bims-placeb Biomed News
on Placental cell biology
Issue of 2026–08–23
fourteen papers selected by
Carlos M Guardia, National Institute of Environmental Health Sciences



  1. EMBO Rep. 2026 Aug 20.
      The expansion and differentiation of trophoblast stem (TS) cells are critical for defining fundamental properties of the placenta. Specialized trophoblast cells called extravillous trophoblast (EVT) cells in human and invasive trophoblast cells in rat, exit the placenta, enter and transform the uterus. This includes the restructuring of uterine spiral arteries, essential for the transfer of nutrients to the fetus. Mechanisms governing invasive trophoblast cell differentiation remain poorly understood. Here, we investigate peroxisome proliferator-activated receptor gamma (PPARG) as a potential regulator of EVT/invasive trophoblast cell development. In first trimester human placentas, PPARG is expressed in the EVT cell column and increases in amount as human TS cells differentiate into EVT cells. PPARG disruption impairs EVT cell differentiation and alters the expression of genes controlling EVT cell lineage development. Rat invasive trophoblast cells similarly express PPARG. Conditional inactivation of PPARG within rat invasive trophoblast cells establishes PPARG as an essential cell-autonomous regulator of invasive trophoblast cells in vivo. In conclusion, PPARG is a conserved regulator of placentation and is essential for directing trophoblast cell-guided uterine transformation.
    DOI:  https://doi.org/10.1038/s44319-026-00896-0
  2. Hum Reprod. 2026 Aug 22. pii: deag132. [Epub ahead of print]
       STUDY QUESTION: What is the contribution of cyclin-dependent kinase inhibitor 1C (CDKN1C) to the regulation of extravillous trophoblast (EVT) cell differentiation and function?
    SUMMARY ANSWER: Cell cycle regulators CDKN1C, cyclin-dependent kinase 7 (CDK7), and cyclin E1 (CCNE1) contribute to the development of a healthy placenta by promoting trophoblast stem (TS) cell differentiation to the invasive EVT cell lineage.
    WHAT IS KNOWN ALREADY: Early in gestation, cytotrophoblast cells expand and then differentiate into terminal cell lineages, including EVT cells, which invade into uterine tissue and facilitate redirection of maternal resources to the fetus. Cyclin-dependent kinase inhibitor 1C (CDKN1C) is a cell cycle regulator implicated in placental development.
    STUDY DESIGN, SIZE, DURATION: In this study, we used control versus gene-silenced human trophoblast stem cells to assess mechanisms regulating human TS cell differentiation to the EVT cell lineage. An 8-day EVT cell differentiation protocol was utilized. RNA sequencing data include n = 3 for control EVT cells and n = 3 for gene-silenced cells. Assessment of cell counts, DNA content, qPCR, and migration assays were performed with between n = 3 and n = 6.
    PARTICIPANTS/MATERIALS, SETTING, METHODS: In situ hybridization was used to evaluate CDKN1C, CDK7, and CCNE1 transcript expression in human placental tissue sections. A human trophoblast stem cell model was utilized to assess the contributions of CDKN1C, CDK7, and CCNE1 to EVT cell development. Gene perturbation was achieved through lentiviral delivery of short-hairpin RNAs to XY (CT29) and XX (CT27) human TS cell lines. Characterization of cell models and effects of gene silencing were measured by assessing cell morphology and number, reverse transcriptase-quantitative polymerase chain reaction, western blotting, flow cytometry, and co-immunoprecipitation.
    MAIN RESULTS AND THE ROLE OF CHANCE: CDKN1C was expressed in EVT cells of the placenta and in EVT cells derived from TS cells. Disruption of CDKN1C in TS cells affected cell proliferation, morphology, DNA content, migration, and transcript profiles. CDKN1C is a known modulator of CDK-CCN complexes. CDK7 and CCNE1 were prominently expressed in EVT cells of the placenta and in EVT cells derived from TS cells. CDKN1C was also shown to physically interact with CDK7 and CCNE1. Loss of CDK7 or CCNE1 impaired EVT cell differentiation.
