This provides a significant improvement in the time efficiency of this assay while maintaining the highly resolved subcellular quantification as well as the kinetic parameters necessary to capture the detail of mitochondrial behavior in its native cytoarchitectural environment.
Mitochondrial dynamics play a role in many cellular processes including respiration, calcium regulation, and apoptosis1,2,3,13. The structure of the mitochondrial network affects the function of mitochondria, and the way they interact with the rest of the cell. Undergoing constant division and fusion, mitochondrial networks attain various shapes ranging from highly fused networks, to being more fragmented. Interestingly, Alzheimer's disease, Parkinson's disease, Charcot Marie Tooth 2A, and dominant optic atrophy have been correlated with altered mitochondrial morphology, namely fragmented networks4,10,13. Often times, upon fragmentation, mitochondria become depolarized, and upon accumulation this leads to impaired cell function18. Mitochondrial fission has been shown to signal a cell to progress toward apoptosis. It can also provide a mechanism by which to separate depolarized and inactive mitochondria to keep the bulk of the network robust14. Fusion of mitochondria, on the other hand, leads to sharing of matrix proteins, solutes, mtDNA and the electrochemical gradient, and also seems to prevent progression to apoptosis9. How fission and fusion of mitochondria affects cell homeostasis and ultimately the functioning of the organism needs further understanding, and therefore the continuous development and optimization of how to gather information on these phenomena is necessary.
Existing mitochondrial fusion assays have revealed various insights into mitochondrial physiology, each having its own advantages. The hybrid PEG fusion assay7, mixes two populations of differently labeled cells (mtRFP and mtYFP), and analyzes the amount of mixing and colocalization of fluorophores in fused, multinucleated, cells. Although this method has yielded valuable information, not all cell types can fuse, and the conditions under which fusion is stimulated involves the use of toxic drugs that likely affect the normal fusion process. More recently, a cell free technique has been devised, using isolated mitochondria to observe fusion events based on a luciferase assay1,5. Two human cell lines are targeted with either the amino or a carboxy terminal part of Renilla luciferase along with a leucine zipper to ensure dimerization upon mixing. Mitochondria are isolated from each cell line, and fused. The fusion reaction can occur without the cytosol under physiological conditions in the presence of energy, appropriate temperature and inner mitochondrial membrane potential. Interestingly, the cytosol was found to modulate the extent of fusion, demonstrating that cell signaling regulates the fusion process 4,5. This assay will be very useful for high throughput screening to identify components of the fusion machinery and also pharmacological compounds that may affect mitochondrial dynamics. However, more detailed whole cell mitochondrial assays will be needed to complement this in vitro assay to observe these events within a cellular environment.
A technique for monitoring whole-cell mitochondrial dynamics has been in use for some time and is based on a mitochondrially-targeted photoactivatable GFP (mtPAGFP)6,11. Upon expression of the mtPAGFP, a small portion of the mitochondrial network is photoactivated (10-20%), and the spread of the signal to the rest of the mitochondrial network is recorded every 15 minutes for 1 hour using time lapse confocal imaging. Each fusion event leads to a dilution of signal intensity, enabling quantification of the fusion rate. Although fusion and fission are continuously occurring in cells, this technique only monitors fusion as fission does not lead to a dilution of the PAGFP signal6. Co-labeling with low levels of TMRE (7-15 nM in INS1 cells) allows quantification of the membrane potential of mitochondria. When mitochondria are hyperpolarized they uptake more TMRE, and when they depolarize they lose the TMRE dye. Mitochondria that depolarize no longer have a sufficient membrane potential and tend not to fuse as efficiently if at all. Therefore, active fusing mitochondria can be tracked with these low levels of TMRE9,15. Accumulation of depolarized mitochondria that lack a TMRE signal may be a sign of phototoxicity or cell death. Higher concentrations of TMRE render mitochondria very sensitive to laser light, and therefore great care must be taken to avoid overlabeling with TMRE. If the effect of depolarization of mitochondria is the topic of interest, a technique using slightly higher levels of TMRE and more intense laser light can be used to depolarize mitochondria in a controlled fashion (Mitra and Lippincott-Schwartz, 2010). To ensure that toxicity due to TMRE is not an issue, we suggest exposing loaded cells (3-15 nM TMRE) to the imaging parameters that will be used in the assay (perhaps 7 stacks of 6 optical sections in a row), and assessing cell health after 2 hours. If the mitochondria appear too fragmented and cells are dying, other mitochondrial markers, such as dsRED or Mitotracker red could be used instead of TMRE.
The mtPAGFP method has revealed details about mitochondrial network behavior that could not be visualized using other methods. For example, we now know that mitochondrial fusion can be full or transient, where matrix content can mix without changing the overall network morphology. Additionally, we know that the probability of fusion is independent of contact duration and organelle dimension, is influenced by organelle motility, membrane potential and history of previous fusion activity8,15,16,17.
In this manuscript, we describe a methodology for scaling up the previously published protocol using mtPAGFP and 15nM TMRE8 in order to examine multiple cells at a time and improve the time efficiency of data collection without sacrificing the subcellular resolution. This has been made possible by the use of an automated microscope stage, and programmable image acquisition software. Zen software from Zeiss allows the user to mark and track several designated cells expressing mtPAGFP. Each of these cells can be photoactivated in a particular region of interest, and stacks of confocal slices can be monitored for mtPAGFP signal as well as TMRE at specified intervals. Other confocal systems could be used to perform this protocol provided there is an automated stage that is programmable, an incubator with CO2, and a means by which to photoactivate the PAGFP; either a multiphoton laser, or a 405 nm diode laser.

