...
首页> 外文期刊>Cardiovascular Research >Shear stress and spiral artery remodelling: the effects of low shear stress on trophoblast-induced endothelial cell apoptosis.
【24h】

Shear stress and spiral artery remodelling: the effects of low shear stress on trophoblast-induced endothelial cell apoptosis.

机译:剪应力和螺旋动脉重塑:低剪应力对滋养细胞诱导的内皮细胞凋亡的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

AIMS: In the first trimester of pregnancy, placental trophoblasts migrate along uterine spiral arteries (SA) and replace endothelial cells (EC) lining these vessels by mechanisms involving EC apoptosis. Inadequate SA remodelling has been associated with pre-eclampsia and intra-uterine growth restriction. Until 10-12 weeks of gestation, trophoblasts plug SA, preventing maternal blood flow into the intervillous space and resulting in high resistance, low shear flow in these vessels. We aimed to determine the effect of shear stress on trophoblast-induced EC apoptosis. METHODS AND RESULTS: Trophoblasts and human umbilical vein endothelial cells (HUVECs) were cultured for 13-31 h under shear stresses from 0.02 to 7 dyne/cm(2). Apoptosis was quantified by time-lapse microscopy. Treatment with tumour necrosis factor alpha/actinomycin D increased apoptotic death in all cell types (P < 0.01). However, trophoblasts cultured in 3 dyne/cm(2) underwent less apoptosis than those in 0.5 dyne/cm(2) cultures (P < 0.05). Trophoblasts cultured on HUVEC monolayers at 0.5 or 3 dyne/cm(2) significantly induced apoptosis in directly adjacent HUVECs, in comparison to HUVECs >2 cells away or HUVEC only controls (P < 0.05), and this was mediated by Fas/Fas-ligand mechanisms. The amount of induced apoptosis decreased from 0.5 to 3 dyne/cm(2) cultures (P < 0.05), and trophoblasts failed to significantly induce HUVEC apoptosis in 5 or 7 dyne/cm(2) cultures. CONCLUSION: The survival advantage of trophoblasts over EC at low shear stress, and the inhibition of trophoblast-induced EC apoptosis with increasing shear stress, suggests that low shear stresses in plugged first-trimester SA may aid trophoblast-induced EC apoptosis involved in SA remodelling.
机译:目的:在妊娠的前三个月中,胎盘滋养细胞沿子宫螺旋动脉(SA)迁移,并通过涉及EC凋亡的机制替代位于这些血管内的内皮细胞(EC)。 SA重塑不足与子痫前期和子宫内生长受限有关。直到妊娠10-12周为止,滋养细胞都会堵塞SA,阻止母体血液流入小毛孔腔,并导致这些血管的阻力高,剪切力低。我们旨在确定剪应力对滋养细胞诱导的EC凋亡的影响。方法和结果:滋养层细胞和人脐静脉内皮细胞(HUVEC)在0.02至7达因/厘米(2)的剪切应力下培养13-31小时。通过延时显微镜对细胞凋亡进行定量。用肿瘤坏死因子α/放线菌素D处理可增加所有细胞类型的凋亡死亡(P <0.01)。但是,在3达因/厘米(2)中培养的滋养细胞比在0.5达因/厘米(2)文化中的滋养细胞凋亡更少(P <0.05)。在HUVEC单层以0.5或3达因/厘米(2)的浓度滋养细胞,相比于距离超过2个细胞的HUVEC或仅HUVEC的对照,显着诱导了直接相邻的HUVEC的凋亡(P <0.05),这是由Fas / Fas-介导的。配体机制。诱导的细胞凋亡量从0.5达因/厘米(2)培养物减少(P <0.05),并且滋养细胞未能显着诱导5或7达因/厘米(2)培养物中的HUVEC凋亡。结论:在低切应力下,滋养层细胞比EC具有存活优势,且随着切应力的增加,对滋养层诱导的EC细胞凋亡的抑制作用表明,早孕SA中低切应力可能有助于滋养层诱导的EC细胞凋亡,参与SA重塑。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号