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Transfection is the process of deliberately introducing naked or purified nucleic acids into eukaryotic cells.[1][2] It may also refer to other methods and cell types, although other terms are often preferred: "transformation" is typically used to describe non-viral DNA transfer in bacteria and non-animal eukaryotic cells, including plant cells. In animal cells, transfection is the preferred term as transformation is also used to refer to progression to a cancerous state (carcinogenesis) in these cells. Transduction is often used to describe virus-mediated gene transfer into eukaryotic cells.[2][3]

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 (i.e. tricalcium phosphate), by electroporation, by cell squeezing 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.


The meaning of the term has evolved.[4] The original meaning of transfection was "infection by transformation", i.e., introduction of genetic material, 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.


There are various methods of introducing foreign DNA into a eukaryotic cell: some rely on physical treatment (electroporation, cell squeezing, nanoparticles, magnetofection); others rely on chemical materials or biological particles (viruses) that are used as carriers. Gene delivery is, for example, one of the steps necessary for gene therapy and the genetic modification of crops. There are many different methods of gene delivery developed for various types of cells and tissues, from bacterial to mammalian. Generally, the methods can be divided into two categories: non-viral and viral.[5]

Non-viral methods include physical methods such as electroporation, microinjection, gene gun, impalefection, hydrostatic pressure, continuous infusion, and sonication and chemical, such as lipofection, which is a lipid-mediated DNA-transfection process utilizing liposome vectors. It can also include the use of polymeric gene carriers (polyplexes).[6]

Virus mediated gene delivery utilizes the ability of a virus to inject its DNA inside a host cell. A gene that is intended for delivery is packaged into a replication-deficient viral particle. Viruses used to date include retrovirus, lentivirus, adenovirus, adeno-associated virus and herpes simplex virus. However, there are drawbacks to using viruses to deliver genes into cells. Viruses can only deliver very small pieces of DNA into the cells, it is labor-intensive and there are risks of random insertion sites, cytopathic effects and mutagenesis.

Nonviral methods[edit]

Chemical-based transfection[edit]

Chemical-based transfection can be divided into several kinds: cyclodextrin,[7] polymers,[8] liposomes, or nanoparticles[9] (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[10] (see also[11]). 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. This process has been a preferred method of identifying many oncogenes.[12]
  • Other methods use highly branched organic compounds, so-called dendrimers, to bind the DNA and get it into the cell.
  • Another method is the use of cationic polymers such as DEAE-dextran or polyethylenimine (PEI). The negatively charged DNA binds to the polycation and the complex is taken up by the cell via endocytosis.
  • Lipofection (or liposome transfection) is a technique used to inject genetic material into a cell by means of liposomes, which are vesicles that can easily merge with the cell membrane since they are both made of a phospholipid bilayer.[13] Lipofection generally uses a positively charged (cationic) lipid (cationic liposomes or mixtures) to form an aggregate with the negatively charged (anionic) genetic material.[14] This transfection technology performs the same tasks as other biochemical procedures utilizing polymers, DEAE-dextran, calcium phosphate, and electroporation. The efficiency of lipofection can be improved by treating transfected cells with a mild heat shock.[15]
  • FuGENE is a reagent capable of directly transfecting a wide variety of cells with high efficiency and low toxicity.[16][17]

Non-chemical methods[edit]

Electroporator with square wave and exponential decay waveforms for in vitro, in vivo, adherent cell and 96 well electroporation applications. Manufactured by BTX Harvard Apparatus, Holliston MA USA.
  • Electroporation (gene electrotransfer) is a popular method, where transient increase in the permeability of cell membrane is achieved when the cells are exposed to short pulses of an intense electric field.
  • Cell squeezing is a method invented in 2012 by Armon Sharei, Robert Langer and Klavs Jensen at MIT. It enables delivery of molecules into cells via cell membrane deformation. It is a high throughput vector-free microfluidic platform for intracellular delivery. It reduces the possibility of toxicity or off-target effects as it does not rely on exogenous materials or electrical fields.[18]
  • Sonoporation uses high-intensity ultrasound to induce pore formation in cell membranes. This pore formation is attributed mainly to the cavitation of gas bubbles interacting with nearby cell membranes since it is enhanced by the addition of ultrasound contrast agent, a source of cavitation nuclei.
  • 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.[19] In this technique, one cell at a time is treated, making it particularly useful for single cell analysis.
  • Protoplast fusion is a technique in which transformed bacterial cells are treated with lysozyme in order to remove the cell wall. Following this, fusogenic agents (e.g., Sendai virus, PEG, electroporation) are used in order to fuse the protoplast carrying the gene of interest with the target recipient cell. A major disadvantage of this method is that bacterial components are non-specifically introduced into the target cell as well.
  • 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 is a method used in mice and rats, but to a lesser extent in larger animals, in which 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.[20][21][22]

