bims-placeb Biomed News
on Placental cell biology
Issue of 2026–03–22
eleven papers selected by
Carlos M Guardia, National Institute of Environmental Health Sciences



  1. Trends Mol Med. 2026 Mar 18. pii: S1471-4914(26)00039-0. [Epub ahead of print]
      The placenta is an essential organ that supports fetal development during pregnancy. The establishment of human trophoblast stem cells has enhanced our understanding of placental development; however, their limited diversity constrains our ability to capture interindividual variation. Patient-specific trophoblast stem cells (pTSCs), derived from induced pluripotent stem cells, fibroblasts, cytotrophoblasts, or chorionic villus tissue, retain the unique genetic and epigenetic backgrounds of individual patients. Notably, chorionic villus-derived trophoblast stem cells can be obtained without terminating a pregnancy, allowing for integration with prospective clinical data. pTSCs, therefore, provide powerful platforms to investigate the pathogenesis of placental disorders, assess individual risk, and advance personalized therapeutic strategies. This review highlights recent advances in pTSC derivation and discusses their potential applications.
    Keywords:  chorionic villus sampling; patient-specific; placenta; placental disorders; trophoblast stem cells
    DOI:  https://doi.org/10.1016/j.molmed.2026.02.009
  2. PLoS One. 2026 ;21(3): e0328123
      Cannabis use during pregnancy continues to increase with smoking remaining the most common mode of consumption. While clinical studies highlight an association between prenatal cannabis use and adverse pregnancy outcomes, less is known about placental outcomes, even though many of the reported pregnancy outcomes are thought to be mediated via placental dysfunction. Here, we established a mouse model of gestational cannabis smoke exposure to investigate the impacts on fetal outcomes and placental structure and function. Pregnant CD1 mice were exposed daily to Δ9-tetrahydrocannabinol (THC)-dominant cannabis smoke (12-14% THC, 0-2% CBD) or filtered air from embryonic day (E)6.5 to E18.5 or parturition. Cannabinoid analyses in cannabis smoke-exposed, paired maternal and fetal livers revealed total THC and 11-Nor-9-carboxy-THC (THCA) concentrations of 135.95 ± 13.60 ng/g and 30.84 ± 4.68 ng/g, respectively. Moreover, Cyp1a1, a smoke-inducible enzyme, was induced by 4-fold in cannabis smoke-exposed placentae. No changes in offspring body weights were observed; however, there was a marked decrease in the brain-to-body weight ratio of exposed postnatal day 1 (PND1) offspring. Placentae from exposed dams were significantly reduced in size, with altered zonation marked by a significantly decreased junctional zone and increased labyrinth zone. Key trophoblast differentiation markers (Tfap2c, Tpbpa, Pcdh12) and placental endocrine regulators (Pl2, Igf1r) were significantly downregulated following cannabis smoke exposure in placentas. Furthermore, transcript levels of placental nutrient and vascularization markers, Glut1, Vegfa and Pparg were significantly decreased in cannabis smoke-exposed placentas. By employing a physiologically relevant platform of prenatal cannabis exposure in vivo we demonstrate the adverse effects of prenatal cannabis smoke exposure on placental structure and function as well as on fetal brain growth.
    DOI:  https://doi.org/10.1371/journal.pone.0328123
  3. Life Sci. 2026 Mar 19. pii: S0024-3205(26)00147-5. [Epub ahead of print]393 124338
       AIMS: Advanced maternal age (AMA), increasingly prevalent worldwide, is linked to obstetric risk even in clinically uncomplicated pregnancies. Mitochondria are essential for trophoblast metabolism and stress adaptation, and their alteration is associated with gestational pathologies. However, it remains unclear whether maternal age alone alters placental mitochondrial homeostasis.
    MATERIALS AND METHODS: Human placentas from AMA and control pregnancies were analysed by transmission electron microscopy (TEM) to assess mitochondrial ultrastructure and mitochondria-endoplasmic reticulum contacts (MERCs). Western blotting was used to evaluate regulators of mitochondrial fusion, fission, and mitophagy.
    KEY FINDINGS: placentas from AMA pregnancies showed a significant increase in mitochondrial number in both syncytiotrophoblast and cytotrophoblast cells, with regional variation between maternal and foetal sides. Despite increased abundance, mitochondria were smaller (reduced area and perimeter), indicating a fragmented phenotype, while circularity was unchanged. MERCs exhibited decreased distance and increased ER coverage, suggesting enhanced stress signaling and fission. Western blotting revealed decreased MFN1 with increased OPA1 and DRP1 expression, whereas MFN2, FIS1, and DNM2 remained unchanged. Mitophagy markers were dysregulated, with reduced OPTN and BNIP3 but elevated FUNDC1.
