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皮质类固醇可诱导人真皮微血管内皮细胞增殖,但在体外不影响肿瘤坏死因子或白细胞介素-1β诱导的细胞间黏附分子-1表达。

Corticosteroids induce proliferation but do not influence TNF- or IL-1 beta-induced ICAM-1 expression of human dermal microvascular endothelial cells in vitro.

作者信息

Hettmannsperger U, Tenorio S, Orfanos C E, Detmar M

机构信息

Department of Dermatology, University Medical Center Steglitz, Free University of Berlin, Germany.

出版信息

Arch Dermatol Res. 1993;285(6):347-51. doi: 10.1007/BF00371835.

Abstract

The effects of hydrocortisone, dexamethasone, betamethasone 17-valerate and clobetasol propionate at concentrations of 10(-5)-10(-12) M on the proliferation of human dermal microvascular endothelial cells (HDMEC) were studied in vitro. In addition, confluent HDMEC were treated with TNF (1000 U/ml) or IL-1 beta (1000 U/ml) alone or in combination with the corticosteroids (10(-5) M, 10(-6) M) for 24 h, and cytokine-induced expression of intercellular adhesion molecule-1 (ICAM-1) was assessed by immunocytochemistry. Controls were treated either with growth medium or with the corticosteroids alone. All tested corticosteroids stimulated HDMEC growth after 4 and 6 days of treatment in a dose-dependent manner, as assessed by 3H-thymidine incorporation and the 4-methyl-umbelliferyl heptanoate (MUH) assay. The minimal effective concentration was 10(-9) M for hydrocortisone, 10(-10) M for dexamethasone and betamethasone, and 10(-12) M for clobetasol. In untreated and in corticosteroid-treated cultures, less than 5% of the cells expressed ICAM-1. TNF and IL-1 beta were strong inducers of ICAM-1 expression on 74% and 82% of the cells, respectively. None of the tested corticosteroids significantly influenced cytokine-induced ICAM-1 expression, suggesting that the anti-inflammatory effects of corticosteroids are not related to ICAM-1 modulation on HDMEC.

摘要

体外研究了浓度为10^(-5)-10^(-12)M的氢化可的松、地塞米松、倍他米松17-戊酸酯和丙酸氯倍他索对人真皮微血管内皮细胞(HDMEC)增殖的影响。此外,将汇合的HDMEC单独或与皮质类固醇(10^(-5)M、10^(-6)M)联合用TNF(1000U/ml)或IL-1β(1000U/ml)处理24小时,并通过免疫细胞化学评估细胞因子诱导的细胞间粘附分子-1(ICAM-)的表达。对照组用生长培养基或单独用皮质类固醇处理。通过3H-胸腺嘧啶核苷掺入和4-甲基伞形酮庚酸酯(MUH)测定法评估,所有测试的皮质类固醇在处理4天和6天后均以剂量依赖性方式刺激HDMEC生长。氢化可的松的最小有效浓度为10^(-9)M,地塞米松和倍他米松为10^(-10)M,丙酸氯倍他索为10^(-12)M。在未处理和皮质类固醇处理的培养物中,不到5%的细胞表达ICAM-1。TNF和IL-1β分别是74%和82%的细胞上ICAM-1表达的强诱导剂。所测试的皮质类固醇均未显著影响细胞因子诱导的ICAM-1表达,这表明皮质类固醇的抗炎作用与HDMEC上的ICAM-1调节无关。

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