POSTMORTEM DELAY EFFECTS ON NEUROGLIAL CELLS AND BRAIN MACROPHAGES FROM LEWIS RATS WITH ACUTE EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS - AN IMMUNOHISTOCHEMICAL AND CYTOCHEMICAL STUDY

Citation
Cja. Degroot et al., POSTMORTEM DELAY EFFECTS ON NEUROGLIAL CELLS AND BRAIN MACROPHAGES FROM LEWIS RATS WITH ACUTE EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS - AN IMMUNOHISTOCHEMICAL AND CYTOCHEMICAL STUDY, Journal of neuroimmunology, 59(1-2), 1995, pp. 123-134
Citations number
26
Categorie Soggetti
Neurosciences,Immunology
Journal title
ISSN journal
01655728
Volume
59
Issue
1-2
Year of publication
1995
Pages
123 - 134
Database
ISI
SICI code
0165-5728(1995)59:1-2<123:PDEONC>2.0.ZU;2-6
Abstract
The effects of increasing postmortem delay (PMD) times on morphologica l, immunological and functional characteristics of various brain cells both in situ and in vitro were studied in postmortem brain tissue der ived from rats with acute experimental allergic encephalomyelitis (EAE ). A decline of the brain tissue structure was first noted after a PMD of 6 h. Radial glia in the cerebellum were frequently interrupted and retractions artifacts appeared around brain cells. However, even afte r the longest PMD interval of 18 h the quality of the cell and tissue structure was still good enough for immunohistochemical characterizati on. Immunohistochemical staining of frozen and fixed rat brain tissue sections resulted in an enhancement of the immunoreactivity after a PM D of 4 h, using a panel of mono and polyclonal antibodies directed aga inst glial fibrillary acidic protein (GFAP), basement membranes (lamin in), brain macrophage antigens (ED1 and ED2), and various immunologica lly important surface molecules, such as major histocompatibility comp lex (MHC) class II (Ia) antigen (OX6), CR3 complement receptor (ED8), and leukocyte common antigen (OX1). No increase in staining intensitie s with the ED1, ED8 and OX6 mAbs specific for macrophage antigens coul d be detected on brain macrophages that were isolated from brain tissu e of rats with EAE obtained after various PMD intervals. Irrespective of the PMD interval, viable astrocyte cell cultures were obtained with comparable staining intensities for GFAP. These cultured astrocytes w ere capable of ingesting Latex beads and were highly proliferative as measured by BrdU uptake, at all investigated PMDs. Thus, even after lo ng PMD intervals, brain material can be used successfully. Other data suggest that the situation is similar to human brain material, even th ough the PMD times may be somewhat different.