Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarker

Preterm birth may have a pathological impact on intrauterine development of the fetal brain, resulting in developmental disabilities. In this study, we examine the expression of soluble Fms-like tyrosine kinase 1 (sFLT-1) and placental growth factor (PlGF), which is one of the vascular endothelial g...

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Main Authors: Sama Hussein, Weina Ju, Stephanie Pizzella, Michael Flory, Chu Chu, Yong Wang, Nanbert Zhong
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-12-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.1024587/full
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author Sama Hussein
Weina Ju
Stephanie Pizzella
Michael Flory
Chu Chu
Yong Wang
Nanbert Zhong
author_facet Sama Hussein
Weina Ju
Stephanie Pizzella
Michael Flory
Chu Chu
Yong Wang
Nanbert Zhong
author_sort Sama Hussein
collection DOAJ
description Preterm birth may have a pathological impact on intrauterine development of the fetal brain, resulting in developmental disabilities. In this study, we examine the expression of soluble Fms-like tyrosine kinase 1 (sFLT-1) and placental growth factor (PlGF), which is one of the vascular endothelial growth factors (VEGFs), as these play a key role in angiogenesis; in particular, we examine their effect on the sFLT-1/PlGF ratio in cases of preterm birth as compared to typical pregnancies. Enzyme-linked immunosorbent assay was performed on samples of maternal-derived plasma and extracellular vesicles-exosomes (EVs-EXs) isolated at the third trimester, consisting of 17 samples from cases of preterm birth and 38 control cases. Our results showed that both sFLT-1 (P=0.0014) and PlGF (P=0.0032) were significantly downregulated in cases of preterm birth compared to controls, while the sFLT-1/PIGF ratio was significantly (P=0.0008) increased in EVs-EXs, but not in maternal plasma. Our results suggest that this reduced expression of sFLT-1 and PlGF with an elevated sFLT-1/PlGF ratio in EVs-EXs may represent a potential biomarker for prediction of PTB.
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spelling doaj.art-1ea8fc20a7a0405397a8382f73e2e8552022-12-22T11:24:43ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922022-12-011310.3389/fendo.2022.10245871024587Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarkerSama Hussein0Weina Ju1Stephanie Pizzella2Michael Flory3Chu Chu4Yong Wang5Nanbert Zhong6New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, United StatesNew York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, United StatesDepartment of Obstetrics and Gynecology, School of Medicine, Washington University, St. Louis, MO, United StatesNew York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, United StatesNew York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, United StatesDepartment of Obstetrics and Gynecology, School of Medicine, Washington University, St. Louis, MO, United StatesNew York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, United StatesPreterm birth may have a pathological impact on intrauterine development of the fetal brain, resulting in developmental disabilities. In this study, we examine the expression of soluble Fms-like tyrosine kinase 1 (sFLT-1) and placental growth factor (PlGF), which is one of the vascular endothelial growth factors (VEGFs), as these play a key role in angiogenesis; in particular, we examine their effect on the sFLT-1/PlGF ratio in cases of preterm birth as compared to typical pregnancies. Enzyme-linked immunosorbent assay was performed on samples of maternal-derived plasma and extracellular vesicles-exosomes (EVs-EXs) isolated at the third trimester, consisting of 17 samples from cases of preterm birth and 38 control cases. Our results showed that both sFLT-1 (P=0.0014) and PlGF (P=0.0032) were significantly downregulated in cases of preterm birth compared to controls, while the sFLT-1/PIGF ratio was significantly (P=0.0008) increased in EVs-EXs, but not in maternal plasma. Our results suggest that this reduced expression of sFLT-1 and PlGF with an elevated sFLT-1/PlGF ratio in EVs-EXs may represent a potential biomarker for prediction of PTB.https://www.frontiersin.org/articles/10.3389/fendo.2022.1024587/fullsFlt-1placental growth factorbiomarkerpreterm (birth)PTBextracellular vehicles (EVs)
spellingShingle Sama Hussein
Weina Ju
Stephanie Pizzella
Michael Flory
Chu Chu
Yong Wang
Nanbert Zhong
Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarker
Frontiers in Endocrinology
sFlt-1
placental growth factor
biomarker
preterm (birth)
PTB
extracellular vehicles (EVs)
title Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarker
title_full Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarker
title_fullStr Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarker
title_full_unstemmed Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarker
title_short Reduced expression in preterm birth of sFLT-1 and PlGF with a high sFLT-1/PlGF ratio in extracellular vesicles suggests a potential biomarker
title_sort reduced expression in preterm birth of sflt 1 and plgf with a high sflt 1 plgf ratio in extracellular vesicles suggests a potential biomarker
topic sFlt-1
placental growth factor
biomarker
preterm (birth)
PTB
extracellular vehicles (EVs)
url https://www.frontiersin.org/articles/10.3389/fendo.2022.1024587/full
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