Cargando…

Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta

The offspring of mothers with gestational diabetes mellitus (GDM) are at a higher risk for metabolic dysregulation and neurodevelopmental impairment. Evidence suggests that serotonin, which is present in both the placenta and the brain, programs the development and growth of the fetal brain. In the...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Jae Yen, Lee, Kyung Eun, Byeon, Eun Jeong, Choi, Jieun, Kim, Sa Jin, Shin, Jae Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695704/
https://www.ncbi.nlm.nih.gov/pubmed/36431006
http://dx.doi.org/10.3390/life12111869
_version_ 1784838129230807040
author Song, Jae Yen
Lee, Kyung Eun
Byeon, Eun Jeong
Choi, Jieun
Kim, Sa Jin
Shin, Jae Eun
author_facet Song, Jae Yen
Lee, Kyung Eun
Byeon, Eun Jeong
Choi, Jieun
Kim, Sa Jin
Shin, Jae Eun
author_sort Song, Jae Yen
collection PubMed
description The offspring of mothers with gestational diabetes mellitus (GDM) are at a higher risk for metabolic dysregulation and neurodevelopmental impairment. Evidence suggests that serotonin, which is present in both the placenta and the brain, programs the development and growth of the fetal brain. In the current study, we tested the hypothesis that GDM affects the methylation of the serotonin transporter gene (SLC6A4) and serotonin receptor gene (HTR2A) in the placenta. Ninety pregnant women were included in this study. Thirty mothers were diagnosed with GDM, and sixty mothers served as controls in a 1:2 ratio. Ten CpG sites within the promoter regions of SLC6A4 and HTR2A were analyzed using pyrosequencing. The relative expression of genes involved in DNA methylation was evaluated using real-time PCR. The average DNA methylation of placental SLC6A4 was higher in the GDM group than in the control group (2.29 vs. 1.16%, p < 0.001). However, the average DNA methylation level of HTR2A did not differ between the two groups. SLC6A4 methylation showed a positive correlation with maternal plasma glucose level and neonatal birth weight percentile and a negative correlation with the neonatal head circumference percentile. This finding suggests that epigenetic modification of the placental serotonin system may affect placental adaptation to a harmful maternal environment, thereby influencing the long-term outcome in the offspring.
format Online
Article
Text
id pubmed-9695704
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96957042022-11-26 Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta Song, Jae Yen Lee, Kyung Eun Byeon, Eun Jeong Choi, Jieun Kim, Sa Jin Shin, Jae Eun Life (Basel) Article The offspring of mothers with gestational diabetes mellitus (GDM) are at a higher risk for metabolic dysregulation and neurodevelopmental impairment. Evidence suggests that serotonin, which is present in both the placenta and the brain, programs the development and growth of the fetal brain. In the current study, we tested the hypothesis that GDM affects the methylation of the serotonin transporter gene (SLC6A4) and serotonin receptor gene (HTR2A) in the placenta. Ninety pregnant women were included in this study. Thirty mothers were diagnosed with GDM, and sixty mothers served as controls in a 1:2 ratio. Ten CpG sites within the promoter regions of SLC6A4 and HTR2A were analyzed using pyrosequencing. The relative expression of genes involved in DNA methylation was evaluated using real-time PCR. The average DNA methylation of placental SLC6A4 was higher in the GDM group than in the control group (2.29 vs. 1.16%, p < 0.001). However, the average DNA methylation level of HTR2A did not differ between the two groups. SLC6A4 methylation showed a positive correlation with maternal plasma glucose level and neonatal birth weight percentile and a negative correlation with the neonatal head circumference percentile. This finding suggests that epigenetic modification of the placental serotonin system may affect placental adaptation to a harmful maternal environment, thereby influencing the long-term outcome in the offspring. MDPI 2022-11-13 /pmc/articles/PMC9695704/ /pubmed/36431006 http://dx.doi.org/10.3390/life12111869 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Song, Jae Yen
Lee, Kyung Eun
Byeon, Eun Jeong
Choi, Jieun
Kim, Sa Jin
Shin, Jae Eun
Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta
title Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta
title_full Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta
title_fullStr Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta
title_full_unstemmed Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta
title_short Maternal Gestational Diabetes Influences DNA Methylation in the Serotonin System in the Human Placenta
title_sort maternal gestational diabetes influences dna methylation in the serotonin system in the human placenta
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695704/
https://www.ncbi.nlm.nih.gov/pubmed/36431006
http://dx.doi.org/10.3390/life12111869
work_keys_str_mv AT songjaeyen maternalgestationaldiabetesinfluencesdnamethylationintheserotoninsysteminthehumanplacenta
AT leekyungeun maternalgestationaldiabetesinfluencesdnamethylationintheserotoninsysteminthehumanplacenta
AT byeoneunjeong maternalgestationaldiabetesinfluencesdnamethylationintheserotoninsysteminthehumanplacenta
AT choijieun maternalgestationaldiabetesinfluencesdnamethylationintheserotoninsysteminthehumanplacenta
AT kimsajin maternalgestationaldiabetesinfluencesdnamethylationintheserotoninsysteminthehumanplacenta
AT shinjaeeun maternalgestationaldiabetesinfluencesdnamethylationintheserotoninsysteminthehumanplacenta