posted on 2012-02-14, 01:12authored byLars Kuerschner, Doris Richter, Hans Kristian Hannibal-Bach, Anne Gaebler, Andrej Shevchenko, Christer S. Ejsing, Christoph Thiele
Cells were incubated with 50 µM of c16:5-alkyl-glycerol (A, C, D) or c20:5-alkyl-glycerol (B) for different pulse times (A & B), 2 h (C) or 0.5 h (D). Cellular lipids were extracted and analyzed by TLC for fluorescent metabolites, which were identified by comigrating lipid standards (A & B). Living cells were imaged using two-photon-excitation microscopy (C) or epifluorescence microscopy (D). Merged color images show ether lipids in green and LDs, mitochondria, or lysosomes stained by LD540, Mitotracker, or Lysotracker, respectively, in red (D). Bars, 20 µm. ori, origin of application.