An Introduction to Transfection, Transfection Protocol and Applications
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The ability to alter the genetic composition of living cells has revolutionized biology. Scientific advances, from treating genetic disorders through gene therapy to reprograming skin cells into neurons, have been made possible by the increasing proficiency in introducing foreign nucleic acids (DNA and RNA) into cells using a technique known as transfection.
What is transfection?
How does transfection work?
- Physical methods including electroporation and gene gun
- Chemical methods including lipofection
- Viral methods
What’s the difference between stable transfection and transient transfection?
Example transfection protocol
Transfection vs transduction
Applications of transfection
In 1928, Griffith proposed the “transforming principle” having observed that bacterial cells could take up foreign hereditary genetic material.1 This led to the discovery of DNA as that genetic material,2 a discovery that enabled great strides in science. In the 1960s, viruses were employed to transfer genetic material into animal cells in a controlled manner and it was shown that foreign genetic material could be expressed in animal cells; this opened up the possibility of gene therapy.3 The simultaneous advances in the field of recombinant technology – the discovery of plasmids4 followed by an increased application of plasmids in the 1970s and the discovery of restriction enzymes5,6 – facilitated the manipulation of genes. Around the same time, chemical and physical methods of introducing the genetic material into cells, such as electroporation,7 calcium phosphate transfection8 and liposomal9 transfection were also developed, thus providing a plethora of methods to deliver the modified genes into cells of interest.
With the development of transfection methods, many discoveries in basic and translational sciences have been possible and the technique has a plethora of applications in biology. This includes understanding the role of target genes in healthy and diseased cells, unraveling molecular pathways, designing gene therapeutic approaches, cellular reprograming and many more. Thus, transfection is now an indispensable molecular and cell biology laboratory technique. In this article, we discuss the fundamentals of transfection and provide an overview of some of the commonly employed methods. A sample protocol that can be used as a starting point is included and finally, we consider some of the key applications of transfection.
What is transfection?
Transfection is a commonly used technique employed to transfer foreign nucleic acids into eukaryotic cells.10 The purpose of transfection is to alter the genetic content of the host cells, thus changing the expression of desired genes in these cells.
It is important here to distinguish between the terms transfection and transformation. While the term transfection is used when the host cells are eukaryotic, the term transformation is used to denote the transfer of nucleic acids to bacterial cells. This distinction is vital because in higher eukaryotic cells, transformation refers to the process by which the cells become malignant.11
How does transfection work?
The primary objective of a transfection technique is to ensure that the desired foreign nucleic acid can cross the cell membrane and that a substantial amount of that nucleic acid is protected from degradation to allow its expression within the cell. The transfer of nucleic acids into host cells can be achieved through various physical, chemical and biological methods. In most of these cases, the cellular uptake of the nucleic acids is mediated through endocytosis12 of the nucleic acid along with a carrier (Figure 1). A portion of these nucleic acids can avoid lysosomal degradation through what is known as endosomal escape and make their way to the nucleus where they can be transcribed to affect gene expression. While this is not an exhaustive list of the methodologies employed to achieve transfection, we summarize here some of the most commonly used transfection methods.
Figure 1: Diagrammatic representation of the generalized mechanism of transfection.
Physical methods including electroporation and gene gun
Physical methods of transfection apply electrical, mechanical or thermal forces13 to facilitate nucleic acid entry into host cells. Some examples include microinjection, electroporation, biolistic transfection (gene gun), sonoporation, magnetofection and laser optoporation. While the microinjection method employs a special needle to inject the nucleic acids directly into the cells, the other physical methods involve inducing transient and reversible permeabilization of the cell membrane while simultaneously placing the nucleic acids in the vicinity of the permeabilized membrane.14 In electroporation, short and intense electrical pulses are applied to achieve transient permeabilization of the cell membrane. Similarly, ultrasound waves achieve transient cell membrane permeabilization in the case of sonoporation; and the same effect is achieved using controlled exposure to a laser beam in the case of laser optoporation. Biolistic approaches propel naked DNA coated with heavy metal particles into the cell using gas discharge. Magnetofection utilizes magnetic nanoparticles to guide the nucleic acids to the cell membrane where they can be taken up by the process of endocytosis. Physical methods of transfection have the advantage that they do not pose an immunogenic risk like viral methods and are not restricted in the length of the nucleic acid sequences that can be used like viral and some chemical methods. However, these methods require dedicated and expensive equipment and reagents, and they often offer low transfection efficiencies with high cellular mortality.
