EARLY CHANGES OF MACROPHAGE-LIKE IMMUNOREACTIVITY IN THE RAT INFERIOR OLIVE AFTER INTRAPERITONEAL 3-ACETYLPYRIDINE INJECTION

被引:14
作者
OGAWA, M
ARAKI, M
NAITO, M
TAKEYA, M
TAKAHASHI, K
YOSHIDA, M
机构
[1] JICHI MED SCH,DEPT ANAT,TOCHIGI,JAPAN
[2] KUMAMOTO UNIV,SCH MED,DEPT PATHOL 2,KUMAMOTO 860,JAPAN
关键词
MICROGLIA; MACROPHAGE; 3-ACETYLPYRIDINE; RAT; BRAIN;
D O I
10.1016/0006-8993(93)91226-I
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Early changes of macrophage-like immunoreactivity were observed in the inferior olive after intraperitoneal injection of 3-acetylpyridine (3AP) using seven monoclonal antibodies recognizing macrophage subpopulations (OX-42, OX-6, ED-1, RM-1, TRPM-1, TRPM-2, and TRPM-3). Both resting and activated forms of microglia were stained with OX-42 and TRPM-2. Some of activated microglia reacted to OX-6 and/or ED-1. Neither resting nor activated microglia reacted to any of RM-1, TRPM-1, and TRPM-3. Four h after 3AP injection, the processes of OX-42-positive microglia had increased in number and became thicker than resting microglia. Between 24 h and the 7th day after 3AP injection (day 7), OX-42-positive Microglia gradually increased in number. At 24 h after 3AP injection, round cells appeared that stained with all seven antibodies. These disappeared by day 3. Double staining indicated that OX-42-positive activated microglia on day 7 were divided into subpopulations by their immunoreactivity to ED-1. We suggest that the round cells derived from blood monocytes and entered the brain only transiently while OX-42-positive activated microglia originated from parenchymal resting microglia and continued to increase in number after the disappearance of the round cells.
引用
收藏
页码:135 / 140
页数:6
相关论文
共 20 条
[1]   MICROGLIAL RESPONSE TO 6-HYDROXYDOPAMINE-INDUCED SUBSTANTIA NIGRA LESIONS [J].
AKIYAMA, H ;
MCGEER, PL .
BRAIN RESEARCH, 1989, 489 (02) :247-253
[2]   THE KINETICS AND MORPHOLOGICAL-CHARACTERISTICS OF THE MACROPHAGE MICROGLIAL RESPONSE TO KAINIC ACID-INDUCED NEURONAL DEGENERATION [J].
ANDERSSON, PB ;
PERRY, VH ;
GORDON, S .
NEUROSCIENCE, 1991, 42 (01) :201-214
[3]   BEHAVIOURAL CHANGES AND NEUROPATHOLOGICAL FEATURE IN RATS INTOXICATED WITH 3-ACETYLPYRIDINE [J].
DENK, H ;
HAIDER, M ;
KOVAC, W ;
STUDYNKA, G .
ACTA NEUROPATHOLOGICA, 1968, 10 (01) :34-&
[4]   HISTOLOGICAL EVIDENCE SUPPORTING INFERIOR OLIVE AS MAJOR SOURCE OF CEREBELLAR CLIMBING FIBERS IN RAT [J].
DESCLIN, JC .
BRAIN RESEARCH, 1974, 77 (03) :365-384
[5]   OLIVOCEREBELLAR SYSTEM .2. SOME ULTRASTRUCTURAL CORRELATES OF INFERIOR OLIVE DESTRUCTION IN THE RAT [J].
DESCLIN, JC ;
COLIN, F .
BRAIN RESEARCH, 1980, 187 (01) :29-46
[6]   EFFECTS OF 3-ACETYLPYRIDINE ON CENTRAL NERVOUS-SYSTEM OF RAT, AS DEMONSTRATED BY SILVER METHODS [J].
DESCLIN, JC ;
ESCUBI, J .
BRAIN RESEARCH, 1974, 77 (03) :349-364
[7]  
DIJKSTRA CD, 1985, IMMUNOLOGY, V54, P589
[8]   CHARACTERIZATION OF 2 NEW MONOCLONAL-ANTIBODIES DIRECTED AGAINST RAT MICROGLIA [J].
GEHRMANN, J ;
KREUTZBERG, GW .
JOURNAL OF COMPARATIVE NEUROLOGY, 1991, 313 (03) :409-430
[9]   FORMATION OF MICROGLIA-DERIVED BRAIN MACROPHAGES IS BLOCKED BY ADRIAMYCIN [J].
GRAEBER, MB ;
STREIT, WJ ;
KREUTZBERG, GW .
ACTA NEUROPATHOLOGICA, 1989, 78 (04) :348-358
[10]   AXOTOMY OF THE RAT FACIAL-NERVE LEADS TO INCREASED CR3 COMPLEMENT RECEPTOR EXPRESSION BY ACTIVATED MICROGLIAL CELLS [J].
GRAEBER, MB ;
STREIT, WJ ;
KREUTZBERG, GW .
JOURNAL OF NEUROSCIENCE RESEARCH, 1988, 21 (01) :18-24