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环孢素A抑制角质形成细胞细胞因子基因的表达。

Cyclosporin A inhibits keratinocyte cytokine gene expression.

作者信息

Won Y H, Sauder D N, McKenzie R C

机构信息

Division of Dermatology, University of Toronto, Sunnybrook Health Science Centre, Ontario, Canada.

出版信息

Br J Dermatol. 1994 Mar;130(3):312-9. doi: 10.1111/j.1365-2133.1994.tb02926.x.

Abstract

The immunosuppressive peptide cyclosporin A (CyA) is an extremely effective therapy for severe recalcitrant psoriasis, although its mechanism of action is unknown. In this study, we examined the effect of CyA on keratinocyte growth and cytokine expression, and showed that CyA inhibits the growth of murine and human keratinocytes (KC) and KC cell lines. In addition, CyA inhibits the expression of cytokine genes in a dose-dependent fashion. After 2 days' incubation with 20 microM CyA, interleukin-1 alpha (IL-1 alpha), interleukin-1 beta (IL-1 beta), and interleukin 8 (IL-8) mRNA were decreased by 4-fold, 3.3-fold and 3.3-fold, respectively, in COLO-16, a keratinocyte cell line. IL-1 biological activity recovered from COLO-16 culture supernatants decreased to one-fifth of that of controls. In the murine KC cell line PAM 212, 10 microM CyA treatment for 2 days downregulated IL-1 alpha, tumour necrosis factor-alpha (TNF-alpha) and IL-1 receptor by 60%, but had no effect on the message for interleukin 3 (IL-3), granulocyte-macrophage colony-stimulating factor (GM-CSF), ornithine decarboxylase and beta-actin. Cells cultured for 5 days in the presence of CyA required much lower concentrations (2 microM) to achieve the same degree of inhibition of IL-1 alpha. Similar tissue concentrations of CyA have been reported in psoriatics undergoing CyA therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

免疫抑制肽环孢菌素A(CyA)是治疗严重顽固性银屑病的一种极其有效的疗法,尽管其作用机制尚不清楚。在本研究中,我们检测了CyA对角质形成细胞生长和细胞因子表达的影响,结果表明CyA可抑制小鼠和人角质形成细胞(KC)及KC细胞系的生长。此外,CyA以剂量依赖方式抑制细胞因子基因的表达。在角质形成细胞系COLO-16中,用20μM CyA孵育2天后,白细胞介素-1α(IL-1α)、白细胞介素-1β(IL-1β)和白细胞介素8(IL-8)的mRNA分别下降了4倍、3.3倍和3.3倍。从COLO-16培养上清液中回收的IL-1生物活性降至对照组的五分之一。在小鼠KC细胞系PAM 212中,用10μM CyA处理2天可使IL-1α、肿瘤坏死因子-α(TNF-α)和IL-1受体下调60%,但对白细胞介素3(IL-3)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)、鸟氨酸脱羧酶和β-肌动蛋白的信息没有影响。在CyA存在下培养5天的细胞达到相同程度的IL-1α抑制所需的浓度要低得多(2μM)。接受CyA治疗的银屑病患者体内也有类似的CyA组织浓度报道。(摘要截短于250字)

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