Kyorin University School of Medicine, Department of Obstetrics and Gynecology, Tokyo 181-8611, Japan.
Endocr J. 2020 Aug 28;67(8):819-825. doi: 10.1507/endocrj.EJ20-0037. Epub 2020 May 21.
Pregnant women with obesity are at increased risk of parturition dysfunction; however, the biological mechanism has remained unknown. We hypothesized that molecules circulating in the serum of pregnant women with obesity may induce the aberrant expression of contraction-associated proteins (CAPs), leading to insufficient uterine contractions. This study aimed to investigate the effects of maternal serum on CAPs expression by human uterine smooth muscle cells (UtSMCs) and elucidate the influence of maternal obesity. Blood samples were collected from singleton pregnant women at 36-41 weeks of gestation before the onset of labor. UtSMCs were incubated in the serum, and the mRNA expressions of PTGFR, OXTR, GJA1, and PTGS2 were examined by RT-PCR. Progranulin (PGRN) is a circulating glycoprotein associated with insulin resistance characterized by the accumulation of visceral fat. The serum PGRN levels of the samples were measured by ELISA. After incubated with PGRN (100-1,000 ng/mL), mRNA expression of PTGFR, OXTR, and GJA1 and protein expression of CX43 were examined by RT-PCR and western blotting, respectively. The mRNA expressions of PTGFR, OXTR, and GJA1 showed significantly negative correlations with gestational weight gain (GWG). Serum PGRN levels showed a significantly positive correlation with GWG. High levels of PGRN suppressed the mRNA expression of GJA1 and the protein expression of CX43. The change in maternal serum induced by GWG suppressed the CAPs expression by UtSMCs. PGRN is one of the factors in the serum responsible for inhibiting the expression of CX43.
肥胖孕妇分娩功能障碍的风险增加;然而,其生物学机制尚不清楚。我们假设肥胖孕妇血清中的分子可能会诱导收缩相关蛋白 (CAPs) 的异常表达,导致子宫收缩不足。本研究旨在探讨母体血清对人子宫平滑肌细胞 (UtSMCs) 中 CAPs 表达的影响,并阐明母体肥胖的影响。采集单胎孕妇在分娩前 36-41 周的血液样本。将 UtSMCs 在血清中孵育,并用 RT-PCR 检测 PTGFR、OXTR、GJA1 和 PTGS2 的 mRNA 表达。颗粒蛋白前体 (PGRN) 是一种与胰岛素抵抗相关的循环糖蛋白,其特征是内脏脂肪堆积。通过 ELISA 测量样品的血清 PGRN 水平。用 PGRN(100-1000ng/ml)孵育后,通过 RT-PCR 和 Western blot 分别检测 PTGFR、OXTR 和 GJA1 的 mRNA 表达以及 CX43 的蛋白表达。PTGFR、OXTR 和 GJA1 的 mRNA 表达与 GWG 呈显著负相关。血清 PGRN 水平与 GWG 呈显著正相关。高水平的 PGRN 抑制 GJA1 的 mRNA 表达和 CX43 的蛋白表达。GWG 引起的母体血清变化抑制了 UtSMCs 中 CAPs 的表达。PGRN 是抑制 CX43 表达的血清因子之一。