    LARGE SCALE DATA: RNA-seq datasets are available at the Gene Expression Omnibus database under accession number GSE316875.
    LIMITATIONS, REASONS FOR CAUTION: In vitro experiments were used to evaluate contribution of cell cycle regulators to EVT cell development. Therefore, these methods do not completely recapitulate the in vivo cell environment.
    WIDER IMPLICATIONS OF THE FINDINGS: Collectively, these findings demonstrate the importance CDKN1C in regulating EVT cell differentiation and link its actions, at least in part, to CDK7 and CCNE1.
    FUNDING: Supported by an NIH F31predoctoral fellowship to RLS (HD104495), an NIH K99/R00 grants to KMV (HD107262) and AMI (HD115834), P20GM113117 to DKJ, NIH grants (HD020676, HD105734, HD112559), The Sosland Foundation, and the Donald C. Johnson Research Endowment Fund.
    DISCLOSURES: No disclosures to report.
    Keywords:  CCNE1; CDK7; CDKN1C; placenta; trophoblast
    DOI:  https://doi.org/10.1093/humrep/deag132
  3. Hum Reprod Update. 2026 Aug 20. pii: dmag025. [Epub ahead of print]
       BACKGROUND: The global expansion of assisted reproductive technologies (ART), including in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI), has raised concerns regarding the impact on placental development and susceptibility to pregnancy complications. Oxygen tension is a central regulator of placental biology, acting both as a physiological developmental signal and, when dysregulated, as a driver of pathology. Early placentation occurs in a naturally low-oxygen environment that is essential for trophoblast specification, invasion, immune-vascular crosstalk, and angiogenesis. These processes are coordinated by hypoxia-inducible factor (HIF) signaling and related oxygen-sensing pathways.
    OBJECTIVE AND RATIONALE: This review examines the dual role of oxygen in placental development and disease, with particular emphasis on the molecular mechanisms that regulate hypoxia responses during normal and pathological placentation. We further evaluate emerging evidence that ART alters early embryonic and placental programming and propose a mechanistic framework in which ART-induced developmental reprogramming increases susceptibility to hypoxic maladaptation later in pregnancy.
    SEARCH METHODS: Literature searches were conducted in PubMed and Google Scholar up to June 2026 using combinations of the terms 'hypoxia,' 'placenta,' 'HIF signaling,' 'assisted reproductive technology,' 'in vitro fertilization,' and 'embryo culture.' Studies were limited to English-language publications, with emphasis on human studies and mechanistic investigations in experimental animal and stem cell models.
    OUTCOMES: Oxygen tension emerges as a master regulator of placental development. Genetic and experimental studies demonstrate that precise temporal and spatial regulation of HIF signaling, including distinct contributions of HIF-1α and HIF-2α, is essential for trophoblast differentiation, placental morphogenesis, vascular development, and fetal viability. Physiological hypoxia orchestrates normal placentation, whereas sustained or dysregulated activation of hypoxia-responsive pathways contributes to an angiogenic imbalance, inflammation, oxidative stress, mitochondrial dysfunction, regulated cell death, and placental insufficiency. Increasing evidence suggests that ART may perturb this tightly regulated developmental program at its earliest stages. Exposure of preimplantation embryos to non-physiological culture conditions can alter their metabolic state, redox homeostasis, epigenetic regulation, and trophectoderm gene expression. These early perturbations may persist into placental development, resulting in impaired trophoblast differentiation and invasion, altered angiogenic signaling, and heightened sensitivity to hypoxic stress. Collectively, findings from experimental models, human placental studies, and emerging single-cell and spatial omics approaches support a model in which ART-induced developmental reprogramming predisposes the placenta to hypoxic maladaptation, thereby increasing susceptibility to disorders such as preeclampsia and fetal growth restriction.
    WIDER IMPLICATIONS: ART-associated placental hypoxia may originate from altered embryonic programming during preimplantation development rather than arising solely from placental pathology that develops later in pregnancy. Integrating developmental biology, oxygen-sensing pathways, and multi-omic approaches may facilitate the identification of early biomarkers, optimization of embryo culture conditions, and development of targeted strategies to improve maternal and fetal health.
