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由于血小板与补体相互作用,血小板参与免疫反应。

Participation of the blood platelet in immune reactions due to platelet-complement interaction.

作者信息

Spycher M O, Nydegger U E

机构信息

ZLB Zentrallaboratorium Blutspendedienst SRK, Bern Switzerland.

出版信息

Infusionsther Transfusionsmed. 1995 Feb;22(1):36-43. doi: 10.1159/000223090.

Abstract

OBJECTIVE

Review of different aspects of the primary interaction of complement with blood platelets in immunological reactions and the effect on platelet activation in healthy people and patients.

DATA SOURCES AND SELECTION CRITERIA

Relevant original papers and review articles mainly of the English-written literature.

RESULTS

Besides their major role in hemostasis and wound healing, blood platelets are involved in immunological reactions. They are not only able to interact with IgG through Fc receptors (FcR), they also react with complement components. This review summarizes interactions of complement with mainly human platelets. Such interactions may occur through complement receptors of the plasma membrane (e.g. C1q receptor, complement receptors 2 and 4), but also in a receptor-independent way including activation of the platelet by the membrane attack complex of complement C5b-9. In addition, activation of complement at the surface of the platelets may be induced after binding of anti-platelet antibodies to membrane glycoproteins (e.g. GpIIb/IIIa, GpIb/IX) or after binding of platelet-nonspecific immune complexes via FcR. Complement activation in turn may be regulated by various means including specific plasma or membrane proteins [e.g. decay-accelerating factor (DAF), membrane cofactor protein (MCP), membrane inhibitor of reactive lysis (MIRL), C8-binding protein (C8bp, homologous restriction factor hrf)]. As a further way of self-protection against complement attack, platelets may actively release C5b-9, deposited at the surface as C5b-9-enriched membrane vesicles.

CONCLUSIONS

Two lines of interaction of platelet with complement can be distinguished. On the one hand, platelets are equipped with membrane proteins which protect them from complement attack against themselves. On the other hand, membrane receptors for activated complement components as well as for IgG are expressed on the surface, which enable the platelet to intervene in immunological reactions. This property varies between platelets of different species and needs further investigation also in view of the platelet as an intersection between immunology and hemostasis.

摘要

目的

综述补体在免疫反应中与血小板初次相互作用的不同方面,以及对健康人和患者血小板活化的影响。

资料来源与选择标准

主要为英文撰写的相关原始论文和综述文章。

结果

血小板除了在止血和伤口愈合中起主要作用外,还参与免疫反应。它们不仅能够通过Fc受体(FcR)与IgG相互作用,还能与补体成分发生反应。本综述总结了补体与主要人类血小板的相互作用。这种相互作用可能通过质膜的补体受体(如C1q受体、补体受体2和4)发生,也可能以不依赖受体的方式发生,包括补体C5b-9的膜攻击复合物激活血小板。此外,抗血小板抗体与膜糖蛋白(如GpIIb/IIIa、GpIb/IX)结合后,或血小板非特异性免疫复合物通过FcR结合后,可诱导血小板表面补体的激活。补体激活反过来可能受到多种方式的调节,包括特定的血浆或膜蛋白[如衰变加速因子(DAF)、膜辅因子蛋白(MCP)、反应性溶解膜抑制剂(MIRL)、C8结合蛋白(C8bp,同源限制因子hrf)]。作为一种针对补体攻击的自我保护的进一步方式,血小板可能会主动释放沉积在表面的富含C5b-9的膜囊泡中的C5b-9。

结论

血小板与补体的相互作用可分为两类。一方面,血小板配备有膜蛋白,可保护它们免受补体对自身的攻击。另一方面,活化补体成分以及IgG的膜受体在表面表达,这使血小板能够干预免疫反应。不同物种的血小板之间这种特性有所不同,鉴于血小板作为免疫学和止血学的交叉点,这也需要进一步研究。

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