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人牙龈成纤维细胞与牙周膜细胞特性的比较。

Comparison of the characteristics of human gingival fibroblasts and periodontal ligament cells.

作者信息

Ogata Y, Niisato N, Sakurai T, Furuyama S, Sugiya H

机构信息

Department of Periodontology, Nihon University School of Dentistry, Matsudo, Japan.

出版信息

J Periodontol. 1995 Dec;66(12):1025-31. doi: 10.1902/jop.1995.66.12.1025.

Abstract

To elucidate the characteristics of human periodontal ligament cells, we compared these cells with gingival fibroblasts isolated from the periodontal tissues of female human subjects. Human periodontal ligament (HPDL) cells had a sharper spindle shape and exhibited a higher growth rate than human gingival fibroblasts (HGF). HPDL cells had a high level of alkaline phosphatase (ALPase) activity, whereas HGF had a low level of such activity. Northern blot analysis demonstrated that HPDL cells produced ALPase mRNA. Decorin and biglycan mRNA were detected in both HPDL cells and HGF, whereas osteocalcin and bone sialoprotein mRNA was not detected in either cells. Both HPDL cells and HGF responded to prostaglandin E2 (PGE2) and isoproterenol, and produced cyclic AMP (cAMP), but did not respond to human 1-34 parathyroid hormone (PTH). Intracellular Ca2+ ([Ca2+]i) was measured in HPDL cells and HGF, using Fura 2-AM. Bradykinin (BK) and histamine (HIS), which are major chemical mediators, caused a transient rise of [Ca2+]i in the presence of extracellular Ca2+. In HGF, but not HPDL cells, HIS induced a biphasic transient peak in [Ca2+]i. BK and HIS increased PGE2 release in both HPDL cells and HGF. However, HGF released a larger amount of PGE2 than HPDL cells. These results demonstrate that HPDL cells have quite different characteristics from HGF. HPDL cells proliferate at a higher rate than HGF, show higher levels of cAMP production and greater ALPase activity, and respond in a different fashion to chemical mediators (BK and HIS) compared with HGF.

摘要

为阐明人牙周膜细胞的特性,我们将这些细胞与从女性人类受试者牙周组织分离出的牙龈成纤维细胞进行了比较。人牙周膜(HPDL)细胞呈更细长的纺锤形,且比人牙龈成纤维细胞(HGF)具有更高的生长速率。HPDL细胞具有高水平的碱性磷酸酶(ALPase)活性,而HGF的这种活性水平较低。Northern印迹分析表明HPDL细胞产生ALPase mRNA。在HPDL细胞和HGF中均检测到核心蛋白聚糖和双糖链蛋白聚糖mRNA,而在这两种细胞中均未检测到骨钙素和骨唾液蛋白mRNA。HPDL细胞和HGF均对前列腺素E2(PGE2)和异丙肾上腺素产生反应,并产生环磷酸腺苷(cAMP),但对人1-34甲状旁腺激素(PTH)无反应。使用Fura 2-AM在HPDL细胞和HGF中测量细胞内Ca2+([Ca2+]i)。缓激肽(BK)和组胺(HIS)是主要的化学介质,在细胞外Ca2+存在的情况下会导致[Ca2+]i短暂升高。在HGF中,而非HPDL细胞中,HIS诱导[Ca2+]i出现双相瞬态峰值。BK和HIS均增加HPDL细胞和HGF中PGE2的释放。然而,HGF释放的PGE2量比HPDL细胞多。这些结果表明HPDL细胞与HGF具有相当不同的特性。HPDL细胞比HGF增殖速率更高,显示出更高水平的cAMP产生和更大的ALPase活性,并且与HGF相比,对化学介质(BK和HIS)的反应方式不同。

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