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基底膜成分和肺成纤维细胞对仓鼠纤维肉瘤中IV型胶原酶和纤溶酶原激活剂的调节作用。

Modulation of type IV collagenase and plasminogen activator in a hamster fibrosarcoma by basement membrane components and lung fibroblasts.

作者信息

Teale D M, Khidair I A, Potter C W, Rees R C

机构信息

Department of Virology, University of Sheffield Medical School, UK.

出版信息

Br J Cancer. 1988 May;57(5):475-80. doi: 10.1038/bjc.1988.110.

Abstract

The effect of basement membrane components (laminin, fibronectin and type IV collagen) and lung fibroblasts on type IV collagenase and plasminogen activator activity was investigated in a primary HSV-2-induced hamster fibrosarcoma, and its in vivo derived sublines and in vitro derived clones of varying metastatic potential. Fibronectin and type IV collagen were ineffective at influencing the expression of either type IV collagenase or plasminogen activator activity. Laminin, however, at concentrations of 1-10 micrograms ml-1 added to the serum-free culture supernatants, increased the release of type IV collagenase by up to 100% for the parental cell line. Three highly metastatic sublines (two from in vivo origin and one from in vitro cloning) showed increases of up to 300%. Non-metastatic sublines (two from in vivo origin and one from in vitro cloning), however, showed no increase in type IV collagenase activity. Plasminogen activator release from either the parental line cell or its metastatic sublines and clones, was unaffected by the addition of laminin. Addition of tumour cells to lung fibroblast monolayers resulted in an increased expression of PA activity in the supernatant, whilst type IV collagenase activity was reduced.

摘要

在原发性单纯疱疹病毒2型诱导的仓鼠纤维肉瘤及其体内衍生的亚系和体外衍生的具有不同转移潜能的克隆中,研究了基底膜成分(层粘连蛋白、纤连蛋白和IV型胶原)和肺成纤维细胞对IV型胶原酶和纤溶酶原激活物活性的影响。纤连蛋白和IV型胶原对IV型胶原酶或纤溶酶原激活物活性的表达没有影响。然而,将浓度为1 - 10微克/毫升的层粘连蛋白添加到无血清培养上清液中,亲代细胞系的IV型胶原酶释放量增加了高达100%。三个高转移性亚系(两个来自体内,一个来自体外克隆)显示增加了高达300%。然而,非转移性亚系(两个来自体内,一个来自体外克隆)的IV型胶原酶活性没有增加。向肺成纤维细胞单层中添加肿瘤细胞导致上清液中PA活性表达增加,而IV型胶原酶活性降低。

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Biosynthesis of type IV procollagens.IV型前胶原的生物合成
Biochemistry. 1980 Apr 1;19(7):1284-9. doi: 10.1021/bi00548a003.

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