Vargha Regina, Bender Thorsten O, Riesenhuber Andrea, Endemann Michaela, Kratochwill Klaus, Aufricht Christoph
Kinderdialyse, Department of Pediatrics, AKH Vienna, Medical University of Vienna, Vienna, Austria.
Nephrol Dial Transplant. 2008 Nov;23(11):3494-500. doi: 10.1093/ndt/gfn353. Epub 2008 Jun 24.
During peritoneal dialysis, mesothelial cells undergo epithelial-to-mesenchymal transition (EMT), resulting in markedly altered protein expression. This potentially includes heat-shock proteins (HSP), the main effectors of cellular repair. Thus, chronic cellular processes, such as EMT, may influence acute stress responses and thus survival of mesothelial cells following non-lethal injury upon exposure to peritoneal dialysis fluid (PDF).
In this study, we investigated the effects of EMT on acute stress responses and cytoresistance in human peritoneal mesothelial cells. In vivo EMT was defined as a fibroblast-like growth pattern in mesothelial cells grown from peritoneal effluents, and in vitro EMT was induced by TGF-beta1 in mesothelial cells grown from omental tissue. Morphologic EMT was validated by western blot analysis of EMT marker proteins (ezrin, alpha-SMA). Expression of HSP and cellular survival was evaluated in a simple in vitro PDF exposure model.
In vivo and in vitro EMT resulted in marked effects on phenotypes of mesothelial cells, associated with differential HSP expression. In vivo 'chronic' EMT resulted in lower expression of HSP-27 and HSP-72, whereas in vitro 'acute' EMT was associated with increased HSP-27 and decreased HSP-72 expression. Following PDF exposure, there were no effects of in vivo EMT on the stress induction of HSP, and survival of epithelial versus fibroblast-like phenotypes was comparable. The non-stressful induction of HSP-27 following TGF-beta1 pretreatment resulted in the attenuated stress induction of HSP, and in improved survival in following PDF exposure.
Taken together, this study confirms that mesothelial cells are not 'unchanged' or 'static targets' during the clinical course of PD treatment. The cellular processes during EMT play a complex role in acute cellular stress response and cytoresistance of mesothelial cells. Sequential analysis at different stages of EMT will be essential to provide more insights on cytoprotective cellular processes in in vitro and in vivo models of PD.
在腹膜透析过程中,间皮细胞经历上皮-间质转化(EMT),导致蛋白质表达显著改变。这可能包括热休克蛋白(HSP),即细胞修复的主要效应因子。因此,诸如EMT等慢性细胞过程可能会影响急性应激反应,进而影响间皮细胞在接触腹膜透析液(PDF)后遭受非致命损伤时的存活。
在本研究中,我们调查了EMT对人腹膜间皮细胞急性应激反应和细胞抗性的影响。体内EMT定义为从腹膜流出物中生长的间皮细胞呈现的成纤维细胞样生长模式,体外EMT则通过转化生长因子-β1(TGF-β1)诱导大网膜组织来源的间皮细胞产生。通过对EMT标志物蛋白(埃兹蛋白、α-平滑肌肌动蛋白)进行蛋白质印迹分析来验证形态学上的EMT。在一个简单的体外PDF暴露模型中评估HSP的表达和细胞存活情况。
体内和体外EMT对间皮细胞表型产生显著影响,与不同的HSP表达相关。体内“慢性”EMT导致HSP-27和HSP-72表达降低,而体外“急性”EMT则与HSP-27表达增加和HSP-72表达降低相关。在PDF暴露后,体内EMT对HSP的应激诱导没有影响,上皮样和成纤维细胞样表型的存活情况相当。TGF-β1预处理后对HSP-27的非应激诱导导致HSP的应激诱导减弱,并改善了PDF暴露后的存活情况。
综上所述,本研究证实间皮细胞在腹膜透析治疗的临床过程中并非“不变”或“静态靶点”。EMT过程中的细胞过程在间皮细胞的急性细胞应激反应和细胞抗性中发挥复杂作用。对EMT不同阶段进行顺序分析对于深入了解腹膜透析体外和体内模型中的细胞保护过程至关重要。