author_facet Kandzija, Neva
Zhang, Wei
Motta‐Mejia, Carolina
Mhlomi, Vuyane
McGowan‐Downey, Jennifer
James, Tim
Cerdeira, Ana Sofia
Tannetta, Dionne
Sargent, Ian
Redman, Christopher W.
Bastie, Claire C.
Vatish, Manu
Kandzija, Neva
Zhang, Wei
Motta‐Mejia, Carolina
Mhlomi, Vuyane
McGowan‐Downey, Jennifer
James, Tim
Cerdeira, Ana Sofia
Tannetta, Dionne
Sargent, Ian
Redman, Christopher W.
Bastie, Claire C.
Vatish, Manu
author Kandzija, Neva
Zhang, Wei
Motta‐Mejia, Carolina
Mhlomi, Vuyane
McGowan‐Downey, Jennifer
James, Tim
Cerdeira, Ana Sofia
Tannetta, Dionne
Sargent, Ian
Redman, Christopher W.
Bastie, Claire C.
Vatish, Manu
spellingShingle Kandzija, Neva
Zhang, Wei
Motta‐Mejia, Carolina
Mhlomi, Vuyane
McGowan‐Downey, Jennifer
James, Tim
Cerdeira, Ana Sofia
Tannetta, Dionne
Sargent, Ian
Redman, Christopher W.
Bastie, Claire C.
Vatish, Manu
Journal of Extracellular Vesicles
Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
Cell Biology
Histology
author_sort kandzija, neva
spelling Kandzija, Neva Zhang, Wei Motta‐Mejia, Carolina Mhlomi, Vuyane McGowan‐Downey, Jennifer James, Tim Cerdeira, Ana Sofia Tannetta, Dionne Sargent, Ian Redman, Christopher W. Bastie, Claire C. Vatish, Manu 2001-3078 2001-3078 Wiley Cell Biology Histology http://dx.doi.org/10.1080/20013078.2019.1617000 <jats:title>ABSTRACT</jats:title><jats:p>Gestational diabetes mellitus (GDM) is the most common metabolic disorder in pregnancy and is characterized by insulin resistance and decreased circulating glucagon‐like peptide‐1 (GLP‐1). GDM resolves rapidly after delivery implicating the placenta in the disease. This study examines the biological functions that cause this pathology. The placenta releases syncytiotrophoblast‐derived extracellular vesicles (STB‐EVs) into the maternal circulation, which is enhanced in GDM. Dipeptidyl peptidase IV (DPPIV) is known to play a role in type 2 diabetes by breaking down GLP‐1, which in turn regulates glucose‐dependent insulin secretion. STB‐EVs from control and GDM women were analysed. We show that normal human placenta releases DPPIV‐positive STB‐EVs and that they are higher in uterine than paired peripheral blood, confirming placental origin. DPPIV‐bound STB‐EVs from normal perfused placentae are dose dependently inhibited with vildagliptin. DPPIV‐bound STB‐EVs from perfused placentae are able to breakdown GLP‐1 <jats:italic>in vitro</jats:italic>. STB‐EVs from GDM perfused placentae show greater DPPIV activity. Importantly, DPPIV‐bound STB‐EVs increase eightfold in the circulation of women with GDM. This is the first report of STB‐EVs carrying a biologically active molecule that has the potential to regulate maternal insulin secretion.</jats:p> Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus Journal of Extracellular Vesicles
doi_str_mv 10.1080/20013078.2019.1617000
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title Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_unstemmed Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_full Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_fullStr Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_full_unstemmed Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_short Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_sort placental extracellular vesicles express active dipeptidyl peptidase iv; levels are increased in gestational diabetes mellitus
topic Cell Biology
Histology
url http://dx.doi.org/10.1080/20013078.2019.1617000
publishDate 2019
physical
description <jats:title>ABSTRACT</jats:title><jats:p>Gestational diabetes mellitus (GDM) is the most common metabolic disorder in pregnancy and is characterized by insulin resistance and decreased circulating glucagon‐like peptide‐1 (GLP‐1). GDM resolves rapidly after delivery implicating the placenta in the disease. This study examines the biological functions that cause this pathology. The placenta releases syncytiotrophoblast‐derived extracellular vesicles (STB‐EVs) into the maternal circulation, which is enhanced in GDM. Dipeptidyl peptidase IV (DPPIV) is known to play a role in type 2 diabetes by breaking down GLP‐1, which in turn regulates glucose‐dependent insulin secretion. STB‐EVs from control and GDM women were analysed. We show that normal human placenta releases DPPIV‐positive STB‐EVs and that they are higher in uterine than paired peripheral blood, confirming placental origin. DPPIV‐bound STB‐EVs from normal perfused placentae are dose dependently inhibited with vildagliptin. DPPIV‐bound STB‐EVs from perfused placentae are able to breakdown GLP‐1 <jats:italic>in vitro</jats:italic>. STB‐EVs from GDM perfused placentae show greater DPPIV activity. Importantly, DPPIV‐bound STB‐EVs increase eightfold in the circulation of women with GDM. This is the first report of STB‐EVs carrying a biologically active molecule that has the potential to regulate maternal insulin secretion.</jats:p>
