Method Article

Transfection of an Inducible Gene Expression System into Cells Expressing a Bacterial Effector Protein

436 views

November 28th, 2025

In This Article

Abstract

Source: Berens, C. et al. Applying an Inducible Expression System to Study Interference of Bacterial Virulence Factors with Intracellular Signaling. J. Vis. Exp. (2015)

This video demonstrates the use of an inducible expression system to identify where the bacterial effector protein CaeB disrupts the host apoptotic cascade. It outlines the steps for transfecting CaeB-expressing cells with a tetracycline-responsive system to induce pro-apoptotic gene expression in order to identify the point of disruption within the cascade.

Protocol

1. Transfection of the Stable Cell Line with the Inducible Expression Vector System

  1. Seed human embryonic kidney (HEK)293 cells stably expressing green fluorescent protein (GFP) or GFP-CaeB in a 12-well plate at a density of 1 x 105 cells/well.
  2. 19 hr post-seeding, co-transfect the cells with the regulator plasmid and response plasmid, either encoding Bax or activated caspase 3.
    1. Co-transfect the stable HEK293 cells with 100 ng of pWHE125-P regulator plasmid (Figure 1) and 100 ng of the response plasmids pWHE655-hBax or pWHE655-revCasp3 (Figure 2) and 0.4 µl of polyethylenimine.
    2. Prepare the deoxyribonucleic acid (DNA) and polyethylenimine transfection reagent each in 75 µl of Opti-MEM medium and incubate for exactly 5 min at room temperature (RT). For complex formation, incubate both mixtures together for 15 min at RT.
  3. Add the polyethylenimine/DNA solution dropwise to the cells and incubate at 37 °C in 5% CO2.

2. Induction of Apoptosis

  1. 5 hr post-transfection, induce expression of the pro-apoptotic proteins by the addition of 1 µg/ml doxycycline to the culture medium. Incubate cells for 18 hr at 37 °C in 5% CO2.

Access restricted. Please log in or start a trial to view this content.

Results

Circular plasmid map pWHE125 5703 bp, diagram of gene elements for DNA cloning and expression.

Figure 1. Schematic overview of the regulatory plasmid pWHE125. Elements essential for propagation in ...

Access restricted. Please log in or start a trial to view this content.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
DMEMLife technologies31966-021
FCSBiochromS0115
Pen/StrepLife technologies15140-122
OptiMEMLife technologies51985
X-tremeGENE 9Roche6365752001
PolyethyleniminePolyscienes23966
DoxycyclineSigma AldrichD9891

Reprints and Permissions

Request permission to reuse the text or figures of this JoVE article

Request Permission

Tags

Tetracycline Inducible SystemPro Apoptotic Protein ExpressionApoptotic Signaling CascadeTransfection Reagent ComplexPolyethylenimine TransfectionDoxycycline InductionHEK293 CellsCaeB Protein

Related Articles