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地塞米松和细胞增殖对人黏膜正常及恶性细胞中基质金属蛋白酶表达的影响

Effects of dexamethasone and cell proliferation on the expression of matrix metalloproteinases in human mucosal normal and malignant cells.

作者信息

Kylmäniemi M, Oikarinen A, Oikarinen K, Salo T

机构信息

Institute of Dentistry, University of Oulu, Finland.

出版信息

J Dent Res. 1996 Mar;75(3):919-26. doi: 10.1177/00220345960750030901.

Abstract

Matrix metalloproteinases (MMPs) have an important role in many biological processes, such as tumor metastasis, wound healing, and inflammation. The regulation of MMPs and their inhibitors is still not known in detail, and the aim of this study was to investigate the effects of dexamethasone on cultured oral benign and malignant cell lines. The expression of MMPs in culture was studied: in four gingival (GF) and one periodontal ligament (PLF) fibroblast cell lines; in six gingival keratinocyte (GK) cell lines; and in UNR (UNR-108, rat osteogenic sarcoma) and SCC (SCC-25, human tongue squamous cell carcinoma) cell lines. In the GFs, PLFs, and UNR cells, only MMP-2 (72 kDa gelatinase) was detected by gelatin zymography, while in most of the GK cell lines only MMP-9 (92 kDa gelatinase) was observed. In confluent SCC cultures, both MMP-2 and MMP-9 were found, while only MMP-2 was seen in rapidly growing SCC cells, demonstrating that cell proliferation influenced gelatinase expression in these cells, but not in the other cell lines studied. Dexamethasone at concentrations of 10(-5) mol/L and 10(-7) mol/L decreased the production of gelatinases in the GFs and PLFs, but not in the GKs, SCC, or UNR cells. The expression of mRNAs for matrix metalloproteinases (MMP-1 [interstitial collagenase] and MMP-2) and their inhibitors (TIMP-1 and TIMP-2) was also studied in the GFs by Northern hybridization. Dexamethasone markedly decreased the amount of MMP-2 mRNA in the GFs. The mRNA level of MMP-1 decreased even more in the same GFs. The mRNA levels for TIMP-1 and TIMP-2 were also decreased by dexamethasone in the GFs. Cell proliferation influenced the degree to which dexamethasone decreased these mRNA levels. The results indicate that glucocorticoids decrease the levels of MMPs and TIMPs in oral fibroblastic cells, whereas they do not appear to affect the production of gelatinases in either normal or malignant oral epithelial cell lines.

摘要

基质金属蛋白酶(MMPs)在许多生物学过程中发挥着重要作用,如肿瘤转移、伤口愈合和炎症。MMPs及其抑制剂的调控机制仍未完全明确,本研究旨在探讨地塞米松对培养的口腔良性和恶性细胞系的影响。研究了培养物中MMPs的表达情况:在四种牙龈(GF)和成纤维细胞系以及一种牙周膜(PLF)细胞系中;在六种牙龈角质形成细胞(GK)细胞系中;以及在UNR(UNR-108,大鼠骨肉瘤)和SCC(SCC-25,人舌鳞状细胞癌)细胞系中。在GF、PLF和UNR细胞中,通过明胶酶谱法仅检测到MMP-2(72 kDa明胶酶),而在大多数GK细胞系中仅观察到MMP-9(92 kDa明胶酶)。在汇合的SCC培养物中,同时发现了MMP-2和MMP-9,而在快速生长的SCC细胞中仅见到MMP-2,这表明细胞增殖影响了这些细胞中明胶酶的表达,但对所研究的其他细胞系没有影响。浓度为10^(-5) mol/L和10^(-7) mol/L的地塞米松降低了GF和PLF中明胶酶的产生,但对GK、SCC或UNR细胞没有影响。还通过Northern杂交研究了GF中基质金属蛋白酶(MMP-1[间质胶原酶]和MMP-2)及其抑制剂(TIMP-1和TIMP-2)的mRNA表达。地塞米松显著降低了GF中MMP-2 mRNA的量。在相同的GF中,MMP-1的mRNA水平下降得更多。地塞米松也降低了GF中TIMP-1和TIMP-2的mRNA水平。细胞增殖影响了地塞米松降低这些mRNA水平的程度。结果表明,糖皮质激素降低了口腔成纤维细胞中MMPs和TIMPs的水平,而它们似乎不影响正常或恶性口腔上皮细胞系中明胶酶的产生。

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