    SIGNIFICANCE: AMA is associated with fragmented and stress-adapted placental mitochondria, showing structural imbalance in dynamics and altered quality control even in the absence of clinical pathology. These features may reflect reduced placental capacity to buffer metabolic and stress challenges and contribute to increased vulnerability in pregnancies of older mothers, positioning mitochondria as a potential target for monitoring and improving outcomes in this population.
    Keywords:  Advanced maternal age; Mitochondria; Mitochondrial dynamics; Placenta; Pregnancy; Transmission electron microscopy
    DOI:  https://doi.org/10.1016/j.lfs.2026.124338
  4. Biol Sex Differ. 2026 Mar 18.
       BACKGROUND: Sex differences in the function and morphology of the human placenta can lead to sex differences in pregnancy outcomes. X chromosome inactivation (XCI) is the primary mechanism for dosage compensation between the sexes, and is strongly associated with X-chromosome promoter DNA methylation (DNAme) in somatic cells. However, in the placenta, low X-chromosome promoter DNAme has been reported. The placenta is a complex organ consisting of cells of different developmental origins, but the sex differences in DNAme by specific cell types have not been investigated.
    METHODS: We examined sex-influenced DNAme from 18 to 19 samples each of endothelial, stromal, cytotrophoblast and Hofbauer cells, sorted from term placentas, as well as matched whole chorionic villi. We also compared these profiles with data from 65 endothelial cell samples from placental chorionic plate arteries and veins (XX = 16, XY = 13) and umbilical cord veins (XX = 22, XY = 14). All data were derived from Illumina Infinium HumanMethylation450 or EPIC DNAme arrays. Sex-stratified analyses of the X/Y and autosomal DNAme were undertaken to identify DNAme differences associated with sex chromosome complement.
    RESULTS: The DNAme distribution on both the X and Y chromosomes differed by cell type. These differences clustered according to the differing developmental origins from extraembryonic mesoderm (endothelial/stromal), trophectoderm (cytotrophoblast) and epiblast (Hofbauer cells), with Hofbauer cells sharing a similar distribution with blood and umbilical endothelial cells. Interestingly, the typical XCI-associated DNAme at promoter CpG islands (CGI) on the X-chromosome of XX cells was absent for endothelial/stromal cells and present only at low levels in trophoblasts, suggesting that de novo establishment of promoter-CGI DNAme on the X-chromosome may differ by cell type.
    CONCLUSION: The lack of X-linked promoter DNAme in extraembryonic mesoderm-derived cells (endothelial/stromal) is consistent with a distinct developmental origin of these populations relative to the other placental and umbilical cell types. Autosomal DNAme also showed cell-type differences in alignment with cellular relationships observed for sex chromosomes. This work suggests the effects of sex chromosome complement on pregnancy outcomes may differ by placental cell type.
    Keywords:  DNA methylation; X chromosome; endothelial cell; placenta; sex
    DOI:  https://doi.org/10.1186/s13293-026-00869-x
  5. Reproduction. 2026 Mar 18. pii: xaag030. [Epub ahead of print]
      Recurrent spontaneous abortion (RSA), defined as the loss of two or more pregnancies before 20 weeks of gestation, remains a challenging clinical problem with largely unknown pathogenesis. In this study, we performed single-cell RNA sequencing analysis of control and RSA villous tissues and identified three subtypes of cytotrophoblasts (CTBs): CTB1, which is mainly involved in protein synthesis; CTB2, a highly proliferative progenitor population; and CTB3, an adhesive and invasive subtype that serves as the precursor of extravillous trophoblasts (EVTs). We also characterized syncytiotrophoblasts (STBs), which are responsible for hormone production. In RSA villi, the functions of both CTBs and STBs were impaired. Notably, CTB2 and CTB3 exhibited pronounced features of cellular senescence, potentially contributing to reduced proliferative and differentiation capacity. These findings suggest that aberrant trophoblast senescence may underlie defective placentation in RSA and highlight potential therapeutic targets for restoring trophoblast function and improving pregnancy outcomes.