Particle-based methods[edit]

  • 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 that 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.[23]
  • 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.
  • Another particle-based method of transfection is known as particle bombardment. The nucleic acid is delivered through membrane penetration at a high velocity, usually connected to microprojectiles.[2]

Other (and hybrid) methods[edit]

Other methods of transfection include nucleofection, which has proved very efficient in transfection of the THP-1 cell line, creating a viable cell line that was able to be differentiated into mature macrophages,[24] and heat shock.

Viral methods[edit]

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. Adenoviral vectors can be useful for viral transfection methods because they can transfer genes into a wide variety of human cells and have high transfer rates.[2] Lentiviral vectors are also helpful due to their ability to transduce cells not currently undergoing mitosis.

Stable and transient transfection[edit]

For some 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[citation needed]. Cell lines expressing the Epstein–Barr virus (EBV) nuclear antigen 1 (EBNA1) or the SV40 large-T antigen, allow episomal amplification of plasmids containing the viral EBV (293E) or SV40 (293T) origins of replication, greatly reducing the rate of dilution.[25]

If it is desired that the transfected gene actually remain 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.

Common agents for selecting stable transfection are:

RNA transfection[edit]

RNA can also be transfected into cells to transiently express its coded protein, or to study RNA decay kinetics. RNA transfection is often used in primary cells that do not divide.

siRNAs can also be transfected to achieve RNA silencing (i.e. loss of RNA and protein from the targeted gene). This has become a major application in research to achieve "knock-down" of proteins of interests (e.g Endothelin-1[26]) with potential applications in gene therapy. Limitation of the silencing approach are the toxicity of the transfection for cells and potential "off-target" effects on the expression of other genes/proteins.

See also[edit]


