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佛波酯对牛淋巴细胞中氨基酸转运加速作用的抑制

Inhibition of phorbol ester-accelerated amino acid transport in bovine lymphocytes.

作者信息

Kensler T W, Wertz P W, Mueller G C

出版信息

Biochim Biophys Acta. 1979 Jun 1;585(1):43-52. doi: 10.1016/0304-4165(79)90323-4.

Abstract

12-O-Tetradecanoylphorbol-13-acetate, a highly active tumor-promoting agent and lymphocyte comitogen, rapidly accelerates the transport of alpha-aminoisobutyric acid in cultured bovine lymphocytes. Structure-activity studies show that the ability of phorbol diesters to accelerate alpha-aminoisobutyric acid uptake runs parallel to their potency as lymphocyte comitogens and as tumor promoters in mouse skin. This phorbol ester-accelerated, amino acid transport is largely insensitive to the inhibition of RNA and protein synthesis by actinomycin D and cycloheximide, respectively, and is insensitive to the inhibition of membrane movement by cytochalasin B and colchicine. Retinoic acid, an antagonist of the tumor-promoting and comitogenic actions of phorbol esters also inhibits the acceleration of amino acid uptake by 12-O-tetradecanoylphorbol-13-acetate; however, the epoxy derivatives of retinoic acid and structurally related analogs, which are potent antagonists of the other aspects of phorbol ester activation of lymphocytes, are inactive in blocking amino acid uptake. Comparative studies in lymphocytes show that this phorbol ester elicits a number of metabolic responses which appear to originate at the cell membrane and that these are differentially antagonized by retinoic acid, the 5,6-epoxide of retinoic acid, and related retinoid analogs.

摘要

12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯是一种高活性的肿瘤促进剂和淋巴细胞促有丝分裂原,它能迅速加速培养的牛淋巴细胞中α - 氨基异丁酸的转运。结构 - 活性研究表明,佛波醇二酯加速α - 氨基异丁酸摄取的能力与其作为淋巴细胞促有丝分裂原以及在小鼠皮肤中作为肿瘤促进剂的效力平行。这种佛波醇酯加速的氨基酸转运在很大程度上不受放线菌素D和环己酰亚胺分别对RNA和蛋白质合成的抑制作用影响,也不受细胞松弛素B和秋水仙碱对膜运动的抑制作用影响。视黄酸是佛波醇酯肿瘤促进和促有丝分裂作用的拮抗剂,它也能抑制12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯对氨基酸摄取的加速作用;然而,视黄酸的环氧衍生物和结构相关类似物虽然是佛波醇酯激活淋巴细胞其他方面的有效拮抗剂,但在阻断氨基酸摄取方面却没有活性。在淋巴细胞中的比较研究表明,这种佛波醇酯引发了许多似乎起源于细胞膜的代谢反应,并且视黄酸、视黄酸的5,6 - 环氧化物以及相关类视黄醇类似物对这些反应有不同程度的拮抗作用。

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