    REGISTRATION NUMBER: N/A.
    Keywords:  ART; HIF signaling; IVF; fetal growth restriction; hypoxia; placenta; preeclampsia; trophoblast
    DOI:  https://doi.org/10.1093/humupd/dmag025
  4. J Virol. 2026 Aug 21. e0030026
      Adverse pregnancy outcomes associated with dengue virus (DENV) infection are a severe manifestation of dengue fever; however, we still poorly understand the underlying mechanisms. Trophoblast dysfunction in the placenta contributes centrally to various pregnancy complications. As the functional unit of the placenta, the syncytiotrophoblast (STB) requires continuous fusion of precursor trophoblasts and adequate energy supply. In this study, we established a model of adverse pregnancy by infecting Ifnar1-/- pregnant mice with DENV-2. We did not detect viral replication within the placental trophoblast layer but observed substantial structural damage to the STB. RNA-seq analysis demonstrated that precursor trophoblasts exhibit disrupted glucose metabolism, and placental tissue upregulates pro-fusion genes-yet fails to complete syncytialization. Metabolic assays revealed reduced ATP levels and elevated lactate concentrations, indicating that an inadequate energy supply impedes trophoblast differentiation. Treatment with the glycolytic inhibitor 2-DG restored oxidative phosphorylation (OXPHOS) activity in the placenta and markedly improved pathological outcomes. Further mechanistic studies established that DENV infection induces oxidative stress, which activates hypoxia-inducible factor Hif1α, leading to subsequent upregulation of lactate dehydrogenase (LDHA) expression. We identify this cascade as a fundamental mechanism underlying metabolic reprogramming in trophoblasts. Our findings not only clarify the key pathological processes driving DENV-induced adverse pregnancy outcomes but also propose novel therapeutic strategies for clinical intervention.IMPORTANCEDengue virus infection during pregnancy is linked to adverse fetal outcomes, but the underlying mechanisms remain unclear. In Ifnar1-/- pregnant mice, we show that fetal growth restriction is driven by disruption of the maternal environment that impairs placental function. We identify syncytiotrophoblast damage and defective trophoblast fusion despite compensatory upregulation of pro-fusion genes. Placental metabolic analysis reveals a shift from oxidative phosphorylation to glycolysis, accompanied by reduced ATP production and impaired syncytialization. Inhibition of glycolysis in vivo partially restores placental structure and improves fetal outcomes, supporting a key role for metabolic reprogramming. Mechanistically, ROS activates HIF-1α and upregulates its downstream target LDHA, thereby linking metabolic reprogramming to placental dysfunction and highlighting this pathway as a potential therapeutic target. These findings reveal a mechanism underlying DENV-associated pregnancy complications and highlight metabolic pathways as potential therapeutic targets.
    Keywords:  adverse pregnancy outcome; dengue virus; metabolic reprogram; syncytialization
    DOI:  https://doi.org/10.1128/jvi.00300-26
  5. Placenta. 2026 Aug 18. pii: S0143-4004(26)00668-5. [Epub ahead of print]183 37-43
       BACKGROUND: Maternal high-fat diet (HFD) contributes to developmental programming through placental adaptations; however, the effects of exposure timing before and during pregnancy remain unclear.
    OBJECTIVE: To investigate the distinct effects of pre-pregnancy and gestational HFD on maternal metabolism, pregnancy outcomes, placental oxidative stress, placental gene-expression adaptations, and gut microbiota in rats.
    METHODS: Female Sprague-Dawley rats were fed a control diet (V) or HFD (H) before and/or during pregnancy, generating four groups (V/V, V/H, H/V, H/H). Maternal metabolic parameters, placental gene expression, oxidative stress, and gut microbiota composition were analyzed at gestational day 21.
