Abstract
Background: Numerous changes in maternal physiology occur during pregnancy that are critical in controlling and maintaining the maternal metabolic adaptations and fetal development. The placenta is the key source through which the fetus receives nutrients, blood, and oxygen for growth. The human placenta releases several molecules into maternal circulation that include hormones, proteins, RNA, and DNA throughout the course of pregnancy. Additionally, extracellular vesicles (EVs) originating from the placenta have been found in the maternal circulation.
Methods: In this review, we discuss the role of EVs in maternal-fetal communication during pregnancy.
Results: EVs originating from the placenta can be divided into 3 categories based on their size and/or origin: exosomes (50 to 150 nm), microvesicles (nm to several μm), and apoptotic bodies or syncytial nuclear aggregates (>1 μm). The cellular microenvironment—such as oxygen tension and glucose concentration—have been found to control EV release from the placenta and their bioactivity on target cells. Furthermore, maternal EVs can stimulate cytokine release from endothelial cells and are involved in several physiologic and pathologic events in pregnancy.
Conclusion: Exosomes provide a way to identify the function and metabolic state of cell origin through their ability to reflect the microenvironment that they are released from. Further understanding of how EVs regulate key events in pregnancy may help elucidate how maternal-fetal communication is established in both normal and pathologic conditions.
INTRODUCTION
The human placenta develops from the implantation of the blastocyst into the uterine wall and becomes a critical transient organ that is unique to pregnancy.1 The placenta provides nutrition, gas exchange, waste removal, and immune support for the fetus and also mediates molecular exchange between the maternal and fetal systems.2
The placenta is the home of trophoblast cells that can be subcategorized as cytotrophoblasts, extravillous trophoblasts, or syncytiotrophoblasts. The placenta releases many different molecules that can alter maternal physiology to accommodate fetal requirements during gestation. The placenta may also influence the physiology of the mother via extracellular vesicles (EVs).3-5
EVs are increasingly released into the maternal circulation as pregnancy progresses, in both healthy and pathologic pregnancies (ie, pregnancies complicated by gestational diabetes mellitus [GDM]) or preeclampsia [PE]) (Figure).4-6 EVs encapsulate a diverse cargo of proteins, lipids, and nucleic acids that are released into the maternal circulation and are subsequently taken up by cells of the maternal immune and vascular systems, thereby modulating the overall maternal physiologic system to adapt to pregnancy-induced changes.4 In complicated pregnancies, this mode of cell signaling plays a role in the manifestation of physical symptoms of disease states, as the release of the EVs is dependent on the microenvironment to which they are exposed.7
Extracellular vesicle (EV) trafficking during pregnancy. EVs—including small EVs such as exosomes and large EVs such as microvesicles and apoptotic bodies—are released from the human placenta into maternal and fetal circulation during pregnancy. Placental EVs present in maternal circulation can interact with maternal tissues and regulate several biologic functions, including maternal immune response, migration/invasion, metabolic adaptation to pregnancy, and vascular reactivity. EVs present in fetal circulation are associated with fetal development. GDM, gestational diabetes mellitus; PE, preeclampsia.
Several recent (2014 through 2020) reviews on EVs during pregnancy have been published,8-11 but this review focuses on EVs during gestation, with emphasis on the trafficking of placental vesicles into maternal circulation to regulate immune and metabolic adaptations in pregnancy.
