The video demonstrates a protocol for transfecting HeLa cells using siRNA, followed by BrdU incorporation to study mitochondrial DNA. It outlines the steps of cell seeding, incubation times, and conditions, emphasizing the experimental setup to analyze BrdU specificity in mitochondrial DNA by using rho0 cells.

cell transfection and 5-bromo-2&#39;-deoxyuridine (brdu) incorporation in hela cells

Cuantificación de alto rendimiento de la síntesis y distribución de ADNmt

For most eukaryotic cells mitochondria are essential organelles, as they play a crucial role in numerous cellular processes. First and foremost, mitochondria are the key energy suppliers of cells1. Mitochondria are also involved in regulating cellular homeostasis (for instance, intracellular redox2 and the calcium balance3), cell signaling4,5, apoptosis6, the synthesis of different biochemical compounds7,8, and the innate immune response9. Mitochondrial dysfunction is associated with various pathological states and human diseases10. 
The functioning of mitochondria depends on the genetic information located in two separate genomes: the nuclear and mitochondrial genomes. The mitochondrial genome encodes a small number of genes compared to the nuclear genome, but all the mtDNA-encoded genes are essential for human life. The mitochondrial protein machinery necessary to maintain the mtDNA is encoded by nDNA. The basic components of the mitochondrial replisome, as well as some mitochondrial biogenesis factors, have already been identified (reviewed in previous research11,12). However, mitochondrial DNA replication and maintenance mechanisms are still far from being understood. In contrast to nDNA, the mitochondrial genome exists in multiple copies, which provides an additional layer for regulating mitochondrial gene expression. Much less is currently known about the distribution and segregation of mtDNA within organelles, to what extent these processes are regulated, and if they are, which proteins are involved13. The segregation pattern is crucial when cells contain a mixed population of wild-type and mutated mtDNA. Their unequal distribution may lead to the generation of cells with a detrimental amount of mutated mtDNA.
So far, the protein factors necessary for mtDNA maintenance have been identified mainly by biochemical methods, bioinformatic analyses, or through disease-associated studies. In this work, in order to ensure a high chance of identifying factors that have previously escaped identification, a different strategy is described. The method is based on the labeling of mtDNA during replication or repair with 5-bromo-2'-deoxyuridine (BrdU), a nucleoside analog of thymidine. BrdU is readily incorporated into nascent DNA strands during DNA synthesis and, in general, is used for monitoring the replication of nuclear DNA14. However, the procedure developed here has been optimized for detecting BrdU incorporated into mtDNA using the immunofluorescence of anti-BrdU antibodies.
The approach allows for the high-throughput quantification of mtDNA synthesis and distribution in human cells cultured in vitro. A high-throughput strategy is necessary to conduct tests under different experimental conditions in a relatively short time; therefore, it is proposed in the protocol to utilize a multi-well format for cell culturing and automated fluorescence microscopy for imaging. The protocol includes the transfection of human HeLa cells with an siRNA library and the subsequent monitoring of mtDNA replication or repair using the metabolic labeling of newly synthesized DNA with BrdU. This approach is combined with immunostaining of the DNA with the help of anti-DNA antibodies. Both parameters are analyzed using quantitative fluorescence microscopy. Additionally, mitochondria are visualized with a specific dye. To demonstrate the specificity of the protocol, BrdU staining was tested on cells devoid of mtDNA (rho0 cells), on HeLa cells upon the silencing of well-known mtDNA maintenance factors, and on HeLa cells after treatment with an mtDNA replication inhibitor. The mtDNA levels were also measured by an independent method, namely qPCR.

Autor destacado: Cuantificación basada en imágenes de alto rendimiento de la síntesis y distribución del ADN mitocondrial  

Cuantificación basada en imágenes de alto rendimiento de la síntesis y distribución del ADN mitocondrial

Watch this Scientific Journal Video about Cell Transfection and 5-Bromo-2'-Deoxyuridine BrdU Incorporation in HeLa Cells at JoVE.com

Cell Transfection and 5-Bromo-2'-Deoxyuridine (BrdU) Incorporation in HeLa Cells  

Transfección celular e incorporación de 5-Bromo-2&#39;-desoxiuridina (BrdU) en células HeLa

Para comenzar la transfección celular, agregue 20 microlitros de la suspensión de células HeLa a los pocillos de placa de 384 pocillos que contienen siRNA diluido para sembrar 700 células HeLa por pocillo. Después de una hora de incubación a temperatura ambiente, coloque la placa del pozo en una incubadora durante 72 horas a 37 grados centígrados y 5% de dióxido de carbono. Para incorporar BrdU en las células transfectadas, agregue 10 microlitros de solución de BrdU 90 micromolares a cada pocillo después de 56 horas de transfección de ARNsi.Incubar las células durante 16 horas a 37 grados centígrados y 5% de dióxido de carbono. La especificidad de la incorporación de BrdU en el ADN mitocondrial de las células HeLa se estudió utilizando células rho0 que carecen de ADN mitocondrial.

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Research

JoVE Journal

Biochemistry

Cell Transfection and 5-Bromo-2&#39;-Deoxyuridine (BrdU) Incorporation in HeLa Cells

183 vistas. Para comenzar la transfección celular, agregue 20 microlitros de la suspensión de células HeLa a los pocillos de placa de 384 pocillos que contienen siRNA diluido para sembrar 700 células HeLa por pocillo. Después de una hora de incubación a temperatura ambiente, coloque la placa del pozo en una incubadora durante 72 horas a 37 grados centígrados y 5% de dióxido de carbono. Para incorporar BrdU en las células transfectadas, agregue 10 microlitros de solución de BrdU 90 micromolares ...

Video: Cell Transfection and 5-Bromo-2'-Deoxyuridine (BrdU) Incorporation in HeLa Cells  

High-Throughput Image-Based Quantification of Mitochondrial DNA Synthesis and Distribution

The vast majority of cellular processes require a continuous supply of energy, the most common carrier of which is the ATP molecule. Eukaryotic cells produce most of their ATP in the mitochondria by oxidative phosphorylation. Mitochondria are unique organelles because they have their own genome that is replicated and passed on to the next generation of cells. In contrast to the nuclear genome, there are multiple copies of the mitochondrial genome in the cell. The detailed study of the mechanisms responsible for the replication, repair, and maintenance of the mitochondrial genome is essential for understanding the proper functioning of mitochondria and whole cells under both normal and disease conditions. Here, a method that allows the high-throughput quantification of the synthesis and distribution of mitochondrial DNA (mtDNA) in human cells cultured in vitro is presented. This approach is based on the immunofluorescence detection of actively synthesized DNA molecules labeled by 5-bromo-2'-deoxyuridine (BrdU) incorporation and the concurrent detection of all the mtDNA molecules with anti-DNA antibodies. Additionally, the mitochondria are visualized with specific dyes or antibodies. The culturing of cells in a multi-well format and the utilization of an automated fluorescence microscope make it easier to study the dynamics of mtDNA and the morphology of mitochondria under a variety of experimental conditions in a relatively short time.

A procedure for studying the dynamics of mitochondrial DNA (mtDNA) metabolism in cells using a multi-well plate format and automated immunofluorescence imaging to detect and quantify mtDNA synthesis and distribution is described. This can be further used to investigate the effects of various inhibitors, cellular stresses, and gene silencing on mtDNA metabolism.

The vast majority of cellular processes require a continuous supply of energy, the most common carrier of which is the ATP molecule. Eukaryotic cells ...