Hi, I am looking for a little advice from anyone who has experience processing lavage fluid into cell pellets that can be sectioned and stained. I need to work out a protocol using lavages from knockout mice that may eventually be used to look at human patients. In both models of disease I expect to collect a lot of macrophages.
After reading, "googling" and looking up articles and the Histonet, I have come up with the following "procedure". I would appreciate advice or ideas from anyone who has performed any part(s) of this type of procedure: 1. Collect lavage in PBS (perform actual lavage on euthanized mouse using PBS as the diluent). Store on ice until I get back to the lab. Question here - because I will be collecting many samples, should I spin them right away or keep them on ice and spin them all at once? Should I add a mucolytic agent (mucolexx or the like) and then store them on ice until I get back to my lab? I know that in mice, although it will be a model that has lung disease, mucus will not be a problem. However, in the human model of the disease it may be an issue. I need to see the effect of the mucolytic agent on the affected cells before using it on the patients' lavages. Does anyone out there use a specific mucolytic agent that they like? I plan on trying 2 - the Mucolexx (MSDS only lists formaldehyde) and Richard Allan Mucolytic agent (MSDS lists formaldehyde, ethylene glycol, methyl alcohol and polyethylene glycol). 2. Spin down cells at 4C for 15 minutes. Remove supernatant. Add fix - either overnight or for a few hours. Question - if I use a mucolytic agent that contains fixative - formaldehyde - do I have to rinse it out (resuspend the cells in PBS or other buffer and spin again) or can I just remove the sup and add a gel (step 4)? Is the mucolytic agent enough of a fixative (the Thermo/Richard Allan and Mucolexx mucolytic agents contain 0.3 or 3 % formaldehyde)? 3. Once the cells are pelleted, should I fix them again or just resuspend them in a gel (something like Histogel or an agar(ose)? Does anyone out there use either of these gels to look at cells? Any preferences? 4. Once the cells are in the gel, fix the cell pellet. (Is this necessary?) 5. Pray and process the pellet into paraffin (and maybe plastic too). Thanks in advance for any help you can give. Jenn Jennifer Johnson Genzyme Corp. Department of Pathology 5 Mountain Road Framingham, MA 01701-9322 Phn - 508-271-3610 Fax - 508-872-9080 _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet