Storogenko M, Pech-Amsellem M A, Kerdine S, Rousselet F, Pallardy M
Immunotoxicologie et Cancérogenèse, Faculté de Pharmacie Paris-Sud, Chatenay-Malabry, France.
Life Sci. 1997;60(17):1487-96. doi: 10.1016/s0024-3205(97)00100-8.
Cyclosporine A (CsA) is a widely used immunosuppressant which possesses significant side effects including nephrotoxicity and systemic arterial hypertension. In this work we evaluated the effects of CsA on human umbilical endothelial cell proliferation (HUVEC). Treatment of endothelial cells with CsA inhibited cell proliferation, and was correlated with an increase of interleukin-6 (IL-6) production and IL-6 mRNA expression. Addition of exogenous IL-6 also significantly altered cell proliferation. Furthermore, neutralization of endogenous IL-6 with a specific monoclonal antibody concomitantly with CsA treatment completely restored HUVEC proliferation. These results suggest that CsA-induced inhibition of HUVEC proliferation is mediated through an augmentation of IL-6 synthesis.
环孢素A(CsA)是一种广泛使用的免疫抑制剂,具有显著的副作用,包括肾毒性和系统性动脉高血压。在这项研究中,我们评估了CsA对人脐静脉内皮细胞增殖(HUVEC)的影响。用CsA处理内皮细胞会抑制细胞增殖,并与白细胞介素-6(IL-6)产生增加和IL-6 mRNA表达增加相关。添加外源性IL-6也显著改变了细胞增殖。此外,用特异性单克隆抗体中和内源性IL-6并同时进行CsA处理可完全恢复HUVEC增殖。这些结果表明,CsA诱导的HUVEC增殖抑制是通过增强IL-6合成介导的。