Nucleotides for application in apoptosis tunel assay apoptosis is the process of an intracellular death program leading to characteristic biochemical and morphological changes within a cell that consequently result in cell death 1. The tunel assay is considered the gold standard for measuring apoptosis because is works on 95% of cells. The method described here has the advantages of simplicity, reliability and reproducibility. The data demonstrates that the delfia dna fragmentation assay is a simple and fast microplate format method, for detection of dna strand breaks in cells.
Sperm dna damage affects the conception rate resulting from human assisted reproduction technology. Detection of apoptosis by tunel assay springerlink. Terminal deoxynucleotidyl transferase dutp nick end labeling tunel is a method for. The comet assay is an extremely sensitive dna damage assay. Tunel is an acronym for terminal deoxynucleotidyl transferase biotindutp nick end labeling. Tunel staining may also be used to detect dna damage associated with nonapoptotic events such as necrotic cell death induced by exposure to toxic compounds and other insults, and tunel staining has also been reported to stain cells undergoing active dna repair. In contrast to tunel, which only stains apoptotic cells, hoechst 33342 stains the dna of all cells.
By using dutps that are labeled with chemical tags that can produce fluorescence or color. Tunel is a method for detecting apoptotic dna fragmentation, widely used to identify and quantify apoptotic cells, or to detect excessive dna breakage in individual cells. In situ cell death detection kit, pod sigmaaldrich. The fluorochromebased tunel assay applicable for flow cytometry, combining the detection of dna strand breaks with respect to the cell cycle phase position, was originally developed by gorczyca et al.
Oct 16, 2015 terminal deoxynucleotidyl transferase dutp nick end labeling is a method for detecting dna fragmentation by labeling the terminal end of nucleic acids. A cellbased dna fragmentation assay in microplate format. The tunel assay allows the in situ detection of apoptosis in tissue sections. Tunel staining protocol for apoptosis detection enzyme. Essentially, anything that can cause dna damage or denaturation except the factors being researched is to be avoided. Terminal deoxynucleotidyl transferase tdt is a templateindependent dna polymerase that is normally active in primitive lymphoid cells to increase receptor diversity. Wallac isoplates tc 1450517 delfia assay buffer 1244111 wallac eusa 1244360.
Tunel staining allows for visualization and quantification of apoptotic cells. Apoptosis detection using terminal transferase and biotin16. Cell death can occur by either of two distinct mechanisms, necrosis or programmed cell death apoptosis. A cautionary note on the use of the tunel stain to determine apoptosis. Looking for online definition of tunel or what tunel stands for. Detection of dna fragmentation in apoptotic cells by tunel. Cleavage of genomic dna during apoptosis may yield.
Caution the label solution contains cacodylate, toxic by inhalation and swallowed, and cobalt dichlo ride, which may cause ca ncer by inhalation. Pdf detection of apoptosis by tunel assay researchgate. Evaluation of sperm dna damage in bulls by tunel assay as a. Alternate fixation methods may be necessary to fully exploit some cell systems. After the discovery of apoptosis, a variety of the existing dna end.
The clickit tunel alexa fluor imaging assay has been tested in hela, a549, and cho k1 cells with a variety of reagents that induce apoptosis including staurosporine figure 6. The tunel assay relies on the presence of nicks in the dna which can be identified by tdt, an enzyme that catalyzes the addition of dutps that are labeled with fluorescein. The tunel assay also gives one more key piece of information which the annexin v assay doesnt. Sharma, edmund sabanegh, reda mahfouz, sajal gupta, aparna thiyagarajan, and ashok agarwal objectives to standardize the tunel assay by establishing inter and intraobserver variability, interassay. The deadend colorimetric tunel system endlabels the fragmented dna of apoptotic cells using a modified. Apr 10, 2014 as apoptosis assays go, tunel technology isnt exactly new, dating back to the early 1990s. Deadend fluorometric tunel system instructions for use of product g3250. Dna fragmentation occurs as one of the final stages of programmed cell death and has long been considered a hallmark of apoptosis as well as one of the defining biochemical events of the pathway.
