Long-lasting perivascular accumulation of major histocompatibility complex class II positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain

被引:36
作者
Kosel, S
Egensperger, R
Bise, K
Arbogast, S
Mehraein, P
Graeber, MB
机构
[1] MAX PLANCK INST PSYCHIAT,DEPT NEUROMORPHOL,D-82152 MARTINSRIED,GERMANY
[2] UNIV MUNICH,INST NEUROPATHOL,MOL NEUROPATHOL LAB,D-80337 MUNICH,GERMANY
[3] HANNOVER MED SCH,INST NEUROPATHOL,MOL NEUROPATHOL LAB,D-30625 HANNOVER,GERMANY
[4] UNIV MUNICH,INST PATHOL,D-80337 MUNICH,GERMANY
关键词
apoptosis; demyelination; microglia; perivascular cells; Wallerian degeneration;
D O I
10.1007/s004010050747
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Six cases of middle cerebral artery occlusion are presented in which the cellular changes accompanying descending degeneration of the lateral corticospinal tract were studied at different time points (5 days-10 years) following the insult. Microglia and perivascular cells were found to ingest large amounts of myelin degradation products, while expressing high levels of major histocompatibility complex (MHC) class II molecules. Activation of perivascular macrophages, as indicated by increased class II expression, lasted for many years and appeared to follow down-regulation of both phagocytic activity and class II expression on parenchymal microglia. TUNEL labeling was absent from both microglia and perivascular cells at all time points investigated. Indirect evidence is presented that microglia may transfer myelin degradation products to the perivascular space. Perivascular cells which express MHC class II molecules constitutively do not appear to leave the perivascular compartment in large numbers and could release myelin degradation products into the cerebrospinal fluid. The possible immunological consequences of these findings are discussed with respect to their possible relevance for antigen presentation and autoimmune central nervous system disease.
引用
收藏
页码:532 / 538
页数:7
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