Angiopoietin-like protein 4 induces growth hormone variant secretion and aggravates insulin resistance during pregnancy, linking obesity to gestational diabetes mellitus.
Chun-Heng KuoShu-Huei WangHsien-Chia JuanSzu-Chi ChenChing-Hua KuoHan-Chun KuoShin-Yu LinHung-Yuan LiPublished in: BioFactors (Oxford, England) (2024)
Angiopoietin-like protein 4 (ANGPTL4) is a secretory glycoprotein involved in regulating glucose homeostasis in non-pregnant subjects. However, its role in glucose metabolism during pregnancy and the pathophysiology of gestational diabetes mellitus (GDM) remains elusive. Thus, this study aimed to clarify the relationship between ANGPTL4 and GDM and investigate the pathophysiology of placental ANGPTL4 in glucose metabolism. We investigated this issue using blood and placenta samples in 957 pregnant women, the human 3A-sub-E trophoblast cell line, and the L6 skeletal muscle cell line. We found that ANGPTL4 expression in the placenta was higher in obese pregnant women than in lean controls. Palmitic acid significantly induced ANGPTL4 expression in trophoblast cells in a dose-response manner. ANGPTL4 overexpression in trophoblast cells resulted in endoplasmic reticulum (ER) stress, which stimulated the expression and secretion of growth hormone-variant (GH2) but not human placental lactogen. In L6 skeletal muscle cells, soluble ANGPTL4 suppressed insulin-mediated glucose uptake through the epidermal growth factor receptor (EGFR)/extracellular signal-regulated kinases 1/2 (ERK 1/2) pathways. In pregnant women, plasma ANGPTL4 concentrations in the first trimester predicted the incidence of GDM and were positively associated with BMI, plasma triglyceride, and plasma GH2 in the first trimester. However, they were negatively associated with insulin sensitivity index ISI 0,120 in the second trimester. Overall, placental ANGPTL4 is induced by obesity and is involved in the pathophysiology of GDM via the induction of ER stress and GH2 secretion. Soluble ANGPTL4 can lead to insulin resistance in skeletal muscle cells and is an early biomarker for predicting GDM.
Keyphrases
- cell death
- cell cycle arrest
- pregnant women
- insulin resistance
- growth hormone
- skeletal muscle
- induced apoptosis
- epidermal growth factor receptor
- type diabetes
- poor prognosis
- metabolic syndrome
- endothelial cells
- adipose tissue
- pregnancy outcomes
- tyrosine kinase
- small cell lung cancer
- weight loss
- signaling pathway
- body mass index
- endoplasmic reticulum
- blood pressure
- endoplasmic reticulum stress
- polycystic ovary syndrome
- blood glucose
- physical activity
- long non coding rna
- high glucose
- advanced non small cell lung cancer
- high resolution
- glycemic control
- pluripotent stem cells