Elizabeth Fragopoulou , Christos Iatrou , Smaragdi Antonopoulou , Xiong-Zhong Ruan , Ray L. Fernando , Stephen H. Powis , John F. Moorhead , Zac Varghese
{"title":"Platelet-activating factor (PAF) increase intracellular lipid accumulation by increasing both LDL and scavenger receptors in human mesangial cells","authors":"Elizabeth Fragopoulou , Christos Iatrou , Smaragdi Antonopoulou , Xiong-Zhong Ruan , Ray L. Fernando , Stephen H. Powis , John F. Moorhead , Zac Varghese","doi":"10.1016/j.lab.2006.01.004","DOIUrl":null,"url":null,"abstract":"<div><p>Intra- and extracellular lipid accumulation and the production of inflammatory mediators by renal and accessory cells may play an important role in the initiation and progression of these lesions. Platelet activating factor (PAF) is a biologically active phospholipid that is produced by various cells upon activation by different stimuli. It has been suggested that PAF plays a role in atherogenesis, and several studies indicated its participation in the pathogenesis of renal diseases. The aim of this study is to investigate the role of PAF on intracellular lipid accumulation and gene regulation of lipoprotein receptors in human mesangial cells (HMCs). A human mesangial cell line (HMC) was used to study the effects of PAF on foam cell formation by Oil red O staining and on the expression of LDLr, SR-AI, and PAF-R mRNA using RT-PCR. Native LDL caused foam cell formation in HMC in the presence of PAF. PAF enhanced LDLr expression and overrode LDL receptor suppression induced by a high concentration of LDL. Moreover, it enhanced SR-AI expression. PAF also caused increase in PAF-R expression. The above data suggest that PAF enhances its own receptor expression and then increases lipid accumulation by dysregulating LDL receptor regulation and inducing scavenger receptor expression in HMCs. These results suggest that PAF has a potential role in lipid mediated renal injury.</p></div>","PeriodicalId":16273,"journal":{"name":"Journal of Laboratory and Clinical Medicine","volume":"147 6","pages":"Pages 281-289"},"PeriodicalIF":0.0000,"publicationDate":"2006-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.lab.2006.01.004","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Laboratory and Clinical Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002221430600059X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10
Abstract
Intra- and extracellular lipid accumulation and the production of inflammatory mediators by renal and accessory cells may play an important role in the initiation and progression of these lesions. Platelet activating factor (PAF) is a biologically active phospholipid that is produced by various cells upon activation by different stimuli. It has been suggested that PAF plays a role in atherogenesis, and several studies indicated its participation in the pathogenesis of renal diseases. The aim of this study is to investigate the role of PAF on intracellular lipid accumulation and gene regulation of lipoprotein receptors in human mesangial cells (HMCs). A human mesangial cell line (HMC) was used to study the effects of PAF on foam cell formation by Oil red O staining and on the expression of LDLr, SR-AI, and PAF-R mRNA using RT-PCR. Native LDL caused foam cell formation in HMC in the presence of PAF. PAF enhanced LDLr expression and overrode LDL receptor suppression induced by a high concentration of LDL. Moreover, it enhanced SR-AI expression. PAF also caused increase in PAF-R expression. The above data suggest that PAF enhances its own receptor expression and then increases lipid accumulation by dysregulating LDL receptor regulation and inducing scavenger receptor expression in HMCs. These results suggest that PAF has a potential role in lipid mediated renal injury.
细胞内和细胞外脂质积累以及肾细胞和副细胞炎症介质的产生可能在这些病变的发生和发展中起重要作用。血小板活化因子(PAF)是一种具有生物活性的磷脂,由各种细胞在不同刺激下活化产生。已有研究表明PAF在动脉粥样硬化中起作用,一些研究表明它参与肾脏疾病的发病机制。本研究旨在探讨PAF在人系膜细胞(HMCs)细胞内脂质积累和脂蛋白受体基因调控中的作用。采用油红O染色法研究PAF对人肾小球系(HMC)泡沫细胞形成的影响,RT-PCR法研究PAF对LDLr、SR-AI和PAF- r mRNA表达的影响。在PAF存在的情况下,天然LDL引起HMC中的泡沫细胞形成。PAF增强了LDLr的表达,并覆盖了高浓度LDL诱导的LDL受体抑制。同时增强SR-AI的表达。PAF也引起PAF- r表达升高。上述数据表明,PAF通过失调LDL受体的调节,诱导清道夫受体的表达,在hmc中增强其自身受体的表达,进而增加脂质积累。这些结果表明PAF在脂质介导的肾损伤中具有潜在的作用。