Transfection is the process of deliberately introducing nucleic acids into cells. The term is used notably for non-viral methods in eukaryotic cells.[1] It may also refer to other methods and cell types, although other terms are preferred: "transformation" is more often used to describe non-viral DNA transfer in bacteria, non-animal eukaryotic cells and plant cells - a distinctive sense of transformation refers to spontaneous genetic modifications (mutations to cancerous cells (carcinogenesis), or under stress (UV irradiation)). Transduction is often used to describe virus-mediated DNA transfer. The word transfection is a blend of trans- and infection.
Genetic material (such as supercoiled plasmid DNA or siRNA constructs), or even proteins such as antibodies, may be transfected.
Transfection of animal cells typically involves opening transient pores or "holes" in the cell membrane, to allow the uptake of material. Transfection can be carried out using calcium phosphate, by electroporation, or by mixing a cationic lipid with the material to produce liposomes, which fuse with the cell membrane and deposit their cargo inside.
Transfection can result in unexpected morphologies and abnormalities in target cells.
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Contents
- 1 Terminology
- 2 Methods
- 2.1 Chemical-based transfection
- 2.2 Non chemical methods
- 2.3 Particle-based methods
- 2.4 Viral methods
- 2.5 Other (and hybrid) methods
- 3 Stable and transient transfection
- 4 RNA transfection
- 5 See also
- 6 References
- 7 External links
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Terminology
The meaning of the term has evolved.[2] The original meaning of transfection was "infection by transformation," i.e., introduction of DNA (or RNA) from a prokaryote-infecting virus or bacteriophage into cells, resulting in an infection. Because the term transformation had another sense in animal cell biology (a genetic change allowing long-term propagation in culture, or acquisition of properties typical of cancer cells), the term transfection acquired, for animal cells, its present meaning of a change in cell properties caused by introduction of DNA.
Methods
There are various methods of introducing foreign DNA into a eukaryotic cell: some rely on physical treatment (electroporation, nanoparticles, magnetofection), other on chemical materials or biological particles (viruses) that are used as carriers.
Chemical-based transfection
Chemical-based transfection can be divided into several kinds: cyclodextrin,[3] polymers,[4] liposomes, or nanoparticles [5] (with or without chemical or viral functionalization. See below).
- One of the cheapest methods uses calcium phosphate, originally discovered by F. L. Graham and A. J. van der Eb in 1973[6] (see also [7]). HEPES-buffered saline solution (HeBS) containing phosphate ions is combined with a calcium chloride solution containing the DNA to be transfected. When the two are combined, a fine precipitate of the positively charged calcium and the negatively charged phosphate will form, binding the DNA to be transfected on its surface. The suspension of the precipitate is then added to the cells to be transfected (usually a cell culture grown in a monolayer). By a process not entirely understood, the cells take up some of the precipitate, and with it, the DNA.
- Other methods use highly branched organic compounds, so-called dendrimers, to bind the DNA and get it into the cell.
- A very efficient method is the inclusion of the DNA to be transfected in liposomes, i.e. small, membrane-bounded bodies that are in some ways similar to the structure of a cell and can actually fuse with the cell membrane, releasing the DNA into the cell. For eukaryotic cells, transfection is better achieved using cationic liposomes (or mixtures), because the cells are more sensitive. See lipofection for more details.
- Another method is the use of cationic polymers such as DEAE-dextran or polyethylenimine. The negatively charged DNA binds to the polycation and the complex is taken up by the cell via endocytosis.
Non chemical methods
- Electroporation is a popular method, although requiring an instrument and affecting the viability of many cell types, that also creates micro-sized holes transiently in the plasma membrane of cells under an electric discharge.
- Similarly, transfection applying sonic forces to cells, referred as Sono-poration.
- Optical transfection is a method where a tiny (~1 µm diameter) hole is transiently generated in the plasma membrane of a cell using a highly focused laser. This technique was first described in 1984 by Tsukakoshi et al., who used a frequency tripled Nd:YAG to generate stable and transient transfection of normal rat kidney cells.[8] In this technique, one cell at a time is treated, making it particularly useful for single cell analysis.
- Gene electrotransfer is a technique that enables transfer of genetic material into prokaryotic or eukaryotic cells. It is based on a physical method named electroporation, where transient increase in the permeability of cell membrane is achieved when submitted to short and intense electric pulses.
- Impalefection is a method of introducing DNA bound to a surface of a nanofiber that is inserted into a cell. This approach can also be implemented with arrays of nanofibers that are introduced into large numbers of cells and intact tissue.
