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1
Human rheumatoid synovial cell stimulation by the membrane attack complex and other pore-forming toxins in vitro: the role of calcium in cell activation.膜攻击复合物及其他成孔毒素对人类风湿性滑膜细胞的体外刺激:钙在细胞活化中的作用
Immunology. 1990 Nov;71(3):312-6.
2
Stimulation of human rheumatoid synovial cells by non-lethal complement membrane attack.非致死性补体膜攻击对人类风湿性滑膜细胞的刺激作用。
Immunology. 1990 Feb;69(2):237-42.
3
Complement membrane attack complex, perforin, and bacterial exotoxins induce in K562 cells calcium-dependent cross-protection from lysis.补体膜攻击复合物、穿孔素和细菌外毒素可诱导K562细胞产生对裂解的钙依赖性交叉保护作用。
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4
In vivo and in vitro evidence of cell recovery from complement attack in rheumatoid synovium.
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5
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Clin Exp Immunol. 1988 Sep;73(3):473-8.
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7
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An investigation of cell proliferation and soluble mediators induced by interleukin 1beta in human synovial fibroblasts: comparative response in osteoarthritis and rheumatoid arthritis.白细胞介素1β诱导人滑膜成纤维细胞的细胞增殖及可溶性介质的研究:骨关节炎与类风湿关节炎的比较反应
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ATP and UTP activate calcium-mobilizing P2U-like receptors and act synergistically with interleukin-1 to stimulate prostaglandin E2 release from human rheumatoid synovial cells.三磷酸腺苷(ATP)和三磷酸尿苷(UTP)激活钙动员型P2U样受体,并与白细胞介素-1协同作用,刺激人类风湿性滑膜细胞释放前列腺素E2。
Arthritis Rheum. 1998 Feb;41(2):246-55. doi: 10.1002/1529-0131(199802)41:2<246::AID-ART8>3.0.CO;2-I.

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1
Therapeutic Efficacy of a Paramyosin-Derived Peptide Modified With a Membrane-Targeting Signal in Mice With Antigen-Induced Arthritis.一种经膜靶向信号修饰的副肌球蛋白衍生肽在抗原诱导性关节炎小鼠中的治疗效果
Front Microbiol. 2020 Dec 23;11:608380. doi: 10.3389/fmicb.2020.608380. eCollection 2020.
2
Comparison of the suppressive effects of soluble CR1 and C5a receptor antagonist in acute arthritis induced in rats by blocking of CD59.可溶性补体受体1(CR1)与C5a受体拮抗剂对通过阻断CD59诱导大鼠急性关节炎的抑制作用比较
Clin Exp Immunol. 2000 Feb;119(2):368-75. doi: 10.1046/j.1365-2249.2000.01127.x.
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Targeting of functional antibody-CD59 fusion proteins to a cell surface.将功能性抗体 - CD59融合蛋白靶向至细胞表面。
J Clin Invest. 1999 Jan;103(1):55-61. doi: 10.1172/JCI4607.

本文引用的文献

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Characterization of human complement components C6 and C7.人类补体成分C6和C7的特性分析
Mol Immunol. 1982 Nov;19(11):1425-31. doi: 10.1016/0161-5890(82)90189-4.
2
Release of arachidonic acid: a new function of the late complement components.花生四烯酸的释放:补体晚期成分的一项新功能。
Immunobiology. 1984 May;166(4-5):473-83. doi: 10.1016/S0171-2985(84)80024-8.
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Measurement of intracellular calcium ions and oxygen radicals in polymorphonuclear leucocyte-erythrocyte 'ghost' hybrids.多形核白细胞-红细胞“空壳”杂交体中细胞内钙离子和氧自由基的测量。
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Stimulation by human interleukin 1 of cartilage breakdown and production of collagenase and proteoglycanase by human chondrocytes but not by human osteoblasts in vitro.在体外,人白细胞介素1刺激人软骨细胞导致软骨分解并产生胶原酶和蛋白聚糖酶,但不刺激人成骨细胞。
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Immunoaffinity purification of human complement component C9 using monoclonal antibodies.使用单克隆抗体对人补体成分C9进行免疫亲和纯化。
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Mechanism of cytolysis by complement.补体介导的细胞溶解机制。
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膜攻击复合物及其他成孔毒素对人类风湿性滑膜细胞的体外刺激:钙在细胞活化中的作用

Human rheumatoid synovial cell stimulation by the membrane attack complex and other pore-forming toxins in vitro: the role of calcium in cell activation.

作者信息

Daniels R H, Williams B D, Morgan B P

机构信息

Department of Medical Biochemistry, University of Wales College of Medicine, Cardiff, U.K.

出版信息

Immunology. 1990 Nov;71(3):312-6.

PMID:2269468
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1384424/
Abstract

The effects of non-lethal amounts of a variety of pore-forming agents on cultured human rheumatoid synovial cells (HRSC) have been investigated. Non-lethal complement membrane attack and non-lethal amounts of melittin, perforin and ionomycin all caused a biphasic release of prostaglandin E2 (PGE2) from HRSC, an early phase of release occurring within 1 hr and a second larger phase commencing after 4 hr and continuing over the 24-hr time-course. Removal of extracellular calcium abolished the release of PGE2 under all conditions of non-lethal attack. Modulation of G-protein activity reduced the second phase of release caused by non-lethal doses of the membrane-attack complex (MAC) from 800 ng/10(6) cells PGE2 to around 300 ng/10(6) cells. Non-lethal levels of the MAC also caused release of interleukin-6 (IL-6) from HRSC over the 24-hr time-course, with levels reaching 550 ng/10(6) cells at 24 hr compared to background levels of 200 ng/10(6) cells. No detectable release of IL-1 alpha could be measured at any time following non-lethal complement membrane attack. These results suggest a role for the MAC as an initiating mediator inducing the inflammation associated with rheumatoid arthritis.

摘要

研究了多种非致死剂量的成孔剂对培养的人类风湿性滑膜细胞(HRSC)的影响。非致死剂量的补体膜攻击复合物以及非致死剂量的蜂毒肽、穿孔素和离子霉素均导致HRSC中前列腺素E2(PGE2)出现双相释放,早期释放在1小时内发生,第二个更大的释放阶段在4小时后开始,并在24小时的时间进程中持续。去除细胞外钙可消除在所有非致死攻击条件下PGE2的释放。G蛋白活性的调节将非致死剂量的膜攻击复合物(MAC)引起的第二阶段释放从800 ng/10⁶个细胞PGE2降低至约300 ng/10⁶个细胞。非致死水平的MAC在24小时的时间进程中也导致HRSC释放白细胞介素-6(IL-6),与200 ng/10⁶个细胞的背景水平相比,24小时时水平达到550 ng/10⁶个细胞。在非致死补体膜攻击后的任何时间均未检测到IL-1α的释放。这些结果表明MAC作为引发介质在诱导与类风湿性关节炎相关的炎症中发挥作用。