    RESULTS: Pre-pregnancy high-fat diet increased maternal body and liver weights and elevated placental oxidative stress, whereas gestational high-fat diet increased adiposity and impaired glucose tolerance and insulin sensitivity without affecting pregnancy outcomes. Placental nutrient transporters, including glucose transporter 1 (Glut1) and solute carrier family 38 (Slc38) members, were mainly regulated by pre-pregnancy diet. Insulin-like growth factor 2 (Igf2) was influenced by gestational diet and its interaction with pre-pregnancy diet, while insulin-like growth factor 2 receptor (Igf2R) and insulin 2 (Ins2) expression were primarily influenced by pre-pregnancy diet. Forkhead box O1 (FoxO1) and Forkhead box O3 (FoxO3) exhibited differential responses to maternal dietary exposure. Gestational HFD also altered gut microbiota composition without affecting microbial diversity.
    CONCLUSION: Pre-pregnancy and gestational HFD exert distinct but complementary effects on maternal metabolism and placental adaptations. These findings highlight the stage-specific impact of maternal nutritional status on developmental programming and placental function.
    Keywords:  DOHaD; Developmental programming; Maternal high-fat diet; Placenta; Transcriptomics
    DOI:  https://doi.org/10.1016/j.placenta.2026.08.335
  6. Placenta. 2026 Aug 13. pii: S0143-4004(26)00651-X. [Epub ahead of print]183 22-29
       INTRODUCTION: The human placental trophoblast layer is a crucial barrier to the transfer of xenobiotics from maternal to fetal fluids. Intercellular spaces between adjacent trophoblast cells are sealed by bicellular and tricellular tight junctions (TJs), which respectively include claudins and angulins. However, which TJ components are involved in the barrier function of placental trophoblast cells remains unclear.
    METHODS: In this study, we used proteins that bind to the extracellular domain of claudins or angulins (hereafter referred to as binders) to investigate the contributions of various TJ components to barrier function in JEG-3 cells, a human trophoblast model.
    RESULTS: In this system, claudin binders enhanced the permeation of paracellular passage markers (dextrans with molecular mass of ≤150 kDa) and thus more effectively attenuated TJ integrity than did angulin binders. Gene expression analysis revealed that claudin-4 and angulin-1 are key components in bicellular and tricellular TJs, respectively.
    CONCLUSIONS: This study is the first to characterize the barrier function of TJ components in JEG-3 cell monolayers, a human trophoblast model.
    Keywords:  Angulin; Claudin; JEG-3; Placenta; Tight junction
    DOI:  https://doi.org/10.1016/j.placenta.2026.08.318
  7. Reprod Toxicol. 2026 Aug 20. pii: S0890-6238(26)00174-7. [Epub ahead of print] 109331
      Plastic production has been increasing exponentially. Throughout their lifespan, plastics degrade into smaller particles that accumulate in our bodies and the environment. Recent studies found these plastic particles can cross the placental barrier and reach the fetus. However, the impact of plastic particles on placental function is still unknown. We hypothesized that nanoplastics would disrupt placental growth and function, specifically focusing on transforming growth factor beta (TGFβ) signaling. To understand the impact of plastic particles on the placenta, we orally exposed pregnant CD-1 mice to 50nm or 200nm polystyrene plastic particles from gestation day 8 to day 15 at a human-relevant concentration of 5mg/kg/day. After euthanasia on day 15, placenta and fetus weights were recorded, and tissues were prepared for histomorphology and gene expression analysis. We observed a statistically significant decrease in the area of the decidua in the placentas for the 200nm treatment group and a borderline significant decrease in decidua area for the 50nm treatment group compared to control. However, when separated by sex, only the male decidua were significantly decreased in the 200nm group. Gene expression analysis of key signaling factors in the TGFβ pathway identified increased expression of Smad2 and Smad3, which may be suppressing estrogen receptor signaling. Overall, both particle sizes disrupted placenta structure and signaling in a sex-dependent manner.