In some cell systems apoptosis may progress without internucleosomal fragmentation of dna such cells will be weakly positive in tunel assay and it will be difficult to identify them. Yet the assay remains popular, in part because it meshes well with other cytological techniques. Terminal deoxynucleotidyl transferase dutp nick end labeling is a method for detecting dna fragmentation by labeling the terminal. Tunel terminal deoxynucleotidyl transferase dutp nick end labeling assays are a valuable method for detecting dna fragmentation, which is a hallmark of apoptosis, or programmed cell death.
A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Apoptotic cells can be detected by terminal deoxynucleotidyl transferase tdtmediated dutp nick end labeling tunel. Detection of apoptosis using the bd annexin v fitc assay. As apoptosis assays go, tunel technology isnt exactly new, dating back to the early 1990s. Necrosis is a pathological process which occurs when cells are exposed to a serious physical or chemical insult. Tunel label is used in combination with tunel enzyme to prepare the tunel reaction mixture. Apobrdu tunel assay kit c cell fixation is an important step in analyzing apoptotic samples. The tdt enzyme binds to the blunt ends of doublestranded dna breaks using a fl uorescent dye system 32. If your tunel assay does not fit the requirements above, send us a quick note or reach us at. The method is based on the ability of tdt to label blunt ends of doublestranded dna breaks independent of a template. Apoptosis detection using terminal transferase and biotin16dutp tunel enzyme method apoptosis detectiontunel staining service.
This is a colorimetric assay that measures the reduction of yellow 34,5dimethythiazol2yl2,5diphenyl tetrazolium bromide mtt by mitochondrial succinate dehydrogenase. Apoptosis is an important biological process during development, and for maintaining tissue homeostasis. I have some mouse mammary gland tissues that are formalin fixed and will be paraffin embedded. The kits are optimized for hcs and provide a choice of three wavelength options to aid in. In situ cell death detection kit, pod y version 15 content version. Hcs apoptosis tunel assay thermo fisher scientific us. In this method, the degree of integration of dutp deoxyuridine triphosphate. Therefore tunel staining may be considered generally as a method for the. Concurrently, the avidinperoxidase labeling assay applicable for light absorption microscope was described by gavrieli et al.
Terminal deoxynucleotidyl transferase dutp nick end labeling tunel is an established method for detecting dna fragments. Furthermore, the clickit tunel assay allows multiplexing with surface and intracellular biomarker detection. However, only an observation in light microscopy with high magnification permits the detection of chromatin condensation and apoptotic bodies. Stridea fluorescence method for direct, specific in situ. Tunelpositive cardiomyocytes show morphological features of. Sharma, edmund sabanegh, reda mahfouz, sajal gupta, aparna thiyagarajan, and ashok agarwal objectives to standardize the tunel assay by establishing inter. Unfixed cells may lose smaller dna fragments, leading to lower signals. Tunel staining allows for visualization and quantification of. Tunel as a test for sperm dna damage in the evaluation of.
Tunel assay is based on incorporation of labeled dutp in the dna mediated by the enzyme. The objective of this study was to adapt the terminal deoxynucleotidyl transferasemediated dutp nick end labeling tunel assay to provide a quality parameter for bull semen based on the detection of sperm dna damage. Analysis of apoptosis by cytometry using tunel assay. Tunel assay kits for apoptosis detection biocompare. Cellular viability xtt assay protocol this assay is based on the conversion of the watersoluble xtt 2,3bis2methoxy4nitro5sulfophenyl2htetrazolium5carboxanilide reagent to an orange formazan product by actively respiring cells. This protocol is used for detection and quantification of apoptosis programmed cell death at single cell level, based on labeling of dna strand breaks tunel technology.