- Hydrodynamic delivery In mice and rats, but to a lesser extent in larger animals, DNA most often in plasmids, including transposons, can be delivered to the liver using hydrodynamic injection that involves infusion of a relatively large volume in the blood in less than 10 seconds; nearly all of the DNA is expressed in the liver by this procedure.[9][10][11]
Particle-based methods
- A direct approach to transfection is the gene gun, where the DNA is coupled to a nanoparticle of an inert solid (commonly gold) which is then "shot" directly into the target cell's nucleus.
- Magnetofection, or Magnet assisted transfection is a transfection method, which uses magnetic force to deliver DNA into target cells. Nucleic acids are first associated with magnetic nanoparticles. Then, application of magnetic force drives the nucleic acid particle complexes towards and into the target cells, where the cargo is released.[12][13][14]
- Impalefection is carried out by impaling cells by elongated nanostructures and arrays of such nanostructures such as carbon nanofibers or silicon nanowires which have been functionalized with plasmid DNA.
Viral methods
DNA can also be introduced into cells using viruses as a carrier. In such cases, the technique is called viral transduction, and the cells are said to be transduced.
Other (and hybrid) methods
Other methods of transfection include nucleofection, heat shock.
Stable and transient transfection
For most applications of transfection, it is sufficient if the transfected genetic material is only transiently expressed. Since the DNA introduced in the transfection process is usually not integrated into the nuclear genome, the foreign DNA will be diluted through mitosis or degraded.
If it is desired that the transfected gene actually remains in the genome of the cell and its daughter cells, a stable transfection must occur. To accomplish this, a marker gene is co-transfected, which gives the cell some selectable advantage, such as resistance towards a certain toxin. Some (very few) of the transfected cells will, by chance, have integrated the foreign genetic material into their genome. If the toxin is then added to the cell culture, only those few cells with the marker gene integrated into their genomes will be able to proliferate, while other cells will die. After applying this selective stress (selection pressure) for some time, only the cells with a stable transfection remain and can be cultivated further.
A common agent for selecting stable transfection is Geneticin, also known as G418, which is a toxin that can be neutralized by the product of the neomycin resistance gene.
RNA transfection
Main article: RNA transfection
RNA can also be transfected into cells to transiently express its coded protein, or to study RNA decay kinetics. The later application is referred as siRNA transfection or RNA silencing, and has become a major application in research (to replace the "knock-down" experiments, to study the expression of proteins, i.e. of Endothelin-1 [15]) with potential applications in gene-therapy.
A limitation of the silencing approach rely on the toxicity of the transfection for cells, and its suspected effect on the expression of other genes/proteins.
See also
- Protofection
- Transformation
- Transduction
- Cationic liposome
- Nucleofection
- Magnet assisted transfection
- Impalefection
References
- ^ http://www.promega.com/paguide/chap12.htm
- ^ "Transfection" at Dorland's Medical Dictionary
- ^ Menuel S, Fontanay S, Clarot I, Duval R.E, Diez L, Marsura A (2008). "Synthesis and Complexation Ability of a Novel Bis- (guanidinium)-tetrakis-(β-cyclodextrin) Dendrimeric Tetrapod as a Potential Gene Delivery (DNA and siRNA) System. Study of Cellular siRNA Transfection". Bioconjugate Chem. 19 (12): 2357–2362. doi:10.1021/bc800193p. PMID 19053312.
- ^ Fischer D, von Harpe A, Kunath K, Petersen H, Li YX, Kissel T (2002). "Copolymers of ethylene imine and N-(2-hydroxyethyl)-ethylene imine as tools to study effects of polymer structure on physicochemical and biological properties of DNA complexes". Bioconjugate Chem. 13 (5): 1124–1133. doi:10.1021/bc025550w.
- ^ http://www.transfection.ws/nanoparticle_based_transfection_reagents
- ^ Graham FL, van der Eb AJ (1973). "A new technique for the assay of infectivity of human adenovirus 5 DNA". Virology 52 (2): 456–67. doi:10.1016/0042-6822(73)90341-3. PMID 4705382.
- ^ Bacchetti S, Graham F (1977). "Transfer of the gene for thymidine kinase to thymidine kinase-deficient human cells by purified herpes simplex viral DNA". Proc Natl Acad Sci USA 74 (4): 1590–4. doi:10.1073/pnas.74.4.1590. PMC 430836. PMID 193108. //www.ncbi.nlm.nih.gov/pmc/articles/PMC430836/.