    Keywords:  developmental exposure; microplastics; nanoplastics; placenta; polystyrene
    DOI:  https://doi.org/10.1016/j.reprotox.2026.109331
  8. bioRxiv. 2026 Aug 05. pii: 2026.08.04.742335. [Epub ahead of print]
      Ebola virus (EBOV) disease (EVD) is a hemorrhagic disease caused by EBOV infection. EVD outcomes in pregnant women are similar to non-pregnant women however, EVD is associated with negative fetal outcomes in ∼99% of cases. There is a critical need for a tractable small animal model to study maternal/fetal transmission of EBOV. We utilized interferon α/β receptor knock out mice infected and authentic EBOV or the model virus, recombinant vesicular stomatitis virus encoding EBOV glycoprotein (rVSV/EBOV). Infection with either virus during late pregnancy resulted in placental infection and vertical transmission to the fetus within 2-3 days. Robust levels of maternal and fetal proinflammatory cytokines were evident by day 5 after EBOV infection. Within the placenta, trophoblasts and endothelial cells were viral antigen positive. Elimination of the endosomal receptor NPC1 in junctional zone trophoblasts reduced placental infection and virus transmission to the fetus. These studies establish an infectious model that provides EBOV trafficking and pathogenesis insights during pregnancy.
    Teaser: This model provides key insights into how viral trafficking and maternal immune responses drive adverse fetal outcomes during gestational Ebola virus infection.
    DOI:  https://doi.org/10.64898/2026.08.04.742335
  9. mBio. 2026 Aug 21. e0156226
      Zika virus (ZIKV) infection during pregnancy can result in severe fetal outcomes, yet the mechanisms of transplacental dissemination remain incompletely defined. We previously showed that ZIKV induces tunneling nanotubes (TNTs), actin-rich intercellular conduits that enable direct cell-to-cell transfer of viral components. Here, we investigated the in vivo role of TNTs in ZIKV maternal-fetal transmission using complementary pregnancy models. A TNT-deficient ZIKV mutant (ZIKVΔTNT), harboring a change between residues 40 and 52 of the nonstructural protein 1 (NS1), showed markedly reduced viral dissemination to maternal and fetal tissues across all models tested, whereas the TNT-competent ZIKV established a robust infection. ZIKVΔTNT infection was associated with reduced placental pathology, altered junctional-to-labyrinth architecture, improved placental efficiency, and protection from fetal growth restriction. Loss of TNT-forming capacity also limited viral persistence despite maternal type III interferon (IFN-λ) responses, suggesting a role for TNTs in immune evasion. Together, these findings provide in vivo evidence that TNTs are a key mechanism by which ZIKV enhances dissemination, promotes placental dysfunction, and drives fetal pathogenesis.IMPORTANCEZika virus infection during pregnancy can cause severe fetal abnormalities, yet how the virus overcomes the placenta remains incompletely understood. Here, we show that ZIKV exploits direct intercellular connections called tunneling nanotubes (TNTs) to facilitate cell-to-cell transmission and impact placental infection and fetal outcomes. Using multiple pregnancy models, we demonstrate that viruses capable of forming these structures disseminate more efficiently, damage the placenta, and lead to fetal growth restriction, whereas TNT-deficient viruses show reduced infection and milder disease. Importantly, TNT-mediated dissemination is associated with viral persistence despite maternal interferon responses, suggesting a role in immune evasion. These findings identify TNTs as a previously underappreciated pathway of viral transmission during pregnancy and suggest new therapeutic targets. More broadly, TNTs may contribute to the pathogenesis of other vertically transmitted or emerging viral infections.
    Keywords:  IFN-λ; NS1; TNT; ZIKV; placenta
    DOI:  https://doi.org/10.1128/mbio.01562-26
  10. Reprod Toxicol. 2026 Aug 21. pii: S0890-6238(26)00177-2. [Epub ahead of print] 109334
       INTRODUCTION: If taken during pregnancy, some psychotropic medications may increase the risk of adverse perinatal outcomes, including reduced birth weight and small for gestational age outcome. A key factor in foetal growth and development is the placental endocrine function, with critical placental hormones including human chorionic gonadotropin (hCG), placental growth factor (PlGF), and leptin. In this in vitro study, we aimed at characterising the impact of psychotropic medications on placental endocrine function.