Chemical methods including lipofection
A number of chemical reagents have been developed to assist DNA/RNA to cross the cell membrane.15 These include cationic lipids, calcium phosphate, cationic polymers and nanoparticles. Transfection using cationic liposomal lipids is termed as lipofection and involves the formation of positively charged lipid aggregates surrounding the negatively charged nucleic acid molecules that can easily merge with the bilipid cell membrane and enter the host cell. Positively charged calcium phosphate molecules form a complex with the negatively charged nucleic acid molecules and generate a precipitate that enters the host cells through endocytosis. The calcium phosphate method of transfection does not require special reagents and is inexpensive. However, this method has limited reproducibility with low transfection efficiency that depends on the cell type. Cationic polymers, such as dendrimers, linear or branched poly (ethylene imine) (PEI), poly (L-lysine) and others are examples of cationic polymers. Several polymeric nanoparticles, solid lipid nanoparticles (SLNP) and inorganic nanoparticles have been used for chemical transfection.12
Viral vectors of transfection offer the highest efficiency and can transfect a large variety of cell types. Virus-mediated biological transfection is termed transduction. Although the term transfection is sometimes used when nucleic acid delivery into host cells is achieved using viral particles, transduction is the correct term that should be used to refer to this process of viral-mediated delivery. Adenoviruses, adeno-associated viruses and retroviruses have been developed for transduction.16 Adenoviruses are double-stranded DNA viruses that can be used to transduce both dividing and non-dividing cells for a short duration. They can elicit strong host immune responses and the experiments with adenoviruses need to be performed in biosafety level 2 laboratories. Adeno-associated viruses (AAV) are single-stranded DNA viruses with an inability to replicate. They induce a weaker immune response in host cells. Retroviruses are RNA viruses that are characterized by the integration of their RNA into the host genome after reverse transcription. This leads to prolonged expression of the gene of interest. Lentiviruses, gammaretroviruses, spumaviruses and alphateroviruses are examples of retroviruses that have been used for biological transfection.12
What’s the difference between stable transfection and transient transfection?
Transfection can be classified as stable or transient (Figure 2) depending on the duration of retention of the genetic material in the host cells.17 If the transfected nucleic acids are incorporated into the host DNA or are retained in the host nucleus as an extrachromosomal element, leading to a permanent change in the expression of the desired gene, the process is termed stable transfection. Stable transfection facilitates constitutive expression of genetic material in cell lines and is useful for the generation of clonal cell lines, large-scale protein production applications and also for stable expression during gene therapy.
Figure 2: Diagram representing the differences between stable and transient transfection.
Transient transfection, on the other hand, does not involve the incorporation of the foreign nucleic acid into the host cell genome, resulting in short-term expression of the target genetic material. The nucleic acids are often removed from the cell as a result of environmental perturbation or cell division. Transient transfection is often used to understand the temporary effect of the change in expression on the desired cellular processes.
Example transfection protocol
Here, we describe a generalized lipofection protocol18 for adherent secondary cell lines and primary cell cultures with plasmid DNA (Figure 3). The quantities of the plasmid DNA and reagents used are applicable for a single well of a 6-well plate and will have to be scaled depending on the size of the culture dish. Lipofection is a relatively low cost, safe, easy and quick method of transfecting cells. While this protocol can be a good starting point, the parameters will have to be standardized and optimized based on the properties of the DNA/RNA as well the host cell type. All procedures are performed under sterile conditions.