  1. ^ Transfection at the US National Library of Medicine Medical Subject Headings (MeSH)
  2. ^ a b c d "Transfection". Protocols and Applications Guide. Promega. 
  3. ^ Transduction, Genetic at the US National Library of Medicine Medical Subject Headings (MeSH)
  4. ^ "Transfection" at Dorland's Medical Dictionary
  5. ^ Kamimura K, Suda T, Zhang G, et al. (2011). "Advances in Gene Delivery Systems". Pharm Med. 25 (5): 293–306. doi:10.2165/11594020-000000000-00000. 
  6. ^ Saul JM, Linnes MP, Ratner BD, Giachelli CM, Pun SH (November 2007). "Delivery of non-viral gene carriers from sphere-templated fibrin scaffolds for sustained transgene expression". Biomaterials. 28 (31): 4705–16. PMID 17675152. doi:10.1016/j.biomaterials.2007.07.026. 
  7. ^ 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): 2357–62. PMID 19053312. doi:10.1021/bc800193p. 
  8. ^ 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): 1124–33. doi:10.1021/bc025550w. 
  9. ^ "Nanoparticle Based Transfection Reagents". Biology Transfection Research Resource. 
  10. ^ 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. PMID 4705382. doi:10.1016/0042-6822(73)90341-3. 
  11. ^ 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. PMC 430836Freely accessible. PMID 193108. doi:10.1073/pnas.74.4.1590. 
  12. ^ Kriegler, Michael (1991). Transfer and Expression: A Laboratory Manual. W. H. Freeman. pp. 96–97. ISBN 0716770040. 
  13. ^ Felgner PL, Gadek TR, Holm M, et al. (November 1987). "Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure". Proc. Natl. Acad. Sci. U.S.A. 84 (21): 7413–7. PMC 299306Freely accessible. PMID 2823261. doi:10.1073/pnas.84.21.7413. 
  14. ^ Felgner JH, Kumar R, Sridhar CN, et al. (January 1994). "Enhanced gene delivery and mechanism studies with a novel series of cationic lipid formulations". J. Biol. Chem. 269 (4): 2550–61. PMID 8300583. 
  15. ^ Pipes, Brian; Vasanwala, Farha (January 2005). "Brief heat shock increases stable integration of lipid-mediated DNA transfections". BioTechniques. 38 (1): 48–52. Retrieved 7 September 2017. 
  16. ^ Jacobsen, Linda B.; Calvin, Susan A.; Colvin, Kim E.; Wright, MaryJo (2004-06-01). "FuGENE 6 Transfection Reagent: the gentle power". Methods. Transfection of Mammalian Cells. 33 (2): 104–112. doi:10.1016/j.ymeth.2003.11.002. 
  17. ^ Hellgren*, I.; Drvota, V.; Pieper, R.; Enoksson, S.; Blomberg, P.; Islam, K. B.; Sylvén, C. (2000-08-01). "Highly efficient cell-mediated gene transfer using non-viral vectors and FuGene™6: in vitro and in vivo studies". Cellular and Molecular Life Sciences CMLS. 57 (8-9): 1326–1333. ISSN 1420-682X. doi:10.1007/PL00000769. 
  18. ^ Sharei A, Zoldan J, Adamo A, Sim WY, Cho N, Jackson E, Mao S, Schneider S, Han MJ, Lytton-Jean A, Basto PA, Jhunjhunwala S, Lee J, Heller DA, Kang JW, Hartoularos GC, Kim KS, Anderson DG, Langer R, Jensen KF (February 2013). "A vector-free microfluidic platform for intracellular delivery". Proc. Natl. Acad. Sci. U.S.A. 110 (6): 2082–7. PMC 3568376Freely accessible. PMID 23341631. doi:10.1073/pnas.1218705110. 
  19. ^ Tsukakoshi M, Kurata S, Nomiya Y, et al. (1984). "A Novel Method of DNA Transfection by Laser Microbeam Cell Surgery". Applied Physics B: Photophysics and Laser Chemistry. 35 (3): 135–140. Bibcode:1984ApPhB..35..135T. doi:10.1007/BF00697702. 
  20. ^ Zhang G, Budker V, Wolff JA (July 1999). "High levels of foreign gene expression in hepatocytes after tail vein injections of naked plasmid DNA". Hum. Gene Ther. 10 (10): 1735–7. PMID 10428218. doi:10.1089/10430349950017734. 
  21. ^ Zhang G, Vargo D, Budker V, Armstrong N, Knechtle S, Wolff JA (October 1997). "Expression of naked plasmid DNA injected into the afferent and efferent vessels of rodent and dog livers". Hum. Gene Ther. 8 (15): 1763–72. PMID 9358026. doi:10.1089/hum.1997.8.15-1763. 
  22. ^ Bell JB, Podetz-Pedersen KM, Aronovich EL, Belur LR, McIvor RS, Hackett PB (2007). "Preferential delivery of the Sleeping Beauty transposon system to livers of mice by hydrodynamic injection". Nat Protoc. 2 (12): 3153–65. PMC 2548418Freely accessible. PMID 18079715. doi:10.1038/nprot.2007.471. 
  23. ^ "Magnetofection — Magnetic assisted transfection & transduction". OzBiosciences—The art of delivery systems. 
  24. ^ Schnoor M, Buers I, Sietmann A, et al. (May 2009). "Efficient non-viral transfection of THP-1 cells". J. Immunol. Methods. 344 (2): 109–15. PMID 19345690. doi:10.1016/j.jim.2009.03.014. 
  25. ^ Durocher Y, Perret S, Kamen A (January 2002). "High-level and high-throughput recombinant protein production by transient transfection of suspension-growing human 293-EBNA1 cells". Nucleic Acids Res. 30 (2): E9. PMC 99848Freely accessible. PMID 11788735. doi:10.1093/nar/30.2.e9. 
  26. ^ Mawji IA, Marsden PA (June 2006). "RNA transfection is a versatile tool to investigate endothelin-1 posttranscriptional regulation". Exp. Biol. Med. (Maywood). 231 (6): 704–8. PMID 16740984. 

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