Mitochondrial fusion was measured by tracking the equilibration of photoconverted matrix-targeted GFP across the mitochondrial network over time. Thus far, only one cell could be subjected to an hour long kinetic analysis at a time. We present a method that simultaneously measures multiple cells, thereby speeding up the data collection process.

Uma resolução mais rápida, alta, MTPA-GFP baseada em ensaio de fusão mitocondrial aquisição de dados cinéticos de várias células em paralelo usando microscopia confocal

Mitochondrial fusion plays an essential role in mitochondrial calcium homeostasis, bioenergetics, autophagy and quality control. Fusion is quantified in ...

Expression of Fluorescent Fusion Proteins in Murine Bone Marrow-derived Dendritic Cells and Macrophages

Dendritic cells and macrophages are crucial cells that form the first line of defense against pathogens. They also play important roles in the initiation of an adaptive immune response. Experimental work with these cells is rather challenging. Their abundance in organs and tissues is relatively low. As a result, they cannot be isolated in large numbers. They are also difficult to transfect with cDNA constructs. In the murine model, these problems can be partially overcome by in vitro differentiation from bone marrow progenitors in the presence of M-CSF for macrophages or GM-CSF for dendritic cells. In this way, it is possible to obtain large amounts of these cells from very few animals. Moreover, bone marrow progenitors can be transduced with retroviral vectors carrying cDNA constructs during early stages of cultivation prior to their differentiation into bone marrow derived dendritic cells and macrophages. Thus, retroviral transduction followed by differentiation in vitro can be used to express various cDNA constructs in these cells. The ability to express ectopic proteins substantially extends the range of experiments that can be performed on these cells, including live cell imaging of fluorescent proteins, tandem purifications for interactome analyses, structure-function analyses, monitoring of cellular functions with biosensors and many others. In this article, we describe a detailed protocol for retroviral transduction of murine bone marrow derived dendritic cells and macrophages with vectors coding for fluorescently-tagged proteins. On the example of two adaptor proteins, OPAL1 and PSTPIP2, we demonstrate its practical application in flow cytometry and microscopy. We also discuss the advantages and limitations of this approach.

In this article, we provide a detailed protocol for the expression of fluorescent fusion proteins in murine bone marrow derived dendritic cells and macrophages. The method is based on the transduction of bone marrow progenitors with retroviral constructs followed by differentiation into macrophages and dendritic cells in vitro.

Expressão de proteínas da fusão fluorescente em murino derivadas da medula óssea as células dendríticas e macrófagos

Dendritic cells and macrophages are crucial cells that form the first line of defense against pathogens. They also play important roles in the initiation ...

LDL Cholesterol Uptake Assay Using Live Cell Imaging Analysis with Cell Health Monitoring

The regulation of LDL cholesterol uptake through LDLR-mediated endocytosis is an important area of study in various major pathologies including metabolic disorder, cardiovascular disease, and kidney disease. Currently, there is no available method to assess LDL uptake while simultaneously monitoring for health of the cells. The current study presents a protocol, using a live cell imaging analysis system, to acquire serial measurements of LDL influx with concurrent monitoring for cell health. This novel technique is tested in three human cell lines (hepatic, renal tubular epithelial, and coronary artery endothelial cells) over a four-hour time course. Moreover, the sensitivity of this technique is validated with well-known LDL uptake inhibitors, Dynasore and recombinant PCSK9 protein, as well as by an LDL uptake promoter, Simvastatin. Taken together, this method provides a medium-to-high throughput platform for simultaneously screening pharmacological activity as well as monitoring of cell morphology, hence cytotoxicity of compounds regulating LDL influx. The analysis can be used with different imaging systems and analytical software.

This protocol provides an efficient approach to measuring LDL cholesterol uptake with real time influx rates using a live cell imaging system in various cell types. This technique provides a platform to screen the pharmacological activity of compounds affecting LDL influx while monitoring for cell morphology and hence potential cytotoxicity.

Ensaio de absorção de LDL colesterol usando célula viva análise com célula de imagem monitoramento de integridade

The regulation of LDL cholesterol uptake through LDLR-mediated endocytosis is an important area of study in various major pathologies including metabolic ...

