Different
hepatic cell types are isolated from male Sprague-Dawley rats
following standard enzymatic perfusion and differential centrifugation
techniques. Freshly isolated cells are then washed in PBS
and fixed immediately in 4% formaldehyde for 1 hour. Cells
are then spun down and carefully resuspended in pre-warmed
1% agarose (an inert material) and quickly cooled down on
ice. Once cells are embedded in agarose they are again fixed
in 4% formaldehyde over-night and processed as a piece of
tissue in an automated tissue processor. Cells are embedded
in paraffin blocks that will serve as donors and 1.5 mm cores
are punched from the different cell types to build up the
recipient block cell array.
Applications:
This organ-specific cell model offers
the possibility to perform a variety of protein expression
hepatic studies such as antibody screening using immunocytochemical
techniques as well as in situ hybridization studies.