Inoviq Limited, Notting Hill, Australia; Translational Extracellular Vesicles in Obstetrics and Gynae-Oncology Group, The University of Queensland Centre for Clinical Research, Royal Brisbane and Women's Hospital, Faculty of Medicine, The University of Queensland, Brisbane, QLD, 4029, Australia.
Translational Extracellular Vesicles in Obstetrics and Gynae-Oncology Group, The University of Queensland Centre for Clinical Research, Royal Brisbane and Women's Hospital, Faculty of Medicine, The University of Queensland, Brisbane, QLD, 4029, Australia.
Placenta. 2024 Nov;157:5-13. doi: 10.1016/j.placenta.2024.02.007. Epub 2024 Feb 23.
The field of extracellular vesicle (EV) signalling has the potential to transform our understanding of maternal-fetal communication and affords new opportunities for non-invasive prenatal testing and therapeutic intervention. EVs have been implicated in implantation, placentation, maternal adaptation to pregnancy and complications of pregnancy, being detectable in maternal circulation as early as 6 weeks of pregnancy. EVs of differing biogenic origin, composition and bioactivity are released by cells to maintain homoeostasis. Induction of EV signalling is associated with aberrant cellular metabolism and manifests as changes in EV concentrations and/or composition. Characterizing such changes affords opportunity to develop more informative diagnostics and efficacious interventions. To develop accurate and reliable EV-based diagnostics requires: identification of disease-associated biomarkers in specific EV subpopulations; and rapid, reproducible and scalable sample processing. Conventional isolation methods face challenges due to co-isolation of particles with similar physicochemical properties. Methods targeting specific vesicle-surface epitopes and compatible with automated platforms show promise. Effective EV therapeutics require precise targeting, achieved through genetic engineering to release EVs expressing cell-targeting ligands and carrying therapeutic payloads. Unlike cell-based therapies, this approach offers advantages including: low immunogenicity; stability; and long-term storage. Although EV diagnostics and therapeutics in reproductive biology are nascent, available technologies can enhance our understanding of EV signalling between mother and fetus, its role in pregnancies and improve outcomes.
细胞外囊泡(EV)信号领域有可能改变我们对母婴通讯的理解,并为非侵入性产前检测和治疗干预提供新的机会。EV 参与了着床、胎盘形成、母体对妊娠的适应以及妊娠并发症,早在妊娠 6 周时就可以在母体循环中检测到。不同生物起源、组成和生物活性的 EV 由细胞释放以维持内稳态。EV 信号的诱导与异常细胞代谢有关,并表现为 EV 浓度和/或组成的变化。表征这种变化为开发更具信息性的诊断和有效的干预提供了机会。为了开发准确可靠的基于 EV 的诊断方法,需要:在特定的 EV 亚群中识别与疾病相关的生物标志物;以及快速、可重复和可扩展的样本处理。由于类似的物理化学性质,常规的分离方法面临着共同分离颗粒的挑战。针对特定囊泡表面表位的方法与自动化平台兼容,显示出前景。有效的 EV 治疗需要精确的靶向,通过基因工程实现,释放表达细胞靶向配体并携带治疗有效载荷的 EV。与基于细胞的治疗方法不同,这种方法具有以下优点:低免疫原性;稳定性;和长期储存。尽管生殖生物学中的 EV 诊断和治疗仍处于起步阶段,但现有技术可以增强我们对母婴之间 EV 信号、其在妊娠中的作用以及改善妊娠结局的理解。