Weston K M, Raison R L
Department of Cell and Molecular Biology, University of Technology, Sydney, NSW, Australia.
J Cell Biochem. 1998 Feb 1;68(2):164-73.
We have examined the cytolytic effects of the membrane-active peptide, melittin, on a human lymphoblastoid cell line (HMy2) in the context of the use of melittin as the toxic component of an immunotoxin. The toxicity of melittin for HMy2 cells was linear over the concentration range 0.875-3.5 microM. Increased incubation times failed to result in significant cell death at concentrations of melittin below 0.875 microM. Kinetic analysis revealed that the cytolytic activity of melittin was independent of time of exposure beyond 90 min. Flow cytometric analysis of HMy2 cells incubated with FITC-labeled melittin demonstrated that the cells could incorporate up to 2.5 x 10(5) FITC-melittin molecules per cell with no reduction in viability. Extrapolation of this data indicates that 10(6) melittin molecules per cell are required for maximum cytotoxicity to HMy2 cells. Further analysis of HMy2 cells that incorporated melittin, but that remained viable, revealed that these cells were able to reduce the number of melittin molecules per cell over time. The data indicate a potential threshold value for the number of melittin molecules that may be required to be delivered to the cell surface in the form of an immunotoxin if effective selective cell death is to be achieved.
我们研究了膜活性肽蜂毒素在作为免疫毒素的毒性成分使用时,对人淋巴母细胞系(HMy2)的细胞溶解作用。在0.875 - 3.5微摩尔的浓度范围内,蜂毒素对HMy2细胞的毒性呈线性关系。在蜂毒素浓度低于0.875微摩尔时,延长孵育时间并未导致显著的细胞死亡。动力学分析表明,超过90分钟后,蜂毒素的细胞溶解活性与暴露时间无关。对用异硫氰酸荧光素(FITC)标记的蜂毒素孵育的HMy2细胞进行流式细胞术分析表明,细胞每单位可摄取多达2.5×10⁵个FITC - 蜂毒素分子,且活力未降低。根据这些数据推断,对HMy2细胞产生最大细胞毒性需要每单位细胞10⁶个蜂毒素分子。对摄取了蜂毒素但仍存活的HMy2细胞的进一步分析表明,随着时间推移,这些细胞能够减少每单位细胞内蜂毒素分子的数量。数据表明,如果要实现有效的选择性细胞死亡,以免疫毒素形式递送至细胞表面的蜂毒素分子数量可能存在一个潜在阈值。