Role of melatonin receptor 1B gene polymorphism and its effect on the regulation of glucose transport in gestational diabetes mellitus.
- Author:
Lijie WEI
1
;
Yi JIANG
1
;
Peng GAO
1
;
Jingyi ZHANG
1
;
Xuan ZHOU
1
;
Shenglan ZHU
1
;
Yuting CHEN
1
;
Huiting ZHANG
1
;
Yuanyuan DU
1
;
Chenyun FANG
1
;
Jiaqi LI
2
;
Xuan GAO
1
;
Mengzhou HE
1
;
Shaoshuai WANG
1
;
Ling FENG
1
;
Jun YU
3
Author Information
- Publication Type:Journal Article
- Keywords: Gestational diabetes mellitus (GDM); Glucose transporters (GLUTs); Glucose uptake; Melatonin receptor 1B (MTNR1B); Peroxisome proliferator-activated receptor γ (PPARγ); Single nucleotide polymorphism (SNP)
- MeSH: Female; Humans; Pregnancy; Blood Glucose/metabolism*; Diabetes, Gestational/metabolism*; Glucose/metabolism*; Melatonin/metabolism*; Polymorphism, Genetic; PPAR gamma; Receptor, Melatonin, MT2/genetics*
- From: Journal of Zhejiang University. Science. B 2023;24(1):78-88
- CountryChina
- Language:English
- Abstract: Melatonin receptor 1B (MT2, encoded by the MTNR1B gene), a high-affinity receptor for melatonin, is associated with glucose homeostasis including glucose uptake and transport. The rs10830963 variant in the MTNR1B gene is linked to glucose metabolism disorders including gestational diabetes mellitus (GDM); however, the relationship between MT2-mediated melatonin signaling and a high birth weight of GDM infants from maternal glucose abnormality remains poorly understood. This article aims to investigate the relationship between rs10830963 variants and GDM development, as well as the effects of MT2 receptor on glucose uptake and transport in trophoblasts. TaqMan-MGB (minor groove binder) probe quantitative real-time polymerase chain reaction (qPCR) assays were used for rs10930963 genotyping. MT2 expression in the placenta of GDM and normal pregnant women was detected by immunofluorescence, western blot, and qPCR. The relationship between MT2 and glucose transporters (GLUTs) or peroxisome proliferator-activated receptor γ (PPARγ) was established by western blot, and glucose consumption of trophoblasts was measured by a glucose assay kit. The results showed that the genotype and allele frequencies of rs10830963 were significantly different between GDM and normal pregnant women (P<0.05). The fasting, 1-h and 2-h plasma glucose levels of G-allele carriers were significantly higher than those of C-allele carriers (P<0.05). Besides, the protein and messenger RNA (mRNA) expression of MT2 in the placenta of GDM was significantly higher than that of normal pregnant women (P<0.05). Melatonin could stimulate glucose uptake and GLUT4 and PPARγ protein expression in trophoblasts, which could be attenuated by MT2 receptor knockdown. In conclusion, the rs10830963 variant was associated with an increased risk of GDM. The MT2 receptor is essential for melatonin to raise glucose uptake and transport, which may be mediated by PPARγ.
