Figure 1.
Effect of growth factors on the synthesis of PLs by human osteoarthritic FLS as modulated by inhibitors of cell signalling pathways. (A,B) Effect of TGF-β1 as modulated by TGF-βR1 inhibitor. The percentages of labelled PL classes from the total corresponding labelled and unlabelled PL classes are presented. FLS were first pre-treated for 30 min with 10 µM TGF-βR1 kinase inhibitor SB431542, and then treated with 10 ng/ml TGF-β1 for 16 hours in the presence of stable isotope-labelled PL precursors. (C,D) Effect of IGF-1 on PL biosynthesis as modulated by inhibitors of PI3K and ERK. The percentages of labelled PL classes from the total corresponding labelled and unlabelled PL classes are presented. FLS were first pre-treated for 30 min with 10 µM LY294002 inhibitor (PI3K) or 1 µM SCH772984 inhibitor (ERK), and then treated with 100 ng/ml IGF-1 for 16 hours in the presence of stable isotope-labelled PL precursors. Data are expressed as means ± SDs (n = 5). *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001. PC = phosphatidylcholines; PE = phosphatidylethanolamines; PE P = phosphatidylethanolamine-based plasmalogens; SM = sphingomyelins; LPC = lysophosphatidylcholines.