Terminal deoxynucleotidyl transferase dutp nick end labeling. Strong evidence of apoptosis, following ischaemia and epilepsy, has been recently provided by combining genomic dna gel electrophoresis, light and electron microscopy and in situ dnabreak labelling. Terminal deoxynucleotidyl transferase tdt dutp nickend labeling tunel assay detects apoptotic cells at their terminal stage when there is extensive dna degradation. Oh dna ends using the terminal deoxynucleotidyl transferase, recombinant, enzyme rtdt, which forms a polymeric tail using the principle of the tunel tdtmediated dutp nickend labeling assay. Nucleotides for application in apoptosis tunel assay. This sensitivity needs to be handled carefully as it is also vulnerable to physical changes which can affect the reproducibility of results. I have read that tunel assays done on ffpe tissues is digestiondependant. The assay is commonly called tunel, the acronym of t erminal deoxynucleotidyl transferasemediated du tp n ick e nd l abeling. Tunel positive cardiomyocytes show morphological features of apoptosis and the typical ladder pattern in dna. In fact, this acronym is a misnomer because not only dutp but variety of other deoxynucleotides, indirectly or directly fluorochrometagged, are being used in different variants of the tunel assay. Evaluation of sperm dna damage in bulls by tunel assay as. The deadend colorimetric tunel system labels fragmented dna in situ and has been tested in all of these systems.
Dna fragmentation represents a characteristic hallmark of apoptosis. The presence of these groups is considered an established marker of apoptosis. To avoid the loss of fragmented dna and to allow enzyme and nucleotide entrance, cells need to be fixed and. Tunel assay on skeletal tissue sections to detect cell death. Because every research is unique, wimasis tunel assay tool is engineered with the flexibility to adapt to the needs of every researcher. In this assay, an enzyme called terminal deoxynucleotidyl transferase catalyzes the addition of dutp nucleotides to the free 3 ends of fragmented dna. The viability assay most commonly used throughout the world is the mtt assay, first described by tim mosmann in 1983. Tdt is expressed in certain immune cells and acts during vdj recombination the process that generates antibody diversity. Detection of apoptosis using the bd annexin v fitc assay on. Dna fragmentation can be detected in situ within the nuclei of fixed cells and tissues where the integrity of the dna and the free 3 hydroxyl groups at the sites of cleavage have been preserved by. This is a sensitive and efficient method for screening potential inducers of apoptosis. Tunel as a test for sperm dna damage in the evaluation of male infertility rakesh k.
Oh dna ends using the terminal deoxynucleotidyl transferase, recombinant, rtdt enzyme. One benefit of using a tunel assay for apoptosis research is the ability to detect surface and intracellular biomarkers on the same sample, says guffey. The tunel staining tunel assay method relies on the enzyme terminal deoxynucleotide transferase tdt, which attaches deoxynucleotides to the 3hydroxyl terminus of dna breaks. This assay uses a nuclear stain to identify cells and a tunel label to measure dna strand breaks. In this chapter, we describe a stepbystep protocol for fluorescent tunel staining in tissue sections of the developing skeleton. A cautionary note on the use of the tunel stain to. The assay relies on the use of terminal deoxynucleotidyl transferase tdt, an enzyme that catalyzes attachment of deoxynucleotides, tagged with a fluorochrome or another marker, to 3hydroxyl termini of dna double strand breaks. The fixation procedure only takes a little while and is a paraformaldehydeethanol fixation.
Detection of apoptotic cells in tissue samples currently relies on the tunel assay. The deadend fluorometric tunel system measures nuclear dna fragmentation, an important biochemical hallmark of apoptosis in many cell types. The tacs tdt kits contain a highly purified form of the tdt enzyme for the enzymatic incorporation of biotinylated nucleotides. Oh termini in singlestranded breaks in highmolecularweight nuclear dna fragments.
