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一种使用经甲基泼尼松龙处理的人血清制备EAC14中间细胞的简化方法。

A simplified method for the preparation of EAC14 intermediate cells using human serum treated with methylprednisolone.

作者信息

Kitamura F, Shimada K, Suzuki T, Nishioka K

出版信息

J Immunol Methods. 1985 Dec 27;85(2):363-70. doi: 10.1016/0022-1759(85)90145-0.

DOI:10.1016/0022-1759(85)90145-0
PMID:3908568
Abstract

The inhibitory effect of methylprednisolone 21-succinate ester (MPS) on the activities of complement components in human serum was studied by incubating human serum with various concentrations of MPS at 37 degrees C for 30 min and then measuring the residual activity of each component in human serum. The formation of EAC1 and EAC14 by C1 and C4 respectively, were only weakly inhibited by MPS at a final concentration of 10 mg/ml. In contrast, the same concentration of MPS completely inhibited the capacity of C2, C3, C5 and C6-9 to induce respective succeeding intermediates. On the basis of these findings a simplified method was devised for the preparation of EAC14 intermediates using human serum pretreated with MPS.

摘要

通过将人血清与不同浓度的琥珀酸甲泼尼龙(MPS)在37℃孵育30分钟,然后测定人血清中各成分的残余活性,研究了琥珀酸甲泼尼龙(MPS)对人血清中补体成分活性的抑制作用。最终浓度为10mg/ml时,MPS仅对分别由C1和C4形成的EAC1和EAC14有微弱抑制作用。相比之下,相同浓度的MPS完全抑制了C2、C3、C5和C6-9诱导各自后续中间体的能力。基于这些发现,设计了一种使用经MPS预处理的人血清制备EAC14中间体的简化方法。

相似文献

1
A simplified method for the preparation of EAC14 intermediate cells using human serum treated with methylprednisolone.一种使用经甲基泼尼松龙处理的人血清制备EAC14中间细胞的简化方法。
J Immunol Methods. 1985 Dec 27;85(2):363-70. doi: 10.1016/0022-1759(85)90145-0.
2
A simplified method for the preparation of EAC14.一种制备EAC14的简化方法。
J Immunol Methods. 1980;39(1-2):25-9. doi: 10.1016/0022-1759(80)90290-2.
3
New methods for the preparation of the cellular intermediate EAC14.制备细胞中间体EAC14的新方法。
J Immunol Methods. 1986 Dec 24;95(2):277-81. doi: 10.1016/0022-1759(86)90416-3.
4
Surface modulation of classical pathway activation: C2 and C3 convertase formation and regulation on sheep, guinea pig, and human erythrocytes.经典途径激活的表面调节:绵羊、豚鼠和人红细胞上C2和C3转化酶的形成与调节
J Immunol. 1983 Jul;131(1):403-8.
5
The bovine complement system.牛补体系统。
Adv Exp Med Biol. 1981;137:413-30.
6
In vitro inhibition of the classical pathway of human complement by polymyxin B.
Biochem Pharmacol. 1987 Sep 15;36(18):2927-30. doi: 10.1016/0006-2952(87)90204-8.
7
Effects of zinc chloride on guinea pig complement component activity in vitro: concentration-dependent inhibition and enhancement.氯化锌对豚鼠补体成分活性的体外影响:浓度依赖性抑制和增强作用。
Infect Immun. 1979 Feb;23(2):424-31. doi: 10.1128/iai.23.2.424-431.1979.
8
EAC4 and EAC14 production without purified Ci.在没有纯化的Ci的情况下生产EAC4和EAC14。
J Immunol. 1975 Dec;115(6):1625-30.
9
Monoclonal antibodies against components of the classical pathway of complement.针对补体经典途径成分的单克隆抗体。
Complement Inflamm. 1989;6(3):166-74. doi: 10.1159/000463092.
10
Inhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranes.衰变加速因子(DAF)整合到细胞膜后对细胞表面补体激活的抑制作用。
J Exp Med. 1984 Nov 1;160(5):1558-78. doi: 10.1084/jem.160.5.1558.

引用本文的文献

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Mechanism of killing of Giardia lamblia trophozoites by complement.补体杀灭蓝氏贾第鞭毛虫滋养体的机制。
J Clin Invest. 1987 May;79(5):1296-302. doi: 10.1172/JCI112952.
2
Lysis of complement-sensitive Entamoeba histolytica by activated terminal complement components. Initiation of complement activation by an extracellular neutral cysteine proteinase.活化的末端补体成分对补体敏感的溶组织内阿米巴的溶解作用。细胞外中性半胱氨酸蛋白酶引发补体激活。
J Clin Invest. 1990 Dec;86(6):1815-22. doi: 10.1172/JCI114911.
3
Mechanism of resistance to complement-mediated killing of bacteria encoded by the Salmonella typhimurium virulence plasmid gene rck.
鼠伤寒沙门氏菌毒力质粒基因rck编码的细菌对补体介导杀伤的抗性机制。
J Clin Invest. 1992 Sep;90(3):953-64. doi: 10.1172/JCI115972.