Fig. 1From: Fatty acids abrogate the growth-suppressive effects induced by inhibition of cholesterol flux in pancreatic cancer cellsMajor lipid classes and LD storage in HPDE and PDAC cells. A. TLC images showing major lipid classes in HPDE and PDAC cells cultured in DMEM supplemented with 10% FBS. Band intensity was quantified relative to total lipids of the same sample. Lipid standard mixture (Std.) contains 1 µg for each lipid; B. LD storage in HPDE and PDAC cells cultured in DMEM supplemented with 10% FBS. Cells were stained with BODIPY 493/503 to visualize LDs (green), Phallodin-CF568 to visualize cytoskeleton (red), and Hoechst 33,342 to visualize nuclei (blue); C-D. Quantification of LD content in HPDE and PDAC cells cultured in DMEM, supplemented with 10% or 1% FBS, or 1% FBS plus OA (150 µM), or OA (50 µM) and FC (50 µM). Results are presented as means ± SD (n = 3) in A and means ± 95% confidence interval (n = 30–35 images) in C and D. *p < 0.05 comparing PDAC cells with HPDE cells; #p < 0.05 comparing control with OA or OA + FC. CE cholesteryl ester, DAG diacylglycerol, FBS fetal bovine serum, FC free cholesterol, FFA free fatty acids, LD lipid droplet, MAG monoacylglycerol, OA oleic acid, PL phospholipids, TAG triacylglycerol, TLC thin-layer chromatographyBack to article page