GENERAL CHARACTERISTICS OF EXTRACELLULAR VESICLES
Investigation of the potential role of EVs in intercellular communication has been an area of growing research.12 EVs are lipid bilayer structures measuring 50 nm to several μm that are released from a multitude of different cell types, including trophoblasts,13 erythrocytes,14 and endothelial cells,15 into the extracellular environment. Within their lipid bilayer membrane, EVs contain RNA, DNA, and proteins, which are hypothesized to modulate the bioactivity of specifically targeted cells.16 Studies published in 2014 and 2018 have demonstrated that EVs may affect cellular adaptations to physiologic changes during gestation, including immune responses, migration, and invasion of placental cells.17,18
The different types of EVs—exosomes, microvesicles, and apoptotic bodies—can be categorized on the basis of their size, surface markers, and content.12 Exosomes are a specific type of EV (50 to 150 nm) that arise from the inward budding of the plasma membrane, forming multivesicular bodies that internalize to form intraluminal vesicles and are then released into the extracellular environment as exosomes. As a result of their mode of formation, exosomes are enriched with intracellular proteins such as CD63, CD9, and CD81. Exosomes are distinguished from other EV cells by their distinct cup-shaped morphology and a buoyant density in a sucrose gradient, ranging from 1.13 to 1.19 g/mL. Compared to exosomes, microvesicles are different in size and originate in a different manner. Microvesicles can be as small as exosomes or as large as a few μm in size and are derived from plasma membrane secretion through direct budding of the membrane itself in response to cellular activation or in response to stress.19 Similarly, apoptotic bodies differ from exosomes in size (>1 μm) and through their formation via membrane blebbing, membrane protrusion, and formation of distinct bodies.
Regardless of their origin and size, EVs play important roles in cell communication and act as key regulators in disease states and healthy conditions. In the context of pregnancy, the placenta releases a wide range of EVs that are identified in the maternal circulation in both normal pregnancies and pregnancies with complications.
PLACENTAL VESICLES IN MATERNAL CIRCULATION
Exosomes are released from different organs, including the placenta, in both normal and pathologic conditions.5 Placental exosomes are hypothesized to regulate the establishment of maternal-fetal circulation via remodeling of spiral arteries. Upon implantation, the blastocyst adheres to the endothelium of the placenta, and the trophoblastic cells of the fetus differentiate into an inner cytotrophoblast and an outer syncytiotrophoblast layer. As the blastocyst continues to grow, the cytotrophoblast layer forms a layer of multinucleated syncytiotrophoblasts. Within this layer, the cytotrophoblast releases proteolytic enzymes, while the syncytiotrophoblast layer extends finger-like projections into the endometrium and replaces the endothelial cells of the uterine spiral arteries, establishing a connection between the growing embryo and maternal blood. This normal physiologic process is thought to be mediated at least in part by cell-to-cell communication via EVs and is complete by 10 weeks of gestation.
Evidence of EV release by extravillous trophoblasts has been demonstrated through the detection of soluble proteins such as human leukocyte antigen G (HLA-G).20 Whereas HLA-G is expressed only in extravillous trophoblasts, HLA-G+-EVs have been detected in pregnancy.21 An analysis of EVs released from extravillous trophoblasts using Swan71 cell line isolation showed that the EVs release exosomes.22 The findings of this study strongly indicate that extravillous trophoblasts not only release microvesicles but specifically exosomes.
The amount and type of EVs released are affected by the microenvironment.23,24 In a comparison of pregnant and nonpregnant women, the concentration of exosomes was approximately 50-fold greater in pregnant women.25 The increased concentration may be attributable in part to the contribution of placental-specific exosomes that have been identified in maternal circulation as early as approximately 6 weeks of gestational age.9 Specifically, placental-alkaline phosphatase-positive (PLAP+)-EVs were detected in the maternal circulation throughout pregnancy.5 The PLAP+-EVs can be isolated from the plasma of pregnant women and increase during the first 12 weeks of gestation.5 The increased presence of these EVs may be because of the changes and adaptations in maternal physiology.
