MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus

The role of microRNA (miRNA) in gestational diabetes mellitus has been widely investigated during the last decade. However, the altering effect of miR-6869-5p on immunity and placental microenvironment in gestational diabetes mellitus is largely unknown. In our study, the expression of miR-6869-5p w...

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Main Authors: Pingping Wang, Zhenzhi Ma, Zengyan Wang, Ximei Wang, Guifeng Zhao, Zengfang Wang
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2021/6696636
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author Pingping Wang
Zhenzhi Ma
Zengyan Wang
Ximei Wang
Guifeng Zhao
Zengfang Wang
author_facet Pingping Wang
Zhenzhi Ma
Zengyan Wang
Ximei Wang
Guifeng Zhao
Zengfang Wang
author_sort Pingping Wang
collection DOAJ
description The role of microRNA (miRNA) in gestational diabetes mellitus has been widely investigated during the last decade. However, the altering effect of miR-6869-5p on immunity and placental microenvironment in gestational diabetes mellitus is largely unknown. In our study, the expression of miR-6869-5p was documented to be significantly decreased in placenta-derived mononuclear macrophages, which was also negatively related to PTPRO. Besides, PTPRO was negatively regulated by miR-6869-5p in placenta-derived mononuclear macrophages. In vitro, miR-6869-5p inhibited macrophage proliferation demonstrated by EdU and CCK-8 experiments. The inflammatory response in macrophages was also significantly inhibited by miR-6869-5p, which could regulate PTPRO as a target documented by luciferase reporter assay. Moreover, miR-6869-5p promoted M2 macrophage polarization and thus restrain inflammation. Accordingly, miR-6869-5p is involved in maintaining placental microenvironment balance by preventing from inflammation and inducing M2 macrophages in gestational diabetes mellitus.
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institution Kabale University
issn 0962-9351
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language English
publishDate 2021-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-b1a9d8a10038439f8d06d2ad519dd2c42025-02-03T05:49:18ZengWileyMediators of Inflammation0962-93511466-18612021-01-01202110.1155/2021/66966366696636MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes MellitusPingping Wang0Zhenzhi Ma1Zengyan Wang2Ximei Wang3Guifeng Zhao4Zengfang Wang5Department of Gynecology and Obstetrics, the Affiliated Hospital of Maternal and Child Health, Weifang Medical University, Weifang 261000, ChinaDepartment of Pharmacy, the First Affiliated Hospital of Weifang Medical University, Weifang 261000, ChinaOperating Room, Zhucheng People’s Hospital, Zhucheng 262200, ChinaDepartment of Gynecology and Obstetrics, the Affiliated Hospital of Maternal and Child Health, Weifang Medical University, Weifang 261000, ChinaDepartment of Antenatal Diagnosis, the First Affiliated Hospital of Maternal and Child Health, Weifang Medical University, Weifang 261000, ChinaDepartment of Gynecology and Obstetrics, the Affiliated Hospital of Maternal and Child Health, Weifang Medical University, Weifang 261000, ChinaThe role of microRNA (miRNA) in gestational diabetes mellitus has been widely investigated during the last decade. However, the altering effect of miR-6869-5p on immunity and placental microenvironment in gestational diabetes mellitus is largely unknown. In our study, the expression of miR-6869-5p was documented to be significantly decreased in placenta-derived mononuclear macrophages, which was also negatively related to PTPRO. Besides, PTPRO was negatively regulated by miR-6869-5p in placenta-derived mononuclear macrophages. In vitro, miR-6869-5p inhibited macrophage proliferation demonstrated by EdU and CCK-8 experiments. The inflammatory response in macrophages was also significantly inhibited by miR-6869-5p, which could regulate PTPRO as a target documented by luciferase reporter assay. Moreover, miR-6869-5p promoted M2 macrophage polarization and thus restrain inflammation. Accordingly, miR-6869-5p is involved in maintaining placental microenvironment balance by preventing from inflammation and inducing M2 macrophages in gestational diabetes mellitus.http://dx.doi.org/10.1155/2021/6696636
spellingShingle Pingping Wang
Zhenzhi Ma
Zengyan Wang
Ximei Wang
Guifeng Zhao
Zengfang Wang
MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus
Mediators of Inflammation
title MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus
title_full MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus
title_fullStr MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus
title_full_unstemmed MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus
title_short MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus
title_sort mir 6869 5p induces m2 polarization by regulating ptpro in gestational diabetes mellitus
url http://dx.doi.org/10.1155/2021/6696636
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