The macrophage and the apoptotic cell: an innate immune interaction viewed simplistically?

被引:214
作者
Gregory, CD [1 ]
Devitt, A [1 ]
机构
[1] Univ Edinburgh, MRC, Ctr Inflammat Res, Coll Med & Vet Med, Edinburgh EH8 9XD, Midlothian, Scotland
关键词
apoptosis; cell interactions; inflammation : inflammatory mediators including eicosanoids; macrophages; monocytes; phagocytosis;
D O I
10.1111/j.1365-2567.2004.01959.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages play important roles in the clearance of dying and dead cells. Typically, and perhaps simplistically, they are viewed as the professional phagocytes of apoptotic cells. Clearance by macrophages of cells undergoing apoptosis is a non-phlogistic phenomenon which is often associated with actively anti-inflammatory phagocyte responses. By contrast, macrophage responses to necrotic cells, including secondarily necrotic cells derived from uncleared apoptotic cells, are perceived as proinflammatory. Indeed, persistence of apoptotic cells as a result of defective apoptotic-cell clearance has been found to be associated with the pathogenesis of autoimmune disease. Here we review the mechanisms by which macrophages interact with, and respond to, apoptotic cells. We suggest that macrophages are especially important in clearing cells at sites of histologically visible, high-rate apoptosis and that, otherwise, apoptotic cells are removed largely by non-macrophage neighbours. We challenge the view that necrotic cells, including persistent apoptotic cells are, of necessity, proinflammatory and immunostimulatory and suggest that, under appropriate circumstances, persistent apoptotic cells can provide a prolonged anti-inflammatory stimulus.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 126 条
  • [31] A receptor for phosphatidylserine-specific clearance of apoptotic cells
    Fadok, VA
    Bratton, DL
    Rose, DM
    Pearson, A
    Ezekewitz, RAB
    Henson, PM
    [J]. NATURE, 2000, 405 (6782) : 85 - 90
  • [32] Loss of phospholipid asymmetry and surface exposure of phosphatidylserine is required for phagocytosis of apoptotic cells by macrophages and fibroblasts
    Fadok, VA
    de Cathelineau, A
    Daleke, DL
    Henson, PM
    Bratton, DL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) : 1071 - 1077
  • [33] FADOK VA, 1992, J IMMUNOL, V148, P2207
  • [34] Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-β, PGE2, and PAF
    Fadok, VA
    Bratton, DL
    Konowal, A
    Freed, PW
    Westcott, JY
    Henson, PM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (04) : 890 - 898
  • [35] Differential effects of apoptotic versus lysed cells on macrophage production of cytokines: Role of proteases
    Fadok, VA
    Bratton, DL
    Guthrie, L
    Henson, PM
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 166 (11) : 6847 - 6854
  • [36] FADOK VA, 1999, COLD SPRING HARB LAB, P64
  • [37] Phagocytosis and development: back to the future
    Franc, NC
    White, K
    Ezekowitz, RAB
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (01) : 47 - 52
  • [38] Uptake of apoptotic cells drives the growth of a pathogenic trypanosome in macrophages
    Freire-de-Lima, CG
    Nascimento, DO
    Soares, MBP
    Bozza, PT
    Castro-Faria-Neto, HC
    de Mello, FG
    DosReis, GA
    Lopes, MF
    [J]. NATURE, 2000, 403 (6766) : 199 - 203
  • [39] Difference in the way of macrophage recognition of target cells depending on their apoptotic states
    Fujii, C
    Shiratsuchi, A
    Manaka, J
    Yonehara, S
    Nakanishi, Y
    [J]. CELL DEATH AND DIFFERENTIATION, 2001, 8 (11) : 1113 - 1122
  • [40] Antiinflammatory effects of CD95 ligand (FasL)-induced apoptosis
    Gao, YK
    Herndon, JM
    Zhang, H
    Griffith, TS
    Ferguson, TA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (05) : 887 - 896