For a follow up to our last blog we want to talk about maintaining healthy cells over the holiday period spanning Christmas and New Year. Ok, if you are like our CEO you don’t really want to be thinking about the office Christmas party so early, but end of year is creeping up on us. Most labs, academic and industry, will have some time off. It is often a problem keeping your cell cultures in good condition so that when you return in 2017 you can pick up that important protein expression project without too much delay. Given that most insect cell lines (usually Spodoptera frugiperda or Trichoplusia ni cell lines) need to be sub cultured at least twice a week if they are grown as suspension/shake cultures, how will they survive for this protracted period?
It is probably pointless trying to keep a suspension healthy cell culture going for more than 5 days. Even if they are seeded very thinly they will eventually become very dense or at the other extreme possibly not grow at all (cells in serum-free medium don’t like to be over diluted). You will almost certainly return in the New Year to a dead flask of cells.
You might think that it is time to return to your frozen stocks of healthy cells and start afresh in January. This isn’t a bad idea, particularly if you have had your current stocks in culture for a while. The only problem is that even with a batch of cells frozen at a high density it takes a while to amplify them to quantities sufficient for use in experiments.
An alternative is to assign the task of keeping healthy cells going over the break to the most junior member of the lab. This isn’t very fair and runs the risk of a resentful or hungover member of staff contaminating the lot!
Probably the best option is to remove your cells from suspension cultures to monolayers in flasks and grow them at a lower temperature for the duration. We recommend a temperature of 20-21°C, which is often the ambient level in most air conditioned labs. You might also have an incubator you could drop to this temperature for the period. This is particularly useful if your air conditioner system is turned off over the break. The size of flask you use depends on the numbers of healthy cells you wish to have available for rapid use in the New Year. These can be seeded with various densities of cells. For example, 175cm2 flasks could be set up with 10e6, 2.5 x 10e6 or 5 x 10e6 cells in 15mls medium. This gives a reasonable spread of cell densities so that at least one flask survives.
When you return after the holiday break and want to return your healthy cells to suspension culture don’t forget that the best way to remove them from the attached state is to tap them firmly on the lab bench. Don’t use a cell scraper as this can result in a very high mortality rate.
If you follow the above advice, you should be able to return to the lab in 2017 and have your insect cell-based research up and running in no time.
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