Nuffield Department of Obstetrics & Gynaecology, University of Oxford, Womens Centre Level 3, John Radcliffe Hospital, Oxford OX3 9DU, UK.
Nuffield Department of Obstetrics & Gynaecology, University of Oxford, Womens Centre Level 3, John Radcliffe Hospital, Oxford OX3 9DU, UK.
Eur J Obstet Gynecol Reprod Biol. 2014 Jan;172:32-5. doi: 10.1016/j.ejogrb.2013.10.022. Epub 2013 Oct 25.
Cell injury releases actin, the most abundant cell protein. Gelsolin and vitamin D binding protein (VDBP) together depolymerise and clear cell-free actin. Impaired actin clearance is associated with several diseases and correlates with clinical outcome. The actin scavenging system was investigated in pre-eclampsia (PE), a procoagulant and proinflammatory state with placental and vascular damage.
Plasma gelsolin and actin free VDBP (AFVDBP) were measured in PE (early onset <33weeks; late onset ≥36weeks), matched normal pregnant (normP) and non-pregnant (nonPr) women, using commercially available ELISAs. Longitudinal samples from normP and women who subsequently developed PE were also analysed.
Plasma gelsolin fell during pregnancy (p=0.0002), with a concomitant rise in actin-free VDBP (p<0.001). Gelsolin concentrations were only significantly lower in established PE (p<0.05) when compared to non-pregnant controls.
We have shown that the components of the actin clearance system, gelsolin and AFVDBP, are altered in normal pregnancy and further changes occur in established PE, suggesting depleted actin clearance in PE. Whether this is a cause or consequence of PE pathophysiology requires further investigation.
细胞损伤会释放肌动蛋白,这是细胞中含量最丰富的蛋白质。凝溶胶蛋白和维生素 D 结合蛋白(VDBP)共同使无细胞肌动蛋白解聚和清除。细胞内肌动蛋白清除功能受损与多种疾病相关,并与临床结果相关。本研究旨在探讨子痫前期(PE)中肌动蛋白清除系统的变化,PE 是一种存在胎盘和血管损伤的促凝和促炎状态。
采用商业 ELISA 法检测早发型(<33 周)和晚发型(≥36 周)子痫前期、匹配的正常妊娠(normP)和非妊娠(nonPr)妇女的血浆凝溶胶蛋白和无细胞游离 VDBP(AFVDBP)。还分析了 normP 妇女和随后发生 PE 的妇女的纵向样本。
血浆凝溶胶蛋白在妊娠期间下降(p=0.0002),同时伴随游离 VDBP 浓度升高(p<0.001)。与非妊娠对照组相比,仅在已确诊的 PE 患者中,凝溶胶蛋白浓度显著降低(p<0.05)。
我们已经表明,正常妊娠时肌动蛋白清除系统的组成部分,即凝溶胶蛋白和 AFVDBP,发生改变,而在已确诊的 PE 中进一步发生变化,提示 PE 中肌动蛋白清除功能受损。这种情况是 PE 病理生理学的原因还是结果,需要进一步研究。