    METHODS: We focused on often used psychotropic medications at concentrations up to 30µM and including concentrations attained in blood plasma in (non-pregnant) patients. Their effects on the secretion of hCG, PlGF, and leptin were investigated in a well-established model of human trophoblasts (BeWo cells). Since intact cell viability and metabolic activity are required for hormone production, these aspects were studied beforehand.
    RESULTS: Citalopram (at 30µM), sertraline and aripiprazole (at ≥10µM) markedly reduce cell viability, whereas quetiapine (at 30µM) slightly decreases it and diazepam and zolpidem (each up to 30µM) do not affect it. Experiments with subtoxic concentrations of the medications reveal no effects on either metabolic activity or on the production of the hormone hCG. The production of PlGF varies slightly and depending on the medication tested. Diazepam and quetiapine (at 30µM) markedly impair leptin production.
    DISCUSSION: Our findings reveal marked differences in how various medications affected cell viability and hormone production. Whether these effects could be related to changes in clinical outcomes such as birth weight and small-for-gestational-age requires further investigation.
    Keywords:  birth weight; diazepam; leptin; pregnancy; psychotropic; quetiapine
    DOI:  https://doi.org/10.1016/j.reprotox.2026.109334
  11. Theriogenology. 2026 Aug 11. pii: S0093-691X(26)00322-5. [Epub ahead of print]266 118132
      Pre-weaning mortality remains a major constraint to productivity and animal welfare in modern swine production and has not declined proportionally with improvements in genetics, nutrition, and housing. Mortality is commonly attributed to crushing, starvation, or impaired temperature regulation. However, accumulating evidence indicates that these outcomes frequently represent the final manifestations of compromised neonatal viability rather than independent primary causes. Selection for increased litter size has altered the intrauterine environment, such that uterine capacity and placental development limit fetal growth. Resulting variation in fetal development produces neonates with differing physiological reserves at birth, including reduced energy stores and impaired thermoregulatory capacity in vulnerable individuals. Parturition imposes an additional hypoxic and metabolic challenge. Prolonged farrowing and increased birth intervals due to large litter sizes expose fetuses to intermittent reductions in oxygen supply, and tolerance to this stress depends on developmental condition. Piglets that recover rapidly establish thermoregulation, locomotor activity, and adequate colostrum intake whereas compromised piglets exhibit delayed standing, poor suckling, and reduced vigor. These impairments initiate a cascade of impaired temperature regulation, inadequate energy intake, and inactivity that predisposes affected piglets to the commonly recorded causes of death. This review integrates evidence from fetal development, placental biology, parturition physiology, and neonatal adaptation to propose a unified model of pre-weaning mortality. Early mortality in pigs is best interpreted as a consequence of neonatal viability at birth, shaped by prenatal and perinatal processes, rather than solely a failure of postnatal management. Improving survival will therefore require strategies that enhance utero-placental function and neonatal resilience in addition to farrowing management.
    Keywords:  Intrauterine growth restriction; Neonatal physiology; Neonatal viability; Piglet survival; Pre-weaning mortality
    DOI:  https://doi.org/10.1016/j.theriogenology.2026.118132
  12. J Vis Exp. 2026 Aug 18.
      SASH1 is a signal adaptor protein involved in cell growth, apoptosis, and immune regulation, and has been increasingly studied in tumor and immune cells. Emerging evidence suggests that SASH1 plays an important role in inflammatory responses and cellular homeostasis, processes that are closely associated with the development of PE. This study aimed to determine whether SASH1 contributes to trophoblast apoptosis and inflammatory responses in PE and whether P-EXOS exerts protective effects through SASH1 regulation. In this study, three PE-related transcriptomic datasets (GSE75010, GSE10588, and GSE60438) were analyzed to identify shared differentially expressed genes (DEGs), followed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses. Machine learning algorithms were further applied to screen key candidate genes, and single-cell RNA sequencing data were used to characterize cellular heterogeneity in placental tissue and to determine cell type-specific expression patterns. SASH1 was identified as a consensus candidate gene and was significantly upregulated in trophoblast cells from PE samples. In vitro, a hypoxia-treated HTR-8/SVneo trophoblast cell model was established, combined with SASH1 knockdown, SASH1 overexpression, and co-culture with P-EXOS. Functional experiments showed that knockdown of SASH1 significantly suppressed hypoxia-induced trophoblast apoptosis and reduced the secretion of pro-inflammatory cytokines, including IL-6, IL-1β, and TNF-α, whereas SASH1 overexpression promoted apoptosis and inflammatory responses. In addition, P-EXOS treatment markedly reduced SASH1 expression at both mRNA and protein levels and attenuated hypoxia-induced trophoblast injury, while SASH1 overexpression largely abolished these protective effects. Taken together, these findings indicate that SASH1 plays a critical role in trophoblast apoptosis and inflammatory responses in PE. P-EXOS may alleviate hypoxia-induced trophoblastic injury by suppressing SASH1 expression, providing new insights into the molecular mechanisms and potential therapeutic targets for PE.
