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用佛波醇肉豆蔻酸酯乙酸盐处理小鼠L细胞可诱导一种纤溶酶原激活物抑制剂的分泌,该抑制剂可与人及小鼠尿激酶和人组织纤溶酶原激活物结合。

Treatment of mouse L-cells with phorbol myristate acetate induces the secretion of a plasminogen activator inhibitor which binds to human and mouse urokinase and human tissue plasminogen activator.

作者信息

Rehemtulla A, Gates J, Hart D A

机构信息

Department of Microbiology and Infectious Disease, University of Calgary Health Sciences Centre, Alberta, Canada.

出版信息

Comp Biochem Physiol B. 1987;88(1):277-83. doi: 10.1016/0305-0491(87)90114-3.

Abstract
  1. Serum-free conditioned medium from L-cells or L-cells treated with the tumor-promotor phorbol myristate acetate (PMA) was analyzed for plasminogen activator (PA) and plasminogen activator inhibitor (PAI) activity. Conditioned medium from control or PMA-treated cells did not contain detectable PA activity when assayed by SDS-PAGE and zymography. 2. Conditioned medium from PMA-treated cells, but not control cells, contained a PAI of Mr = 40,000 da when assayed by reverse zymography. 3. The L-cell PAI formed SDS-stable complexes with purified human (homo sapiens) urokinase and tissue plasminogen activator, as well as, mouse (Mus musculus) urinary PA. 4. These results indicate that biochemical and immunological differences between human and mouse urokinase and human urokinase and human tissue plasminogen activator do not influence the interaction of the L-cell PAI with these enzymes.
摘要
  1. 对来自L细胞或用肿瘤促进剂佛波酯肉豆蔻酸酯乙酸酯(PMA)处理的L细胞的无血清条件培养基进行纤溶酶原激活剂(PA)和纤溶酶原激活剂抑制剂(PAI)活性分析。通过SDS-PAGE和酶谱法检测时,对照细胞或PMA处理细胞的条件培养基中未检测到PA活性。2. 通过反向酶谱法检测时,PMA处理细胞的条件培养基中含有一种分子量为40,000道尔顿的PAI,而对照细胞的条件培养基中则没有。3. L细胞PAI与纯化的人(智人)尿激酶、组织纤溶酶原激活剂以及小鼠(小家鼠)尿PA形成SDS稳定复合物。4. 这些结果表明,人尿激酶与小鼠尿激酶以及人尿激酶与人体组织纤溶酶原激活剂之间的生化和免疫学差异不影响L细胞PAI与这些酶的相互作用。

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