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乙醛修饰的血清蛋白抑制有丝分裂原刺激的人淋巴细胞转化。

Acetaldehyde-modified serum proteins inhibit mitogen-stimulated human lymphocyte transformation.

作者信息

Wickramasinghe S N, Barden G

机构信息

Department of Haematology, Medical School, Imperial College of Science, St Mary's Campus, Norfolk Place, London.

出版信息

Br J Haematol. 1989 Sep;73(1):23-8. doi: 10.1111/j.1365-2141.1989.tb00213.x.

Abstract

Sera obtained from healthy volunteers immediately before and 8 h after the rapid consumption of 1.2 g ethanol/kg body weight were dialysed against RPMI 1640 and added ab initio to microcultures of normal human lymphocytes containing 1-3 micrograms phytohaemagglutinin (PHA)/ml or 2-8 micrograms pokeweed mitogen (PWM)/ml. When compared with the pre-alcohol sera, the post-alcohol sera inhibited lymphocyte transformation after 48 h incubation with either mitogen. In other experiments, acetaldehyde-albumin complexes were generated by reacting solutions of human serum albumin with 45-720 microM acetaldehyde, and the same quantity of either unmodified albumin or acetaldehyde-modified albumin was included in freshly-prepared lymphocyte microcultures containing 3 micrograms PHA/ml or 8 micrograms PWM/ml. When compared with unmodified albumin, acetaldehyde-modified albumin inhibited lymphocyte transformation after 48 h of culture with either mitogen. The inhibition of lymphocyte transformation caused by post-alcohol sera and acetaldehyde-modified albumin was partially corrected after treatment of the proteins with 1.55 mM sodium borohydride at a pH of 9.5. The data indicate that post-alcohol sera contain a non-dialysable activity which inhibits mitogen-stimulated lymphocyte transformation in vitro and that at least part of this activity may reside in acetaldehyde-modified serum albumin.

摘要

从健康志愿者身上采集的血清,在快速摄入1.2克乙醇/千克体重之前及之后8小时立即获取,将其对RPMI 1640进行透析,并从头添加到含有1 - 3微克植物血凝素(PHA)/毫升或2 - 8微克商陆有丝分裂原(PWM)/毫升的正常人淋巴细胞微培养物中。与饮酒前血清相比,饮酒后血清在与任何一种有丝分裂原孵育48小时后均抑制淋巴细胞转化。在其他实验中,通过使人血清白蛋白溶液与45 - 720微摩尔乙醛反应生成乙醛 - 白蛋白复合物,并将相同量的未修饰白蛋白或乙醛修饰白蛋白包含在新鲜制备的含有3微克PHA/毫升或8微克PWM/毫升的淋巴细胞微培养物中。与未修饰白蛋白相比,乙醛修饰白蛋白在与任何一种有丝分裂原培养48小时后均抑制淋巴细胞转化。用1.55毫摩尔硼氢化钠在pH 9.5条件下处理蛋白质后,饮酒后血清和乙醛修饰白蛋白对淋巴细胞转化的抑制作用得到部分纠正。数据表明,饮酒后血清含有一种不可透析的活性物质,它在体外抑制有丝分裂原刺激的淋巴细胞转化,并且这种活性至少部分可能存在于乙醛修饰的血清白蛋白中。

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