[Histonet] RE: PCR and ISH in fixed tissues
histojock <@t> hotmail.com
Tue Jul 5 20:05:58 CDT 2005
Here's what I know:
The issue isn't whether or not you can "do" RNA work on fixed tissues, it's
whether or not you can trust the result.
At my former place of employment we ran a study comparing ISH and IHC
results on FFPE and matched snap frozen specimens. The frozen results were
always rock steady and matched the IHC dead on. The ISH on FFPE was all over
the map - when you actually got staining that was. Results I've seen from
other places follow the same pattern. Absolutely no consistancy with the
fixed material and much, much tougher to optimize the signal.
I know that fixation procedure is a least partly to blame for this. If the
initial specimen was a big piece you'll often see less signal in the center
as it took longer for fixative to infiltrate there. Where perfusion isn't an
option, a lot of researchers will insist on cutting their animal specimens
into tiny little pieces and dropping them in fixative as quickly as possible
to prevent this. Real pain to work with those!
You also might as well forget about anything that was embedded before the
age of buffered formalin. Formic acid is death to nucleic acids. Old,
unbuffered formalin that's gone acidic is a sure way to kill an ISH signal.
I've never seen even a hint of a signal out of anything embedded pre-1980's
Finally, keep in mind that different species of RNA are subject to different
rates of degradation. I've seen FFPE specimens that showed great results for
total RNA, but were useless when probed for a specific species. This is
particularly true if you try standardizing against an rRNA which is almoist
necer a good idea.
All of the above do not apply if you use snap frozen material. Never had any
problems at all with it.
I'm not doubting that some places do ISH on fixed slides and get a signal
from it. The literature is full a this and some times that's all you've got
so you go with it. Given the choice, though, I'd stick with the frozen stuff
every time despite the extra hassle involved. If you do use fixed stuff only
trust it for localization, not quantitation.
>My boss is submitting a grant and he does not believe that you can do
>PCR (RT) or ISH with fixed tissues. I thought you could but I don't
>know any details. Could someone elaborate? Is there a particular way
>the tissue should be fixed? In other words do I have to use FFPE
>sections or can I use 4% paraformaldehyde perfusion?
>Any advice would be helpful.
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