Dalloul A H, Arock M, Fourcade C, Béranger J Y, Jaffray P, Debré P, Mossalayi M D
Laboratoire d'Immunologie, Centre National de la Recherche Scientifique URA625, CHU Pitié-Salpêtrière, Paris, France.
J Clin Invest. 1992 Oct;90(4):1242-7. doi: 10.1172/JCI115986.
Human epidermal keratinocytes (EK) secrete factors able to sustain the proliferation of early myeloid cells and, in particular, the generation of basophils. This activity was previously attributed to IL-3, although no definitive in situ demonstration of this cytokine was provided. In regard to the possible physiological relevance of these data, we investigated herein the nature of EK-derived factors responsible for basophil promotion. Our data show that EK-derived supernatants (EK-sup) contain IL-3 as well as soluble CD23 (sCD23), both known for their colony stimulating activity. Messenger RNA for IL-3 and CD23 were also detected in EK. Blocking experiments using specific neutralizing monoclonal antibodies (mAb) further indicate that EK-derived basophil promoting activity is mainly due to the presence of IL-3 and sCD23 in EK-sup. Furthermore, by contrast to IL-3, sCD23 secretion by EK is cortisone sensitive and highly enhanced by IL-4, suggesting distinct regulatory mechanisms for their production.
人表皮角质形成细胞(EK)分泌的因子能够维持早期髓样细胞的增殖,尤其是嗜碱性粒细胞的生成。这种活性先前被归因于白细胞介素-3(IL-3),尽管没有提供该细胞因子的确切原位证明。关于这些数据可能的生理相关性,我们在此研究了负责促进嗜碱性粒细胞生成的EK衍生因子的性质。我们的数据表明,EK衍生的上清液(EK-sup)含有IL-3以及可溶性CD23(sCD23),二者均因其集落刺激活性而闻名。在EK中也检测到了IL-3和CD23的信使核糖核酸。使用特异性中和单克隆抗体(mAb)的阻断实验进一步表明,EK衍生的促进嗜碱性粒细胞生成的活性主要归因于EK-sup中存在IL-3和sCD23。此外,与IL-3不同,EK分泌的sCD23对可的松敏感,且被IL-4高度增强,这表明它们的产生存在不同的调节机制。