Microglia kill amyloid-β1-42 damaged neurons by a CD14-dependent process

被引:35
作者
Bate, C
Veerhuis, R
Eikelenboom, P
Williarns, A
机构
[1] Univ Glasgow, Sch Vet, Dept Vet Pathol, Inst Comparat Med, Glasgow G61 1QH, Lanark, Scotland
[2] Vrije Univ Amsterdam, Med Ctr, Neurosci Res Inst, Grad Sch Neurosci Amsterdam,Dept Pathol, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Neurosci Res Inst, Grad Sch Neurosci Amsterdam,Dept Psychiat, Amsterdam, Netherlands
[4] Univ London Royal Vet Coll, Dept Pathol & Infect Dis, N Mymms AL9 7TA, Herts, England
关键词
Alzheimer's disease; amyloid-beta; CD14; microglia; neurotoxicity;
D O I
10.1097/01.wnr.0000132203.76836.16
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activated microglia are closely associated with neuronal damage in Alzheimer's disease. In the present study, neurons exposed to low concentrations of amyloid-beta(1-42), a toxic fragment of the amyloid-beta protein, were killed by microglia in a process that required cell-cell contact. Pre-treating microglia with polyclonal antibodies to the CD14 protein, or treating neurons exposed to amyloid-beta(1-42) with a CD14-IgG chimera, prevented the killing of amyloid-beta(1-42) damaged neurons by microglia. Moreover, microglia from CD14 null mice failed to kill amyloid-beta(1-42) damaged neurons. Increased neuronal survival was accompanied by a significant reduction in the production of interleukin-6 indicative of reduced microglial activation. These results indicate an important role for CD14 in the recognition and subsequent killing of amyloid-beta damaged neurons by microglia.
引用
收藏
页码:1427 / 1430
页数:4
相关论文
共 13 条
  • [1] Killing of prion-damaged neurones by microglia
    Bate, C
    Reid, S
    Williams, A
    [J]. NEUROREPORT, 2001, 12 (11) : 2589 - 2594
  • [2] Frequency of stages of Alzheimer-related lesions in different age categories
    Braak, H
    Braak, E
    [J]. NEUROBIOLOGY OF AGING, 1997, 18 (04) : 351 - 357
  • [3] Neuroinflammation in Alzheimer's disease and prion disease
    Eikelenboom, P
    Bate, C
    Van Gool, WA
    Hoozemans, JJM
    Rozemuller, JM
    Veerhuis, R
    Williams, A
    [J]. GLIA, 2002, 40 (02) : 232 - 239
  • [4] ElKhoury J, 1996, NATURE, V382, P716
  • [5] Biomedicine - A portrait of Alzheimer secretases - New features and familiar faces
    Esler, WP
    Wolfe, MS
    [J]. SCIENCE, 2001, 293 (5534) : 1449 - 1454
  • [6] The LPS receptor (CD14) links innate immunity with Alzheimer's disease
    Fassbender, K
    Walter, S
    Kuhl, S
    Landmann, R
    Ishii, K
    Bertsch, T
    Stalder, AK
    Muehlhauser, F
    Liu, Y
    Ulmer, AJ
    Rivest, S
    Lentschat, A
    Gulbins, E
    Jucker, M
    Staufenbiel, M
    Brechtel, K
    Walter, J
    Multhaup, G
    Penke, B
    Adachi, Y
    Hartmann, T
    Beyreuther, K
    [J]. FASEB JOURNAL, 2004, 18 (01) : 203 - 205
  • [7] APOPTOSIS MEDIATED NEUROTOXICITY INDUCED BY CHRONIC APPLICATION OF BETA-AMYLOID FRAGMENT 25-35
    FORLONI, G
    CHIESA, R
    SMIROLDO, S
    VERGA, L
    SALMONA, M
    TAGLIAVINI, F
    ANGERETTI, N
    [J]. NEUROREPORT, 1993, 4 (05) : 523 - 526
  • [8] Integrin Mac-1 and beta-amyloid in microglial release of nitric oxide
    Goodwin, JL
    Kehrli, ME
    Uemura, E
    [J]. BRAIN RESEARCH, 1997, 768 (1-2) : 279 - 286
  • [9] ACTIVATION OF MICROGLIAL CELLS BY BETA-AMYLOID PROTEIN AND INTERFERON-GAMMA
    MEDA, L
    CASSATELLA, MA
    SZENDREI, GI
    OTVOS, L
    BARON, P
    VILLALBA, M
    FERRARI, D
    ROSSI, F
    [J]. NATURE, 1995, 374 (6523) : 647 - 650
  • [10] CD14 is a component of multiple recognition systems used by macrophages to phagocytose apoptotic lymphocytes
    Schlegel, RA
    Krahling, S
    Callahan, MK
    Williamson, P
    [J]. CELL DEATH AND DIFFERENTIATION, 1999, 6 (06) : 583 - 592