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肿瘤启动子佛波酯(PMA)可刺激经莫洛尼氏肉瘤病毒(MSV)转化的3T3细胞中鼠原尿激酶的合成与分泌:这是由尿激酶mRNA含量增加介导的。

Tumor promoter PMA stimulates the synthesis and secretion of mouse pro-urokinase in MSV-transformed 3T3 cells: this is mediated by an increase in urokinase mRNA content.

作者信息

Belin D, Godeau F, Vassalli J D

出版信息

EMBO J. 1984 Aug;3(8):1901-6. doi: 10.1002/j.1460-2075.1984.tb02065.x.

DOI:10.1002/j.1460-2075.1984.tb02065.x
PMID:6541126
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC557615/
Abstract

In mouse MSV-3T3 cells the synthesis of the urokinase form of plasminogen activator was increased 10-fold after addition of the tumor promoter phorbol-12-myristate-13-acetate (PMA). PMA also stimulated the secretion of the protein into the culture medium, mostly in the form of enzymatically inactive pro-urokinase. When assayed by injecting RNA into Xenopus laevis oocytes, the concentration of functional urokinase mRNA was found to be 6- to 10-fold higher in the PMA-treated cells; a similar increase in urokinase mRNA content was measured by hybridisation with a mouse urokinase cDNA probe. Thus, the induction of plasminogen activator by PMA in MSV-3T3 cells is accounted for by an increased content of urokinase mRNA.

摘要

在小鼠MSV - 3T3细胞中,加入肿瘤促进剂佛波醇 - 12 - 肉豆蔻酸酯 - 13 - 乙酸酯(PMA)后,尿激酶型纤溶酶原激活剂的合成增加了10倍。PMA还刺激该蛋白分泌到培养基中,大多以无酶活性的尿激酶原形式存在。通过将RNA注射到非洲爪蟾卵母细胞中进行检测时,发现经PMA处理的细胞中功能性尿激酶mRNA的浓度高6至10倍;用小鼠尿激酶cDNA探针杂交测量,尿激酶mRNA含量也有类似增加。因此,PMA对MSV - 3T3细胞中纤溶酶原激活剂的诱导作用是由尿激酶mRNA含量增加所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/ddbf5d7aeb03/emboj00312-0229-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/e83a8a273b3b/emboj00312-0227-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/33e271595e0d/emboj00312-0227-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/ea4ceab63bfb/emboj00312-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/6ea328bb2c05/emboj00312-0228-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/e64564fb25e1/emboj00312-0229-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/ddbf5d7aeb03/emboj00312-0229-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/e83a8a273b3b/emboj00312-0227-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/33e271595e0d/emboj00312-0227-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/ea4ceab63bfb/emboj00312-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/6ea328bb2c05/emboj00312-0228-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/e64564fb25e1/emboj00312-0229-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2a/557615/ddbf5d7aeb03/emboj00312-0229-b.jpg

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