TY - JOUR
T1 - Differences in glycolysis and mitochondrial respiration between cytotrophoblast and syncytiotrophoblast in-vitro
T2 - Evidence for sexual dimorphism
AU - Bucher, Matthew
AU - Kadam, Leena
AU - Ahuna, Kylia
AU - Myatt, Leslie
N1 - Funding Information:
Funding: This research was funded by the National Institutes of Health, Grant number HD095610 (LM).
Funding Information:
This research was funded by the National Institutes of Health, Grant number HD095610 (LM). The authors thank the Labor and Delivery Department at OHSU and the Maternal and Fetal Research Team for coordinating the collection of the placentas. We also thank all the women who participated in this study by donating their placentas, and the Maloyan lab for helping collect and process placentas and isolate trophoblasts.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - In the placenta the proliferative cytotrophoblast cells fuse into the terminally differentiated syncytiotrophoblast layer which undertakes several energy-intensive functions including nutrient uptake and transfer and hormone synthesis. We used Seahorse glycolytic and mitochondrial stress tests on trophoblast cells isolated at term from women of healthy weight to evaluate if cyto-trophoblast (CT) and syncytiotrophoblast (ST) have different bioenergetic strategies, given their different functions. Whereas there are no differences in basal glycolysis, CT have significantly greater glycolytic capacity and reserve than ST. In contrast, ST have significantly higher basal, ATP-coupled and maximal mitochondrial respiration and spare capacity than CT. Consequently, under stress conditions CT can increase energy generation via its higher glycolytic capacity whereas ST can use its higher and more efficient mitochondrial respiration capacity. We have previously shown that with adverse in utero conditions of diabetes and obesity trophoblast respiration is sexually dimor-phic. We found no differences in glycolytic parameters between sexes and no difference in mito-chondrial respiration parameters other than increases seen upon syncytialization appear to be greater in females. There were differences in metabolic flexibility, i.e., the ability to use glucose, glutamine, or fatty acids, seen upon syncytialization between the sexes with increased flexibility in female trophoblast suggesting a better ability to adapt to changes in nutrient supply.
AB - In the placenta the proliferative cytotrophoblast cells fuse into the terminally differentiated syncytiotrophoblast layer which undertakes several energy-intensive functions including nutrient uptake and transfer and hormone synthesis. We used Seahorse glycolytic and mitochondrial stress tests on trophoblast cells isolated at term from women of healthy weight to evaluate if cyto-trophoblast (CT) and syncytiotrophoblast (ST) have different bioenergetic strategies, given their different functions. Whereas there are no differences in basal glycolysis, CT have significantly greater glycolytic capacity and reserve than ST. In contrast, ST have significantly higher basal, ATP-coupled and maximal mitochondrial respiration and spare capacity than CT. Consequently, under stress conditions CT can increase energy generation via its higher glycolytic capacity whereas ST can use its higher and more efficient mitochondrial respiration capacity. We have previously shown that with adverse in utero conditions of diabetes and obesity trophoblast respiration is sexually dimor-phic. We found no differences in glycolytic parameters between sexes and no difference in mito-chondrial respiration parameters other than increases seen upon syncytialization appear to be greater in females. There were differences in metabolic flexibility, i.e., the ability to use glucose, glutamine, or fatty acids, seen upon syncytialization between the sexes with increased flexibility in female trophoblast suggesting a better ability to adapt to changes in nutrient supply.
KW - Cytotrophoblast
KW - Glycolysis
KW - Metabolism
KW - Mitochondrial respiration
KW - Placenta
KW - Placental metabolism
KW - Sexual dimorphism
KW - Syncytio-trophoblast
KW - Trophoblast glycolysis
KW - Trophoblast mitochondrial respiration
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U2 - 10.3390/ijms221910875
DO - 10.3390/ijms221910875
M3 - Article
C2 - 34639216
AN - SCOPUS:85116533639
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 19
M1 - 10875
ER -