Figure 3: Steps involved in transfection of adherent cells using liposomal transfection reagents.
A) Before transfection:
Plasmid DNA: The quality of plasmid DNA is very important for efficient transfection. The gene of interest is usually cloned into an appropriate plasmid DNA backbone downstream from a suitable promoter. A pure and concentrated plasmid DNA preparation is required for transfection.
Plating of cells: The host cells are trypsinized, counted and plated onto an appropriate culture dish in complete culture media 18–24 h before transfection. The cell numbers need to be adjusted so that they reach a confluency of 50–75% at the time of transfection. Care must be taken to avoid contamination and maintain optimal cell health.
- Plasmid DNA is diluted in 100 µL of commercially available, specialized transfection media or serum-free, antibiotic-free cell culture media. The amount of plasmid DNA used will depend on the size of the culture dish in which the cells have been plated and needs to be optimized for the DNA preparation and cell line. It is common to use 1–8 µg of plasmid DNA per well for a 6-well dish.
- The commercially available lipofection reagent of choice (2.5–50 µL) is diluted in 100 µL of transfection media or serum-free, antibiotic-free media.
- The plasmid and lipofection reagent dilutions are mixed well and incubated for 30 min at room temperature.
- After incubation, 800 µL of transfection or serum-free, antibiotic-free media is added to the mix to make up the transfection volume to 1 mL.
- The plate containing the cells is removed from the 5% CO2 incubator, the complete culture media removed, each well rinsed with 500 µL transfection media and the transfection mix prepared in the previous step is added gently to the cells. The cells are incubated with the transfection mix for 6–24 h at 37 ℃ in the 5% CO2 incubator.
The transfection mix is replaced with 3 mL of complete culture media in each well. The cells are incubated for at least 48 h at 37 ℃ in the 5% CO2 incubator. The health of the cells should be monitored regularly.
Transfection vs transduction
We have previously described the biological methods of transfection that employ viruses for the delivery of nucleic acids. The term transduction is often used to describe virus-mediated delivery of nucleic acids into host cells. Bacteriophages were first shown to transduce bacterial cells in 1952.19 Since then, viral vectors have been developed to deliver genetic material into host cells by exploiting the natural propensity of certain viruses to transduce cells. Table 1 summarizes the differences between non-viral transfection and transduction.
Table 1: Comparison of transfection and transduction.
Delivery of foreign nucleic acids using non-viral methods
Delivery of foreign nucleic acids using viral vectors
Gene-transfer efficiency depends on the type of cells, media conditions etc. and is relatively low
Greater gene transfer efficiency
Serum in the media interferes with cellular uptake of nucleic acids
Transduction can be performed in the presence of serum
These methods are relatively harmless to the lab personnel
Viral contamination needs to be carefully handled. Appropriate biosafety measures should be practiced
Often requires specialized equipment and/or special reagents
Relatively easy to perform
Some methods and reagents can be cytotoxic
Viral infection of cells may induce cytopathic effects, such as insertional mutagenesis and immunogenicity
Physical methods, such as electroporation, gene gun and microinjection, and chemical methods, such as lipofection and calcium phosphate transfection, are examples of transfection
Viral transduction is mediated by DNA viruses, such as adenovirus and adeno-associated virus and RNA viruses, such as lentiviruses
Applications of transfection
Transfection methods have a wide range of applications. Here, a few of them have been briefly described.
Gene therapy: Gene therapy refers to treating genetic diseases by either silencing a defective gene, replacing a defective gene with the corrected version or amplifying the expression of a gene. Over the years, gene therapy has been used to treat diseases such as sickle cell anemia, beta thalassemia, Duchenne’s muscular dystrophy and hemophilia.20
DNA vaccines: DNA vaccines are vaccines that transfect host cells with engineered DNA plasmids to facilitate the expression of recombinant antigens in vivo.21 These antigens are recognized by the host’s body and stimulate the generation of adaptive immunity. The entry of DNA plasmids into host cells is achieved through in vivo electroporation.
