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抗体依赖性细胞毒性:细胞松弛素和微管破坏剂的调节作用

Antibody-dependent cytotoxicity: modulation by the cytochalasins and microtubule-disruptive agents.

作者信息

Gelfand E W, Morris S A, Resch K

出版信息

J Immunol. 1975 Mar;114(3):919-24.

PMID:1112985
Abstract

Cytochalasin B was shown to inhibit lysis of antibody-coated target cells by effector cells from rabbit spleen and lymph node. The inhibitory activity was dose-dependent and reversible. At low concentrations of cytochalasin B (0.15 to 0.3 mug/ml) enhancement of antibody-dependent cytotoxicity was observed. The drug appeared to act at an early stage of the lytic pathway after effector cell-target cell interaction, but before triggering of the cytotoxic event. Cytochalasin A was shown to be a more potent but similarly reversible inhibitor of antibody-dependent cytotoxicity. No enhancement of cytotoxicity was seen at non-inhibitory concentrations of cytochalasin A. The microtubule-disruptive agents colchicine (10-4 M), vinblastine (10-5 M) and colcemid (10-6 M) did not influence antibody-dependent cytotoxicity at concentrations which were not toxic to the effector cells. Our results suggest that antibody-dependent cytotoxicity is a surface membrane-initiated process and microtubule-associated functions are not essential.

摘要

细胞松弛素B被证明可抑制兔脾脏和淋巴结中的效应细胞对抗体包被的靶细胞的裂解作用。其抑制活性呈剂量依赖性且可逆。在低浓度的细胞松弛素B(0.15至0.3微克/毫升)时,观察到抗体依赖性细胞毒性增强。该药物似乎作用于效应细胞与靶细胞相互作用后、细胞毒性事件触发前的裂解途径早期阶段。细胞松弛素A被证明是一种更有效的但同样可逆的抗体依赖性细胞毒性抑制剂。在细胞松弛素A的非抑制浓度下未观察到细胞毒性增强。微管破坏剂秋水仙碱(10⁻⁴M)、长春碱(10⁻⁵M)和秋水仙酰胺(10⁻⁶M)在对效应细胞无毒的浓度下不影响抗体依赖性细胞毒性。我们的结果表明,抗体依赖性细胞毒性是一个由表面膜启动的过程,与微管相关的功能并非必不可少。

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