Department of Endocrinology, Fifth People's Hospital, Fudan University, Shanghai 200240, China; Discipline of Pathology, Bosch Institute and School of Medical Sciences, University of Sydney, 2006, Australia.
Department of Endocrinology, Fifth People's Hospital, Fudan University, Shanghai 200240, China.
J Reprod Immunol. 2017 Nov;124:8-14. doi: 10.1016/j.jri.2017.09.011. Epub 2017 Sep 28.
Gestational diabetes mellitus (GDM) is still a clinical challenge around world. Inflammation contributes to the pathogenesis of GDM, the precise underlying mechanism remains to be explored. IL-37 and 38 play important role in autoimmunity, but their role in the development of GDM is unclear. Using histopathology and immunohistochemistry, the thickness of the umbilical artery, the area of capillaries within the placental chorionic villi, and the production of IL-37/38 were determined. Placental mRNA of IL-37/IL-38 from GDM and Non-GMD was measured using qRT-PCR. serum IL-37/IL38 levels were evaluated, using ELISA. IL-37 was reduced 49%, 48% or 57% in chorionic villi of placentas (P<0.05), umbilical artery (P<0.05), or umbilical vein (P<0.05) from GDM women, respectively, compared to that from non-GDM women. In contrast, IL-38 was increased 3.3, 2.6, or 2.6 fold in chorionic villi (P<0.01), umbilical artery (P<0.05), umbilical vein (P<0.05) from GDM women, respectively, compared to that from non-GDM women. IL-37 in GDM placentas or serum was reduced ∼52% or 33%, compared to that from Non-GDM subjects, respectively; whereas IL-38 in the GDM placentas or serum was increased by 1.6 fold or 1.3 fold, compare to that from Non-GDM, respectively. Our data suggest that IL-37 protect pregnant women from the development of GDM. IL-38 produced in the chorionic villi and umbilical cords may be a response to local inflammation during the development of GDM. Such a dysregulated micro-environment may contribute to the development of GDM via an immune-mediated mechanism. These data may provide useful information for the intervention for GDM.
妊娠期糖尿病(GDM)仍然是全球临床面临的挑战。炎症导致 GDM 的发病机制,其潜在的精确机制仍有待探索。IL-37 和 38 在自身免疫中发挥重要作用,但它们在 GDM 发展中的作用尚不清楚。使用组织病理学和免疫组织化学方法,确定了脐带动脉的厚度、胎盘绒毛膜绒毛内毛细血管的面积以及 IL-37/38 的产生。使用 qRT-PCR 测量 GDM 和非 GDM 胎盘的 IL-37/IL-38 胎盘 mRNA。使用 ELISA 评估血清 IL-37/IL38 水平。与非 GDM 女性相比,GDM 女性胎盘绒毛膜(P<0.05)、脐带动脉(P<0.05)或脐带静脉(P<0.05)的 IL-37 分别减少了 49%、48%或 57%。相比之下,GDM 女性的绒毛膜(P<0.01)、脐带动脉(P<0.05)和脐带静脉(P<0.05)中的 IL-38 分别增加了 3.3、2.6 和 2.6 倍。与非 GDM 女性相比。与非 GDM 受试者相比,GDM 胎盘或血清中的 IL-37 分别减少了约 52%或 33%;而 GDM 胎盘或血清中的 IL-38 分别增加了 1.6 倍或 1.3 倍。我们的数据表明,IL-37 可保护孕妇免受 GDM 的发展。绒毛膜和脐带中产生的 IL-38 可能是 GDM 发展过程中局部炎症的反应。这种失调的微环境可能通过免疫介导的机制导致 GDM 的发展。这些数据可能为 GDM 的干预提供有用信息。