This Protocol is listed in the following Categories:
Cell and tissue culture, Isolation, purification and separation, Model organisms

Author(s): Benno Weigmann, Ingrid Tubbe, Daniel Seidel, Alex Nicolaev, Christoph Becker & Markus F Neurath
Affiliation(s): I. Med. Clinic, Immunological Laboratory, Johannes-Gutenberg University, Obere Zahlbacherstrasse 63
DOI: 10.1038/nprot.2007.315

Isolation and subsequent analysis of murine lamina propria mononuclear cells from colonic tissue

Studies on colonic cells in the lamina propria (LP) of mice are important for understanding the cellular and immune responses in the gut, especially in inflammatory bowel diseases (such as morbus crohn and colitis ulcerosa). This protocol details a method to isolate LP cells and characterize freshly isolated cells by quality control experiments to obtain cells that can be used for further investigations. After different steps of digestion of the tissue using collagenase, DNase and dispase, the resulting cells are purified using Percoll gradient. The success of the isolation can be analyzed by cell viability test (Trypan Blue exclusion test) and by flow cytometric analysis to assess apoptosis. Finally, the isolated cells can be used for further investigations like comparative studies of mRNA expression, cell-proliferation assay or protein analysis. This protocol can be completed within 6–7 h.

Comments

This protocol calls for a rather high concentration of amphotericin B (5ug/ml) to be used in the culture media. What effect does this concentration have on the LPLs? Can a lower concentration be used and still be protective?

The high concentration of Amphotericin B in the solution prevents of being contaminated with fungi. A lower concentration can of course be used for the preparation. The protection depends from washing the colon in the first steps. If you wash intensively you can lower the concentration.

Has anyone actually compared using isolations with and without Amphotericin B? I follow the current protocols in immunology (unit 3.19 basic protocol 3) and do not use it. I'd think this would be an issue only if the cells are to be cultured, as opposed to stained for flow immediately upon isolation.

Post a comment


Extra navigation

Search Protocols

Feedback

3 comments have been posted on this protocol

ADVERTISEMENT