Biosynthesis and Metabolism of 2-Iodohexadecanal in Cultured Dog Thyroid Cells

2-Iodohexadecanal (2-IHDA) is a major thyroid iodolipid. It mimics the main regulatory effects of iodide on thyroid metabolism: inhibition of H 2 O 2 production and of adenylyl cyclase. The biosynthesis of 2-IHDA and its metabolism have been investigated in cultured dog thyroid cells maintained in a differentiated state by forskolin. Incubation of these cells with [9,10- 3 H]hexadecan-1-ol or [9,10- 3 H]palmitic acid labeled several phospholipids, but [9,10- 3 H]hexadecan-1-ol was selectively incorporated into plasmenylethanolamine. In the presence of an exogenous H 2 O 2 generating system (glucose oxidase), iodide induced the production of [9,10- 3 H]2-IHDA from [9,10- 3 H]hexadecan-1-ol-labeled cells but not from [9,10- 3 H]palmitic acid-labeled cells. 2-IHDA was also generated during the lactoperoxidase-catalyzed iodination of brain and heart plasmalogens, and of ethyl hexadec-1-enyl ether, a synthetic vinyl ether-containing compound. Taken together, these results show that thyroid 2-IHDA is derived from plasmenylethanolamine via an attack of reactive iodine on the vinyl ether group. 2-Iodohexadecan-1-ol (2-IHDO) was also detected in these studies; it was formed later than 2-IHDA, and thyroid cells converted exogenous 2-IHDA into 2-IHDO in a time-dependent way. The ratio of 2-IHDO/2-IHDA increased with H 2 O 2 production and decreased as a function of iodide concentration. An aldehyde-reducing activity was detected in subcellular fractions of the horse thyroid. No formation of 2-iodohexadecanoic acid could be detected. Reduction into the biologically inactive 2-IHDO is thus a major metabolic pathway of 2-IHDA in dog thyrocytes.