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author Kandzija, Neva, Zhang, Wei, Motta‐Mejia, Carolina, Mhlomi, Vuyane, McGowan‐Downey, Jennifer, James, Tim, Cerdeira, Ana Sofia, Tannetta, Dionne, Sargent, Ian, Redman, Christopher W., Bastie, Claire C., Vatish, Manu
author_facet Kandzija, Neva, Zhang, Wei, Motta‐Mejia, Carolina, Mhlomi, Vuyane, McGowan‐Downey, Jennifer, James, Tim, Cerdeira, Ana Sofia, Tannetta, Dionne, Sargent, Ian, Redman, Christopher W., Bastie, Claire C., Vatish, Manu, Kandzija, Neva, Zhang, Wei, Motta‐Mejia, Carolina, Mhlomi, Vuyane, McGowan‐Downey, Jennifer, James, Tim, Cerdeira, Ana Sofia, Tannetta, Dionne, Sargent, Ian, Redman, Christopher W., Bastie, Claire C., Vatish, Manu
author_sort kandzija, neva
container_issue 1
container_start_page 0
container_title Journal of Extracellular Vesicles
container_volume 8
description <jats:title>ABSTRACT</jats:title><jats:p>Gestational diabetes mellitus (GDM) is the most common metabolic disorder in pregnancy and is characterized by insulin resistance and decreased circulating glucagon‐like peptide‐1 (GLP‐1). GDM resolves rapidly after delivery implicating the placenta in the disease. This study examines the biological functions that cause this pathology. The placenta releases syncytiotrophoblast‐derived extracellular vesicles (STB‐EVs) into the maternal circulation, which is enhanced in GDM. Dipeptidyl peptidase IV (DPPIV) is known to play a role in type 2 diabetes by breaking down GLP‐1, which in turn regulates glucose‐dependent insulin secretion. STB‐EVs from control and GDM women were analysed. We show that normal human placenta releases DPPIV‐positive STB‐EVs and that they are higher in uterine than paired peripheral blood, confirming placental origin. DPPIV‐bound STB‐EVs from normal perfused placentae are dose dependently inhibited with vildagliptin. DPPIV‐bound STB‐EVs from perfused placentae are able to breakdown GLP‐1 <jats:italic>in vitro</jats:italic>. STB‐EVs from GDM perfused placentae show greater DPPIV activity. Importantly, DPPIV‐bound STB‐EVs increase eightfold in the circulation of women with GDM. This is the first report of STB‐EVs carrying a biologically active molecule that has the potential to regulate maternal insulin secretion.</jats:p>
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spelling Kandzija, Neva Zhang, Wei Motta‐Mejia, Carolina Mhlomi, Vuyane McGowan‐Downey, Jennifer James, Tim Cerdeira, Ana Sofia Tannetta, Dionne Sargent, Ian Redman, Christopher W. Bastie, Claire C. Vatish, Manu 2001-3078 2001-3078 Wiley Cell Biology Histology http://dx.doi.org/10.1080/20013078.2019.1617000 <jats:title>ABSTRACT</jats:title><jats:p>Gestational diabetes mellitus (GDM) is the most common metabolic disorder in pregnancy and is characterized by insulin resistance and decreased circulating glucagon‐like peptide‐1 (GLP‐1). GDM resolves rapidly after delivery implicating the placenta in the disease. This study examines the biological functions that cause this pathology. The placenta releases syncytiotrophoblast‐derived extracellular vesicles (STB‐EVs) into the maternal circulation, which is enhanced in GDM. Dipeptidyl peptidase IV (DPPIV) is known to play a role in type 2 diabetes by breaking down GLP‐1, which in turn regulates glucose‐dependent insulin secretion. STB‐EVs from control and GDM women were analysed. We show that normal human placenta releases DPPIV‐positive STB‐EVs and that they are higher in uterine than paired peripheral blood, confirming placental origin. DPPIV‐bound STB‐EVs from normal perfused placentae are dose dependently inhibited with vildagliptin. DPPIV‐bound STB‐EVs from perfused placentae are able to breakdown GLP‐1 <jats:italic>in vitro</jats:italic>. STB‐EVs from GDM perfused placentae show greater DPPIV activity. Importantly, DPPIV‐bound STB‐EVs increase eightfold in the circulation of women with GDM. This is the first report of STB‐EVs carrying a biologically active molecule that has the potential to regulate maternal insulin secretion.</jats:p> Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus Journal of Extracellular Vesicles
spellingShingle Kandzija, Neva, Zhang, Wei, Motta‐Mejia, Carolina, Mhlomi, Vuyane, McGowan‐Downey, Jennifer, James, Tim, Cerdeira, Ana Sofia, Tannetta, Dionne, Sargent, Ian, Redman, Christopher W., Bastie, Claire C., Vatish, Manu, Journal of Extracellular Vesicles, Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus, Cell Biology, Histology
title Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_full Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_fullStr Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_full_unstemmed Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_short Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
title_sort placental extracellular vesicles express active dipeptidyl peptidase iv; levels are increased in gestational diabetes mellitus
title_unstemmed Placental extracellular vesicles express active dipeptidyl peptidase IV; levels are increased in gestational diabetes mellitus
topic Cell Biology, Histology
url http://dx.doi.org/10.1080/20013078.2019.1617000