Granulocytes in the subarachnoid space of humans and rabbits with bacterial meningitis undergo apoptosis and are eliminated by macrophages

被引:20
作者
Nau, R
Zettl, U
Gerber, J
Trostdorf, F
Michel, U
Böttcher, T
Schmidt, H
Adler, S
Brück, W
机构
[1] Univ Gottingen, Dept Neurol, D-37075 Gottingen, Germany
[2] Univ Gottingen, Dept Neuropathol, D-3400 Gottingen, Germany
[3] Univ Rostock, Dept Neurol, D-18055 Rostock, Germany
关键词
cell death; inflammation; leukocytes; central nervous system; Streptococcus pneumoniae;
D O I
10.1007/s004010050921
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The contribution of leukocyte apoptosis to the resolution of meningeal inflammation in bacterial meningitis was studied in the cerebrospinal fluid (CSF) and in meningeal infiltrates of humans and rabbits by in situ tailing, flow cytometry, agarose gel electrophoresis, and electron microscopy. In humans, the rate of apoptotic granulocytes was 21.0 +/- 20.8% (n = 11) in cytocentrifuge preparations and 3.3 +/- 3.4 (n = 14) in putride infiltrates of autopsy cases (P = 0.02). In rabbits, CSF pleocytosis peaked 8 h after the initiation of antibiotic treatment (5311 +/- 3122/mu l). At this time, the rate of apoptotic granulocytes was 15.2 +/- 7.3% in CSF and 1.8 +/- 1.4% in the meningeal infiltrates (each group n = 6, P = 0.007). Thereafter, the rate of apoptotic granulocytes in CSF declined below 10%. In humans and rabbits, bands representing internucleosomal fragments of approximately 180 base pairs and multiples thereof were documented on agarose gels. Phagocytosis of apoptotic granulocytes by macrophages was visualized by light and electron microscopy. In conclusion, during resolution of subarachnoid space inflammation in bacterial meningitis, a substantial fraction of granulocytes undergoes apoptosis. These granulocytes are removed by phagocytosis by macrophages. Apoptosis is more frequent in granulocytes floating in the CSF than in adherent cells.
引用
收藏
页码:472 / 480
页数:9
相关论文
共 42 条
[1]   CEREBROSPINAL-FLUID CELL COUNTS AND CHEMISTRIES IN BACTERIAL-MENINGITIS [J].
AREVALO, CE ;
BARNES, PF ;
DUDA, M ;
LEEDOM, JM .
SOUTHERN MEDICAL JOURNAL, 1989, 82 (09) :1122-1127
[2]  
Bellingan GJ, 1996, J IMMUNOL, V157, P2577
[3]  
Bradbury MW, 1981, AM J PHYSL REN FLUID, V9, P329, DOI DOI 10.1152/AJPRENAL.1981.240.4.F329
[4]   PASSAGE OF INTACT IRON-LABELLED ERYTHROCYTES FROM SUBARACHNOID SPACE TO SYSTEMIC CIRCULATION IN DOGS [J].
BRADFORD, FK ;
JOHNSON, PC .
JOURNAL OF NEUROSURGERY, 1962, 19 (04) :332-+
[5]   Inflammatory central nervous system demyelination: Correlation of magnetic resonance imaging findings with lesion pathology [J].
Bruck, W ;
Bitsch, A ;
Kolenda, H ;
Bruck, Y ;
Stiefel, M ;
Lassmann, H .
ANNALS OF NEUROLOGY, 1997, 42 (05) :783-793
[6]   THE BIOCHEMISTRY OF CELL-DEATH BY APOPTOSIS [J].
BURSCH, W ;
KLEINE, L ;
TENNISWOOD, M .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1990, 68 (09) :1071-1074
[7]  
COHEN JJ, 1993, IMMUNOL TODAY, V14, P126, DOI 10.1016/0167-5699(93)90214-6
[8]  
COLOTTA F, 1992, BLOOD, V80, P2012
[9]  
COX G, 1995, J IMMUNOL, V154, P4719
[10]   DRAINAGE OF BRAIN EXTRACELLULAR FLUID INTO BLOOD AND DEEP CERVICAL LYMPH AND ITS IMMUNOLOGICAL SIGNIFICANCE [J].
CSERR, HF ;
HARLINGBERG, CJ ;
KNOPF, PM .
BRAIN PATHOLOGY, 1992, 2 (04) :269-276