Problem with Passaging MEFs - (Sep/02/2010 )
Hi. I'm new to stem cell culture, as is my lab, hence i have no one to refer to. i have problem in passaging the MEF. the strain i use is ICR mice. initial culture is fine, but they don't attach to the culture dishes in passage 1. a senior was able to obtain passage 1 once, but by using 20% FBS instead of 10% to passage. even then, she could not proceed to passage 2. any comments? every journal i read uses 10% FBS. this problem is rather unusual. what could be wrong? below is my protocol:
1. Remove 13.5 day pups and transfer into PBS- solution.
2. Remove limbs, internal organs etc.
3. Wash in another PBS- solution.
4. Mince using fine forcep and blade for 5 minutes.
5. Transfer into trypsin-EDTA solution. Further mince for a few minutes.
6. Transfer the solution into a beaker and stir with magnetic stirrer for 20 minutes.
7. Filter into conical tube using nylon (as substitute for cell strainer)
8. Add DMEM with 3% penicilin-streptomycin and 10% FBS at ratio of 1:1.15 DMEM
9. Centrifuge for 5 minutes.
10. Prepare culture dish by adding DMEM solution
11. Aspirate the supernatant out from the conical tube. Add DMEM into the pellet and suck in and out to produce single cells.
12. Transfer the cells to the culture dishes. Incubate.
13. The medium is replaced the next day.
1. Remove media from MEF culture dishes.
2. Wash 2-3 times with PBS-.
3. Deatch the cells using trypsin for 3-5 minutes.
4. Add 1ml of DMEM with 1% penicilin-streptomycin and 10% FBS into conical tube.
5. Fill the conical tubes with detached cells. Add with DMEM.
6. Centrifuge for 5 minutes.
7. Prepare culture dishes by adding DMEM.
8. Aspirate and discard supernatang from conical tubes.
9. Add 2 ml DMEM into tube and suck in and out to dissociate the cells.
10. Place the cells into culture dishes.
11 Incubate and replace the medium 2 days later.
i'm trully grateful of any advices. thank you.
Do you also remove the heads in step 2 of your MEF prep?
And your trypsin step seems a little long to me- our MEF lift really easy so I typically incubate no more than a minute or so.
Also, how hard do you split the cells when passaging? Our MEF can't cope with more than a 1 to 6 split, but are happiest with 1 to 4.
Yeah I agree, they dont like trypsin, and they like to be crowed...to use 20% FCS helps
Thank you for the replies.
I did remove the head when preparing the MEF. for the trypsinization, i basically spray the trypsin onto the cells on the dish, then suck n spray again until they detach. i don't incubate. is my method bad for the cells? do u think i should just place the trypsin into the culture dish, incubate for 3 mins, then let them detach themselves? also, when passaging, i split them to 1 to 3 or 1 to 4.
perhaps you can suggest a quick, efficient way of trypsinization? i have also thought of reducing the concentration of trypsin. any comments? thanks
Hmm not sure about the constant "suck n spray" method, I think you are better off leaving the tryp on for say 1 min, tapping the edge of the dish to loosen the cells and then checking under the microscope for detachment. If you monitor them as they are lifting under the microscope, you should be able to see what time is optimal for them.
That said, I'm not sure if this is the cause of your problem.
Any chance of posting a pic of your cells to see if there is anything unusual that we could pick up?
Also, I routinely culture without antibiotics. For several reasons: 1. that antibiotics can affect your cells, 2. that antibiotics can maintain low level contamination undetectable (so called cryptic contamination), 3. it keeps me on my toes with my aseptic technique.
Sorry I can't be more help to you.
Thanks for your advice. I haven't been able to obtain the pics yet, but once i did, i will upload it. Also, i'll keep on trying and will post the progress.
Attached are pictures taken during primary culture, and first passage. the first picture clearly shows attachment, while the same cannot be said for the 2nd picture. they were taken 3 days after passaging. pls advice. thx
It is kind of hard to see from the pics, but in the second one- the cells look attached to me, but at a very low density.
You said you are splitting them 1 to 3 or 1 to 4, so the density shouldn't be this low. Are you sure all of your cells have lifted before you passage them to fresh plates/dishes? Do you check under the microscope?
With MEF at this low a density, I'm not surprised they aren't growing.
its hard to see but the morphology of the first pic is bit odd to me,
maybe because of confluency. I usually will not make my MEF 100 % confluent like that.
Maybe you should culture less cell for P0 to give cell a room to grow.