Gene silencing: Transfection of cells with RNA interference (RNAi) molecules such as small interfering RNA (siRNA), which disintegrate the mRNA, or micro-RNA (miRNA), which suppress the translation of the gene of interest, leads to gene knockdown. Gene silencing can also be achieved using the CRISPR/Cas9 system.
Stable cell line generation: Stable transfection is used to generate stable cell lines that express a recombinant protein constitutively. These stable cell lines are extremely useful for large scale production of recombinant proteins. Stable cell lines that express recombinant proteins or have gene knock in/down are often used to study cellular processes and understand the structures of proteins22 in laboratories.
Virus production: Viral vectors for applications such as gene therapy involve the insertion of the desired gene into the viral plasmid backbone. The plasmids encoding the different components of the viral vector are transfected into a secondary cell line for assembly and large-scale production of the viruses. Moreover, viral production is employed for the generation of recombinant viruses such as, the influenza A virus, to study the effects of novel mutations and viral strains on the ability of the virus to infect and the efficiency of vaccines.23
Large-scale protein production: Recombinant proteins have many applications in therapeutics and several monoclonal antibodies, hormones, enzymes and clotting factors are produced as recombinant proteins on an industrial scale.24 Further, the rapidly progressing field of precision cellular agriculture, which is a sustainable alternative to traditional agriculture, employs transfection as an important step to enable lab-based production of future foods such as, milk, eggs and plant hemoglobin.25 Large-scale production of recombinant proteins has been achieved through transfection of recombinant DNA into mammalian cells, bacteria, yeast, plant and insect cells.
Stem cell reprograming and differentiation: Somatic cells can be reprogramed into induced pluripotent stem cells (iPSCs), which can be differentiated into specific cell types by inducing the expression of certain transcription factors. The development of iPSC technology has been possible thanks to the ability to transfect the genes required for reprograming and differentiation of the stem cells. This technology has led to the development of cellular models of human diseases and has immense therapeutic potential.26,27
1. Griffith F. The significance of pneumococcal types. J Hyg (Lond). 1928;27(2):113-159. doi:10.1017/s0022172400031879
2. Avery OT, Macleod CM, McCarty M. Studies on the chemical nature of the substance inducing transformation of pneumococcal types : induction of transformation by a deoxyribonucleic acid fraction isolated from pneumococcus type III. J Exp Med. 1944;79(2):137-158. doi:10.1084/jem.79.2.137
3. Rogers S, Pfuderer P. Use of viruses as carriers of added genetic information. Nature. 1968;219(5155):749-751. doi:10.1038/219749a0
4. Lederberg J. Cell genetics and hereditary symbiosis. Physiol Rev. 1952;32(4):403-430. doi:10.1152/physrev.1918.104.22.1683
5. Danna K, Nathans D. Specific cleavage of simian virus 40 DNA by restriction endonuclease of Hemophilus influenzae. Proc Natl Acad Sci U S A. 1971;68(12):2913-2917. doi:10.1073/pnas.68.12.2913
6. Smith HO, Wilcox KW. A restriction enzyme from Hemophilus influenzae. I. Purification and general properties. J Mol Biol. 1970;51(2):379-391. doi:10.1016/0022-2836(70)90149-x
7. Neumann E, Schaefer-Ridder M, Wang Y, Hofschneider PH. Gene transfer into mouse lyoma cells by electroporation in high electric fields. EMBO J. 1982;1(7):841-845. doi:10.1002/j.1460-2075.1982.tb01257.x
