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首页> 外文期刊>British Journal of Cancer >Cytotoxicity of weak electrolytes after the adaptation of cells to low pH: role of the transmembrane pH gradient
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Cytotoxicity of weak electrolytes after the adaptation of cells to low pH: role of the transmembrane pH gradient

机译:细胞适应低pH后弱电解质的细胞毒性:跨膜pH梯度的作用

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摘要

Theory suggests that the transmembrane pH gradient may be a major determinant of the distribution of lipophilic weak electrolytes across the cell membrane. The present study evaluates the extent to which this factor contributes to pH-dependent changes in the cytotoxicity of two such chemotherapeutic drugs: chlorambucil and mitoxantrone. Experiments were performed with two cell types of the same origin but exhibiting different pH gradients at the same extracellular pH (pHe): CHO cells cultured under normal physiological conditions (pH 7.4) and acid-adapted cells obtained by culturing under low pH conditions (6.8). Over the pHe range examined (6.0-7.6), the difference between intracellular pH (pHi) and pHe increased with decreasing pHe. Acid-adapted cells were more resistant to acute changes in pHi than normal cells, resulting in substantially larger gradients in these cells. Drug cell survival curves were performed at pHe values of 6.4, 6.8 and 7.4. The cytotoxicity of chlorambucil, a weak acid, increased with decreasing pHe, and low pH-adapted cells were more sensitive than normal cells at the same pHe. In contrast, for the weak base, mitoxantrone, cytotoxicity increased with pHe and was more pronounced in normal cells. As predicted by the theory, the cytotoxicity of both drugs changed exponentially as a function of the pH gradient, regardless of cell type. For mitoxantrone, the rate of such change in cytotoxicity with the gradient was approximately two times greater than for chlorambucil. This difference is probably due to the presence of two equally ionizable crucial groups on mitoxantrone vs one group on chlorambucil. It is concluded that the cellular pH gradient plays a major role in the pH-dependent modulation of cytotoxicity in these weak electrolytes. The data obtained also suggest that a pronounced differential cytotoxicity may be expected in vivo in tumour vs normal tissue. In comparison with normal cells at a pHe of 7.4 (a model of cells in normal tissues), acid-adapted cells at a pHe of 6.8 (a model of cells distal from supplying blood vessels in tumours) were more sensitive to chlorambucil, with a dose-modifying factor of approximately 6, and were more resistant to mitoxantrone by a factor of 14.
机译:理论表明跨膜pH梯度可能是亲脂性弱电解质在细胞膜上分布的主要决定因素。本研究评估了这种因素在两种化学疗法药物:苯丁酸氮芥和米托蒽醌的细胞毒性中对pH依赖性改变的贡献程度。实验是使用两种来源相同但在相同的细胞外pH(pHe)下具有不同pH梯度的细胞类型进行的:在正常生理条件下(pH 7.4)培养的CHO细胞和在低pH条件下(6.8)培养获得的酸适应细胞)。在检查的pHe范围内(6.0-7.6),细胞内pH(pHi)和pHe之间的差异随pHe的降低而增加。酸适应细胞比普通细胞更能抵抗pHi的急性变化,从而导致这些细胞中的梯度明显变大。在pHe值为6.4、6.8和7.4时进行药物细胞存活曲线。苯丁酸氮芥(一种弱酸)的细胞毒性随pHe的降低而增加,并且在相同pHe下,低pH适应性细胞比正常细胞更敏感。相反,对于弱碱米托蒽醌,细胞毒性随pHe增加而增加,在正常细胞中更为明显。如该理论所预测,两种药物的细胞毒性均随pH梯度呈指数变化,而与细胞类型无关。对于米托蒽醌,这种细胞毒性随梯度的变化速率大约是苯丁酸氮芥的两倍。这种差异可能是由于米托蒽醌上有两个可电离的关键基团与苯丁酸氮芥上的一个基团存在。结论是,在这些弱电解质中,细胞pH梯度在细胞毒性的pH依赖性调节中起主要作用。获得的数据还表明,在体内与正常组织相比,肿瘤在体内有望表现出明显的细胞毒性。与pHe值为7.4的正常细胞(正常组织中的细胞模型)相比,pHe值为6.8的酸适应性细胞(远离肿瘤中供应血管的细胞模型)对苯丁酸氮芥更加敏感,剂量调节因子约为6,对米托蒽醌的耐药性提高14倍。

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