Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ 07110, USA.
Hackensack University Medical Center, Department of Pediatrics, Hackensack Meridian Health, Hackensack, NJ 07601, USA.
Int J Mol Sci. 2024 May 7;25(10):5102. doi: 10.3390/ijms25105102.
Placenta Accreta Spectrum (PAS) is a life-threatening condition in which placental trophoblastic cells abnormally invade the uterus, often up to the uterine serosa and, in extreme cases, tissues beyond the uterine wall. Currently, there is no clinical assay for the non-invasive detection of PAS, and only ultrasound and MRI can be used for its diagnosis. Considering the subjectivity of visual assessment, the detection of PAS necessitates a high degree of expertise and, in some instances, can lead to its misdiagnosis. In clinical practice, up to 50% of pregnancies with PAS remain undiagnosed until delivery, and it is associated with increased risk of morbidity/mortality. Although many studies have evaluated the potential of fetal biomarkers circulating in maternal blood, very few studies have evaluated the potential of circulating placental extracellular vesicles (EVs) and their miRNA contents for molecular detection of PAS. Thus, to purify placental EVs from maternal blood, we customized our robust ultra-sensitive immuno-purification assay, termed EV-CATCHER, with a monoclonal antibody targeting the membrane Placental Alkaline Phosphatase (PLAP) protein, which is unique to the placenta and present on the surface of placental EVs. Then, as a pilot evaluation, we compared the miRNA expression profiles of placental EVs purified from the maternal plasma of women diagnosed with placenta previa (controls, = 16); placenta lying low in uterus but not invasive) to those of placental EVs purified from the plasma of women with placenta percreta (cases, = 16), PAS with the highest level of invasiveness. Our analyses reveal that miRNA profiling of PLAP EVs purified from maternal plasma identified 40 differentially expressed miRNAs when comparing these two placental pathologies. Preliminary miRNA pathway enrichment and gene ontology analysis of the top 14 upregulated and top nine downregulated miRNAs in PLAP EVs, purified from the plasma of women diagnosed with placenta percreta versus those diagnosed with placenta previa, suggests a potential role in control of cellular invasion and motility that will require further investigation.
胎盘植入谱系疾病(PAS)是一种危及生命的病症,其中胎盘滋养细胞异常侵入子宫,通常可达子宫浆膜层,在极端情况下,还可侵入子宫壁以外的组织。目前,临床上尚无 PAS 的非侵入性检测方法,只能通过超声和 MRI 进行诊断。鉴于视觉评估的主观性,PAS 的检测需要高度的专业知识,并且在某些情况下可能导致误诊。在临床实践中,高达 50%的 PAS 妊娠直到分娩时仍未被诊断出来,并且与发病率/死亡率增加相关。尽管许多研究评估了循环于母体外周血中的胎儿生物标志物的潜力,但很少有研究评估循环胎盘细胞外囊泡(EVs)及其 miRNA 内容物用于 PAS 的分子检测。因此,为了从母体外周血中纯化胎盘 EVs,我们使用针对胎盘碱性磷酸酶(PLAP)蛋白的单克隆抗体定制了我们强大的超灵敏免疫纯化检测法,称为 EV-CATCHER,PLAP 蛋白是胎盘所特有的,存在于胎盘 EVs 的表面。然后,作为初步评估,我们比较了诊断为前置胎盘(对照组,n = 16)和胎盘植入(病例组,n = 16)的女性的母体外周血中纯化的胎盘 EVs 的 miRNA 表达谱。我们的分析表明,比较这两种胎盘病变时,从母体外周血中纯化的 PLAP-EVs 的 miRNA 图谱鉴定出 40 个差异表达的 miRNA。对从诊断为胎盘植入的女性血浆中纯化的 PLAP-EVs 中上调前 14 位和下调前 9 位 miRNA 的 miRNA 通路富集和基因本体分析初步表明,其在控制细胞侵袭和迁移方面具有潜在作用,这需要进一步研究。