{"title":"Three-dimensional microarchitecture of the human placental villous tree in health and disease.","authors":"Nirav Barapatre, Hans-Georg Frank","doi":"10.3389/fcell.2025.1639740","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Placental dysfunction plays a central role in pregnancy complications such as fetal growth restriction (FGR), preeclampsia (PE), and gestational diabetes mellitus (GDM). Recent advances in 3D microscopy and stereological analysis have revealed microanatomical changes not detectable by conventional histology.</p><p><strong>Objective: </strong>To summarise key morphological and cellular alterations in the human placenta across FGR, PE, and GDM, with a focus on architecture of the villous tree, proliferative trophoblast dynamics, and sex-specific adaptations.</p><p><strong>Methods: </strong>A synthesis of quantitative 3D histological studies was undertaken, focusing on villous compartment volumes, trophoblast proliferation markers (PCNA), nuclear distribution patterns, and branching indices in placentas from affected and control pregnancies.</p><p><strong>Results: </strong>FGR placentas exhibit central loss of contractile villi (C-villi), increased syncytial nuclear density, and abolished sexual dimorphism. In PE, peripheral villous volume (NC-villi) is reduced, with marked increased proliferation of trophoblast in female placentas and disrupted nuclear spacing. GDM placentas show a global reduction in villous branching and altered proliferative dynamics of villous trophoblast, particularly in females, already in the absence of placental macrosomia.</p><p><strong>Conclusion: </strong>Despite distinct clinical profiles, FGR, PE, and GDM exhibit specific yet partially overlapping placental microstructural pathologies, characterised by trophoblast dysregulation and sex-specific adaptations. These findings underscore the significance of fetal sex and quantitative three-dimensional morphometry in advancing our understanding of placental disease mechanisms.</p>","PeriodicalId":12448,"journal":{"name":"Frontiers in Cell and Developmental Biology","volume":"13 ","pages":"1639740"},"PeriodicalIF":4.6000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12457310/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Cell and Developmental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fcell.2025.1639740","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Placental dysfunction plays a central role in pregnancy complications such as fetal growth restriction (FGR), preeclampsia (PE), and gestational diabetes mellitus (GDM). Recent advances in 3D microscopy and stereological analysis have revealed microanatomical changes not detectable by conventional histology.
Objective: To summarise key morphological and cellular alterations in the human placenta across FGR, PE, and GDM, with a focus on architecture of the villous tree, proliferative trophoblast dynamics, and sex-specific adaptations.
Methods: A synthesis of quantitative 3D histological studies was undertaken, focusing on villous compartment volumes, trophoblast proliferation markers (PCNA), nuclear distribution patterns, and branching indices in placentas from affected and control pregnancies.
Results: FGR placentas exhibit central loss of contractile villi (C-villi), increased syncytial nuclear density, and abolished sexual dimorphism. In PE, peripheral villous volume (NC-villi) is reduced, with marked increased proliferation of trophoblast in female placentas and disrupted nuclear spacing. GDM placentas show a global reduction in villous branching and altered proliferative dynamics of villous trophoblast, particularly in females, already in the absence of placental macrosomia.
Conclusion: Despite distinct clinical profiles, FGR, PE, and GDM exhibit specific yet partially overlapping placental microstructural pathologies, characterised by trophoblast dysregulation and sex-specific adaptations. These findings underscore the significance of fetal sex and quantitative three-dimensional morphometry in advancing our understanding of placental disease mechanisms.
期刊介绍:
Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board.
The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology.
With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.