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佛波酯可诱导脂皮质素(膜联蛋白)1转位至U937细胞膜,但地塞米松则不能。

Translocation of lipocortin (annexin) 1 to the membrane of U937 cells induced by phorbol ester, but not by dexamethasone.

作者信息

Kang S A, Cho Y J, Moon H B, Na D S

机构信息

Department of Biochemistry, University of Ulsan, Seoul, Korea.

出版信息

Br J Pharmacol. 1996 Apr;117(8):1780-4. doi: 10.1111/j.1476-5381.1996.tb15354.x.

Abstract
  1. Induction of lipocortin 1 secretion by dexamethasone has been demonstrated, although the secretory mechanism is still unknown. We have studied the effects of 12-tetradecanoyl phorbol 13-acetate (TPA) and/or dexamethasone on the expression, translocation, and secretion of lipocortin 1 in U937 cells. 2. The expression of lipocortin 1 and its mRNA increased during TPA-induced differentiation of U937 cells to a maximum of 1.9 fold and 8.2 fold, respectively, after 48 h. Both the protein and the mRNA levels decreased after 48 h. 3. TPA caused the translocation of lipocortin 1 from the cytosol to the membrane of U937 cells in a time-dependent manner, as determined by Western blot analysis. The translocation was concurrent with the differentiation of the cells. After 48 h of TPA treatment, 82.6 +/- 6.5% of lipocortin 1 was present in the membrane fraction compared to 41.6 +/- 1.7% in untreated cells. 4. The amount of lipocortin 1 that was externally bound (associated) with the membrane increased to 3.2 fold as the cytosol to membrane translocation of lipocortin 1 increased. 5. Dexamethasone decreased the externally bound lipocortin 1, but had no effect on the cytosol to membrane translocation. 6. This offers a model system with which the function and the secretion mechanism of lipocortin 1 can be studied. Our data is consistent with the hypothesis that the secretory mechanism is through an unknown pathway, involving the translocation of lipocortin 1 from the cytosol to the internal membranes, and then, its secretion to the external membrane.
摘要
  1. 地塞米松诱导脂皮质素1分泌已得到证实,但其分泌机制仍不清楚。我们研究了12-十四酰佛波醇-13-乙酸酯(TPA)和/或地塞米松对U937细胞中脂皮质素1的表达、转位和分泌的影响。2. 在TPA诱导U937细胞分化过程中,脂皮质素1及其mRNA的表达在48小时后分别增加至最大值,分别为1.9倍和8.2倍。48小时后蛋白质和mRNA水平均下降。3. 如通过蛋白质印迹分析所确定的,TPA以时间依赖性方式导致脂皮质素1从U937细胞的胞质溶胶转位至膜。这种转位与细胞分化同时发生。TPA处理48小时后,82.6±6.5%的脂皮质素1存在于膜组分中,而未处理细胞中为41.6±1.7%。4. 随着脂皮质素1从胞质溶胶到膜的转位增加,与膜外部结合(关联)的脂皮质素1的量增加至3.2倍。5. 地塞米松减少了外部结合的脂皮质素1,但对胞质溶胶到膜的转位没有影响。6. 这提供了一个模型系统,通过该系统可以研究脂皮质素1的功能和分泌机制。我们的数据与以下假设一致,即分泌机制是通过一条未知途径,涉及脂皮质素1从胞质溶胶转位至内膜,然后分泌至外膜。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d60c/1909567/ac2ead1b4909/brjpharm00097-0179-a.jpg

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