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1
C4a: An Anaphylatoxin in Name Only.C4a:徒有虚名的过敏毒素。
J Innate Immun. 2015;7(4):333-9. doi: 10.1159/000371423. Epub 2015 Feb 6.
2
[Atopic dermatitis. II. The status of complement proteins and the pathogenetic role of anaphylatoxins C4a, C3a and C5a].[特应性皮炎。II. 补体蛋白状态及过敏毒素C4a、C3a和C5a的致病作用]
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3
Comparative structural anatomy of the complement anaphylatoxin proteins C3a, C4a and C5a.补体过敏毒素蛋白C3a、C4a和C5a的比较结构解剖学
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Anaphylatoxin levels in human aqueous humor.人房水中过敏毒素水平。
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Generation of human C3a, C4a, and C5a anaphylatoxins by protein A of Staphylococcus aureus and immobilized protein A reagents used in serotherapy of cancer.金黄色葡萄球菌蛋白A及用于癌症血清疗法的固定化蛋白A试剂产生人C3a、C4a和C5a过敏毒素。
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Anaphylatoxin generation in multisystem organ failure.多系统器官衰竭中的过敏毒素生成
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本文引用的文献

1
Complement anaphylatoxin C4a inhibits C5a-induced neointima formation following arterial injury.补体过敏毒素C4a抑制动脉损伤后C5a诱导的新生内膜形成。
Mol Med Rep. 2014 Jul;10(1):45-52. doi: 10.3892/mmr.2014.2176. Epub 2014 Apr 24.
2
Interplay between invertebrate C3a with vertebrate macrophages: functional characterization of immune activities of amphioxus C3a.无脊椎动物 C3a 与脊椎动物巨噬细胞的相互作用:文昌鱼 C3a 的免疫活性功能特征。
Fish Shellfish Immunol. 2013 Oct;35(4):1249-59. doi: 10.1016/j.fsi.2013.07.049. Epub 2013 Aug 15.
3
Complement anaphylatoxin C3a is a potent inducer of embryonic chick retina regeneration.补体过敏毒素 C3a 是胚胎鸡视网膜再生的有效诱导剂。
Nat Commun. 2013;4:2312. doi: 10.1038/ncomms3312.
4
International Union of Basic and Clinical Pharmacology. [corrected]. LXXXVII. Complement peptide C5a, C4a, and C3a receptors.国际基础和临床药理学联合会。[更正]。LXXXVII. 补体肽 C5a、C4a 和 C3a 受体。
Pharmacol Rev. 2013 Jan;65(1):500-43. doi: 10.1124/pr.111.005223.
5
The complement system: an unexpected role in synaptic pruning during development and disease.补体系统:在发育和疾病过程中突触修剪中的意外作用。
Annu Rev Neurosci. 2012;35:369-89. doi: 10.1146/annurev-neuro-061010-113810.
6
Complement fragment C3a controls mutual cell attraction during collective cell migration.补体片段 C3a 控制细胞集体迁移过程中的细胞间相互吸引。
Dev Cell. 2011 Dec 13;21(6):1026-37. doi: 10.1016/j.devcel.2011.10.012. Epub 2011 Nov 24.
7
Structural mechanisms of constitutive activation in the C5a receptors with mutations in the extracellular loops: molecular modeling study.C5a 受体胞外环突变导致组成性激活的结构机制:分子建模研究。
Proteins. 2012 Jan;80(1):71-80. doi: 10.1002/prot.23162. Epub 2011 Sep 30.
8
Complement regulates CD4 T-cell help to CD8 T cells required for murine allograft rejection.补体调节 CD4 T 细胞向 CD8 T 细胞的辅助作用,这对于小鼠同种异体移植物排斥反应是必需的。
Am J Pathol. 2011 Aug;179(2):766-74. doi: 10.1016/j.ajpath.2011.04.038. Epub 2011 Jun 23.
9
Anti-complement component C5 mAb synergizes with CTLA4Ig to inhibit alloreactive T cells and prolong cardiac allograft survival in mice.抗补体成分 C5 mAb 与 CTLA4Ig 协同作用,抑制同种反应性 T 细胞,延长小鼠心脏移植物的存活时间。
Am J Transplant. 2011 Jul;11(7):1397-406. doi: 10.1111/j.1600-6143.2011.03561.x. Epub 2011 Jun 10.
10
γδT-cell function in sepsis is modulated by C5a receptor signalling.γδT 细胞在脓毒症中的功能受 C5a 受体信号的调节。
Immunology. 2011 Jul;133(3):340-9. doi: 10.1111/j.1365-2567.2011.03445.x. Epub 2011 Apr 19.

C4a:徒有虚名的过敏毒素。

C4a: An Anaphylatoxin in Name Only.

作者信息

Barnum Scott R

机构信息

Departments of Microbiology and Neurobiology, University of Alabama at Birmingham, Birmingham, Ala., USA.

出版信息

J Innate Immun. 2015;7(4):333-9. doi: 10.1159/000371423. Epub 2015 Feb 6.

DOI:10.1159/000371423
PMID:25659340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6738802/
Abstract

Activation of complement leads to generation of the 3 anaphylatoxins C3a, C4a, and C5a. Although all 3 peptides are structurally similar, only C3a and C5a share a similar functional profile that includes the classic inflammatory activities and, more recently, developmental homing and regenerative properties among others. In contrast, the functional profile of C4a is questionable in most cases owing to contamination of C4a preparations with physiologically relevant levels of C3a and/or C5a. Combined with the absence of an identified C4a receptor and the inability of C4a to signal through the C3a and C5a receptors, it is clear that C4a should not be included in the family of complement anaphylatoxins.

摘要

补体激活会导致产生三种过敏毒素C3a、C4a和C5a。尽管这三种肽在结构上相似,但只有C3a和C5a具有相似的功能特征,包括典型的炎症活性,以及最近发现的发育归巢和再生特性等。相比之下,在大多数情况下,由于C4a制剂中含有生理相关水平的C3a和/或C5a而受到污染,C4a的功能特征存在疑问。再加上未发现C4a受体,且C4a无法通过C3a和C5a受体发出信号,显然C4a不应被纳入补体过敏毒素家族。