8. Graham FL, van der Eb AJ. A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology. 1973;52(2):456-467. doi:10.1016/0042-6822(73)90341-3
9. Felgner PL, Gadek TR, Holm M, et al. Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure. Proc Natl Acad Sci U S A. 1987;84(21):7413-7417. doi:10.1073/pnas.84.21.7413
10. Chong ZX, Yeap SK, Ho WY. Transfection types, methods and strategies: A technical review. PeerJ. 2021;9:e11165. doi:10.7717/peerj.11165
11. Seeber F. “Transfection” vs “transformation”: Defining terms. Parasitol Today. 2000;16(9):404. doi:10.1016/s0169-4758(00)01736-1
12. Fus-Kujawa A, Prus P, Bajdak-Rusinek K, et al. An overview of methods and tools for transfection of eukaryotic cells in vitro. Front Bioeng Biotechnol. 2021;9. doi:10.3389/fbioe.2021.701031
13. Fajrial AK, He QQ, Wirusanti NI, Slansky JE, Ding X. A review of emerging physical transfection methods for CRISPR/Cas9-mediated gene editing. Theranostics. 2020;10(12):5532-5549. doi:10.7150/thno.43465
14. Villemejane J, Mir LM. Physical methods of nucleic acid transfer: General concepts and applications. Br J Pharmacol. 2009;157(2):207-219. doi:10.1111/j.1476-5381.2009.00032.x
15. Midoux P, Pichon C, Yaouanc J-J, Jaffrès P-A. Chemical vectors for gene delivery: a current review on polymers, peptides and lipids containing histidine or imidazole as nucleic acids carriers. Br J Pharmacol. 2009;157(2):166-178. doi:10.1111/j.1476-5381.2009.00288.x
16. Bouard D, Alazard-Dany D, Cosset F-L. Viral vectors: From virology to transgene expression. Br J Pharmacol. 2009;157(2):153-165. doi:10.1038/bjp.2008.349
17. Kim TK, Eberwine JH. Mammalian cell transfection: The present and the future. Anal Bioanal Chem. 2010;397(8):3173-3178. doi:10.1007/s00216-010-3821-6
18. Hawley-Nelson P, Ciccarone V, Moore ML. Transfection of cultured eukaryotic cells using cationic lipid reagents. Curr Protoc Mol Biol. 2008;81(1):9.4.1-9.4.17. doi:10.1002/0471142727.mb0904s81
19. Zinder ND, lederberg J. Genetic exchange in Salmonella. J Bacteriol. 1952;64(5):679-699. doi:10.1128/jb.64.5.679-699.1952
20. Bulaklak K, Gersbach CA. The once and future gene therapy. Nat Commun. 2020;11(1):5820. doi:10.1038/s41467-020-19505-2
21. Flingai S, Czerwonko M, Goodman J, Kudchodkar S, Muthumani K, Weiner D. Synthetic DNA vaccines: improved vaccine potency by electroporation and co-delivered genetic adjuvants. Front Immunol. 2013;4:354. doi:10.3389/fimmu.2013.00354
22. Büssow K. Stable mammalian producer cell lines for structural biology. Curr Opin Struct Biol. 2015;32:81-90. doi:10.1016/j.sbi.2015.03.002
23. Hoffmann E, Neumann G, Kawaoka Y, Hobom G, Webster RG. A DNA transfection system for generation of influenza A virus from eight plasmids. Proc Natl Acad Sci U S A. 2000;97(11):6108-6113. doi:10.1073/pnas.100133697
24. Tripathi NK, Shrivastava A. Recent developments in bioprocessing of recombinant proteins: Expression hosts and process development. Front Bioeng Biotechnol. 2019;7:420. doi:10.3389/fbioe.2019.00420
25. Dupuis JH, Cheung LKY, Newman L, Dee DR, Yada RY. Precision cellular agriculture: The future role of recombinantly expressed protein as food. Compr Rev Food Sci Food Saf. 2023;22(2):882-912. doi:10.1111/1541-4337.13094
26. Mertens J, Marchetto MC, Bardy C, Gage FH. Evaluating cell reprogramming, differentiation and conversion technologies in neuroscience. Nat Rev Neurosci. 2016;17(7):424-437. doi:10.1038/nrn.2016.46
27. Madrid M, Sumen C, Aivio S, Saklayen N. Autologous induced pluripotent stem cell-based cell therapies: Promise, progress, and challenges. Curr Protoc. 2021;1(3):e88. doi:10.1002/cpz1.88