Longmuir K J, Rossi M E
Department of Physiology and Biophysics, College of Medicine, University of California, Irvine 92717.
Biochim Biophys Acta. 1988 Jul 1;961(1):144-7. doi: 10.1016/0005-2760(88)90140-3.
Type II cells obtained from fetal rabbit lung tissue in culture were incubated with [14C]palmitic and [14C]stearic acids labeled at either the carboxyl or the terminal methyl groups. Significant chain shortening of [18-14C]stearic acid to radiolabeled palmitic acid was observed, with little chain shortening of palmitic acid to myristic acid. Incorporation of 14C into palmitic acid by beta-oxidation followed by de novo fatty acid biosynthesis was not detectable under the same experimental conditions. The palmitic acid supplied by chain shortening was preferentially incorporated into phosphatidylcholine instead of other lipids. Fatty acid chain-shortening activity in the type II cell appears to be capable of increasing the amount and relative proportion of palmitic acid available for phosphatidylcholine biosynthesis.
将从培养的胎兔肺组织中获得的II型细胞与在羧基或末端甲基标记的[14C]棕榈酸和[14C]硬脂酸一起孵育。观察到[18-14C]硬脂酸显著缩短为放射性标记的棕榈酸,而棕榈酸缩短为肉豆蔻酸的情况很少。在相同实验条件下,未检测到通过β-氧化将14C掺入棕榈酸,随后再进行脂肪酸从头生物合成。通过链缩短提供的棕榈酸优先掺入磷脂酰胆碱而不是其他脂质中。II型细胞中的脂肪酸链缩短活性似乎能够增加可用于磷脂酰胆碱生物合成的棕榈酸的量和相对比例。