共 110 条
Lysophospholipids as mediators of immunity
被引:39
作者:

Lin, DA
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机构:
Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA

Boyce, JA
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机构: Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Rheumatol Immunol & Allergy,Dept Med, Boston, MA 02115 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Rheumatol Immunol & Allergy,Dept Pediat, Boston, MA 02115 USA
来源:
ADVANCES IN IMMUNOLOGY, VOL 89
|
2006年
/
89卷
关键词:
D O I:
10.1016/S0065-2776(05)89004-2
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Lysophospholipids (LPLs) are, lipid-derived signaling molecules exemplified by lysophosphatidic acid (LPA) and sphingosine 1-phosphate (SIP). Originally identified as serum-associated growth factors, these mediators now are known to signal through a family of diverse G protein-coupled receptors (GPCRs). Virtually all cells that participate in the immune response express multiple receptors for LPLs. The development of antibody reagents that recognize the receptors for each LPL and the derivation of receptor-selective agonists and receptor-null mouse strains have provided insights into the widely diverse functions of LPLs in immune responses, particularly the role of S1P in lymphocyte trafficking. This review focuses on the biology of the LPLs as these,molecules relate to functional regulation of immune cells in vitro and to the regulation of integrated immune responses in vivo.
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页码:141 / 167
页数:27
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