Lysophosphatidylcholine induces platelet-derived growth factor gene expression in a human mesangial cell line

Background. Oxidized low-density lipoprotein (oxLDL) has been considered important in the pathogenesis of progressive renal injury. Lysophosphatidylcholine (lysoPC) is a major phospholipid component of oxLDL. On the other hand, platelet-derived growth factor (PDGF) has also been implicated in proliferative disease of the kidney. This study investigated the difference in the potential of PC and lysoPC to induce DNA synthesis and PDGF gene expression in a human glomerular mesangial cell line (HMCL). Methods. DNA synthesis in HMCL was measured by [H-3] thymidine incorporation. The mRNA expression levels of the PDGF A chain and B chain genes were measured using reverse transcription-polymerase chain reaction. Results. LysoPC treatment up-regulated the [H-3] thymidine incorporation level in a dose-dependent fashion. The [H-3] thymidine incorporation level in HMCL coincubated with lysoPC started to increase after 4 hours of treatment, peaked at 24 hours, and decreased thereafter. The level in HMCL incubated with 100 mu M Of lysoPC (palmitoyl or stearoyl) increased to 7- or 10-fold of the control at peak time, respectively. However, PC treatment did not increase [H-3] thymidine incorporation in HMCL. PC treatment did not induce mRNA expression of either PDGF A or B chain genes. LysoPC did not induce PDGF A chain mRNA expression either. The only B chain mRNA expression was induced by lysoPC. The mRNA expression level in HMCL treated with 50 mu M lysoPC for two hours increased to 1.6-fold that of the control. Conclusion. LysoPC may induce DNA synthesis in a mesangial cell through the induction of PDGF BE as an autocrine and paracrine growth factor.