Siglec-8 on human eosinophils and mast cells, and Siglec-F on murine eosinophils, are functionally related inhibitory receptors

被引:131
作者
Bochner, B. S. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Clin Immunol & Allergy, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
INTRAVENOUS IMMUNOGLOBULIN; MSIGLEC-F; DIFFERENTIATION ANTIGENS; GLYCAN ARRAY; MOUSE SIGLEC; BASOPHILS; APOPTOSIS; ANTIBODY; DISTINCT; GENE;
D O I
10.1111/j.1365-2222.2008.03173.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Siglecs (sialic acid-binding, Ig-like lectins) are a family of single-pass transmembrane cell surface proteins found predominantly on leucocytes. Their unique structural characteristics include an N-terminal carbohydrate-binding ('lectin') domain that binds sialic acid, followed by a variable number of Ig-like domains, hence these structures are a subset of the Ig gene superfamily. Another unique feature of Siglecs is that most, but not all, possess so-called immunoreceptor tyrosine-based inhibitory motifs in their cytoplasmic domains, suggesting that these molecules function in an inhibitory capacity. Siglec-8, the eighth member identified at the time, was discovered as part of an effort initiated almost a decade ago to identify novel human eosinophil and mast cell proteins. Since that time, its selective expression on human eosinophils and mast cells has been confirmed. On eosinophils, Siglec-8 engagement results in apoptosis, whereas on mast cells, inhibition of Fc epsilon RI-dependent mediator release, without apoptosis, is seen. It has subsequently been determined that the closest functional paralog in the mouse is Siglec-F, selectively expressed by eosinophils but not expressed on mast cells. Despite only modest homology, both Siglec-8 and Siglec-F preferentially recognize a sulphated glycan ligand closely related to sialyl Lewis X, a common ligand for the selectin family of adhesion molecules. Murine experiments in normal, Siglec-F-deficient mice and hypereosinophilic mice have resulted in similar conclusions that Siglec-F, like Siglec-8, plays a distinctive and important role in regulating eosinophil accumulation and survival in vivo. Given the resurgent interest in eosinophil-directed therapies for a variety of disorders, plus its unique additional ability to also target the mast cell, therapies focusing on Siglec-8 could some day prove to be a useful adjunct to our current armamentarium for the treatment of asthma, allergies and related disorders where overproduction and overactivity of eosinophils and mast cells is occurring. Cite this as: B. S. Bochner, Clinical and Experimental Allergy, 2009 (39) 317-324.
引用
收藏
页码:317 / 324
页数:8
相关论文
共 74 条
[1]   Mechanisms of eosinophilia in the pathogenesis of hypereosinophilic disorders [J].
Ackerman, Steven J. ;
Bochner, Bruce S. .
IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA, 2007, 27 (03) :357-+
[2]   New targets for drug development in asthma [J].
Adcock, Ian M. ;
Caramori, Gaetano ;
Chung, K. Fan .
LANCET, 2008, 372 (9643) :1073-1087
[3]   Molecular analysis of human Siglec-8 orthologs relevant to mouse eosinophils: identification of mouse orthologs of Siglec-5 (mSiglec-F) and Siglec-10 (mSiglec-G) [J].
Aizawa, H ;
Zimmermann, N ;
Carrigan, PE ;
Lee, JJ ;
Rothenberg, ME ;
Bochner, BS .
GENOMICS, 2003, 82 (05) :521-530
[4]   Human eosinophils express two Siglec-8 splice variants [J].
Aizawa, H ;
Plitt, J ;
Bochner, BS .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 109 (01) :176-176
[5]  
ANDREWS RG, 1983, BLOOD, V62, P124
[6]   Cloning and characterization of a novel mouse Siglec, mSiglec-F - Differential evolution of the mouse and human (CD33) Siglec-3-related gene clusters [J].
Angata, T ;
Hingorani, R ;
Varki, NM ;
Varki, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (48) :45128-45136
[7]   The membrane-proximal immunoreceptor tyrosine-based inhibitory motif is critical for the inhibitory signaling mediated by siglecs-7 and-9, CD33-related Siglecs expressed on human monocytes and NK cells [J].
Avril, T ;
Floyd, H ;
Lopez, F ;
Vivier, E ;
Crocker, PR .
JOURNAL OF IMMUNOLOGY, 2004, 173 (11) :6841-6849
[8]   Printed covalent glycan array for ligand profiling of diverse glycan binding proteins [J].
Blixt, O ;
Head, S ;
Mondala, T ;
Scanlan, C ;
Huflejt, ME ;
Alvarez, R ;
Bryan, MC ;
Fazio, F ;
Calarese, D ;
Stevens, J ;
Razi, N ;
Stevens, DJ ;
Skehel, JJ ;
van Die, I ;
Burton, DR ;
Wilson, IA ;
Cummings, R ;
Bovin, N ;
Wong, CH ;
Paulson, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (49) :17033-17038
[9]   Verdict in the case of therapies versus eosinophils: The jury is still out [J].
Bochner, BS .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2004, 113 (01) :3-9
[10]   Mast cells, basophils, and eosinophils: distinct but overlapping pathways for recruitment [J].
Bochner, BS ;
Schleimer, RF .
IMMUNOLOGICAL REVIEWS, 2001, 179 :5-15