    DOI:  https://doi.org/10.3791/71083
  13. J Reprod Immunol. 2026 Aug 12. pii: S0165-0378(26)00117-8. [Epub ahead of print]177 104948
      Chronic chorioamnionitis (CCA) is a placental inflammatory lesion characterized by maternal T cell infiltration and trophoblast apoptosis, resembling allograft rejection. MicroRNA-155 (miR-155) is a central regulator of immune and inflammatory pathways, but its role in CCA remains unclear. This study investigated whether miR-155 contributes to the pathogenesis of CCA by targeting karyopherin α1 (KPNA1) and modulating STAT3 signaling in human trophoblasts. Placental tissues from 28 CCA cases and 16 gestational age-matched controls were analyzed for miR-155 expression using quantitative RT-PCR and in situ hybridization. Functional assays were conducted in Swan 71 trophoblast cells following miR-155 overexpression and siRNA-mediated KPNA1 knockdown. Microarray and qRT-PCR analyses identified gene expression changes, while western blotting and dual-luciferase reporter assays were conducted to evaluate STAT3 activity and direct target binding. miR-155 expression was significantly elevated in CCA fetal membranes. KPNA1 was identified as a direct target of miR-155, and its suppression reduced STAT3 phosphorylation and nuclear translocation. Dual-luciferase assays confirmed that miR-155 binds to the 3' untranslated region of KPNA1 mRNA, thereby inhibiting its translation. These findings suggest that miR-155 downregulates KPNA1, leading to inhibition of STAT3 signaling in trophoblasts, which may contribute to maternal-fetal immune dysregulation and trophoblast apoptosis in CCA. The miR-155-KPNA1-STAT3 axis may represent a potential therapeutic target in pregnancy-related inflammatory disorders.
    Keywords:  Apoptosis; Chronic chorioamnionitis; Immune regulation; KPNA1; MicroRNA-155; STAT3; Trophoblast
    DOI:  https://doi.org/10.1016/j.jri.2026.104948
  14. Phys Rev E. 2026 Jul;114(1-1): 014407
      Extracellular vesicles (EVs) hold great promise in drug delivery, disease diagnosis, and treatment; however, the inability to control EVs biogenesis critically limits their therapeutic and diagnostic potential. Although regulatory mechanisms for biochemical cues have been extensively studied, the principles governing how diverse mechanical cues from the extracellular microenvironment orchestrate EV secretion are poorly understood, hindering the development of scalable production strategies. Here, we resolve this by introducing a theoretical model that identifies membrane reservoir depletion as a universal biophysical switch for EV release. We discover that EV secretion is directly activated by the depletion of the membrane reservoir and the consequent rise in membrane tension. This tension-mediated mechanism provides a unifying framework that reconciles disparate experimental observations under various biophysical perturbations, including cell spreading, osmotic shock, contractile perturbation, and substrate stiffening. Furthermore, we identify the membrane reservoir size as a key intrinsic parameter setting the threshold for mechanical activation of EV secretion, offering a rationale for engineering high-yield producer cell lines. Our work thus establishes a unifying mechanochemical framework for EV secretion, explaining disparate experimental observations and providing a quantitative design principle for optimizing EV production.
    DOI:  https://doi.org/10.1103/n6jp-gg95