Dell Kerstin, Böhler Torsten, Gaedeke Jens, Budde Klemens, Neumayer Hans-Hellmut, Waiser Johannes
Department of Internal Medicine-Nephrology, University Hospital Charité, Campus Mitte, Humboldt-University, Schumannstrasse 20/21, 10117 Berlin, Germany.
Cytokine. 2003 Jun 21;22(6):189-93. doi: 10.1016/s1043-4666(03)00151-0.
Transforming growth factor-beta1 (TGF-beta1) plays a major role in cyclosporine A (CsA) induced glomerulosclerosis. We have recently shown that CsA up-regulates the expression of TGF-beta1 and its receptors type I (TbetaR-I) and type II (TbetaR-II) in rat mesangial cells (MCs). Prostaglandins of the E series (PGEs) are known to exert substantial anti-fibrotic effects. Here, we assessed the effect of PGE1 on CsA induced up-regulation of TGF-beta1, TbetaR-I, TbetaR-II and related matrix production in MCs. Co-incubation with PGE1 reduced CsA induced up-regulation of TGF-beta1 and TbetaR-II at the mRNA and protein level. Alike, PGE1 reduced TbetaR-I protein expression, which is posttranscriptionally up-regulated by CsA. Whereas a low PGE(1) concentration decreased CsA induced production of fibronectin (FN) and plasminogen activator inhibitor type-1 (PAI-1), a higher PGE1 concentration did not change FN production, but further increased PAI-1 production. In vivo studies will show, whether treatment with PGE1 analogues will be useful in preventing CsA induced glomerulosclerosis.
转化生长因子-β1(TGF-β1)在环孢素A(CsA)诱导的肾小球硬化中起主要作用。我们最近发现,CsA可上调大鼠系膜细胞(MCs)中TGF-β1及其I型受体(TβR-I)和II型受体(TβR-II)的表达。已知E系列前列腺素(PGEs)具有显著的抗纤维化作用。在此,我们评估了PGE1对CsA诱导的MCs中TGF-β1、TβR-I、TβR-II上调及相关基质产生的影响。与PGE1共同孵育可在mRNA和蛋白质水平降低CsA诱导的TGF-β1和TβR-II上调。同样,PGE1降低了TβR-I蛋白表达,而TβR-I蛋白表达在转录后被CsA上调。低浓度PGE1可降低CsA诱导的纤连蛋白(FN)和纤溶酶原激活物抑制剂-1(PAI-1)产生,而高浓度PGE1不改变FN产生,但进一步增加PAI-1产生。体内研究将表明,用PGE1类似物治疗是否有助于预防CsA诱导的肾小球硬化。