Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?

IntroductionGestational diabetes mellitus (GDM), a common pregnancy disorder, increases the risk of fetal overgrowth and later metabolic morbidity in the offspring. The placenta likely mediates these sequelae, but the exact mechanisms remain elusive. Mitochondrial dynamics refers to the joining and...

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Main Authors: Joelcio Abbade, Miira Marjuska Klemetti, Abby Farrell, Leonardo Ermini, Taylor Gillmore, Julien Sallais, Andrea Tagliaferro, Martin Post, Isabella Caniggia
Format: Article
Language:English
Published: BMJ Publishing Group 2020-04-01
Series:BMJ Open Diabetes Research & Care
Online Access:https://drc.bmj.com/content/8/1/e000923.full
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spelling doaj-e7b5fd94f89c4520bd11bc6a9ab6e8b62021-06-10T10:02:48ZengBMJ Publishing GroupBMJ Open Diabetes Research & Care2052-48972020-04-018110.1136/bmjdrc-2019-000923Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?Joelcio Abbade0Miira Marjuska Klemetti1Abby Farrell2Leonardo Ermini3Taylor Gillmore4Julien Sallais5Andrea Tagliaferro6Martin Post7Isabella Caniggia8Lunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaLunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaLunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaLunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaLunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaLunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaLunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaDepartment of Physiology and Institute of Medical Sciences, University of Toronto, Toronto, Ontario, CanadaLunenfeld-Tanenbaum Research Institute, Toronto, Ontario, CanadaIntroductionGestational diabetes mellitus (GDM), a common pregnancy disorder, increases the risk of fetal overgrowth and later metabolic morbidity in the offspring. The placenta likely mediates these sequelae, but the exact mechanisms remain elusive. Mitochondrial dynamics refers to the joining and division of these organelles, in attempts to maintain cellular homeostasis in stress conditions or alterations in oxygen and fuel availability. These remodeling processes are critical to optimize mitochondrial function, and their disturbances characterize diabetes and obesity.Methods and resultsHerein we show that placental mitochondrial dynamics are tilted toward fusion in GDM, as evidenced by transmission electron microscopy and changes in the expression of key mechanochemical enzymes such as OPA1 and active phosphorylated DRP1. In vitro experiments using choriocarcinoma JEG-3 cells demonstrated that increased exposure to insulin, which typifies GDM, promotes mitochondrial fusion. As placental ceramide induces mitochondrial fission in pre-eclampsia, we also examined ceramide content in GDM and control placentae and observed a reduction in placental ceramide enrichment in GDM, likely due to an insulin-dependent increase in ceramide-degrading ASAH1 expression.ConclusionsPlacental mitochondrial fusion is enhanced in GDM, possibly as a compensatory response to maternal and fetal metabolic derangements. Alterations in placental insulin exposure and sphingolipid metabolism are among potential contributing factors. Overall, our results suggest that GDM has profound impacts on placental mitochondrial dynamics and metabolism, with plausible implications for the short-term and long-term health of the offspring.https://drc.bmj.com/content/8/1/e000923.full
collection DOAJ
language English
format Article
sources DOAJ
author Joelcio Abbade
Miira Marjuska Klemetti
Abby Farrell
Leonardo Ermini
Taylor Gillmore
Julien Sallais
Andrea Tagliaferro
Martin Post
Isabella Caniggia
spellingShingle Joelcio Abbade
Miira Marjuska Klemetti
Abby Farrell
Leonardo Ermini
Taylor Gillmore
Julien Sallais
Andrea Tagliaferro
Martin Post
Isabella Caniggia
Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?
BMJ Open Diabetes Research & Care
author_facet Joelcio Abbade
Miira Marjuska Klemetti
Abby Farrell
Leonardo Ermini
Taylor Gillmore
Julien Sallais
Andrea Tagliaferro
Martin Post
Isabella Caniggia
author_sort Joelcio Abbade
title Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?
title_short Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?
title_full Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?
title_fullStr Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?
title_full_unstemmed Increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?
title_sort increased placental mitochondrial fusion in gestational diabetes mellitus: an adaptive mechanism to optimize feto-placental metabolic homeostasis?
publisher BMJ Publishing Group
series BMJ Open Diabetes Research & Care
issn 2052-4897
publishDate 2020-04-01
description IntroductionGestational diabetes mellitus (GDM), a common pregnancy disorder, increases the risk of fetal overgrowth and later metabolic morbidity in the offspring. The placenta likely mediates these sequelae, but the exact mechanisms remain elusive. Mitochondrial dynamics refers to the joining and division of these organelles, in attempts to maintain cellular homeostasis in stress conditions or alterations in oxygen and fuel availability. These remodeling processes are critical to optimize mitochondrial function, and their disturbances characterize diabetes and obesity.Methods and resultsHerein we show that placental mitochondrial dynamics are tilted toward fusion in GDM, as evidenced by transmission electron microscopy and changes in the expression of key mechanochemical enzymes such as OPA1 and active phosphorylated DRP1. In vitro experiments using choriocarcinoma JEG-3 cells demonstrated that increased exposure to insulin, which typifies GDM, promotes mitochondrial fusion. As placental ceramide induces mitochondrial fission in pre-eclampsia, we also examined ceramide content in GDM and control placentae and observed a reduction in placental ceramide enrichment in GDM, likely due to an insulin-dependent increase in ceramide-degrading ASAH1 expression.ConclusionsPlacental mitochondrial fusion is enhanced in GDM, possibly as a compensatory response to maternal and fetal metabolic derangements. Alterations in placental insulin exposure and sphingolipid metabolism are among potential contributing factors. Overall, our results suggest that GDM has profound impacts on placental mitochondrial dynamics and metabolism, with plausible implications for the short-term and long-term health of the offspring.
url https://drc.bmj.com/content/8/1/e000923.full
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