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糖皮质激素抑制外周CD4+淋巴细胞的CD40配体表达。

Glucocorticoids inhibit CD40 ligand expression of peripheral CD4+ lymphocytes.

作者信息

Bischof F, Melms A

机构信息

Department of Neurology, Eberhardt Karls University, Tübingen, Germany.

出版信息

Cell Immunol. 1998 Jul 10;187(1):38-44. doi: 10.1006/cimm.1998.1308.

Abstract

The ligand for CD40 (CD40L) is a type II transmembrane glycoprotein that belongs to the tumor necrosis factor superfamily. CD40L expression on peripheral CD4+ cells is increased upon activation and delivers signals to B lymphocytes which constitutively express CD40. We show that dexamethasone in vitro inhibits CD40L expression in a dose-dependent manner in concentrations ranging from 0.1 to 1 mg/mL. Semiquantitative analysis of CD40L mRNA by RT-PCR revealed that this effect was due to inhibition of CD40L transcription. The inhibitory effect of dexamethasone on CD40L expression was reversible and not due to affection of cell viability. Lymphocytes which have been exposed to dexamethasone in vitro retained the ability to express CD40L after incubation in medium alone for 48 h. Dexamethasone also inhibited PMA/ionomycin induced IL-2 and IFN-gamma production but not CD25 and CD69 expression. Glucocorticoids may exert their immunosuppressive effect in part by suppression of CD40L. Regulation of CD40L expression is steroid sensitive and may be similar or in part identical with IL-2 and IFN-gamma regulation.

摘要

CD40的配体(CD40L)是一种II型跨膜糖蛋白,属于肿瘤坏死因子超家族。外周CD4 +细胞上的CD40L表达在激活后增加,并向组成性表达CD40的B淋巴细胞传递信号。我们发现,地塞米松在体外以剂量依赖的方式抑制CD40L的表达,浓度范围为0.1至1 mg/mL。通过RT-PCR对CD40L mRNA进行半定量分析表明,这种作用是由于抑制了CD40L的转录。地塞米松对CD40L表达的抑制作用是可逆的,且不是由于影响细胞活力。在体外暴露于地塞米松的淋巴细胞在单独培养基中孵育48小时后仍保留表达CD40L的能力。地塞米松还抑制PMA/离子霉素诱导的IL-2和IFN-γ产生,但不抑制CD25和CD69表达。糖皮质激素可能部分通过抑制CD40L发挥其免疫抑制作用。CD40L表达的调节对类固醇敏感,可能与IL-2和IFN-γ调节相似或部分相同。

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