4.3 Article

Down-regulation of microRNA-30d-5p is associated with gestational diabetes mellitus by targeting RAB8A

期刊

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jdiacomp.2021.107959

关键词

GDM; miR-30d-5p; Trophoblastic cell; Cell function; RAB8A

资金

  1. National Natural Science Foundation of China [81771590]
  2. Research fund of National Research Institute for Family Planning [2020GJZ02]

向作者/读者索取更多资源

The study found that the expression of miR-30d-5p is down-regulated in the placenta of patients with gestational diabetes mellitus (GDM). The research results suggest that miR-30d-5p affects trophoblast cell function by targeting RAB8A, providing new insights into the pathogenesis of GDM.
Gestational Diabetes Mellitus (GDM) is a complicated clinical process, and metabolic disorders during pregnancy are closely related to the structure and function of the placenta. The aberrant expression of miRNAs in the placenta may play a role in the occurrence and development of GDM. Analysis of microRNA (miRNA) expression signature in placenta showed that the level of miR-30d-5p was significantly down-regulated in GDM patients. This study aims to explore the possible mechanism of GDM under the regulation of miR-30d-5p. In situ hybridization and qRT-PCR assay showed that miR-30d expression down-regulated in the placentas from GDM patients compared with normal control group. The trophoblast cells proliferation and glucose uptake capacity were increased, the ability of migration and invasion were also improved after inhibiting the function of endogenous mature miR30d-5p. Bioinformatics analysis and luciferase reporter assays showed that miR-30d-5p binds to the 3 ' UTR of RAB8A mRNA, resulting in RAB8A suppression. Moreover, the down-regulation of RAB8A could attenuate the increase in trophoblast cell proliferation, migration, invasion and glucose uptake induced by miR-30d-5p functional inhibitor. These data imply that miR-30d-5p expression is down-regulated in placental tissue from GDM patients and affects trophoblast cell functions by targeting RAB8A, which may provide new insight into the pathogenesis of GDM. (c) 2021 Elsevier Inc. All rights reserved.

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