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四环素对UMR 106 - 01大鼠成骨细胞骨肉瘤细胞中胶原酶活性的影响。

The effect of tetracyclines on collagenase activity in UMR 106-01 rat osteoblastic osteosarcoma cells.

作者信息

Ramamurthy N S, Vernillo A T, Lee H M, Golub L M, Rifkin B R

机构信息

Department of Oral Medicine and Pathology, New York University College of Dentistry 10010.

出版信息

Res Commun Chem Pathol Pharmacol. 1990 Dec;70(3):323-35.

PMID:1965517
Abstract

Previous studies demonstrated that tetracyclines (TCs) inhibited Type I (interstitial) and Type IV collagenases from different mammalian sources, but there are no studies of TCs effect on osteoblast collagenase (C'ase). The present study assessed the effect of TCs on C'ase activity from osteosarcoma cells. Semiconfluent UMR 106-01 cells were treated with minocycline or chemically modified tetracycline (CMT) at 10 micrograms/ml in the presence or absence of bovine parathyroid hormone, b-PTH-(1-34), at 10(-7)M for 24, 48, 72 and 96 hours. Media were collected at each time point and assayed following concentration, destruction of TIMP by reduction/alkylation, activation with p-aminophenylmercuric acetate (APMA), and incubation with 3H-methylated collagen substrate (approximately 100,000 dpm) at 27 degrees C for 18 hours. Collagenase activity from media was also analyzed by SDS-PAGE and fluorography. b-PTH appeared to stimulate C'ase 60-fold compared to controls; minocycline and CMT reduced PTH stimulation approximately 65% and 90%, respectively. Moreover, TCs incubated with partially purified osteoblastic collagenase directly, inhibited its activity in vitro as indicated by a lack of degradation to collagen alpha A chains. Therefore, TCs ability to inhibit bone resorption in organ culture, reported previously, may be due, in part, to reduced osteoblast collagenase activity.

摘要

以往研究表明,四环素(TCs)可抑制来自不同哺乳动物来源的I型(间质)和IV型胶原酶,但尚无关于TCs对成骨细胞胶原酶(C'ase)作用的研究。本研究评估了TCs对骨肉瘤细胞C'ase活性的影响。将半汇合的UMR 106 - 01细胞在存在或不存在10(-7)M牛甲状旁腺激素b - PTH-(1 - 34)的情况下,用10微克/毫升米诺环素或化学修饰四环素(CMT)处理24、48、72和96小时。在每个时间点收集培养基,经浓缩、通过还原/烷基化破坏组织金属蛋白酶抑制因子(TIMP)、用对氨基苯基汞乙酸盐(APMA)激活,并在27℃与3H - 甲基化胶原底物(约100,000 dpm)孵育18小时后进行检测。培养基中的胶原酶活性也通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)和荧光显影进行分析。与对照组相比,b - PTH似乎可使C'ase活性刺激60倍;米诺环素和CMT分别使PTH刺激降低约65%和90%。此外,直接与部分纯化的成骨细胞胶原酶一起孵育的TCs在体外抑制了其活性,这表现为对胶原αA链缺乏降解。因此,先前报道的TCs在器官培养中抑制骨吸收的能力可能部分归因于成骨细胞胶原酶活性的降低。

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