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Protocol for Transduction of Human Embryonic Stem Cells (hESCs) using Lentiviral Vectors

By: Dr. Rick Cohen, BioFiles 2008, 3.11, 21.

BioFiles 2008, 3.11, 21.

Dr. Rick Cohen
Director, hESC Core Facility, Rutgers


Materials


  • 24-well culture dishes (Cat. No. CLS3526)
  • Puromycin solution (Cat. No. P9620)
  • Dispase II freshly prepared in media (Cat. No. D4693)
  • Feeder free hESC media
  • Matrigel basement membrane
  • DMEM/F12 media
  • MISSION® shRNA lentiviral particles
  • Hexadimethrine bromide (Cat. No. H9268)

Feeder free cultures of hESCs must be used to avoid loss of lentivirus into the feeder layer. The Stem Cell Research Center uses feeder free hESC media with Matrigel to successfully infect H1 and H9 hESC lines with both self-generated and Sigma-Aldrich® MISSION Lentiviral Particles. When the colonies are large, beginning to merge, and have centers that are dense and phase-bright compared to their edges, the hESC lines are ready to passage. This usually occurs 5-7 days after seeding, and the cells can be split 1:6 to 1:10. During the course of the transduction, cells are periodically passaged using a fresh working solution of 1 mg/ml dispase II diluted in DMEM/F-12 media. All materials that come in contact with viral material should be soaked in 10% bleach solution and disposed of carefully using biosafety level two protocols.


Protocol


Prior to transduction, establish the Puromycin Kill Curve. Determine the minimal concentration to kill all non-transduced cells. Use a range starting from 1-10 μg/ml of puromycin on the cells.

Transduction Procedure

Day 0
0.1 Passage cells when 8-% confluent with large colonies approximately 24 hr prior to initial transduction using dispase at 1 mg/ml.
0.2 Seed hESC cultures at a high density (1:3 is recommended) into a 24-well culture dish, taking care to maintain cells as aggregates of approximately 50-60 μm in diameter

Day 1 (late afternoon)
1.1 Feed hESC cells with 500 μl of prewarmed (37°C) mTeSR1 containing 6 μg/ml of polybrene (Hexadimethrine bromide)
1.2 Replace cultures into incubator for 15 minutes.
1.3 Add the desired amount of virus particles to the culture medium.

NOTE: For the initial transduction of hESC lines, Dr. Cohen’s lab uses 10 μl of 1x106 TU/ml viral particles for H1 and H9 hESC lines. Since an exact cell cound cannon be determined from the previous day’s plating due to extreme aggregation of the cells (ranging from 50 to 200 cells per clump), a precise MOI cannot be calculated. The most effective amount of virus particles to be added should be determined empirically for each cell line.
1.4 Incubate for 18-20 hr at 37°C with 5% CO2 and 95% humidity.

Day 2 (mid-day)
2.1 Remove medium, and replace with 500 μl of pre-warmed media supplemented with 6 μg/ml of polybrene
2.2 Replace cultures into incubator for 15 minutes.
2.3 Add three times the initial amount (from day 1) of viral particles to the culture medium.
NOTE: Dr. Cohen’s lab uses 30 μl of 1x106 TU/ml viral particles for the secondary infection

Days 3 and 4 (morning)
Remove medium daily and replace with 500 ml pre-warmed media without polybrene

Days 5-8
Remove media daily and replace with 500 ul of pre-warmed media supplemented with puromycin. Dr. Cohen’s lab determined that a final concentration of 1 μg/ml puromycin worked best to select for successfully transduced H1 and H9 hESCs. Again, a puromycin kill curve should be run prior to any transduction experiment requiring puromycin selection.

Day 9+
To determine the efficacy of shRNA-mediated knockdown, carry out molecular assays to quantify mRNA and protein levels. Be sure to compare to appropriate controls.
For subsequent analysis of additional time points, continue culturing hESCs with puromycin-supplemented media

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Materials

     

References

  1. Nature Methods 2006, 3(8), 637-646

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