Cargando…

Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta

BACKGROUND: Exposure to diabetes in utero influences future metabolic health of the offspring. MicroRNAs (miRNA) are small non-coding RNAs that may contribute mechanistically to the effects on offspring imparted by diabetes mellitus (DM) during pregnancy. We hypothesized that exposure to DM during p...

Descripción completa

Detalles Bibliográficos
Autores principales: Shah, Kruti B., Chernausek, Steven D., Teague, April M., Bard, David E., Tryggestad, Jeanie B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854929/
https://www.ncbi.nlm.nih.gov/pubmed/32663836
http://dx.doi.org/10.1038/s41390-020-1060-x
_version_ 1783646163630555136
author Shah, Kruti B.
Chernausek, Steven D.
Teague, April M.
Bard, David E.
Tryggestad, Jeanie B.
author_facet Shah, Kruti B.
Chernausek, Steven D.
Teague, April M.
Bard, David E.
Tryggestad, Jeanie B.
author_sort Shah, Kruti B.
collection PubMed
description BACKGROUND: Exposure to diabetes in utero influences future metabolic health of the offspring. MicroRNAs (miRNA) are small non-coding RNAs that may contribute mechanistically to the effects on offspring imparted by diabetes mellitus (DM) during pregnancy. We hypothesized that exposure to DM during pregnancy influences select miRNAs in fetal circulation, in human umbilical vein endothelial cells (HUVEC), and placenta. METHODS: miRNA abundance was quantified using real-time PCR from RNA isolated from umbilical cord serum exosomes, HUVEC and placenta exposed to diabetes or normoglycemia during pregnancy. The abundance of each of these miRNAs was determined by comparison to a known standard and the relative expression assessed using the 2(−ΔΔCt) method. Multivariable regression models examined the associations between exposure to diabetes during pregnancy and miRNA expression. RESULTS: miR-126–3p was highly abundant in fetal circulation, HUVEC and placenta. Diabetes exposure during pregnancy resulted in lower expression of miR-148a-3p and miR-29a-3p in the HUVEC. In the placenta, for miR-126–3p, there was a differential effect of DM by birthweight between DM versus control group, expression being lower at the lower birth weight, however not different at the higher birthweight. CONCLUSION: Exposure to DM during pregnancy alters miRNA expression in the offspring in a tissue specific manner.
format Online
Article
Text
id pubmed-7854929
institution National Center for Biotechnology Information
language English
publishDate 2020
record_format MEDLINE/PubMed
spelling pubmed-78549292021-05-15 Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta Shah, Kruti B. Chernausek, Steven D. Teague, April M. Bard, David E. Tryggestad, Jeanie B. Pediatr Res Article BACKGROUND: Exposure to diabetes in utero influences future metabolic health of the offspring. MicroRNAs (miRNA) are small non-coding RNAs that may contribute mechanistically to the effects on offspring imparted by diabetes mellitus (DM) during pregnancy. We hypothesized that exposure to DM during pregnancy influences select miRNAs in fetal circulation, in human umbilical vein endothelial cells (HUVEC), and placenta. METHODS: miRNA abundance was quantified using real-time PCR from RNA isolated from umbilical cord serum exosomes, HUVEC and placenta exposed to diabetes or normoglycemia during pregnancy. The abundance of each of these miRNAs was determined by comparison to a known standard and the relative expression assessed using the 2(−ΔΔCt) method. Multivariable regression models examined the associations between exposure to diabetes during pregnancy and miRNA expression. RESULTS: miR-126–3p was highly abundant in fetal circulation, HUVEC and placenta. Diabetes exposure during pregnancy resulted in lower expression of miR-148a-3p and miR-29a-3p in the HUVEC. In the placenta, for miR-126–3p, there was a differential effect of DM by birthweight between DM versus control group, expression being lower at the lower birth weight, however not different at the higher birthweight. CONCLUSION: Exposure to DM during pregnancy alters miRNA expression in the offspring in a tissue specific manner. 2020-07-14 2021-04 /pmc/articles/PMC7854929/ /pubmed/32663836 http://dx.doi.org/10.1038/s41390-020-1060-x Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Shah, Kruti B.
Chernausek, Steven D.
Teague, April M.
Bard, David E.
Tryggestad, Jeanie B.
Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta
title Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta
title_full Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta
title_fullStr Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta
title_full_unstemmed Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta
title_short Maternal Diabetes Alters microRNA Expression in Fetal Exosomes, Human Umbilical Vein Endothelial Cells and Placenta
title_sort maternal diabetes alters microrna expression in fetal exosomes, human umbilical vein endothelial cells and placenta
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854929/
https://www.ncbi.nlm.nih.gov/pubmed/32663836
http://dx.doi.org/10.1038/s41390-020-1060-x
work_keys_str_mv AT shahkrutib maternaldiabetesaltersmicrornaexpressioninfetalexosomeshumanumbilicalveinendothelialcellsandplacenta
AT chernausekstevend maternaldiabetesaltersmicrornaexpressioninfetalexosomeshumanumbilicalveinendothelialcellsandplacenta
AT teagueaprilm maternaldiabetesaltersmicrornaexpressioninfetalexosomeshumanumbilicalveinendothelialcellsandplacenta
AT barddavide maternaldiabetesaltersmicrornaexpressioninfetalexosomeshumanumbilicalveinendothelialcellsandplacenta
AT tryggestadjeanieb maternaldiabetesaltersmicrornaexpressioninfetalexosomeshumanumbilicalveinendothelialcellsandplacenta