    Keywords:  cellular senescence; placental dysfunction; recurrent spontaneous abortion; single-cell RNA sequencing; trophoblast
    DOI:  https://doi.org/10.1093/reprod/xaag030
  6. Environ Sci Technol. 2026 Mar 16.
      Per- and polyfluoroalkyl substances (PFASs) are persistent pollutants that cross the placental barrier, yet their transfer dynamics and developmental impacts remain unclear. We quantified 16 PFASs in maternal serum, cord serum, and maternal/fetal placental surfaces from 102 mother-infant pairs, calculated transfer efficiencies, and evaluated associations with neonatal growth and 12-month development. Mediation analysis assessed the role of maternal glucose regulation in linking PFAS exposure to early life growth outcomes. All 16 PFASs were detected, with mean ∑16PFAS concentrations of 5.26 ng/mL in maternal serum, 3.52 ng/mL in cord serum, and 1.15 and 0.97 ng/mg on maternal and fetal placental surfaces, respectively. Average transfer efficiencies were 45% (maternal to cord) and 73% (maternal to fetal surface), with several PFASs exceeding 100%. Prenatal PFAS exposure correlated with elevated maternal, fetal, and neonatal glucose and reduced postnatal growth, with maternal glucose mediating up to 23.19% of the effect, implicating glucose dysregulation a key pathway. The findings provide quantitative evidence implicating glucose-regulatory pathways in PFAS-induced maternal-fetal health effects and, using multiple matched biospecimens per mother-infant pair, offer a comprehensive view of PFAS transport across the maternal-fetal interface. A 12-month follow-up confirmed persistent growth impairment, reinforcing the need to regulate emerging PFAS and monitor metabolic outcomes.
    Keywords:  PFAS; fetal exposure; glucose metabolism; maternal transfer; pregnancy
    DOI:  https://doi.org/10.1021/acs.est.5c16089
  7. Cannabis Cannabinoid Res. 2026 Apr;11(2): 130-137
       BACKGROUND: Pregnant people use cannabidiol (CBD) to treat nausea, insomnia, anxiety, and pain. However, CBD crosses the placenta and enters the fetal brain, where it can affect several targets important for brain development. While consumption of high doses of CBD during pregnancy has been shown to disrupt offspring neurodevelopment, pain sensitivity, and cognitive behavior in mice, lower doses have not been assessed.
    METHODOLOGY: We administered 10 mg/kg/day CBD by oral gavage to pregnant C57Bl6 mice from embryonic day 5 through birth. We used the puzzle box, the forced swim test, and Hargreaves thermal sensitivity behavior tests and electrophysiology to determine how prenatal CBD exposure affects postnatal behavior and prefrontal cortex physiology.
    RESULTS: We show that oral consumption of 10 mg/kg/day CBD during pregnancy increases thermal pain sensitivity in male mouse offspring. Furthermore, the same dose impairs cognition and reduces excitability of the prefrontal cortex in female mouse offspring.
    CONCLUSION: These data show that lower doses of CBD consumption during pregnancy can impair fetal brain development and postnatal behavior.
    Keywords:  CBD; behavior; brain development; cannabidiol; fetal exposure; prenatal exposure
    DOI:  https://doi.org/10.1177/25785125251413416
  8. Curr Opin Physiol. 2026 Mar;pii: 100902. [Epub ahead of print]47
      Autophagy is an evolutionarily conserved catabolic process whereby damaged organelles, misfolded proteins, and lipid droplets are sequestered, degraded, and recycled. Definitive etiological links connect dysregulated autophagy to chronic cardiometabolic, neurodegenerative, and inflammatory diseases, along with cancer. Autophagy also fulfills key roles in normal reproduction and fertility, with placental autophagy being crucial for proper trophoblast syncytialization. Dysregulations in placental autophagy have been shown to occur in response to maternal under- and overnutrition, gestational diabetes, and preeclampsia. This review summarizes the roles of autophagy in placental function in both healthy and complicated pregnancies.
    Keywords:  defective autophagy; developmental programming; gestational diabetes; maternal obesity; maternal undernutrition; placenta; preeclampsia
    DOI:  https://doi.org/10.1016/j.cophys.2026.100902
  9. Curr Top Dev Biol. 2026 ;pii: S0070-2153(26)00015-3. [Epub ahead of print]166 121-133
      Faithful chromosome segregation emerges from the mutual cooperation of chromosomes and spindle microtubules. Textbook models of mitosis traditionally emphasize centrosome-driven spindle formation and chromosome capture. However, early mammalian development proceeds under constraints which are incompatible which a centrosome-driven model. Here, we briefly review the non-standard mechanisms of chromosome organization operating during early mouse development. We propose that these mechanisms, despite their differences, reflect a conserved set of organizational principles adapted to distinct developmental contexts.