The standard apobrdu kit au1001 is a two color tunel terminal deoxynucleotide transferase dutp nick end labeling assay for labeling dna breaks and total cellular dna to detect apoptotic cells by flow or image cytometry. Assay principle the deadend colorimetric tunel system endlabels the fragmented dna of apoptotic cells using a modified tunel method. The two existing techniques that can be used for direct microscopy detection of dna breaks in situ, namely terminal deoxynucleotidyl transferase dutp nickend labeling tunel, for dsbs or the nick translation nt, for ssbs assay 11,12, usually rely on. The invitrogen clickit tunel alexa fluor imaging assay kits are fast and efficient and offer precise, quantitative data even with high levels of apoptotic cells. The mtt enters the cells and passes into the mitochondria where it is reduced to an insoluble, coloured dark purple formazan product. The deadend fluorometric tunel system measures the fragmented dna of apoptotic cells by catalytically incorporating fluorescein12dutp at 3. In a tunel assay, an enzyme known as terminal deoxynucleotidyl transferase tdt identifies nicks, or points of fragmentation. Shop online for a wide selection of promega deadend colorimetric tunel system a modified tunel assay designed for simple, rapid detection of apoptotic cells in situ at the. This technical bulletin includes protocols for detecting apoptosis in both tissue sections section 3. Apoptosis is a physiological and controlled process by which unwanted or useless cells are eliminated during development and other normal. One of the hallmarks of apoptosis is the nuclear dna fragmentation by nucleases. View full assay principle apoptotic cells can be detected by terminal deoxynucleotidyl transferase tdtmediated dutp nick end labeling tunel. Tunel is listed in the worlds largest and most authoritative dictionary database of abbreviations and acronyms. The assay relies on the use of terminal deoxynucleotidyl transferase tdt, an enzyme that.
The tunel assay is most commonly used to detect cells undergoing apoptosis, which is a form of programmed cell death. The amount of dna fragmentation was determined by tunel assay using a commercially available kit in situ cell death detection kit, fluorescein, roche, indianapolis, in, usa, whereby the free 3oh ends of dna are labeled with fluorescein conjugated dutp by the enzyme terminal deoxynucleotidyl transferase. Apoptosis detection using terminal transferase and biotin16dutp tunel enzyme method apoptosis detection tunel staining service. To avoid the loss of fragmented dna and to allow enzyme and nucleotide entrance, cells need to be fixed and subsequently permeabilized prior. Rudimentary assay details have been omitted for the sake of brevity. Clickit tunel alexa fluor imaging assay protocol thermo. Tunel assay is a method that takes advantage of this feature to detect apoptotic cells. It requires a minimum of a two color flow cytometer with a green fluorescence 515nm and red fluorescence635nm detector. Terminal deoxynucleotidyl transferase tdt dutp nickend labeling tunel assay has been designed to detect apoptotic cells that undergo extensive dna degradation during the late stages of apoptosis.
Tunel fluorescence assay is a wellestablished, fast, and simple nonradioactive technique to detect and quantify neurons undergoing apoptosis. Detection of dna fragments in situ using the terminal deoxyribonucleotidyl transferase tdtmediated biotin16dutp nickend labelling tunel assay is now commonly used to investigate apoptosis. Here, we describe a protocol in which cells are treated with tunel reagent and counterstained with hoechst 33342. Trevigen has developed a series of tunelbased assay kits for the in situ detection of apoptosis with colorimetric and fluorometric options. Nucleotides for application in apoptosis tunel assay jena.
Detection of apoptosis using the bd annexin v fitc assay on the bd facsverse system bd biosciences august 2011 introduction apoptosis is a normal genetically programmed process that occurs during embryonic development, as well as in maintenance of tissue homeostasis, under pathological conditions, and in aging. This colorimetric assay uses reduction of a yellow tetrazolium salt 3 4,5dimethyl thiazol 2yl2,5di phenyl tetrazolium bromide, or mtt to measure cellular metabolic activity as a proxy for cell viability. The principle of tunel assay relies on terminal deoxynucleotidyl transferase tdtmediated addition of a modified dutp xdutp to 3oh ends of dna fragments that are generated as a result of apoptosis induction. A failure of cells to undergo apoptosis is a common feature of many cancers 2 thus investigation. Mix 45 l tunel label with 5 l tunel enzyme prior to use. This is one of the advantages of the tunel assay because not only does it tell you if your cells are apoptotic, but it also tells you where in the cell cycle the cells are apoptotic.
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