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纤溶酶原激活可改变静止的3T3细胞单层的形态并启动生长。

Plasminogen activation transforms the morphology of quiescent 3T3 cell monolayers and initiates growth.

作者信息

Whur P, Silcox J J, Boston J A, Williams D C

出版信息

Br J Cancer. 1979 Jun;39(6):718-30. doi: 10.1038/bjc.1979.126.

Abstract

Plasminogen activator of cell origin converts the plasma protein plasminogen to the proteolytic enzyme plasmin. Recently, high levels of activator have been observed to be particularly associated with tumours and transformed cells, and a functional relationship between plasminogen activation and malignancy has been proposed. In this paper we have attempted to induce transformation-like morphology and growth in a population of confluent quiescent cells in tissue culture, by inducing plasminogen activation. Untransformed 3T3 cells grown to confluence in plasminogen-free medium were subjected to plasminogen activation by the addition of urokinase and plasminogen or plasminogen-containing acid-treated serum, or plasmin. Under these conditions, the previously well ordered monolayers became disrupted, with multilayering, and discontinuities in the cell sheet, and the cells simultaneously grew to significantly higher densities. Removal of the plasmin-containing medium supplements effected some restoration of normal morphology. Thus, lhen plasmin was present 3T3 cells did not become transformed, but expresses transformation-like features. Well ordered monolayer morphology and quiescence in 3T3 cells at confluence are therefore dependent upon the absence of plasminogen activation.

摘要

细胞源纤溶酶原激活剂可将血浆蛋白纤溶酶原转化为蛋白水解酶纤溶酶。最近,人们观察到高水平的激活剂与肿瘤和转化细胞特别相关,并提出了纤溶酶原激活与恶性肿瘤之间的功能关系。在本文中,我们试图通过诱导纤溶酶原激活,在组织培养中汇合的静止细胞群体中诱导出类似转化的形态和生长。在无纤溶酶原的培养基中生长至汇合的未转化3T3细胞,通过添加尿激酶和纤溶酶原或含纤溶酶原的酸处理血清或纤溶酶来进行纤溶酶原激活。在这些条件下,先前排列良好的单层细胞变得紊乱,出现多层结构,细胞片层出现间断,并且细胞同时生长到显著更高的密度。去除含纤溶酶的培养基补充物后,细胞形态部分恢复正常。因此,当纤溶酶存在时,3T3细胞不会发生转化,但表现出类似转化的特征。因此,汇合状态下3T3细胞排列良好的单层形态和静止状态取决于纤溶酶原激活的缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6bb/2009998/5fe850b4ffb6/brjcancer00152-0109-a.jpg

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