- ^ M. Tsukakoshi, S. Kurata, Y. Nomiya, et al., "A Novel Method of DNA Transfection by Laser Microbeam Cell Surgery". Applied Physics B-Photophysics and Laser Chemistry. 35(3): 135-140 (1984)
- ^ Zhang, G., Budker, V. and Wolff, J.A. (1999) High levels of foreign gene expression in hepatocytes after tail vein injections of naked plasmid DNA. Hum. Gene Ther., 10, 1735-1737.
- ^ Zhang, G., Vargo, D., Budker, V., N., A., Knechtle, S. and Wolff, J.A. (1997) Expression of naked plasmid DNA injected into the afferent and efferent vessels of rodent and dog livers. Hum. Gene Ther., 8, 1763-1772.
- ^ Bell, J.B., Podetz-Pedersen, K., Aronovich, E.L., Belur, L.R., McIvor, R.S. and Hackett, P.B. (2007) Preferential delivery of the Sleeping Beauty transposon system to livers of mice by hydrodynamic injection. Nat. Protocols, 2, 3153-3165.
- ^ Bertram, J. (2006) MATra - Magnet Assisted Transfection: Combining Nanotechnology and Magnetic Forces to Improve Intracellular Delivery of Nucleic Acids. Current Pharmaceutical Biotechnology 7, 277-28
- ^ http://www.magnet-assisted-transfection.com/naps/naps_fr02_01.html
- ^ http://www.promokine.info/products/cell-transfection/magnet-assisted-transfection/
- ^ Mawji et al used this technique to evaluate the kinetics of Endothelin-1 RNA decay in primary endothelial cells: Mawji et al. "RNA transfection is a versatile tool to investigate endothelin-1 posttranscriptional regulation." Exp Biol Med. 2006 Jun;231(6):704-8. PMID 16740984
External links
- Transfection at the US National Library of Medicine Medical Subject Headings (MeSH)
- Biology Research Resource - Articles and Forums about Transfection
- Transfection at eMedicine Dictionary
- Overview of transfection methods in Nature Methods 2, 875 - 883 (2005)
- Research in optical transfection at the University of St Andrews
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Genetics: homologous recombination / mobile genetic elements
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| Primarily prokaryotic |
Conjugation · Transduction · Transformation
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| Occurs in eukaryotes |
Transfection · Chromosomal crossover · Gene conversion · Fusion gene · Horizontal gene transfer · Sister chromatid exchange · Transposon
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B bsyn: dna (repl, cycl, reco, repr) · tscr (fact, tcrg, nucl, rnat, rept, ptts) · tltn (risu, pttl, nexn) · dnab, rnab/runp · stru (domn, 1°, 2°, 3°, 4°)
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Genetic engineering
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Genetically
modified
organisms |
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Mammals
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Mouse (Knockout mouse · Oncomouse) · Enviropig · Herman the Bull · Knockout rat
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Crops
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Maize
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MON 802 · MON 809 · MON 810 · MON 832 · MON 863 · MIR162 · MIR604 · BT11 · BT11 x GA21 · BT11 x MIR162 x MIR604 · BT11 x MIR604
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Potato
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Amflora
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Rice
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Golden rice
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Soybean
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Roundup Ready soybean · Vistive Gold
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Tomato
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Fish tomato · Flavr Savr
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Cotton
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Bt cotton
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Other
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Tobacco · Arabidopsis · Canola · Brinjal · Rose · Wheat · Common Weed
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Fish
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Glofish · Salmon
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Bacteria and viruses
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Ice-minus bacteria · Hepatitis B vaccine · Onyx-015
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| Processes |
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Inserting DNA
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Biolistics · Agrobacteria · Transfection · Electroporation · Microinjection · Viral transformation · Lipofection
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Types
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Recombinant DNA · Transgenesis · Cisgenesis
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| Uses |
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In agriculture
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Food (Controversy) · Pharming (Molecular farming) · Companies (Monsanto · Syngenta · Bayer · DuPont Pioneer · Dow AgroSciences · BASF)
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In humans and diagnostics
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Gene therapy · Genetic enhancement
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In research
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Gene knockout · Gene knockdown · Gene targeting
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| Related articles |
Transgene · Detection of genetically modified organisms · Genetic pollution · Genetic engineering in fiction · Reverse transfection
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| Regulation |
Regulation of the release of GMOs · Regulation of GMOs in the European Union · Regulation of GMOs in Switzerland · Cartagena Protocol on Biosafety
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| Similar fields |
Synthetic biology · Cloning · Stem cell research
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Biology · Genetics · Biotechnology · Bioethics
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