Changes in the cellular microenvironment, such as hypoxia or increased glucose concentration, also affect EV release. These different microenvironments can also affect vesicle content and the bioactivity of target cells.23,26 In pregnancies with increased stress, such as those complicated by GDM6 and PE,27 more EVs are released. For example, the circulation in women affected by PE contains approximately 40% greater number of EVs compared to healthy, pregnant women.28 Furthermore, studies have demonstrated that changes in the microenvironment can alter the secretion of EVs from cytotrophoblast cells and in turn affect vesicle content and bioactivity.23,24 Exosomes released from the placenta have been shown to decrease insulin sensitivity and glucose uptake in skeletal muscles, contributing to the pathophysiology of GDM.29 Also, exosomes released from other types of cells can affect placental function and are involved in regulating the physiologic and pathologic mechanisms in pregnancy. For example, exosomes released from adipocytes can mediate changes in placental metabolic status and contribute to GDM.30 Hence, the cross-communication between different organs and the placenta via exosomes is crucial in mediating the maternal metabolic changes in pregnancy.31
As previously stated, the role of exosomes in the remodeling of spiral arteries from a high-resistance, low-capacitance system to a low-resistance, high-capacitance system has been studied.13,26,27 Furthermore, studies have found that states of abnormal placentation, such as PE, have increased concentrations of circulating placental-derived EVs.27,28,32 All of these findings suggest that EVs have a significant role during pregnancy. The Table summarizes published studies characterizing EVs during gestation.5,6,14,25,28,33-43 Future studies are required to develop a proper understanding of the mechanisms of exosome release and their effect on the target cells, which could give insight into their role as markers for the diagnosis of pregnancy complications.
Studies of Extracellular Vesicles in Maternal and Fetal Circulation
POTENTIAL ROLES OF EXTRACELLULAR VESICLES DURING GESTATION
In normal physiology, EVs from the placenta balance both immunosuppressive and proinflammatory cytokines to support fetal establishment and curtail rejection. Because a fetus is antigenically unique from the mother, maternal immune responses against the growing organism must at least in some part be avoided by inhibiting maternal T lymphocyte (T cell) and natural killer (NK) cell activation.44 As stated previously, exosomes correlationally increase with increasing gestational age,5,6 and several studies have explored the potential role of placental-derived exosomes in regulating maternal immune response during pregnancy.20,45-48
More specifically, immune adaptations in pregnancy are believed to be largely attributable to the expression and production of different cytokines that are thought to be regulated by EVs.18,49 Throughout pregnancy, proinflammatory and anti-inflammatory stages allow for the development, maturation, and parturition of the fetus.49 Placental EVs are believed to have a role in modulating these proinflammation and anti-inflammation states by modulating cytokine release.6,20 A method through which this regulation occurs could be via the expression of UL16 binding protein 1-5 (ULBP1-5) and major histocompatibility complex (MHC) class I chain-related gene protein (MIC) on the surface of placenta-derived exosomes.48 The interaction with these ligands causes the selective and dose-dependent downregulation of receptor NKG2D, which is present in NK cells, CDC8+, and gamma delta T cells, without affecting the lytic pathway through perforin.48 Exosomes also have a role in expression of components of the B7 family of ligands including B7-H3, which causes downregulation of T cell activation.20 HLA-G5 isoform incorporation within exosomes is another important aspect of exosome involvement, as this class of molecules has been shown to protect fetal tissue from maternal immune cell attack.20
More specifically, placental EVs inhibit maternal immunity and promote fetal survival through the expression of specific immunoregulatory molecules.45,47,48 For instance, syncytin-1 is present in placental EV cells. In normal pregnancies, syncytin-1 suppresses the production of tumor necrosis factor alpha (TNF-α) and interferon gamma (IFN-γ), inflammatory regulators that have links to early pregnancy loss and PE.50,51 In a related manner, maternal EVs can also be proinflammatory, causing a systemic inflammatory state and resulting in pathologic pregnancies. Studies have shown that placental EVs can induce release of proinflammatory cytokines, including TNF-α, macrophage inflammatory protein (MIP)-1α, interleukin (IL)-1α, -6, -8, and -1β from endothelial cells and activate macrophages to release proinflammatory IL-1β.6,52 The activation of phagocytic cells, including macrophages and monocytes, is particularly important, as they regulate maternal immune response to maintain a normal pregnancy and also protect against infection.52,53 Similarly, monocyte internalization of EVs trigger their migration and the production of IL-1β, IL-6, granulocyte colony stimulating factor (G-CSF), and TNF-α.53
Alterations in the levels of inflammatory cytokines in pregnancy result in metabolic disorders such as GDM and PE. The amount of cytokine release is particularly evident in obese pregnant women.54 Because of the compounded effect of placental cytokine release and also cytokine release by adipose tissue, the inflammatory pathways are heightened.55 Increased body mass index in pregnancy has been shown to be associated with elevated levels of monocyte chemoattractant protein-1 (MCP-1) and TNF-α and increased activation of the p38 mitogen-activated protein kinases (MAPK) and signal transducer and activator of transcription 3 (STAT3) inflammatory pathways.56 These proinflammatory states may modify placental function and in turn have fetal effects.