Effect of Fluorescent Proteins on Fusion Partners Using Polyglutamine Toxicity Assays in Yeast

For the investigation of protein localization and trafficking using live cell imaging, researchers often rely on fusing their protein of interest to a fluorescent reporter. The constantly evolving list of genetically encoded fluorescent proteins (FPs) presents users with several alternatives when it comes to fluorescent fusion design. Each FP has specific optical and biophysical properties that can affect the biochemical, cellular, and functional properties of the resulting fluorescent fusions. For instance, several FPs tend to form nonspecific oligomers that are susceptible to impede on the function of the fusion partner. Unfortunately, only a few methods exist to test the impact of FPs on the behavior of the fluorescent reporter. Here, we describe a simple method that enables the rapid assessment of the impact of FPs using polyglutamine (polyQ) toxicity assays in the budding yeast Saccharomyces cerevisiae. PolyQ-expanded huntingtin proteins are associated with the onset of Huntington&#39;s disease (HD), where the expanded huntingtin aggregates into toxic oligomers and inclusion bodies. The aggregation and toxicity of polyQ expansions in yeast are highly dependent on the sequences flanking the polyQ region, including the presence of fluorescent tags, thus providing an ideal experimental platform to study the impact of FPs on the behavior of their fusion partner.

This article describes protocols to assess the effect of fluorescent proteins on the aggregation and toxicity of misfolded polyglutamine expansion for the rapid evaluation of a newly uncharacterized fluorescent protein in the context of fluorescent reporters.

Efeito de proteínas fluorescentes na fusão parceiros usando Polyglutamine ensaios de toxicidade em levedura

For the investigation of protein localization and trafficking using live cell imaging, researchers often rely on fusing their protein of interest to a ...

Exploiting Live Imaging to Track Nuclei During Myoblast Differentiation and Fusion

Nuclear positioning within cells is important for multiple cellular processes in development and regeneration. The most intriguing example of nuclear positioning occurs during skeletal muscle differentiation. Muscle fibers (myofibers) are multinucleated cells formed by the fusion of muscle precursor cells (myoblasts) derived from muscle stem cells (satellite cells) that undergo proliferation and differentiation. Correct nuclear positioning within myofibers is required for the proper muscle regeneration and function. The common procedure to assess myoblast differentiation and myofiber formation relies on fixed cells analyzed by immunofluorescence, which impedes the study of nuclear movement and cell behavior over time. Here, we describe a method for the analysis of myoblast differentiation and myofiber formation by live cell imaging. We provide a software for automated nuclear tracking to obtain a high-throughput quantitative characterization of nuclear dynamics and myoblast behavior (i.e., the trajectory) during differentiation and fusion.

Skeletal muscle differentiation is a highly dynamic process, which particularly relies on nuclear positioning. Here, we describe a method to track nuclei movements by live cell imaging during myoblast differentiation and myotube formation and to perform a quantitative characterization of nuclei dynamics by extracting information from automatic tracking.

Explorando a imagem ao vivo aos núcleos de pista durante a diferenciação de Myoblast e fusão

Nuclear positioning within cells is important for multiple cellular processes in development and regeneration. The most intriguing example of nuclear ...

Production of IgG Fusion Proteins Transiently Expressed in Nicotiana benthamiana

High demand for antibodies as therapeutic interventions for various infectious, metabolic, autoimmune, neoplastic, and other diseases creates a growing need in developing efficient methods for recombinant antibody production. As of 2019, there were more than 70 FDA-approved monoclonal antibodies, and there is exponential growth potential. Despite their promise, limiting factors for widespread use are manufacturing costs and complexity. Potentially, plants offer low-cost, safe, and easily scalable protein manufacturing&#160;strategies. Plants like Nicotiana benthamiana not only can correctly fold and assemble complex mammalian proteins but also can add critical post-translational modifications similar to those offered by mammalian cell cultures. In this work, by using native GFP and an acid-stable variant of green fluorescent protein (GFP) fused to human monoclonal antibodies, we were able to visualize the entire transient antibody expression and purification process from N. benthamiana plants. Depending on the experiment&#39;s purpose, native GFP fusion can ensure easier visualization during the expression phase in the plants, while acid-stable GFP fusion allows for visualization during downstream processing. This scalable and straightforward procedure can be performed by a single researcher to produce milligram quantities of highly pure antibody or antibody fusion proteins in a matter of days using only a few small plants. Such a technique can be extended to the visualization of any type of antibody purification process and potentially many other proteins, both in plant and other expression systems. Moreover, these techniques can benefit virtual instructions and be executed in a teaching laboratory by undergraduate students possessing minimal prior experience with molecular biology techniques, providing a foundation for project-based exploration with real-world applications.

Production of IgG Fusion Proteins Transiently Expressed in Nicotiana benthamiana

We describe here a simple method for expression, extraction, and purification of recombinant human IgG fused to GFP in Nicotiana benthamiana. This protocol can be extended to purification and visualization of numerous proteins that utilize column chromatography. Moreover, the protocol is adaptable to the in-person and virtual college teaching laboratory, providing project-based exploration.

Produção de Proteínas IgG Fusion Transitóriamente Expressa em Nicotiana benthamiana

High demand for antibodies as therapeutic interventions for various infectious, metabolic, autoimmune, neoplastic, and other diseases creates a growing ...