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Expression of Dual-Specificity Phosphatase 9 in Placenta and Its Relationship with Gestational Diabetes Mellitus

Overview
Journal J Diabetes Res
Publisher Wiley
Specialty Endocrinology
Date 2019 Nov 28
PMID 31772940
Citations 2
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Abstract

Introduction: The aim of the present study was to examine placental levels of DUSP9 mRNA and protein and to investigate the potential role of DUSP9 in the development of gestational diabetes mellitus (GDM).

Methods: Placental tissues from pregnant women with GDM ( = 17) and normal healthy pregnant women ( = 16) were collected at delivery. The expression of DUSP9 mRNA in placental tissue was analyzed by real-time PCR, while the expression of DUPS9 protein was evaluated by immunohistochemistry and western blot. Differences in the expression levels of DUSP9 mRNA and protein between the two groups were assessed, as well as potential correlations between DUSP9 mRNA expression levels and relevant clinical indicators.

Results: Blood glucose levels were significantly higher in the GDM group than in the control group, based on an oral glucose tolerance test. DUSP9 protein was expressed in the placental cytotrophoblasts in both groups, and placental levels of DUSP9 protein and mRNA were significantly higher in women with GDM. Placental DUSP9 mRNA levels in all 33 women correlated moderately with delivery gestational week ( = 0.465, = 0.006), fasting plasma glucose ( = 0.350, = 0.046), 1-hour postload plasma glucose ( = 0.363, = 0.038), and 2-hour postload plasma glucose ( = 0.366, = 0.036), but not with maternal age, preconception body mass index, prenatal body mass index, or neonatal birth weight. Multiple linear regression analysis indicated that delivery gestational week was an influence factor of DUSP9 mRNA levels ( = 0.026, < 0.05).

Conclusions: DUSP9 upregulation in the placenta of GDM pregnant women may promote insulin resistance, which may correlate with the occurrence of GDM. But there is still possibility that DUSP9 upregulation was the results of insulin resistance and/or hyperglycemia. Further research is needed to explore the role of DUSP9 in GDM.

Citing Articles

miR-132-3p Modulates DUSP9-Dependent p38/JNK Signaling Pathways to Enhance Inflammation in the Amnion Leading to Labor.

Zhong Z, Liu Z, Zheng R, Chai J, Jiang S Int J Mol Sci. 2022; 23(3).

PMID: 35163786 PMC: 8836965. DOI: 10.3390/ijms23031864.


DUSP9, a Dual-Specificity Phosphatase with a Key Role in Cell Biology and Human Diseases.

Khoubai F, Grosset C Int J Mol Sci. 2021; 22(21).

PMID: 34768967 PMC: 8583968. DOI: 10.3390/ijms222111538.

References
1.
Patti M, Kahn C . The insulin receptor--a critical link in glucose homeostasis and insulin action. J Basic Clin Physiol Pharmacol. 1999; 9(2-4):89-109. DOI: 10.1515/jbcpp.1998.9.2-4.89. View

2.
Wang X, Zhang L, Ou G, Wei Q, Wu L, Chen Q . [Association of DUSP9 gene polymorphisms with gestational diabetes mellitus]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019; 36(3):267-270. DOI: 10.3760/cma.j.issn.1003-9406.2019.03.019. View

3.
Saltiel A, Kahn C . Insulin signalling and the regulation of glucose and lipid metabolism. Nature. 2001; 414(6865):799-806. DOI: 10.1038/414799a. View

4.
Al-Daghri N, Alkharfy K, Alokail M, Alenad A, Al-Attas O, Mohammed A . Assessing the contribution of 38 genetic loci to the risk of type 2 diabetes in the Saudi Arabian Population. Clin Endocrinol (Oxf). 2013; 80(4):532-7. DOI: 10.1111/cen.12187. View

5.
Muda M, Boschert U, Smith A, Antonsson B, Gillieron C, Chabert C . Molecular cloning and functional characterization of a novel mitogen-activated protein kinase phosphatase, MKP-4. J Biol Chem. 1997; 272(8):5141-51. DOI: 10.1074/jbc.272.8.5141. View