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引导组织再生后回收的附着于膜上的细胞的蛋白酶谱

Protease repertoires of cells adherent to membranes recovered after guided tissue regeneration.

作者信息

Wakabayashi R C, Wong F, Richards D W, Johnson P W

机构信息

Department of Stomatology, University of California San Francisco, USA.

出版信息

J Periodontal Res. 1996 Apr;31(3):171-80. doi: 10.1111/j.1600-0765.1996.tb00481.x.

Abstract

Guided tissue regeneration is a clinical procedure used to restore mineralized tissue that has been lost to periodontal disease or after tooth extraction. The procedure makes use of Gore-tex membranes or Gore-tex augmentation membranes (GTAM) to prevent migration of keratinocytes and gingival fibroblasts into healing wounds. To begin to characterize the regenerative cells associated with these membranes, human cells have been rescued from membranes retrieved after bone-inductive procedures. Cell lines were established from tissue adherent to Gore-tex membranes used to regenerate bone around periodontally compromised teeth, and from tissue adherent to GTAM used in edentulous ridge augmentation procedures or in conjunction with implant placement. Cell lines were screened for mineralized nodule formation in vitro prior to their subsequent analysis. All but one of the lines selected for this study formed mineralized nodules in vitro with cells from GTAM tending to form nodules more quickly than cells from Gore-tex. Zymograms and Western blots were used to compare protease profiles of these cells with those of human gingival fibroblasts, keratinocytes and periodontal ligament (PDL) cells. All cell types except for keratinocytes produced a 72 kD protease. In contrast, keratinocytes were the only cells that produced 92 kD gelatinase. In some cell lines, notably those removed from patients after short periods of regeneration, collagenase was the major protease detected on gelatin substrate gels. Some of these cell lines also produced additional proteases including a low molecular weight protease (30 kD) not seen in gingival fibroblasts, PDL cells or keratinocytes.

摘要

引导组织再生是一种临床操作,用于修复因牙周病或拔牙而丧失的矿化组织。该操作利用戈尔特斯膜或戈尔特斯增强膜(GTAM)来防止角质形成细胞和牙龈成纤维细胞迁移至愈合伤口。为了开始鉴定与这些膜相关的再生细胞,已从骨诱导操作后取出的膜中拯救出人类细胞。细胞系是从附着于用于在牙周受损牙齿周围再生骨的戈尔特斯膜的组织中建立的,以及从附着于用于无牙颌嵴增高手术或与种植体植入联合使用的GTAM的组织中建立的。在后续分析之前,对细胞系进行了体外矿化结节形成的筛选。本研究选择的细胞系中,除一个外,其他所有细胞系在体外均形成了矿化结节,且来自GTAM的细胞比来自戈尔特斯膜的细胞更倾向于更快地形成结节。酶谱分析和蛋白质免疫印迹法用于比较这些细胞与人类牙龈成纤维细胞、角质形成细胞和牙周膜(PDL)细胞的蛋白酶谱。除角质形成细胞外,所有细胞类型均产生一种72 kD的蛋白酶。相反,角质形成细胞是唯一产生92 kD明胶酶的细胞。在一些细胞系中,尤其是那些在短时间再生后从患者体内取出的细胞系,胶原酶是在明胶底物凝胶上检测到的主要蛋白酶。其中一些细胞系还产生了其他蛋白酶,包括一种在牙龈成纤维细胞、PDL细胞或角质形成细胞中未见到的低分子量蛋白酶(30 kD)。

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