Département de Pédiatrie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, Québec, Canada.
Département d'Obstétrique et de Gynécologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, Québec, Canada.
J Clin Endocrinol Metab. 2019 Nov 1;104(11):5157-5169. doi: 10.1210/jc.2018-02693.
Underlying mechanisms leading to gestational diabetes mellitus (GDM) are still under investigation, and it is unclear whether the placenta plays a role in triggering glucose intolerance or if its functions are modified in response to the hyperglycemia. Circulating miRNAs are involved in placental development and function and are encapsulated in extracellular vesicles (EVs).
To compare differential expression of miRNAs in circulating EVs in pregnancies complicated by GDM vs controls.
This was a case-control study nested in a prospective pregnancy cohort including 23 women with GDM and 46 matched controls. The presence of serum EVs in early pregnancy was validated by transmission electron microscopy. Placental dimensions were assessed at 11 to 13 weeks of gestation. Differential expression of 17 miRNAs encapsulated in EVs (miR‒122-5p, miR‒132-3p, miR-1323, miR‒182-3p, miR‒210-3p, miR‒29a-3p, miR‒29b-3p, miR‒342-3p, miR‒517-5p, miR‒517a-3p, miR‒518b, miR-520h, miR‒525-5p, miR‒136-5p, miR‒342-3p, miR‒376c-5p, and miR‒494-3p) was assessed using quantitative reverse transcription PCR.
EVs were present in the early phase of placentation (6 to 15 weeks of gestation) in both cases and controls. No differences were observed for placental dimensions and estimated placental volume between GDM and control groups. Ten miRNAs (miR‒122-5p; miR‒132-3p; miR‒1323; miR‒136-5p; miR‒182-3p; miR‒210-3p; miR‒29a-3p; miR‒29b-3p; miR‒342-3p, and miR-520h) showed significantly higher levels in GDM cases than in controls (P ≤ 0.05). Bioinformatics analysis showed that these miRNAs are involved in trophoblast proliferation/differentiation as well as in insulin secretion/regulation and glucose transport in pregnant women.
The miRNA content of blood EVs may be a promising avenue for studying the early effect of impaired glucose metabolism on placental development.
导致妊娠期糖尿病(GDM)的潜在机制仍在研究中,尚不清楚胎盘在引发葡萄糖耐量异常中是否起作用,还是其功能因高血糖而改变。循环 microRNAs 参与胎盘发育和功能,并被包裹在细胞外囊泡(EVs)中。
比较 GDM 孕妇与对照组循环 EVs 中 microRNAs 的差异表达。
这是一项病例对照研究,嵌套在一个前瞻性妊娠队列中,包括 23 名 GDM 孕妇和 46 名匹配的对照组。通过透射电子显微镜验证早期妊娠血清 EVs 的存在。在妊娠 11 至 13 周时评估胎盘尺寸。使用定量逆转录 PCR 评估包裹在 EVs 中的 17 种 microRNAs(miR-122-5p、miR-132-3p、miR-1323、miR-182-3p、miR-210-3p、miR-29a-3p、miR-29b-3p、miR-342-3p、miR-517-5p、miR-517a-3p、miR-518b、miR-520h、miR-525-5p、miR-136-5p、miR-342-3p、miR-376c-5p 和 miR-494-3p)的差异表达。
在病例和对照组中,EVs 均存在于胎盘形成的早期阶段(妊娠 6 至 15 周)。GDM 组和对照组之间的胎盘尺寸和估计胎盘体积无差异。10 种 microRNAs(miR-122-5p;miR-132-3p;miR-1323;miR-136-5p;miR-182-3p;miR-210-3p;miR-29a-3p;miR-29b-3p;miR-342-3p 和 miR-520h)在 GDM 病例中的水平明显高于对照组(P≤0.05)。生物信息学分析表明,这些 microRNAs 参与滋养层细胞的增殖/分化以及孕妇的胰岛素分泌/调节和葡萄糖转运。
血液 EVs 的 microRNA 含量可能是研究葡萄糖代谢受损对胎盘发育早期影响的有前途的途径。