Real-Time Tracking of BODIPY-C12 Long-Chain Fatty Acid in Human Term Placenta Reveals Unique Lipid Dynamics in Cytotrophoblast Cells

被引:54
作者
Kolahi, Kevin [1 ,2 ]
Louey, Samantha [1 ]
Varlamov, Oleg [5 ]
Thornburg, Kent [1 ,2 ,3 ,4 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Biomed Engn, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Ctr Dev Hlth, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Knight Cardiovasc Inst, Portland, OR 97201 USA
[4] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97201 USA
[5] Oregon Natl Primate Res Ctr, Div Diabet Obes & Metab, Beaverton, OR USA
来源
PLOS ONE | 2016年 / 11卷 / 04期
关键词
COA SYNTHETASE 5; TROPHOBLAST CELLS; TRANSPORT; METABOLISM; FUSION; DIFFERENTIATION; IDENTIFICATION; INVOLVEMENT; PROTEINS; MODEL;
D O I
10.1371/journal.pone.0153522
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While the human placenta must provide selected long-chain fatty acids to support the developing fetal brain, little is known about the mechanisms underlying the transport process. We tracked the movement of the fluorescently labeled long-chain fatty acid analogue, BODIPY-C-12, across the cell layers of living explants of human term placenta. Although all layers took up the fatty acid, rapid esterification of long-chain fatty acids and incorporation into lipid droplets was exclusive to the inner layer cytotrophoblast cells rather than the expected outer syncytiotrophoblast layer. Cytotrophoblast is a progenitor cell layer previously relegated to a repair role. As isolated cytotrophoblasts differentiated into syncytialized cells in culture, they weakened their lipid processing capacity. Syncytializing cells suppress previously active genes that regulate fatty-acid uptake (SLC27A2/FATP2, FABP4, ACSL5) and lipid metabolism (GPAT3, LPCAT3). We speculate that cytotrophoblast performs a previously unrecognized role in regulating placental fatty acid uptake and metabolism.
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页数:23
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