Kull F C
Molecular Biology Department, Burroughs Wellcome Co., Research Triangle Park, N.C.
Nat Immun Cell Growth Regul. 1988;7(5-6):254-65.
The in vitro cytotoxic capacity (if not every pleiotropic property) of tumor necrosis factor (TNF) begins by interaction with specific high affinity cell surface receptors. The characterization of receptors and ligand kinetics is reviewed in relationship to cytotoxicity. Decreased receptor number and affinity correlate with sensitivity within a given cell line. In L-M cells (a sensitive tumorigenic fibroblast), TNF induces a biphasic downregulation of receptors. Internalized ligand and receptors are largely cleared before the onset of cell death. Drugs affecting cytotoxicity may act primarily on an early 'association' stage (ligand receptor interaction, internalization or perhaps signal transduction) or on a later 'lytic' stage. Phorbol myristate acetate is an example of the former, while chloroquine, cholera toxin and dibutyryl cyclic AMP are examples of the latter.
肿瘤坏死因子(TNF)的体外细胞毒性能力(即便不是其所有多效性特性)始于与特定高亲和力细胞表面受体的相互作用。本文综述了受体及配体动力学特性与细胞毒性的关系。在给定细胞系中,受体数量和亲和力的降低与敏感性相关。在L-M细胞(一种敏感的致瘤性成纤维细胞)中,TNF可诱导受体的双相下调。在细胞死亡发生之前,内化的配体和受体大部分已被清除。影响细胞毒性的药物可能主要作用于早期的“结合”阶段(配体-受体相互作用、内化或可能的信号转导)或后期的“裂解”阶段。佛波酯肉豆蔻酸酯是前者的一个例子,而氯喹、霍乱毒素和二丁酰环磷腺苷是后者的例子。