Effect of glutathione content on cellular uptake and growth inhibitory activity of prostaglandin A2 in L-1210 cells.

Eicosanoids Pub Date : 1992-01-01
K Ohno, M Hirata, S Narumiya, M Fukushima
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Abstract

Prostaglandin A2 (PGA2) is known to be actively incorporated into mammalian cells and thereby evokes its biological effects. To explore the transport mechanism of PGA2 and the possible role of cellular glutathione (GSH) in the transport process, we prepared GSH-enriched and -depleted L-1210 cells and then incubated with [3H] PGA2. In GSH-depleted cells, the total amount of PGA2 incorporated was reduced to about 50% of that in the control and GSH-enriched cells, accompanied by marked reduction of the PG in the cytosol but not in the nuclei. The kinetics of uptake revealed that the apparent Vmax was reduced by GSH depletion. Subsequent study of L-1210 cells under culture conditions provided similar results; GSH-depletion caused suppression of PG uptake and a reduction in the amount of PGA2 in cytosol, while its nuclear accumulation was little influenced. Comparison of the effect of PGA2 on the growth of control and GSH-depleted cells showed that the PG suppressed cell proliferation to the same extent. Our results suggest that, though uptake of PGA2 may be significantly influenced, its accumulation, and hence the manifestation of its biological effects are not influenced by GSH status.

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谷胱甘肽含量对L-1210细胞摄取前列腺素A2及生长抑制活性的影响。
已知前列腺素A2 (PGA2)可被积极地结合到哺乳动物细胞中,从而引起其生物学效应。为了探究PGA2的转运机制以及细胞谷胱甘肽(GSH)在转运过程中可能发挥的作用,我们制备了富含GSH和缺乏GSH的L-1210细胞,然后用[3H] PGA2孵育。在gsh缺失的细胞中,PGA2的总掺入量减少到对照和gsh富集细胞的50%左右,细胞质中PG明显减少,但细胞核中PG没有明显减少。摄取动力学表明表观Vmax因GSH耗竭而降低。随后在培养条件下对L-1210细胞的研究也得到了类似的结果;gsh耗竭抑制了PG的摄取,降低了细胞质中PGA2的含量,但对其核积累影响不大。比较PGA2对对照和gsh缺失细胞生长的影响,发现PG对细胞增殖的抑制程度相同。我们的研究结果表明,尽管PGA2的摄取可能受到显著影响,但其积累及其生物学效应的表现不受GSH状态的影响。
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