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肿瘤大鼠上皮细胞产生的胶原酶:分泌调节、分子量特征及纯化

The collagenase produced by neoplastic rat epithelial cells: modulation of secretion, molecular weight characteristics, and purification.

作者信息

Lyons J G, Nethery A, O'Grady R L, Harrop P J

机构信息

Department of Pathology, University of Sydney, NSW, Australia.

出版信息

Matrix. 1989 Jan;9(1):7-16. doi: 10.1016/s0934-8832(89)80012-5.

Abstract

The modulation of the production of collagenase by an epithelial cell line derived from a spontaneously arising rat mammary carcinoma has been studied. The cell line, BC1, was grown permanently under defined serum-free conditions, thus avoiding the poorly characterized and variable effects of serum on collagenase production. Piperazine-N,N'-bis-(2-ethanesulfonic acid) (Pipes), retinoic acid and cytochalasin B all stimulated collagenase secretion, while dexamethasone inhibited it and progesterone, prolactin, prostaglandin E2, and estrogen had no effect. This profile of response to exogenous compounds was distinct from that of cells of mesenchymal origin and from human keratinocytes. For the production of large quantities of collagenase, culture medium was supplemented with Pipes (30 mM, pH 6.8), and retinoic acid (1 microM, on alternate feeds). The collagenase secreted by BC1 cells grown under these conditions was latent and had a molecular mass of 59 kDa. Treatment of the 59 kDa form with trypsin or APMA caused a progressive decrease in molecular mass via 54 kDa and 52 kDa intermediates, to a 48 kDa form. This form was purified to electrophoretic homogeneity by heparin-Sepharose, zinc-chelate-Sepharose, and Sephacryl S-200 chromatography. Five milligrams of purified collagenase were recovered per litre of culture medium.

摘要

对源自自发产生的大鼠乳腺癌的上皮细胞系产生胶原酶的调节作用进行了研究。该细胞系BC1在特定的无血清条件下永久培养,从而避免了血清对胶原酶产生的特征不明确且多变的影响。哌嗪-N,N'-双(2-乙磺酸)(Pipes)、视黄酸和细胞松弛素B均刺激胶原酶分泌,而地塞米松抑制其分泌,孕酮、催乳素、前列腺素E2和雌激素则无影响。这种对外源化合物的反应模式与间充质来源的细胞以及人角质形成细胞不同。为了大量产生胶原酶,在培养基中添加了Pipes(30 mM,pH 6.8)和视黄酸(1 microM,交替添加)。在这些条件下生长的BC1细胞分泌的胶原酶是无活性的,分子量为59 kDa。用胰蛋白酶或APMA处理59 kDa形式的胶原酶会导致分子量通过54 kDa和52 kDa中间体逐渐降低,直至形成48 kDa形式。通过肝素-琼脂糖、锌螯合-琼脂糖和Sephacryl S-200色谱法将这种形式纯化至电泳纯。每升培养基可回收5毫克纯化的胶原酶。

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