Mohamadzadeh M, Ariizumi K, Sugamura K, Bergstresser P R, Takashima A
Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235, USA.
Eur J Immunol. 1996 Jan;26(1):156-60. doi: 10.1002/eji.1830260124.
The common cytokine receptor gamma chain (gamma c) is an indispensable component of interleukin (IL)-2, IL-4, IL-7, IL-9, and IL-15 receptors, and its expression has been detected in several leukocyte populations, including T cells, B cells, monocytes, natural killer cells, and neutrophils. The purpose of this study was to determine whether gamma c receptors are expressed by dendritic cells (DC). Constitutive gamma c mRNA expression was observed by reverse transcription polymerase chain reaction and/or Northern blotting for: (a) Ia+ epidermal Langerhans cells (LC), (b) 4F7+ splenic DC, (c) granulocyte/macrophage colony-stimulated factor-propagated bone marrow-derived DC, and (d) the epidermal-derived DC line, XS52, which retains important functions of epidermal LC. Exposure of XS52 cells to recombinant IL-4 induced a rapid up-regulation of c-myc mRNA expression, and this IL-4-dependent signaling was blocked almost completely by anti-gamma c monoclonal antibody (mAb) TUGm2 in a soluble form. Moreover, c-myc up-regulation was inducible in XS52 cells by the same mAb in an immobilized form. These results imply that molecules recognized by this antibody (i.e. gamma c receptors) are expressed on XS52 cell surfaces. We thus conclude that DC express functional gamma c receptors, which then mediate cytokine-dependent regulation of DC functions.
共同细胞因子受体γ链(γc)是白细胞介素(IL)-2、IL-4、IL-7、IL-9和IL-15受体不可或缺的组成部分,并且已在包括T细胞、B细胞、单核细胞、自然杀伤细胞和中性粒细胞在内的多种白细胞群体中检测到其表达。本研究的目的是确定γc受体是否由树突状细胞(DC)表达。通过逆转录聚合酶链反应和/或Northern印迹观察到以下细胞中γc mRNA的组成性表达:(a)Ia + 表皮朗格汉斯细胞(LC),(b)4F7 + 脾DC,(c)粒细胞/巨噬细胞集落刺激因子扩增的骨髓来源的DC,以及(d)表皮来源的DC系XS52,其保留了表皮LC的重要功能。将XS52细胞暴露于重组IL-4可诱导c-myc mRNA表达快速上调,并且这种IL-4依赖性信号传导几乎完全被可溶性形式的抗γc单克隆抗体(mAb)TUGm2阻断。此外,固定形式的相同mAb可诱导XS52细胞中c-myc上调。这些结果表明该抗体识别的分子(即γc受体)在XS52细胞表面表达。因此,我们得出结论,DC表达功能性γc受体,其随后介导细胞因子依赖性的DC功能调节。