Mast cells, basophils, and eosinophils: distinct but overlapping pathways for recruitment

被引:116
作者
Bochner, BS [1 ]
Schleimer, RF [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Clin Immunol, Baltimore, MD 21224 USA
关键词
D O I
10.1034/j.1600-065X.2001.790101.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
Mast cells, basophils and eosinophils are bone marrow-derived cells that contribute to a variety of allergic and other immune responses. For example, they are relatively abundant at mucosal sires where allergic inflammation is occurring, and their activation and release of preformed and newly-generated mediators at these sires is considered central to the pathophysiology of allergic diseases. Given their involvement in allergic and other diseases, it is important to understand how these cells are selectively recruited into tissues. These cells share many phenotypic features, including those involved in adhesion and migration, yet their localization within a given tissue can be quite distinct. In addition, there are examples of selective recruitment of one cell type without the others. From studies with human cells, it is now clear that mast cells, basophils and eosinophils share a number of recruitment pathways with one another and with other cells, bur that each possesses unique adhesion and migration responses that can contribute to their preferential accumulation. This review will focus on cell surface structures implicated in adhesion and migration responses of human mast cells, basophils and eosinophils. Both shared and selective expression of these molecules will be highlighted, as well as differences in their relative levels of expression. Cell type-specific stimuli that alter adhesion and migration responses will also be considered.
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页码:5 / 15
页数:11
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共 143 条
[61]  
Handzel ZT, 1998, J IMMUNOL, V160, P1279
[62]  
HANSEL TT, 1991, CLIN EXP IMMUNOL, V86, P271
[63]   C3a and C5a stimulate chemotaxis of human mast cells [J].
Hartmann, K ;
Henz, BM ;
KrugerKrasagakes, S ;
Kohl, J ;
Burger, R ;
Guhl, S ;
Haase, I ;
Lippert, U ;
Zuberbier, T .
BLOOD, 1997, 89 (08) :2863-2870
[64]   Chemokine receptor usage by human eosinophils - The importance of CCR3 demonstrated using an antagonistic monoclonal antibody [J].
Heath, H ;
Qin, SX ;
Rao, P ;
Wu, LJ ;
LaRosa, G ;
Kassam, N ;
Ponath, PD ;
Mackay, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (02) :178-184
[65]   Blockade of CD49d (α4 integrin) on intrapulmonary but not circulating leukocytes inhibits airway inflammation and hyperresponsiveness in a mouse model of asthma [J].
Henderson, WR ;
Chi, EY ;
Albert, RK ;
Chu, SJ ;
Lamm, WJE ;
Rochon, Y ;
Jonas, M ;
Christie, PE ;
Harlan, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (12) :3083-3092
[66]   Involvement of α-4 integrins in allergic airway responses and mast cell degranulation in vivo [J].
Hojo, M ;
Maghni, K ;
Issekutz, TB ;
Martin, JG .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (04) :1127-1133
[67]   A role for the C3a anaphylatoxin receptor in the effector phase of asthma [J].
Humbles, AA ;
Lu, B ;
Nilsson, CA ;
Lilly, C ;
Israel, E ;
Fujiwara, Y ;
Gerard, NP ;
Gerard, C .
NATURE, 2000, 406 (6799) :998-1001
[68]  
ILIOPOULOS O, 1992, J IMMUNOL, V148, P2223
[69]   C3a and C5a enhance granulocyte adhesion to endothelial and epithelial cell monolayers: epithelial and endothelial priming is required for C3a-induced eosinophil adhesion [J].
Jagels, MA ;
Daffern, PJ ;
Hugli, TE .
IMMUNOPHARMACOLOGY, 2000, 46 (03) :209-222
[70]   The α4-integrin:: an alternative pathway for neutrophil recruitment? [J].
Johnston, B ;
Kubes, P .
IMMUNOLOGY TODAY, 1999, 20 (12) :545-550