    Keywords:  Actin; Cell division; Cytoskeleton; Meiosis; Microtubules; Mitosis
    DOI:  https://doi.org/10.1016/bs.ctdb.2026.01.015
  10. Sci Rep. 2026 Mar 18.
      Fetal mortality significantly impacts reproductive efficiency in sheep, with approximately 30% of fetuses failing to survive until lambing. In multifetal gestation, partial litter loss (PLL) occurs in 28% to 37% of cases. The biochemical composition of allantoic fluid (ALF), which plays a key role in metabolic regulation and fetal waste clearance, has been shown in other species to reflect fetal development and maturity. However, ALF metabolomics in sheep, especially in relation to PLL, remains unexplored. This study investigated late-gestation fetal mortality in multifetal sheep pregnancies by analyzing maternal metabolic status, placental gene expression, and ALF composition to identify potential metabolic compounds associated with PLL. The study was conducted on 25 ewes, of which 14 experienced PLL, and 11 had vital litters (VL). Plasma analysis revealed that VL ewes have higher β-hydroxybutyrate concentrations than PLL ewes, whereas plasma insulin and cortisol levels are higher in PLL ewes. Analysis of gene expression in the placental cotyledon demonstrated increased androgen receptor expression in PLL pregnancies and trends toward elevated solute carrier family 2 member 1, and reduced nuclear receptor subfamily 3 group C member 1 expression. Insulin-like growth factor 2 expression tended to be higher in VL placentas. Allantocentesis was performed on 25 ewes with multifetal pregnancies (11 VL and 14 PLL). ALF samples were collected from 74 fetuses at 140.4 ± 2.0 days in pregnancy, and 41 samples were selected for metabolomic profiling. Using genomic analysis, 25 ALF samples were confidently matched to individual lambs. Untargeted lipidomics of ALF from 14 lambs in PLL (7 born alive vs. 7 stillborn) revealed 24 differentially abundant lipid compounds. Stillborn lambs exhibited lower phosphatidylglycerol (PG) 15:0_20:1, but higher levels of sphingomyelin (SM), lysophosphatidylcholine (LPC), ether-linked phosphatidylethanolamines (PEs), lysophosphatidylethanolamines (LPEs), and monogalactosyldiacylglycerols (MGDGs). Collectively, PLL in multifetal ewe pregnancies is linked to maternal metabolic imbalance, elevated cortisol levels, dysregulated placental gene expression, and altered ALF lipid profiles in stillborn fetuses. Elevated SM and LPC, and lower PG, suggest immature lungs. These molecular and metabolic signatures may provide new insights into the mechanisms underlying PLL in late-gestation multifetal pregnancies.
    Keywords:  Allantocentesis; Gene expression; Metabolomics; Partial litter loss; Sheep
    DOI:  https://doi.org/10.1038/s41598-026-44636-9
  11. Commun Biol. 2026 Mar 17. pii: 387. [Epub ahead of print]9(1):
      Selective fetal growth restriction (sFGR) in monochorionic diamniotic twins (MCDA) reflects placental dysfunction, but trophoblast adaptation mechanisms remain unclear. Using single-cell RNA sequencing on placental tissues from three paired sFGR, we demonstrate that villous cytotrophoblasts (VCT) in growth-restricted placentas undergo a transition from VCT_TP63, which expresses barrier-associated TP63/SOX6 and maintains cytoskeletal integrity, to VCT_LDHA, a metabolically reprogrammed phenotype marked by LDHA/YY1/RELA activation. Trajectory analysis shows diminished syncytial precursors, suggesting impaired fusion capacity. Immune profiling identifies depleted TREM2+ Hofbauer macrophages and expanded interferon-responsive natural killer (NK) cells. Cell-cell interaction mapping demonstrates enhanced Interferon Gamma (IFNG)-Interferon Gamma Receptor 1 (IFNGR1)-Signal Transducer and Activator of Transcription 1 (STAT1) signaling between VCT_LDHA and immune cells, alongside weakened VCT_TP63-stromal crosstalk. This study defines a maladaptive triad of metabolic stress, inflammation, and structural disintegration in sFGR, contributing to sFGR pathogenesis.
    DOI:  https://doi.org/10.1038/s42003-026-09798-2