Apolipoprotein E suppresses glial cell secretion of TNF alpha

被引:152
作者
Laskowitz, DT [1 ]
Goel, S [1 ]
Bennett, ER [1 ]
Matthew, WD [1 ]
机构
[1] DUKE UNIV,MED CTR,DEPT NEUROBIOL,DURHAM,NC 27710
关键词
apolipoprotein E; TNF alpha; microglia;
D O I
10.1016/S0165-5728(97)00021-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Apolipoprotein E (apoE) is a 299 amino acid protein with multiple biological functions. Initially described in the context of cholesterol metabolism, apoE also has immunomodulatory properties and recent evidence has implicated a role for apoE in neurological disease. One possibility is that apoE, which is the predominant apolipoprotein produced intra-axially, may modify the CNS response to acute and chronic injury. We prepared mixed neuronal-glial cultures from apoE deficient mouse pups and measured secretion of TNF alpha after stimulation with lipopolysaccharide (LPS) in the presence and absence of human recombinant apoE3 and E4. We demonstrate that preincubation with apoE blocks glial secretion of TNF alpha in a dose-dependent manner. This effect is independent of any direct effect of apoE on cell viability and is greatest when apoE is preincubated with the cell culture for 24 h.
引用
收藏
页码:70 / 74
页数:5
相关论文
共 25 条
[1]  
ALBERTS AJ, 1996, STROKE, V27, P183
[2]   Brain injury and inflammation - A putative role of TNF alpha [J].
Arvin, B ;
Neville, LF ;
Barone, FC ;
Feuerstein, GZ .
NEUROPROTECTIVE AGENTS: CLINICAL AND EXPERIMENTAL ASPECTS, 1995, 765 :62-71
[3]  
BUSCIGLIO J, 1995, NATURE, V378, P21
[4]  
CONNOLLY ES, 1996, STROKE, V27, P174
[5]   DIFFERENTIAL SENSITIVITY OF LYMPHOCYTE SUB-POPULATIONS TO SUPPRESSION BY LOW-DENSITY LIPOPROTEIN INHIBITOR, AN IMMUNOREGULATORY HUMAN-SERUM LOW-DENSITY LIPOPROTEIN [J].
CURTISS, LK ;
EDGINGTON, TS .
JOURNAL OF CLINICAL INVESTIGATION, 1979, 63 (02) :193-201
[6]  
CURTISS LK, 1976, J IMMUNOL, V116, P1452
[7]  
Gordon M N, 1993, J Fla Med Assoc, V80, P267
[8]  
HATTORI A, 1993, J BIOL CHEM, V268, P2577
[9]   CYTOKINES MODULATE THE INFLAMMATORY RESPONSE AND CHANGE PERMISSIVENESS TO NEURONAL ADHESION IN INJURED MAMMALIAN CENTRAL-NERVOUS-SYSTEM [J].
LOTAN, M ;
SOLOMON, A ;
BENBASSAT, S ;
SCHWARTZ, M .
EXPERIMENTAL NEUROLOGY, 1994, 126 (02) :284-290
[10]   Arthritis and anti-inflammatory agents as possible protective factors for Alzheimer's disease: A review of 17 epidemiologic studies [J].
McGeer, PL ;
Schulzer, M ;
McGeer, EG .
NEUROLOGY, 1996, 47 (02) :425-432