The outcome of aberrant regulation of inflammatory pathways has been established57-59; however, the molecules specifically responsible for these effects are still not well understood. The content of EVs reflects the cellular microenvironment and the physiologic response to stresses in the microenvironment and thus may be an important aspect in further understanding the physiologic mechanisms in pregnancy. Current data suggest that exosomes in maternal circulation may contribute to development of a proinflammatory environment by transferring specific cargo (protein and microRNAs [miRNAs]) to target cells.
EXTRACELLULAR VESICLES IN FETAL CIRCULATION
Once established, maternal-fetal circulation is a bidirectional system that nonselectively allows for the exchange between mother and fetus of nutrients, oxygen, wastes, and cytokines necessary for fetal growth. Because of the bidirectional passage, pathologic changes affecting maternal adaptations may also complicate the fetus. On the other hand, cellular trafficking from the fetal to maternal compartment leads to fetal microchimerism, and an appropriate maternal immune response to this phenomenon is key for the proper maintenance of pregnancy.60,61 Furthermore, cell-to-cell signaling from mother to fetus in complicated pregnancies helps protect the fetus via compensatory mechanisms.
Exosomes have been isolated from fetal cord blood in several studies33,58-60,62,63; however, Miranda et al examined the contribution of placental exosomes to the total exosome concentration in fetal circulation and found that the concentration of placental exosomes in maternal and fetal circulation is decreased in conditions such as fetal growth restriction and small for gestational age.64 Cleys et al studied the umbilical cord blood and serum in pregnant sheep and showed the presence of placental EVs.65 A comparison between miRNAs of these vesicles isolated from the umbilical cord blood and maternal serum demonstrated a difference in the miRNA content. Further evaluation by bioinformatics analysis revealed that the miRNA in fetal circulation is important for embryonic development, and in states with abnormal stressors on maternal development, the expression profile of exosomes is also altered.62 The proteins that were expressed differently caused different outcomes for regulation of cellular processes, including complement and coagulation cascades, enzyme regulator activity, and extracellular regulation. Identifying placental-specific exosomes in fetal circulation and isolating their specific roles in both healthy and pathologic pregnancies are important areas of research and need further investigation.
CONCLUSION
EVs represent a mechanism of maternal-fetal interaction during gestation. Exosomes provide a way to identify the function and metabolic state of cell origin through their ability to reflect the microenvironment that they are released from and the metabolic state of their cell of origin. Studies have demonstrated that EVs are released from the placenta into the maternal circulation and have a wide range of functions to regulate immunologic responses to pregnancy and to establish the maternal vascular function. Further understanding of how EVs regulate key events in pregnancy may help elucidate how maternal-fetal communication is established in both normal and pathologic conditions.
This article meets the Accreditation Council for Graduate Medical Education and the American Board of Medical Specialties Maintenance of Certification competencies for Patient Care and Medical Knowledge.
ACKNOWLEDGMENTS
Carlos Salomon, PhD, DMedSc, MPhil, BSc is supported by the Lions Medical Research Foundation, Diabetes Australia, and Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT 1170809 and 11190522). Soumyalekshmi Nair, MSc holds a research training program scholarship from The University of Queensland, funded by the Commonwealth Government of Australia. Otherwise, the authors have no financial or proprietary interest in the subject matter of this article.
- ©2020 by the author(s); Creative Commons Attribution License (CC BY)
©2020 by the author(s); licensee Ochsner Journal, Ochsner Clinic Foundation, New Orleans, LA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (creativecommons.org/licenses/by/4.0/legalcode) that permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
