Role of glycosphingolipid-enriched microdomains in innate immunity: Microdomain-dependent phagocytic cell functions

被引:50
作者
Yoshizaki, Fumiko [1 ]
Nakayama, Hitoshi [1 ]
Wahara, Chihiro [1 ]
Takamori, Kenji [1 ]
Ogawa, Hideoki [1 ]
Iwabuchi, Kazuhisa [1 ,2 ]
机构
[1] Juntendo Univ, Inst Environm & Gender Specif Med, Sch Med, Urayasu Shi, Chiba 2790021, Japan
[2] Juntendo Univ, Grad Sch Hlth Care & Nursing, Infect Control Nursing, Chiba, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2008年 / 1780卷 / 03期
关键词
glycosphingolipid; membrane microdomains; lipid rafts; innate immunity; phagocytes; phagocytosis; lactosylceramide; interdigitation; infection; escape; cholesterol; pattern recognition receptors; beta-glucan; phagosome formation; proteomics;
D O I
10.1016/j.bbagen.2007.11.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The innate immune system is the first line of defense against pathogenic microorganisms, such as bacteria, fungi, and viruses. Phagocytes, such as neutrophils and macrophages, play an important role in the innate immune system by recognizing, engulfing, and eliminating pathogens. It has been suggested that lipid membrane microdomains/rafts of phagocytes are involved in these innate immune responses, including superoxide generation, cell migration, and phagocytosis. Lactosylceramide (LacCer), a neutral glycosphingolipid, forms glycosphingolipid-enriched micro-domains together with the Src family kinase, Lyn, on the neutrophil plasma membrane. LacCer-enriched microdomains have been suggested to play important roles in innate immune function of neutrophils. However, the molecular mechanisms underlying these phenomena remain largely unknown. Recent proteomic analyses of microdomains from phagocytes have provided insight into membrane microdomain-mediated functions in the processes of phagocytosis. In this review, we discuss the membrane microdomain-associated immune functions of phagocytes, focusing on those functions of LacCer-enriched microdomains and recent proteomic approaches to determine the molecular mechanisms underlying these functions. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:383 / 392
页数:10
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