巯基化合物恢复视黄酸对HTLV-I (+) T淋巴细胞的生长抑制;维甲酸诱导的成人t细胞白血病细胞生长抑制的可能机制。

J Miyatake, Y Maeda, H Nawata, Y Sumimoto, H Sono, M Sakaguchi, M Matsuda, Y Tatsumi, F Urase, F Horiuchi, K Irimajiri, A Horiuchi
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引用次数: 0

摘要

我们发现视黄酸(RA)对HTLV-I (+) t细胞株(ATL-2和HUT102)有显著的生长抑制作用,但对HTLV-I (-) t细胞株(MOLT-4和Jurkat)没有明显的抑制作用。我们假设RA抑制生长的机制取决于氧化还原电位的不平衡。为了研究外源硫醇化合物对RA诱导HTLV-I (+) t细胞株生长的影响,在不含硫醇的培养基中,分别添加13顺式RA或ATRA,用几种硫醇化合物(硫氧还蛋白、l -胱氨酸和GSH)培养HTLV-I (+) t细胞株。出乎意料的是,巯基化合物单独不能恢复HTLV-I (+) t细胞系的生长抑制。然而,当这些细胞与硫醇化合物预孵育24小时时,13-顺式RA或ATRA未观察到生长抑制。这些结果表明,硫醇类化合物与HTLV-I (+) T细胞对RA的敏感性密切相关,而与HTLV-I (-) T细胞无关,硫醇类化合物在HTLV-I (+) T细胞中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thiol compounds rescue growth inhibition by retinoic acid on HTLV-I (+) T lymphocytes; possible mechanism of retinoic-acid-induced growth inhibition of adult T-cell leukemia cells.

We demonstrated significant growth inhibition by retinoic acid (RA) of HTLV-I (+) T-cell lines (ATL-2 and HUT102), but not HTLV-I (-) T-cell lines (MOLT-4 and Jurkat). We hypothesized that the mechanism of growth inhibition by RA depends on an imbalance in redox potential. To examine the effect of exogenous thiol compounds for the growth of HTLV-I (+) T-cell lines by RA, HTLV-I (+) T-cell lines were cultured with several thiol compounds (thioredoxin, L-cystine, and GSH), following addition of 13-cis RA or ATRA, respectively, in cultured with thiol free medium. Unexpectedly, thiol compounds alone did not restore growth inhibition of HTLV-I (+) T-cell lines. However, when those cells were preincubated with thiol compounds for 24 hours, no growth inhibition by 13-cis RA or ATRA was observed. These results suggest that thiol compounds are associated strongly with sensitivity to RA of HTLV-I (+) T cells, but not of HTLV-I (-) T cells and that thiol compounds serve an important role on HTLV-I (+) T cells.

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